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Page 1
Johanson-Blizzard's Syndrome with a Novel UBR1 Mutation.
Demir D, Kendir Demirkol Y, Gerenli N, Aktaş Karabay E. Demir D, et al. Among authors: gerenli n. J Pediatr Genet. 2020 Sep 4;11(2):147-150. doi: 10.1055/s-0040-1716331. eCollection 2022 Jun. J Pediatr Genet. 2020. PMID: 35769968 Free PMC article.
Hepatopathies in children and adolescents with type 1 diabetes.
Aydın F, Gerenli N, Dursun F, Atasoy TÖ, Kalın S, Kırmızıbekmez H. Aydın F, et al. Among authors: gerenli n. J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):121-126. doi: 10.1515/jpem-2018-0255. J Pediatr Endocrinol Metab. 2019. PMID: 30685742
Growth, tolerance and safety outcomes with use of an extensively hydrolyzed casein-based formula in infants with cow's milk protein allergy.
Kansu A, Urganci N, Bukulmez A, Kutluk G, Gulcu Taskin D, Sahin Keskin L, Igde M, Molon L, Dogan Y, Sekerel BE, Yuksek M, Bostanci I, Gerenli N, Polat E, Dalgic B, Ayyildiz H, Usta M, Basturk A, Yuce Kirmemis O, Tuna Kirsaclioglu C, Gulerman HF, Alptekin Sarioglu A, Erdogan S. Kansu A, et al. Among authors: gerenli n. Front Pediatr. 2023 Jul 31;11:1230905. doi: 10.3389/fped.2023.1230905. eCollection 2023. Front Pediatr. 2023. PMID: 37601126 Free PMC article.
The frequency of Duchenne muscular dystrophy/Becker muscular dystrophy and Pompe disease in children with isolated transaminase elevation: results from the observational VICTORIA study.
Kansu A, Kuloglu Z, Tümgör G, Taşkın DG, Dalgıç B, Çaltepe G, Demirören K, Doğan G, Tuna Kırsaçlıoğlu C, Arslan D, Işık İA, Demir H, Bekem Ö, Şahin Y, Bayrak NA, Selimoğlu MA, Yavuz S, Taşkaya İE, Altay D; VICTORIA Study Group. Kansu A, et al. Front Pediatr. 2023 Sep 25;11:1272177. doi: 10.3389/fped.2023.1272177. eCollection 2023. Front Pediatr. 2023. PMID: 37818166 Free PMC article.
19 results