Prof. Dr. Ayla Güven

Uluslararası hakemli dergilerde yayınlanan makaleler

• A Roxas , A Gihawi, M Makarchuk, J Bryce, M Chen, S.F Ahmed, S.R Ali , A Drake, M Casipe, L Grove, J Idkowiak, R Krone, C Flueck, A Nordenström, N Reisch , H.L. Claahsen – van der Grinten, B.P.H Adriaansen, N.H Birkebaek, S Hannema, M.W O Reilly, L Cussen, S.P Zaric, U Neumann , F Baronio, A Vieites, G.F Alonso, H Elsedfy, I Mazen, A Thankamony, J Witczak, D.A Rees, N Atapattu, S.N Seneviratne, M Cools, Hayat El Kaddouri, Alegria Ferri Perez, A Guven, S Poyrazoglu, A Fu, D Janus, E Globa, S Shenoy, C de Bruin, M Korbonits, S Adam, M Wasniewska , G Russo, F Phan-Hug, W Bonfig, M Salerno, J.W Tomlinson, S Leka-Emiri, L de Vries, I Yarhere, G Guaranga-Filho, J van Eck, T.A.S.S Bachega, N Krone, M De Bono, JH Davies, A Segev-Becker, V Iotova, N Lenherr-Taube, A German, R Giordano, L De Sanctis, U Probst, R Markosyan, D Brewer, E.C Costa, and EA Webb. Glucocorticoid Prescribing Trends in Congenital Adrenal Hyperplasia, 2017 to 2023. Endocr Connect. 2026 Mar 5:EC-25-0565.
• Bosmans J, Herregods N, van Gremberghe I, van den Akker E, Atapattu N, Baronio F, Bettendorf M, Darendeliler F, Deyanova Y, Flück CE, Globa E, Guran T, Guven A, Hannema S, Herrmann G, Iotova V, Konrad D, Lenherr-Taube N, Lichiardopol C, Lucas-Herald A, Markosyan R, Mazen I, Nordenström A, Poyrazoglu S, Probst U, Dacal JL, Seneviratne S, Thankamony A, de Vries L, Vojtkova J, Ahmed SF, Cools M.Growth Patterns and Bone Maturation in Children with Sex Chromosomal (45,X/46,XY) DSD. Eur J Endocrinol. 2026 May 19:lvag092. doi: 10.1093/ejendo/lvag092.
• Lawrence NR, Bacila I, Tonge J, Dawson J, Collins GS, Lang ZQ, Bryce J, Alimussina M, Chen M, Ali SR, Adam S, van den Akker ELT, Bachega TASS, Baronio F, Birkebæk NH, Bonfig W, Claahsen van der Grinten H, Cools M, Costa EC, Debono M, de Vries L, Flück CE, Gazdagh G, Güven A, Hannema SE, Iotova V, van der Kamp HJ, Krone R, Leka-Emiri S, Clemente-León M, Lichiardopol CR, Markosyan RL, Milenkovic T, de Miranda MC, Neumann U, Newell-Price J, Poyrazoğlu Ş, Probst-Scheidegger U, Russo G, De Sanctis L, Seneviratne SN, Stancampiano MR, Tadokoro-Cuccaro R, Thankamony A, Vieites A, Wasniewska M, Yeste D, Tomlinson J, Ahmed SF, Krone N. Blood pressure and its associations in 554 children and young people with CAH.
• Tadokoro-Cuccaro R, Hughes IA, Cools M, van de Vijver K, Bilharinho de Mendonça B, Domenice S, Loch Batista R, Thomazini Dallago R, F Costa E, Lisboa Gomes N, T Maciel-Guerra A, Guerra-Junior G, Gabriel Ribeiro de Andrade J, Lucas-Herald A, Bryce J, Hannema S, Juul A, Globa E, MсElreavey K, Baronio F, Rey R, Lopez Dacal J, Darendeliler F, Poyrazoglu S, Kolesińska Z, Niedziela M, Claahsen-van der Grinten HL, L T van den Akker E, Herrmann G, Atapattu N, Jain V, Sharma R, Bettendorf M, Konrad D, Lenherr-Taube N, Holterhus PM, Fica S, Skae M, Russo G, Stancampiano MR, Gazdagh G, Davies JH, Mohamed Z, Seneviratne SN, Güran T, Güven A, Wasniewska M, Mladenov V, Verkauskas G, Markosyan R, Korbonits M, Hiort O, Frielitz-Wagner IV, Ahmed SF, Thankamony A. Phenotypic Variation and Pubertal Outcomes in Males and Females with 46,XY Partial Gonadal Dysgenesis.J Clin Endocrinol Metab. 2025 Apr 10:dgaf223. doi: 10.1210/clinem/dgaf223.
• Tseretopoulou X, Ali SR, Bryce J, Amin N, Atapattu N, Bachega TASS, Baronio F, Ortolano R, Birkebaek NH, Bonfig W, Cools M, Davies JH, Thomas T, de Vries L, Elsedfy H, Amr NH, Flueck CE, Globa E, Guran T, Yavas-Abali Z, Guven A, Hannema SE, Iotova V, Konrad D, Lenherr-Taube N, Krone NP, Leka-Emiri S, Vlachopapadopoulou E, Lichiardopol C, Marginean O, Markosyan R, Neumann U, Niedziela M, Banaszak-Ziemska M, Phan-Hug F, Poyrazoglu S, Probst-Scheidegger U, Randell T, Russo G, Salerno M, Seneviratne S, Shnorhavorian M, Thankamony A, Tadokoro-Curraro R, van den Akker E, van Eck J, Vieites A, Wasniewska M, Ahmed SF. Temporal Trends in Acute Adrenal Insufficiency Events in Children With Congenital Adrenal Hyperplasia During 2019-2022. J Endocr Soc. 2024 Aug 20;8(10):bvae145.
• Yumusakhuylu Y, Icagasioglu A, Guven A. Anterior Pituitary Hormones are Important in Growth, but does their Deficiency Cause Skeletal Deformity? A Case Report. Curr Health Sci J.2024 Jul-Sep;50(3):448-452.
• Schröder MAM, Neacşu M, Adriaansen BPH, Sweep FCGJ, Ahmed SF, Ali SR, Bachega TASS, Baronio F, Birkebæk NH, de Bruin C, Bonfig W, Bryce J, Clemente M, Cools M, Elsedfy H, Globa E, Guran T, Güven A, Amr NH, Janus D, Taube NL, Markosyan R, Miranda M, Poyrazoğlu Ş, Rees A, Salerno M, Stancampiano MR, Vieites A, de Vries L, Yavas Abali Z, Span PN, Claahsen-van der Grinten HL.Hormonal control during infancy and testicular adrenal rest tumor development in CAH males - a retrospective multi-center cohort study. Eur J Endocrinol. 2023 Oct 17;189(4):460-468. doi: 10.1093/ejendo/lvad143.
• Neumann U, van der Linde A, Krone RE, Krone NP, Güven A, Güran T, Elsedfy H, Poyrazoglu S, Darendeliler F, Bachega TASS, Balsamo A, Hannema SE, Birkebaek N, Vieites A, Thankamony A, Cools M, Milenkovic T, Bonfig W, Costa EC, Atapattu N, de Vries L, Guaragna-Filho G, Korbonits M, Mohnike K, Bryce J, Ahmed SF, Voet B, Blankenstein O, Claahsen-van der Grinten HL.Treatment of congenital adrenal hyperplasia in children aged 0-3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure. Eur J Endocrinol 2022 ;186(5):587-596.
• Demirtas A, Girgin BA, Güven A, Kırmızıbekmez H. Psychometric Properties of the Turkish Version of the Diabetes Strengths and Resilience Measure for Adolescents with Type 1 Diabetes. J Clin Res Pediatric Endocrinol 2022; 14(3):324-333.
• Eylem Kiral, Birgul Kirel, Merve Havan, Mehmet Keskin, Murat Karaoglan, Ahmet Yıldırım, Murat Kangin, Mehmet Nur Talay, Tuba Urun, Umit Altug, Selman Kesici, Erennur Tufan, Ebru Kacmaz, Gurkan Bozan, Ebru Azapagasi, Mutlu Uysal Yazici, Zeynel Abidin Oztürk, Osman Yesilbas, Gulay Karaguzel, Ulkem Barlas, Muhterem Duyu, Merve Boyraz, Esra Sevketoglu, Nihal Akçay, Suna Hancili, Ayla Güven, OGUZ DURSUN, Nazan Ulgen Tekerek, Gokçen Ozcifci, Pınar Yazici, Eda Turanli, Tanıl Kendirli, Fevzi Kahveci, Ayse Filiz Yetimakman, AGOP CITAK, Guntulu Şık, Ibrahim Bingol, Fatih Aygun, Cansu Durak, Resul YILMAZ, Fuat Bugrul, Yusuf Sari, Hakan Tekguç, Hatice Albayrak, Nazik Yener, Hasan Agin, Ekin Sodan, Dincer Yildizdas, Semine Ozdemir Dile, Nilufer Yalindag, Feyza Incekoy Girgin, Nuri Alacakir, Filiz Tutunculer, Mehmet Ozgur Arslanaoglu, Muzaffer Bilgin, Can Aydin, Enver Simsek, Ener Cagri Dinleyici. Increased severe cases and new-onset type 1 diabetes among children presenting with diabetic ketoacidosis during first year of COVID-19 pandemic in Turkey. Frontiers in Pediatrics 2022;10: 926013.
• Lawrence N, Bacila I, Dawson J, Bryce J, Ali SR, van den Akker EL, Bachega TASS, Baronio F, Birkebaek NH, Bonfig W, Claahsen van der Grinten H, Costa EC, de Vries L, Elsedfy H, Güven A, Hannema S, Iotova V, van der Kamp HJ, León MC, Lichiardopol CR, Milenkovic T, Neumann U, Nordenström A, Poyrazoğlu Ş, Probst-Scheidegger U, De Sanctis L, Tadokoro-Cuccaro R, Thankamony A, Vieites A, Yavaş Z, Faisal Ahmed S, Krone N. Analyses of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry. Clin Endocrinol (Oxf). 2022;97(5):551-561.
• Erdogan F, Güven A. Is there a secular trend regarding puberty in children with down syndrome? Front Endocrinol (Lausanne). 2022 Nov 15;13:1001985. doi: 10.3389/fendo.2022.1001985. eCollection 2022.
• Cioana M, Deng J, Nadarajah A, Hou M, Qiu Y, Chen SSJ, Rivas A, Banfield L, Toor PP, Zhou F, Guven A, Alfaraidi H, Alotaibi A, Thabane L, Samaan MC. The Prevalence of Obesity Among Children with Type 2 Diabetes: A systematic review and Meta-analysis. JAMA Netw Open. 2022 Dec 1;5(12):e2247186.
• Ali SR, Bryce J, Haghpanahan H, Lewsey JD, Tan LE, Atapattu N, Birkebaek NH, Blankenstein O, Neumann U, Balsamo A, Ortolano R, Bonfig W, Claahsen-van der Grinten HL, Cools M, Costa EC, Darendeliler F, Poyrazoglu S, Elsedfy H, Finken MJJ, Fluck CE, Gevers E, Korbonits M, Guaragna-Filho G, Guran T, Guven A, Hannema SE, Higham C, Hughes IA, Tadokoro-Cuccaro R, Thankamony A, Iotova V, Krone NP, Krone R, Lichiardopol C, Luczay A, Mendonca BB, Bachega TASS, Miranda MC, Milenkovic T, Mohnike K, Nordenstrom A, Einaudi S, van der Kamp H, Vieites A, de Vries L, Ross RJM, Ahmed SF. Real World Estimates Of Adrenal Insufficiency Related Adverse Events In Children With Congenital Adrenal Hyperplasia. 2021;106(1):e192-e203
• Bacila I, Freeman N, Daniel E, Sandrk M, Bryce J, Ali SR, Yavas Abali Z, Atapattu N, Bachega TA, Balsamo A, Birkebæk N, Blankenstein O, Bonfig W, Cools M, Costa EC, Darendeliler F, Einaudi S, Elsedfy HH, Finken M, Gevers E, Claahsen-van der Grinten HL, Guran T, Güven A, Hannema SE, Higham CE, Iotova V, van der Kamp HJ, Korbonits M, Krone RE, Lichiardopol C, Luczay A, Mendonca BB, Milenkovic T, Miranda MC, Mohnike K, Neumann U, Ortolano R, Poyrazoglu S, Thankamony A, Tomlinson JW, Vieites A, de Vries L, Ahmed SF, Ross RJ, Krone NP.International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia: data from the I-CAH registry. Eur J Endocrinol. 2021 Apr;184(4):553-563.
• Hebenstreit D, Ahmed SF, Krone N, Krall C, Bryce J, Alvi S, Ortolano R, Lima M, Birkebaek N, Bonfig W, Claahsen van der Grinten H, Costa EC, Poyrazoglu S, de Vries L, Flück CE, Guran T, Bugrul F, Güven A, Iotova V, Koehler B, Schröder JT, Konrad D, Gevers E, Krone R, Milenkovic T, Vieites A, Ross R, Tadokoro Cuccaro R, Hughes I, Acerini C, Springer A.Surgical Practice In Girls With Congenital Adrenal Hyperplasia – An International Registry Study. Sex Dev. 2021;15(4):229-235.
• Lucas-Herald AK, Bryce J, Kyriakou A, Ljubicic ML, Arlt W, Audi L, Balsamo A, Baronio F, Bertelloni S, Bettendorf M, Brooke A, Claahsen van der Grinten HL, Davies JH, Hermann G, de Vries L, Hughes IA, Tadokoro-Cuccaro R, Darendeliler F, Poyrazoglu S, Ellaithi M, Evliyaoglu O, Fica S, Nedelea L, Gawlik A, Globa E, Zelinska N, Guran T, Güven A, Hannema SE, Hiort O, Holterhus PM, Iotova V, Mladenov V, Jain V, Sharma R, Jennane F, Johnston C, Guerra Junior G, Konrad D, Gaisl O, Krone N, Krone R, Lachlan K, Li D, Lichiardopol C, Lisa L, Markosyan R, Mazen I, Mohnike K, Niedziela M, Nordenstrom A, Rey R, Skaeil M, Tack LJW, Tomlinson J, Weintrob N, Cools M, Ahmed SF.Gonadectomy in conditions affecting sex development: a registry-based cohort study. Eur J Endocrinol. 2021;184(6):791-801.
• Özcabı B, Vatansever M, Güven A. Hypogonadism: is-it always hypogonadotropic in an adolescent with a cleft palate? A surprising case of Klinefelter syndrome. Cleft Palate Craniofac J2021; 58(6):787-790.
• Çelebi F, Ozcabı B, Güven A. The Relationship Between Obesity, Depressive Symptoms and Sleep Duration in Children and Adolescents. Acta Medica Alanya 2021: 5 (1): 42-47
• Pofi R, Prete A, Thornton-Jones V, Bryce J, Ali SR, Faisal Ahmed S, Balsamo A, Baronio F, Cannuccia A, Guven A, Guran T, Darendeliler F, Higham C, Bonfig W, de Vries L, Bachega TASS, Miranda MC, Mendonca BB, Iotova V, Korbonits M, Krone NP, Krone R, Lenzi A, Arlt W, Ross RJ, Isidori AM, Tomlinson JW. Plasma Renin Measurements are Unrelated to Mineralocorticoid Replacement Dose in Patients With Primary Adrenal Insufficiency. J Clin Endocrinol Metab. 2020;105(1):314-326
• Guran T, Kara C, Yildiz M, Bitkin EC, Haklar G, Lin JC, Keskin M, Barnard L, Anik A, Catli G, Guven A, Kirel B, Tutunculer F, Onal H, Turan S, Akcay T, Atay Z, Yilmaz GC, Mamadova J, Akbarzade A, Sirikci O, Storbeck KH, Baris T, Chung BC, Bereket A. Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases. J Clin Endocrinol Metab. 2020;105(3):e1718-e1728.
• Güven A. Different Potent Glucocorticoids, Different Routes of Exposure but The Same Result: Iatrogenic Cushing’s syndrome and Adrenal Insufficiency.J Clin Res Pediatr Endocrinol 2020;12:383-392
• Güven A, KonradM, SchlingmannKP. Idiopathic infantile hypercalcemia: Mutations in SLC34A1 and CYP24A1 in two siblings and fathers. JPEM 2020;33:1353-1358
• Zou M, Guven A, BinEssa HA, Al-Rijjal RA, Meyer BF, Alzahrani AS and Shi Y (2020) Molecular Analysis of CYP27B1 Mutations in Vitamin D-Dependent Rickets Type 1A:c.590G > A (p.G197D) Missense Mutation Causes a RNA Splicing Error. Front. Genet. 11:607517.
• Kılınc S, Yildiz M, Guven A. Analysis of Metabolic Features and Cardiovascular Risk Factors in a Group of Patients with Turner Syndrome. J Pediatri Endocrinol. 2020; 5(1): 1031.
• Kilinc S, Yildiz M, Guven A. Associated clinical Abnormalities Among Patients with Turner Syndrome. North Clin Istanb. 2020;7:226-230.
• Güven A, Cebeci AN. A Rare Endocrine Manifestation of Down syndrome: Central Precocious Puberty: Three Cases Report. EJMCR 2020; 4: 404-407.
• Abacı A, Çatlı G, Kırbıyık Ö, Şahin NM, Abalı ZY, Ünal E, Şıklar Z, Mengen E, Özen S, Güran T, Kara C, Yıldız M, Eren E, Nalbantoğlu Ö, Güven A, Çayır A, Akbaş ED, Kor Y, Çürek Y, Aycan Z, Baş F, Darcan Ş, Berberoğlu M. Genotype-phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey.J Endocrinol Invest. 2019 Apr;42(4):453-470
• Akıncı A, Turkkahraman D, Tekedereli I, Özer L, Evren B, Sahin İ, Kalkan T, Çürek Y, Çamtosun E, Doğer E, Bideci A, Güven A, Eren E, Sangün Ö, Çayır A, Bilir P, Törel Ergür A, Ercan O. Novel Mutations in Obesity-Related Genes in Turkish Children with Non-Syndromic Early Onset Severe Obesity: A Multicentre Study. J Clin Res Pediatr Endocrinol. 2019;11:341-349
• Kiykim A,Dursun E, Ogulur I,Charbonnier LM, Nain E,Cekic S, Dogruel D, Karaca NE, Cogurlu MT, Bilir OA, Cansever M, Kapaklı H, Baser D, Kasap N, Kutlug S, Altintas DU, Al‐Shaibi A, Agrebi N, Kara M, Guven A, Somer A, Aydogmus C, Ayaz NA, Metin A, Aydogan M, Uncuoglu A, Patiroglu T, Yildiran A, Guner SN,Keles S, Reisli I, Aksu G, Kutukculer N, Kilic SS, Yilmaz M, Karakoc-Aydiner E, Lo B, Ozen A, Chatila TA, MD, Baris S. Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency. J Allergy Clin Immunol Pract. 2019;7:2790-2800
• Celep G, Varol K, Erdoğan Y, Uyar R, Kahraman BA, Güven A. Epididimoorşitle Seyreden Bir Suçiçeği Olgusu, Bir Tesadüften Fazlası mı? J Pediatr Inf 2019;13:105-108
• Ozcabi B, Demirhan S, Akyol M, Ozturkmen Akay H, Güven A. Lipid accumulation Product is a Predictor of Nonalcoholic Fatty Liver Disease in Childhood Obesity. Korean J Pediatr 2019; 62: 450-455.
• Hancili S, Bonnefond A,Philippe J, Vaillant E, De Graeve F, Sand O, Busiah K, Robert JJ, Polak M, Froguel P, Güven A,Vaxillaire M. A novel NEUROG3 mutation in neonatal diabetes associated with a neuro-intestinal syndrome. Pediatric Diabetes. 2018; 19: 381-387
• Johnson MB, De Franco E, Allen HL, Al Senani A, Elbarbary N, Siklar Z, Berberoglu M, Imane Z, Haghighi A, Razavi Z, Ullah I, Alyaarubi S, Gardner D, Güven A, Ellard S, Hattersley AT, Flanagan SE. Erratum. Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes. Diabetes 2017;66:2316-2322. Diabetes. 2018 Jan 5. pii: db18er03b.
• Erol N, Yıldız M, Güven A, Yıldırım A. Cardiac examination in children with Laron syndrome undergoing mecasermin therapy. J Pediatr Endocrinol Metab. 2018 Jun 27;31(6):675-679.
• Kılınç S, Yücel-Yılmaz D, Ardagil A, Apaydın S, Valverde D, Özgül RK, Güven A. Five novel ALMS1 gene mutations in six patients with Alström syndrome. J Pediatr Endocrinol Metab. 2018 Jun 27;31(6):681-687.
• Poyrazoğlu Ş, Bundak R, Yavaş Abalı Z, Önal H, Sarıkaya S, Akgün A, Baş S, Abalı S, Bereket A, Eren E, Tarım Ö, Güven A, Yıldız M, Karaman Aksakal D, Yüksel A, Seymen Karabulut G, Hatun Ş, Özgen T, Cesur Y, Azizoğlu M, Dilek E, Tütüncüler F, Papatya Çakır E, Özcabı B, Evliyaoğlu O, Karadeniz S, Dursun F, Bolu S, Arslanoğlu İ, Yeşiltepe Mutlu G, Kırmızıbekmez H, İşgüven P, Üstyol A, Adal E, Uçar A, Cebeci N, Bezen D, Binay Ç, Semiz S, Korkmaz HA, Memioğlu N, Sagsak E, Peltek HN, Yıldız M, Akçay T, Turan S, Güran T, Atay Z, Akcan N, Çizmecioğlu F, Ercan O, Dağdeviren A, Baş F, İşsever H, Darendeliler F. Incidence of Type 1 Diabetes in Children Aged Below 18 Years During 2013-2015 in Northwest Turkey. J Clin Res Pediatr Endocrinol. 2018 Nov 29;10(4):336-342.
• Özsoy Koyun I, Ardagil Akçakaya A, Simsek B, Güven A, Koyun E. Topographic and refractive findings in osteogenesis imperfecta. Medeniyet Medical Journal. 2018;33: 291-295.
• Güven A, Polat S. Testicular Adrenal Rest Tumor In Brothers With Novel Mutation In 3-Beta Hydroxysteroid Dehydrogenase -2 Gene. J Clin Res Pediatr Endocrinol 2017; 9; 85-90
• Güven A. Seven Cases With Williams Beuren Syndrome: Endocrine Evaluation And Long Term Follow-Up. J Pediatr Endocrinol Metab. 2017; 30:159-165
• Guven A, Roua Al-Rijjal, Huda Binessa, Durmuş Dogan, Yilmaz Kor, Minjing Zou, Namik Kaya, Anwar Al-Enazi, Suna Hancili, Omer Tarim, Essa Baitei, Walaa Kattan, Brian Meyer, Yufei Shi. Mutational Analysis of PHEX, FGF23 and CLCN5 in Patients with Hypophosphatemic Rickets. Clin Endocrinol (Oxf) 2017;87:103-11253-
• İ Öğülür, A Kıykım, E Nain, A Somer, A Güven, S Barış, A Özen, E Karakoç. Protein Expression in the Diagnosis of LRBA Deficiency by Flow Cytometer. Asthma Allergy Immunol 2017;15:1-9
• Cebeci AN, Guven A, Kuru IL. Perinephritic adipose tissue thickness in relation to blood pressure, plasma apaelin and C-reactive protein levels in obese adolescents. Minerva Endocrinol 2016;41: 166-174
• Dursun F, Güven A, Yıldız M. Assessment of Anti-Müllerian Hormone Level in Management of Adolescents with Polycystic Ovary Syndrome. J Clin Res Pediatr Endocrinol. 2016;8:55-60,
• Güven A, Cebeci AN, Ellard S, Flanagan SE. Clinical, genetic characteristics, management and long-term follow up of Turkish patients with congenital hyperinsulinism.. J Clin Res Pediatr Endocrinol. 2016;8:197-204
• Tracy A Briggs; Gillian I Rice; Navid Adib, Lesley Ades; Stephane Barete; Kannan Baskar; Veronique Baudouin, Ayse N. Cebeci, Philippe Clapuyt; David Coman Lien De Somer; Yael Finezilber; Moshe Frydman; Ayla Guven; Sébastien Heritier; Daniela Karall; Muralidhar L Kulkarni; Pierre Lebon; David Levitt, Martine Le Merrer; Agnes Linglart; John H Livingstone; Vincent Navarro; Ericka Okenfuss; Anne Puel; Nicole Revencu; Sabine Scholl-Bürgi;; Marina Vivarelli; Carine Wouters, Brigitte Bader-Meunier; Yanick J Crow. Spondyloenchondrodysplasia due to mutations in ACP5: A comprehensive survey. Journal of Clinical Immunology 2016;36:220-234,
• Şıklar Z, Genens M, Poyrazoğlu Ş, Baş F, Darendeliler F, Bundak R, Aycan Z, Savaş Erdeve Ş, Çetinkaya S, Güven A, Abalı S, Atay Z, Turan S, Kara C, Can Yılmaz G, Akyürek N, Abacı A, Çelmeli G, Sarı E, Yeşilkaya E, Bolu S, Korkmaz HA, Şimşek E, Çatlı G, Büyükinan M, Çayır A, Evliyaoğlu O, İşgüven P, Özgen IT, Hatipoğlu N, Elhan AH, Berberoğlu M. The growth characteristics of patients with Noonan syndrome, and first 3 years results of GH treatment: A Nationwide multicenter study. J Clin Res Pediatr Endocrinol. 2016 2016;8:305-12
• Cebeci AN, Guven A, Mutus M, Zemheri E. ACTH-Independent Cushing Syndrome in an Adolescent Girl due to Micronodular Adrenal Hyperplasia. J Pediatri Endocrinol 2016;1004.
• Cebeci AN, Güven A. Does maternal obesity have an influence on feding behaviour of obese children. Minerva Pediatr 2015;67:481-487.
• Güven A, Cebeci AN, Hancili S. Gonadotropin releasing hormone analog treatment in children with congenital adrenal hyperplasia complicated by central precocious puberty Hormones (Athens). 2015; 14 :65-71,

Yazılan ulusal ve uluslararası kitaplar veya kitaplarda bölümler

• Ayla Güven. Uzun boy ve uzun boyla seyreden aşırı büyüme sendromları. In: Darendeliler F, Aycan Z, Kara C, Özen S, Eren E (eds). Temel Çocuk Endokrinolojisi ve Diyabet. İstanbul Medikal Sağlık ve Yayıncılık Hiz Tic Ltd Şti, 2023. 116-135. ISBN: 978-625-8103-24-3
• Ayla Güven. Mitokondriyal hastalıklarda endokrinopatiler. Ünal uzun Ö, editör. Çocukluk Çağında Mitokondriyal Hastalıklar. 1. Baskı. Ankara: Türkiye klinikleri; 2022. p.58-67.
• Ayla Güven. Uzun Boy. In: Darendeliler F, Aycan Z, Kara C, Özen S, Eren E (eds). Çocuk Endokrinolojisi ve Diyabet. Cilt 1, 1.Baskı, İstanbul Medikal Sağlık ve Yayıncılık Hiz Tic Ltd Şti, 23 Nisan 2021: 290-316. 290-316.ISBN: 978-625-7291-22-4
• Ayla Güven. Aşırı Büyüme. In: Darendeliler F, Aycan Z, Kara C, Özen S, Eren E (eds). Çocuk Endokrinolojisi ve Diyabet. Cilt 1, 1.Baskı,İstanbul Medikal Sağlık ve Yayıncılık Hiz Tic Ltd Şti 23 Nisan 2021: 317-341, 317-341. ISBN: 978-625-7291-22-4
• Ayla Güven. Polikistik Over Sendromunda Tedavi. In: Haspolat YK, Gül T,Yolbaş I, Aktar F (eds). Adolesan Jinekolojisi, Cinius Yayınları, İstanbul,2016 : 209-218.
• Güven A. Hipofiz Fonksiyon Testleri, Endokrin testler, Dinamik Testler. In :Cinaz P,Darendeliler F,Akıncı A,ÖzkanB,Dündar B,Abacı A,Akçay T (eds): Çocuk Endokrinoloji,2.Baskı,2013,771-783
• Güven A. Cushing’s Sendromu ve Perioperatif Yönetim. In: Kurdoğlu S (ed). Çocuklarda Acil Endokrin Hastalıklar, Nobel Tıp Kitabevi, İstanbul, 2013:463-469
• Güven A. Plasentanın endokrin fonksiyonları. In: Kurdoğlu S (ed). Yenidoğan Dönemi Endokrin Hastalıkları, 2011,Nobel Matbaacılık,İstanbul, 7-20
• Güven A. Çocukluk çağında metabolik sendrom. In. Oğuz A (ed). Metabolik Sendrom Yıllığı, Ayrıntı Basımevi, Ankara, 2009,197-212.
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Uluslararası bilimsel toplantılarda sunulan ve bildiri kitabında basılan bildiriler

• Irina A Bacila, Neil R Lawrence, Chamila Balagamage, Jillian Bryce, Salma R Ali, Malika Alimussina, Minglu Chen, Ved Bhushan Arya, Navoda Atapattu, Tânia A Bachega, Pascal Barat, Federico Baronio, Silvano Bertelloni,Niels Birkebæk, Walter Bonfig, Christiaan de Bruin, Hedi Claahsen – van der Grinten, Martine Cools, Eduardo Costa20, Elizabeth Crowne, Justin H Davies22Miguel Debono, Liat de Vries, Katja Dumic Kubat, Heba Elsedfy, Olcay Evliyaoglu, Christa Flüeck, Gabriella Gazdagh, Alina German, Evelien F Gevers, Evgenia Globa, Tulay Guran, Ayla Güven, Laura Guazzarotti, Sabine Hannema, Nihal Hatipoglu, Dominika Janus41Hetty van der Kamp42, Zacharoula Karabouta, Ruth Krone, Nina Lenherr Taube, Sofia Leka-Emiri, Corina Lichiardopol, Mona Mamdouh Hassan, Otilia Marginean, Renata Markosyan, Inas Mazen, Harriet Miles51Anna L Mitchell, Klaus Mohnike, Uta Neumann, Marek Niedziela, Anna Nordenstrom56, Susan M O’Connell, Franziska Phan-Hug, Sukran Poyrazoglu, Ursina Probst-Scheidegger, Rodolfo Rey, Gianni Russo, Mariacarolina Salerno Luisa de Sanctis, Sumudu N Seneviratne, Anat Segev-Becker, Savitha Shenoy, Mars Skae, Ajay Thankamony, Ahmet Ucar, Agustini Utari, Ana Vieites, Malgorzata Wasniewska, S. Faisal Ahmed, Nils P Krone. Real world data analysis of contemporary therapy and its association to anthropometric outcomes in 1500 patients with congenital adrenal hyperplasia (CAH). Horm Res Paediatr 2024;97(suppl 3):43-44. 62nd Annual Meeting of the ESPE. FC4.1
• Aneta Gawlik-Starzyk, Debbie Matthews, Ewa Błaszczyk, Caroline Brain, Berit Öhman Kriström, Sinéad M McGlacken-Byrne, Theo Sas, Janielle van der Velden, Franciska Verlinde, Malgorzata Wasniewska, Arlen Smith, Jakub Gawlik, Navoda Atapattu, Silvano Bertelloni, Gerhard Binder, Tim Cheetham, Heidi L Claahsen-van der Grinten16, Susan M O’Connell, Martine Cools, Mirjam Dirlewanger, Heba Elsedfy, Mohamed A Baky Fahmy, Simona Fica, Christa E. Flück, Evelien F Gevers, Evgenia Globa, Laura Guazzarott, Ayla Guven, Sabine E. Hannema, Gloria Herrmann, Sasha Howard, Violeta Iotova, Dominika Januś, Daniel Konrad, Nils Krone, Aglaia Kyrilli, Sofia Leka-Emiri, Otilia Marginean, Renata Markosyan, Marek Niedziela, Anna Nordenstrom, Monika Obara - Moszynska, Sukran Poyrazoglu, Ursina Probst, Julia Rohayem, Gianni Russo, Marija Šandrk Beslać, Valerie Schwitzgebel, Sumudu Nimali Seneviratne, Savitha Shenoy, Jerzy Starzyk, Gilles Tourlamain, Nina Lenherr Taube, Ahmet Ucar, Agustini Utari, Anna Wędrychowicz, Joanna Wojtyś, Mohamed Zainaba, Jillian Bryce, Minglu Chen, Sanhita Koley, Malika Alimussina, John N.S. Matthews, Syed Faisal Ahmed, Malcolm D.C. Donaldson. Pubertal induction in girls with Turner syndrome retrospective data from the International TS registry. Horm Res Paediatr 2024;97(suppl 3):104-106. 62nd Annual Meeting of the ESPE.RFC 5.6
• Neil R. Lawrence, Irina Bacila, Joseph Tonge, Jeremy Dawson Gary S. Collins, Zi-Qiang Lang, Jillian Bryce, Malika Alimussina, Minglu Chen, Salma R. Ali, Safwaan Adam, Erica L.T. van den Akker, Tânia A.S.S. Bachega, Federico Baronio, Walter Bonfig, Hedi Claahsen-van der Grinten, Martine Cools, Eduardo C. Costa, Miguel Debono, Liat de Vries, Christa Flück, Gabriella Gazdagh, Ayla Güven Sabine Hannema, Violeta Iotova, Hetty J van der Kamp, Ruth Krone, Sofia Leka-Emiri, María Clemente-León Corina R. Lichiardopol, Renata L. Markosyan, Tatjana Milenkovic29, Mirela C. Miranda, Uta Neumann, John Newell-Price1, Şükran Poyrazoğlu, Ursina Probst-Scheidegger, Gianni Russo, Luisa De Sanctis, Sumudu N. Seneviratne, Marianna R. Stancampiano,Rieko Tadokoro-Cuccaro, Ajay Thankamony, Ana Vieites, Malgorzata Wasniewska, Diego Yeste, Jeremy Tomlinson, S. Faisal Ahmed, Nils Krone1,. Variation in Blood Pressure in Young Adults with 21a-Hydroxylase Deficiency: Longitudinal Multilevel Modelling of Data from the I-CAH Registry. Horm Res Paediatr 2024;97(suppl 3):152-153. 62nd Annual Meeting of the ESPE. P1-7
• Neil R. Lawrence, Irina Bacila, Joseph Tonge, Jeremy Dawson, Gary S. Collins2, Zi-Qiang Lang, Jillian Bryce, Malika Alimussina, Minglu Chen, Salma R. Ali, Safwaan Adam, Erica L.T. van den Akker, Tânia A.S.S. Bachega, Federico Baronio, Niels H. Birkebæk, Walter Bonfig, Hedi Claahsen–van der Grinten, Martine Cools, Eduardo C. Costa, Miguel Debono, Liat de Vries, Christa Flück, Gabriella Gazdagh, Ayla Güven, Sabine Hannema, Violeta Iotova, Hetty J. van der Kamp, Ruth Krone, Sofia Leka-Emiri, María Clemente-León, Corina R. Lichiardopol, Renata L. Markosyan, Tatjana Milenkovic, Mirela C. Miranda, Uta Neumann, John Newell-Price, Şükran Poyrazoğlu, Ursina Probst-Scheidegger, Rodolfo Rey, Gianni Russo, Luisa De Sanctis, Sumudu N. Seneviratne, Marianna R. Stancampiano, Rieko Tadokoro-Cuccaro, Ajay Thankamony, Ana Vieites, Malgorzata Wasniewska, Diego Yeste, Jeremy Tomlinson, S. Faisal Ahmed, Nils Krone. Impact of Fludrocortisone on Blood Pressure in Young Children Under 5 with CAH in the I-CAH Registry: Autoregressive Causal Inference Analysis. Horm Res Paediatr 2024;97(suppl 3):153-154. 62nd Annual Meeting of the ESPE. P1-6
• Ayşehan Akıncı, Doğa Turkkahraman, İbrahim Tekedereli, Leyla Ozer, Bahri Evren, Ibrahim Sahin, Tarkan Kalkan, Yusuf Curek, Emine Camtosun, Esra Doger, Aysun Bideci, Ayla Guven, Erdal Eren, Ozlem Sangun, Atilla Cayır, Pelin Bilir, Ayca Torel Ergur, Oya Ercan. The prevalence of monogenic obesity in Turkish children with non-syndromic early onset obesity. A multicenter study. 50th Annual Meeting of the British Society for Paediatric Endocrinology and Diabetes Manchester, UK, 08 Nov 2023 - 10 Nov 2023
• Xanthippi Tseretopoulou, Jillian Bryce, Nadia Amin, Navoda Atapattu, Tania Bachega, Federico Baronio, Walter Bonfig, Justin H Davies, Tessy Thomas, Heba Elsedfy, Evgenia Globa, Natalia Zelinska, Tulay Guran, Abali Zehra Yavas, Ayla Guven, Violeta Iotova, Daniel Konrad, Nina Lenherr-Taube, Sofia Leka-Emiris, Elpis Vlachopapadopoulou, Otilia Marginean, Uta Neumann, Marek Niedzela, Franziska Phan-Hug, Sukran Poyrazoglu, Ursina Probst, Tabitha Randell, Gianni Russo, Salerno Maria Carolina, Margarett Shnorhavorian, Ana Vieites, Malgorzata Wasniewska, Ahmed Syed Faisal. Acute adrenal insufficiency related adverse events in children with congenital adrenal hyperplasia (CAH): Changes during the period 2019-2022 in I-CAH. Society for Endocrinology BES 2023, Glasgow, UK, 13 Nov 2023 - 15 Nov 2023
• Rieko Tadokoro-Cuccaro, Ieuan Hughes, Martine Cools, Koen van de Vijver, Berenice Bilharinho de Mendonça, Sorahia Domenice, Rafael L Batista, Renata Thomazini Dallago, Nathalia Lisboa Gomes, Elaine F Costa, Andréa T. Maciel-Guerra, Gil Guerra-Junior, Juliana Gabriel Ribeiro de Andrade,Angela Lucas-Herald, Jillian Bryce, Sabine Hannema, Anders Juul, Eugenia Globa, Kenneth MсElreavey, Federico Baronio, Jimena Lopez Dacal, Feyza Darendeliler, Sukran Poyrazoglu, Zofia Kolesińska, Marek Niedziela,Hedi L. Claahsen-van der Grinten, Erica L.T. van den Akke, Gloria Herrmann, Navoda Atapattu, Vandana Jain, Rajni Sharma, Markus Bettendorf, Daniel Konrad, Paul Martin Holterhus, Simona Fica, Mars Skae,Gianni Russo, Marianna Rita Stancampiano, Gabriella Gazdagh, Justin H Davies, Zainaba Mohamed, Sumudu Nimali Seneviratne, Tulay Guran, Ayla Güven, Malgorzata Wasniewska, Vilhelm Mladenov, Gilvydas Verkauskas, Renata Markosyan, Marta KorbonitsS Faisal Ahmed, Olaf Hiort, Isabel Wagner, Ajay Thank. Gonadal morphology in 46, XY gonadal dysgenesis: I-DSD Registry-based study. Norm Res Paediatr 2022; 95 (Suppl 2):44. FC 6-3
• Neil R. Lawrence, Irina Bacila, Jeremy Dawson, Salma R. Ali, Erica LT van den Akker, Tânia Aparecida Sartori Sanchez Bachega, Federico Baronio, Niels Holtum Birkebæk, Walter Bonfig, Hedi Claahsen van der Grinten, Martine Cools, Eduardo Correa Costa, Liat de Vries, Christa Flück, Gabriella Gazdagh, Ayla Güven, Sabine Hannema, Violeta Iotova Hetty J van der Kamp, Ruth Krone, Sofia Leka-Emiri, María Clemente León, Corina Raducanu Lichiardopol, Renata L. Markosyan, Tatjana Milenkovic, Mirela Costa de Miranda, Uta Neumann, John Newell-Price, Şükran Poyrazoğlu, Ursina Probst-Scheidegger, Gianni Russo, Luisa De Sanctis, Adam Safwaan, Sumudu Seneviratne, Marianna Rita Stancampiano, Rieko Tadokoro- Cuccar Ajay Thankamony, Ana Vieites, Malgorzata Wasniewsiego Yeste, Eleni Daniel, Jeremy Tomlins. Faisal Ahmed, Nils Krone. Blood pressure (BP) status in Congenital Adrenal Hyperplasia (CAH) – longitudinal analysis of real world data from the I-CAH registry. Horm Res Paediatr 2022;95(suppl 2): 112 (P1-3).
• Xanthippi Tseretopoulou, Salma R. Ali, Jillian Bryce, Atapattu Navoda, Niels H. Birkebaek, Federico Baronio, Walter Bonfig, Hedi L. Claahsen-van der Grinten, Martine Cools, Feyza Darendeliler, Sukran Poyrazoglu, Luisa de Sanctis, Heba Elsedfy, Martijn J.J. Finken, Christa E. Fluck, Evelien Gevers, Marta Korbonits, Tulay Guran, Ayla Guven, Ieuan A. Hughes, Rieko Tadokoro-Cuccaro, Ajay Thankamony, Violeta Iotova, Ruth Krone, Corina Lichiardopol, Berenice B. Mendonca, Tania A. S. S. Bachega, Mirela C. Miranda, Tatjana Milenkovic, Klaus Mohnike, Anna Nordenstrom, Hetty J. van der Kamp, Syed Faisal Ahmed An International Study of the Association between Local Health Care Resources and Acute Adrenal Insufficiency Events in Children with Congenital Adrenal Hyperplasia. P1-582. Horm Res Paediatr 2022;95(suppl 2):401
• Cioana M,Nadarajah A, Hou M, Qiu Y, Chen SS, Rivas A, Deng J, Banfield L, Guven A, Alfaraidi H, Alotaibi A, Thabane L, Samaan MC. Obesity Prevalence in pediatric Type 2 Diabetes Mellitus: A Systematic Review an Meta-Analysis. Canadian Journal of Diabetes 2020; 44: S19
• Doris Hebenstreit, Faisal Ahmed, on behalf of the contributing centres within the I-DSD registry and I-CAH registry, Alexander Springer, Christoph Krall, Nils Krone, Niels Birkebaek, Tatjana Milenkovic, Birgit Koehler, Christa Flueck, Ruth Krone, Antonio Balsamo, Rodolfo Rey, Carlo Acerini, Ayla Guven, Tulay Guran, Feyza Darendeliler, Sabah Alvi , Marta Korbonits, Walter Bonfig, Eduardo Correa Costa, Richard Ross, Violeta Iotova, Daniel Konrad, Jillian Bryce, Hedi Claahsen van der Grinten, Liat de Vries. Contemporary surgical approach in CAH 46XX – Results from the I-DSD/I-CAH Registries. RFC 10.1 ESPE 2019, 19-21 September.Horm Res Paediatr 2019;91(suppl 1):96-97
• Irina-Alexandra Bacila, Oliver Blankenstein, Uta Neumann, Heidi L Claahsen-van der Grinten, Ruth Krone, Tania SS Bachega, Mirela C Miranda, Berenice Mendonca, Niels H Birkebaek, Martine Cools, Tatjana Milenkovic, Walter Bonfig, Jeremy W Tomlinson, Heba Elsedfy, Antonio Balsamo, Rita Ortolano, Sabine Hannema, Claire Higham, Navoda Atapattu, Corina Lichiardopol, Tulay Guran, Zehra Abali, Klaus Mohnike, Martijn JJ Finken, Ana Vieites, Feyza Darendeliler, Ayla Guven, Marta Korbonits, Liat de Vries, Eduardo Costa, Silvia Einaudi, Hetty van der Kamp, Violeta Iotova, Richard Ross, S Faisal Ahmed, Nils Krone.Exploring trends in the glucocorticoid and mineralocorticoid treatment of congenital adrenal hyperplasia by analysing data from the I-CAH registry.47th Meeting of the British Society for Paediatric Endocrinology and Diabetes. Endocrine Abstracts (2019) 66 OC1.1 | DOI: 10.1530/endoabs.66.OC1.1
• Irina-Alexandra Bacila, Oliver Blankenstein, Uta Neumann,Hedi L. Claahsen - van der Grinten, Ruth Krone, Carlo Acerini, Tania S. S. Bachega, Mirella C. Miranda, Berenice Mendonca, Niels H. Birkebaek, Martine Cools, Tatjana Milenkovic, Walter Bonfig, Jeremy Tomlinson, Heba Elsedfy, Antonio Balsamo, Sabine Hannema, Claire Higham, Navoda Atapattu, Corina Lichiardopol, Tulay Guran, Zehra Abali, Klaus Mohnike, Martijn J. J. Finken, Ana Vieites, Feyza Darendeliler, Ayla Guven, Marta Korbonits, Liat de Vrie, Eduardo Costa, Silvia Einaudi, Hetty van der Kamp, Violeta Iotova, Richard Ross, S. Faisal Ahmed, Nils P. Krone. Global Practice of Glucocorticoid and Mineralocorticoid Treatment in Children and Adults with Congenital Adrenal Hyperplasia –Insights from the I-CAH Registry. P1-10. ESPE 2019, 19-21 September, Vienna. Horm Res Paediatr 2019;91(suppl 1):132-133
• Bahar Özcabı, Salih Demirhan, Özden Aksu, Hatice Öztürkmen Akay, Ayla Güven. Waist circumference triglyceride index is useful to predict non-alcoholic fatty liver disease in childhood obesity. P1-48. ESPE 2019, 19-21 September, Vienna. Horm Res Paediatr 2019;91(suppl 1):150-151
• Uta Neumann, Annelieke van der Linde, Ruth Krone, Ayla Guven, Tülay Güran, Heba Elsedfy, Feyza Darendeliler, Tania Bachega, Antonio Balsamo, Sabine Hannema, Niels Birkebaek, Ana Vieites, Carlo Acerini, Martine Cools, Tatjana Milenkovic, Walter Bonfig, Eduardo Costa, Navoda Atapattu, Liat de Vries, Guilherme Filho, Marta Korbonits, Klaus Mohnike, Jillian Bryce, Faisal Ahmed, Bernard Voet, Oliver Blankenstein, Hedi Claahsen van der Grinten. Influence of salt supplementation on drug therapy in children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency aged 0-3 years: Update on a retrospective multicentre analysis using the I-CAH registry. P1-157. ESPE 2019, 19-21 September, Vienna. Horm Res Paediatr 2019;91(suppl 1):204-205.
• Tulay Guran, Cengiz Kara, Melek Yildiz, Eda C. Bitkin, Goncagul Haklar, Jen-Chieh Lin, Lorna C. Gilligan, Lise Barnard, Mehmet Keskin Ahmet Anik Gonul Catli, Ayla Guven, Birgul Kirel, Filiz Tutunculer, Hasan Onal, Serap Turan, Teoman Akcay, Zeynep Atay, Elizabeth S. Baranowski, Gulay C. Yilmaz, Jamala Mamadova, Azad Akbarzade, Onder Sirikci, AghaRza Aghayev, Afra Alkan, Cedric H.L. Shackleton, Karl H. Storbeck, Tugba Baris, Wiebke Arlt, Bon-Chu Chung, Abdullah Bereket.Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3β-hydroxysteroid dehydrogenase 2 deficiency P1-162.ESPE 2019, 19-21 September, Vienna. Horm Res Paediatr 2019;91(suppl 1): 207
• Salma Ali, Eleni Daniel, Jillian Bryce, Adalia Ikiroma, James Lewsey, Richard Ross, Ruth Krone, Carlo Acerini, Nils Krone, Urmi Das, Jeremy Tomlinson, Marta Korbonits, Claire Higham, Feyza Darendeliler, Tulay Guran, Ayla Guven, Navoda Attapatu, Tatjana Milenkovic, Corina Raducanu-Lichiardopol, Sabine Hannema, Hedi Claahsen, Martijn Finken, Federico Baronio, Antonio Balsamo, Silvia Einaudi, Liat de Vries, Andrea Luczay, Uta Neumann, Oliver Blankenstein, Klaus Mohnike, Walter Bonfig, Heba Elsedfy, Niels Birkebaek, Violeta Iotova, Tania Bachega, Berenice Mendonca, Martine Cools, Eduardo Correa Costa,Guilherme Guaragna-Filho, Rodolfo Rey, S. Faisal Ahmed. Development Of An International Benchmark For Sick Day Episodes As A Core Clinical Outcome In People With Congenital Adrenal Hyperplasia P1-167 . ESPE 2019, 19-21 September, Vienna. Horm Res Paediatr 2019;91(suppl 1): 209-210.
• Ayla Güven. Different Potent Glucocorticoids, Different Routes of Exposure but The Same Result: Iatrogenic Cushing’s syndrome and Adrenal Insufficiency P2-13.ESPE 2019, 19-21 September, Vienna. Horm Res Paediatr 2019;91(suppl 1):365
• Ayla Güven, Martin Konrad, Karl Peter Schlingmann. Idiopathic infantile hypercalcemia: Mutations in SLC34A1 and CYP24A1 in two siblings and fathers. P2-53. ESPE 2019, 19-21 September, Vienna. Horm Res Paediatr 2019;91(suppl 1):384-385
• Ayla Güven.Etiologic Classification of 46, XY Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results. P3-243. ESPE 2019, 19-21 September, Vienna. Horm Res Paediatr 2019;91(suppl 1): 607-608.
• Ayla Guven. Etiologic Classification of 46, XX Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results. P2-262. ESPE 2019, 19-21 September, Vienna. Horm Res Paediatr 2019;91(suppl 1):483
• A. Kiykim, E. Dursun, E. Nain, S. Cekic, I. Ogulur, D. Baser, N. Kasap, S. Kutlug, M.T. Cogurlu, M. Kara, A. Guven, A. Somer, C. Aydogmus, A. Yildiran, A. Uncuoglu Aydogan, S. Kilic, E. Karakoc Aydiner, A. Ozen, S. Baris. A Turkish Lrba Deficiency Cohort Providing Clinical And Laboratory Utilities. ESID 2018, 0126, 24 - 27 October 2018, Lizbon, Portekiz
• Ayla Güven, Canan Yıldırımoglu. Different Clinical Findings in Maturity Onset Diabetes of the Young Due to B-Lymphocyte Kinase Gene Mutations. Horm Res Paediatr 2018;90(suppl 1):211-212. DOI: 10.1159/000492307
• Ayla Güven, Canan Yıldırımoglu. Clinical and Genetic Characterizations of Maturity Onset Diabetes of the Young: Single Center Results. Horm Res Paediatr 2018;90(suppl 1) : 237-238.
• Suna Kılınç, Tuğrul Çiçek, Serdar Moralıoğlu, Ayla Güven. A Case of Transverse Testicular Ectopia with Persistant Müllerian Duct Syndrome:a Novel Amh Gene Mutation. Horm Res Paediatr 2018;90(suppl 1) : 591
• Bahar Ozcabi, Salih Demirhan, Mesut Akyol, Hatice Ozturkmen Akay, Ayla Guven. Lipid Accumulation Product Is a Predictor of Non- alcoholic Fatty Liver Disease in Childhood Obesity. Horm Res Paediatr 2018;90(suppl 1): 293
• Elif Gokce Demir, Ayla Guven2, Metin Yildiz.The Reference and Follow-up Signs and Symptoms of the Cases Who Are Diagnosed as Hyperthyroidism. Horm Res Paediatr 2018;90 (suppl 1): 623
• Ayla Güven, Nejat Işık.A Rare Cause of Panhypopituitarism: Nasofrontal Encephalomeningocel. Endoconnect 3. 16-17 May, 2017, Naples, Italy
• Ayla Güven, Federica Buonocore, John Achermann, Tülay Güran. CYP11A1 mutations Results Various Clinical Phenotypes. P1-123. Horm Res Paediatr, 2017; 88 (Suppl 1): 81
• Ayla Güven, Tülay Güran, Nils Krone. 17-Hydroxlase deficiency: Rare Cause of Delayed Puberty. P2-126. Horm Res Paediatr, 2017; 88 (Suppl 1): 266-267
• Ayhan Abaci, MD, Gönül Çatli, Özgür Kirbiyik, Nursel M Sahin, Zehra Y Abali, Edip Ünal, Zeynep Siklar, Eda M Uçaktürk, Samim Özen, Tulay Guran, Cengiz Kara, Melek Yildiz, Erdal Eren, Özlem Nalbantoglu, Ayla Güven, Atilla Çayir, Emine D Akbas, Yilmaz Kor, Yusuf Çürek, Zehra Aycan, Firdevs Bas, Sükran Darcan, Merih Berberoglu. Phenotypic, hormonal and molecular genetic characteristics of 5-alpha reductase type 2 deficiency patients: a multicenter study from Turkey, P3 1500. Horm Res Paediatr, 2017; 88 (Suppl 1): 586.
• Ayla Güven, Hüseyin Onay.Clinical Findings Of A Novel Cyp19a1 (Aromatase) C.1206_1263+106del (P.H402rfsx4) Mutation Causing Virilization Of a 46,XX Newborn. Horm Res Paediatr, 2017; 88 (Suppl 1): 210.
• T. Guran, C. Kara, Z. Atay, A. Akbarzade, G. Can Yılmaz, E. Çelebi Bitkin, T. Akcay, M. Yildiz, A. Guven, G. Çatlı, G. Yeşil, S. Baş, P. Vatansever, G. Haklar, Ö. Sirikçi, S. Turan, A. Bereket.. Evaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency. Clinical Chemistry, Vol. 63, No. 10, Supplement, October 2017
• H. Onay, S. Ozen, T. Sozen Turk, S. Darcan, T. Atik, A. Anik, O. Ercan, O. Evliyaoglu, F. Hazan, A. Abaci, A. Guven, H. Kirmizibekmez, F. Ozkinay. Investigation of androgen receptor (AR) gene mutation spectrum in the turkish patients with disorder of sex development. European Human Genetics Conference 2017, 27-30 May, Denmark. P03.13A.
• Ayla Güven, Elif Gökçe Demir. Cardiovascular Risk and Long Term Follow-up of Turkish Children with Type 2 Diabetes: Single Center Experience. Horm Res Paediatr 2016;86 (Suppl1): 244
• Ayla Güven, İlhan Hazer. Clinical Features of Newborn with Congenital Hypothyroidism Diagnosed by Neonatal Screening: Single Center Experience. Horm Res Paediatr 2016;86 (Suppl1):515
• Ayla Güven, Suna Kılınç, Didem Helvacıoğlu, L.İhsan Kuru. Adrenal Atrophy Secondary to Inappopriate Oral Administration of Exogenous Steroid Presenting With Hypercalcemia. Horm Res Paediatr 2015:84 (Suppl 1): 316
• Ayla Güven, Didem Helvacıoğlu, Suna Kılınç. 11-β-hydroxylase deficiency: 20 Years Follow-Up. Horm Res Paediatr 2015:84 (Suppl 1):326-327
• Ayla Guven, Ayşe Nurcan Cebeci, Yanick Crow. Spondyloenchondrodysplasia with Immune Dysregulation and without Neurological Involvement: Report Two Siblings with ACPS Gene Mutation. Horm Res Paediatr 2015:84 (Suppl 1):347
• Didem Helvacıoğlu, Suna Kılınç, Ayla Güven. Treatment of Life Threatening Hypercalcemia in Two Infants. Horm Res Paediatr 2015:84 (Suppl 1):349
• Suna Kılınç, Ayla Güven, Didem Helvacıoğlu. I am a Boy Since 8-Years Old: Female During Childhood, Virilization at Puberty. Horm Res Paediatr 2015:84 (Suppl 1):399
• Ayla Güven. Evaluation of the Effect of Two Different GnRH-Agonist Therapies on the Antropometric Measurements in Girls with Idiopathic Central Precocious Puberty. Horm Res Paediatr 2015:84 (Suppl 1):542
• Ayla Guven. Seven Cases with Williams Beuren Syndrome: Endocrine Evaluation and Long-Term Follow-up. Horm Res Paediatr 2015:84 (Suppl 1):567-568
• Ayla Güven, Isil Özer & Aylin Ardagil. Kearn-Sayre syndrome associated with adenohypophysis agenesis: long term follow-up . Eur J Endocrinol 2014: 35:796 16th European Congress of Endocrinology 2014, Wrocław, Poland
• Ayla Güven, Sabahat Cam, Aylin Ardagil & Seyma Ozkanli. A new cause of liver cirrohosis in childhood: Long-term uncontrolled obesity. Eur J Endocrinol 2014: 35:797 16th European Congress of Endocrinology 2014, Wrocław, Poland
• Ayla Güven, Mukaddes Kavala, A Nurten Akarsu. Severe Osteogenesis Imperfecta and Epidermolysis Bullosa Simplex Caused by FKBP10 Mutation: New Case. Horm Res 2014: 82 (Suppl1): 53 rd Annual Meeting of ESPE.
• Suna Hancili, Ayla Güven, Süheyla Apaydin, Aylin Ardagil, Diana Valverde Perez.A Rare Cause of Obesity and Type 2 Diabetes: a Novel Alms1 Mutation in Two Siblings with Alström Syndrome Horm Res 2014: 82 (Suppl1): 53 rd Annual Meeting of ESPE.
• Ayla Güven, Suna Hancili, Wiebke Arlt. Hypospadias in a Male Patient with 21-Hydroxylase Deficiency and Atypical Clinical Course: Presentation of Two Brothers. Horm Res 2014: 82 (Suppl1): 53 rd Annual Meeting of ESPE.
• Suna Hancili, Ayla Güven, Ilke Mungan Akin, Ayse Nurcan Cebeci, Sian Edwards. Transient Neonatal Diabetes Mellitus: New Case. Horm Res 2014: 82 (Suppl1): 53 rd Annual Meeting of ESPE.
• Ayla Güven, Didem Helvacıolu, Suna Hancili, Metin Yıldız. The Use of Pamidronate in Pediatric Patients with Disease of Other than Osteogenesis Imperfecta: the Experience of Our Center. Horm Res 2014: 82 (Suppl1): 53 rd Annual Meeting of ESPE.