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Genetic findings in short Turkish children born to consanguineous parents.
Joustra SD, Isik E, Wit JM, Catli G, Anik A, Haliloglu B, Kandemir N, Ozsu E, Hendriks YMC, de Bruin C, Kant SG, Campos-Barros A, Challis RC, Parry D, Harley ME, Jackson A, Losekoot M, van Duyvenvoorde HA. Joustra SD, et al. Among authors: ozsu e. Horm Res Paediatr. 2024 Jun 5. doi: 10.1159/000539696. Online ahead of print. Horm Res Paediatr. 2024. PMID: 38838658
Clinical and Laboratory Characteristics of MODY (Maturity Onset Diabetes of Young) Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.
Özsu E, Çetinkaya S, Bolu S, Hatipoğlu N, Savaş Erdeve Ş, Evliyaoğlu O, Baş F, Çayır A, Dündar İ, Akbaş ED, Uçaktürk SA, Berberoğlu M, Şıklar Z, Özalkak Ş, Muratoğlu Şahin N, Keskin M, Şiraz ÜG, Turan H, Öztürk AP, Mengen E, Sağsak E, Dursun F, Akyürek N, Odabaşı Guneş S, Aycan Z. Özsu E, et al. J Clin Res Pediatr Endocrinol. 2024 Apr 26. doi: 10.4274/jcrpe.galenos.2024.2023-10-16. Online ahead of print. J Clin Res Pediatr Endocrinol. 2024. PMID: 38665000 Free article.
Comprehensive Insights into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes with a Multicenter Approach.
Şıklar Z, Özsu E, Kızılcan Çetin S, Özen S, Çizmecioğlu-Jones F, Balkı HG, Aycan Z, Goksen D, Kilci F, Abseyi SN, Tercan U, Gürpınar G, Poyrazoğlu Ş, Darendeliler F, Demir K, Besci Ö, Özgen İT, Akın SB, Kocabey Sütçü Z, Aykaç Kaplan EH, Çamtosun E, Dundar İ, Sağsak E, Korkmaz HA, Anık A, Yeşiltepe Mutlu G, Özcabi B, Uçar A, Dağdeviren Çakır A, Selver Eklioğlu B, Kırel B, Berberoğu M. Şıklar Z, et al. Among authors: ozsu e. J Clin Res Pediatr Endocrinol. 2024 Apr 26. doi: 10.4274/jcrpe.galenos.2024.2024-1-3. Online ahead of print. J Clin Res Pediatr Endocrinol. 2024. PMID: 38664994 Free article.
Variant characterisation and clinical profile in a large cohort of patients with Ellis-van Creveld syndrome and a family with Weyers acrofacial dysostosis.
Altunoglu U, Palencia-Campos A, Güneş N, Turgut GT, Nevado J, Lapunzina P, Valencia M, Iturrate A, Otaify G, Elhossini R, Ashour A, K Amin A, Elnahas RF, Fernandez-Nuñez E, Flores CL, Arias P, Tenorio J, Chamorro Fernández CI, Güven Y, Özsu E, Eklioğlu BS, Ibarra-Ramirez M, Diness BR, Burnyte B, Ajmi H, Yüksel Z, Yıldırım R, Ünal E, Abdalla E, Aglan M, Kayserili H, Tuysuz B, Ruiz-Pérez V. Altunoglu U, et al. Among authors: ozsu e. J Med Genet. 2024 Mar 26:jmg-2023-109546. doi: 10.1136/jmg-2023-109546. Online ahead of print. J Med Genet. 2024. PMID: 38531627
Familial Clinical Heterogeneity of Medullary Thyroid Cancer with Germline RET S891A Protooncogene Mutation: 7-Year Follow-up with Successful Sorafenib Treatment.
Kizilcan Cetin S, Siklar Z, Ozsu E, Ceran A, Ceyhan K, Aycan Z, Kırmızı A, Dincaslan H, Unal E, Berberoğlu M. Kizilcan Cetin S, et al. Among authors: ozsu e. J Clin Res Pediatr Endocrinol. 2023 Nov 9. doi: 10.4274/jcrpe.galenos.2023.2023-7-13. Online ahead of print. J Clin Res Pediatr Endocrinol. 2023. PMID: 37942886 Free article.
A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review.
Besci Ö, Fırat SN, Özen S, Çetinkaya S, Akın L, Kör Y, Pekkolay Z, Özalkak Ş, Özsu E, Erdeve ŞS, Poyrazoğlu Ş, Berberoğlu M, Aydın M, Omma T, Akıncı B, Demir K, Oral EA. Besci Ö, et al. Among authors: ozsu e. J Clin Endocrinol Metab. 2023 Aug 18;108(9):2371-2388. doi: 10.1210/clinem/dgad099. J Clin Endocrinol Metab. 2023. PMID: 36825860
45 results