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Year Number of Results
2014 1
2015 1
2016 1
2017 4
2018 6
2019 4
2020 6
2021 2
2022 4
2023 6
2024 4

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Page 1
Subclinical hypothyroidism and long QT.
Akın A, Unal E, Yıldırım R, Türe M, Balık H, Haspolat YK. Akın A, et al. Among authors: yildirim r. Pacing Clin Electrophysiol. 2018 Sep;41(9):1277. doi: 10.1111/pace.13453. Epub 2018 Aug 7. Pacing Clin Electrophysiol. 2018. PMID: 30019377 No abstract available.
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets.
Şıklar Z, Turan S, Bereket A, Baş F, Güran T, Akberzade A, Abacı A, Demir K, Böber E, Özbek MN, Kara C, Poyrazoğlu Ş, Aydın M, Kardelen A, Tarım Ö, Eren E, Hatipoğlu N, Büyükinan M, Akyürek N, Çetinkaya S, Bayramoğlu E, Selver Eklioğlu B, Uçaktürk A, Abalı S, Gökşen D, Kor Y, Ünal E, Esen İ, Yıldırım R, Akın O, Çayır A, Dilek E, Kırel B, Anık A, Çatlı G, Berberoğlu M. Şıklar Z, et al. Among authors: yildirim r. J Clin Res Pediatr Endocrinol. 2020 Jun 3;12(2):150-159. doi: 10.4274/jcrpe.galenos.2019.2019.0098. Epub 2019 Sep 13. J Clin Res Pediatr Endocrinol. 2020. PMID: 31514490 Free PMC article.
Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter study.
Tarçın G, Çatlı G, Çetinkaya S, Eren E, Kardelen AD, Akıncı A, Böber E, Kara C, Yıldırım R, Er E, Polat R, Özhan B, Yıldız M, Kor Y, Evliyaoğlu O, Dündar B, Ercan O. Tarçın G, et al. Among authors: yildirim r. Clin Endocrinol (Oxf). 2024 Jan;100(1):19-28. doi: 10.1111/cen.14980. Epub 2023 Oct 10. Clin Endocrinol (Oxf). 2024. PMID: 37814958
Hereditary spherocytosis: evaluation of 68 children.
Konca Ç, Söker M, Taş MA, Yıldırım R. Konca Ç, et al. Among authors: yildirim r. Indian J Hematol Blood Transfus. 2015 Mar;31(1):127-32. doi: 10.1007/s12288-014-0379-z. Epub 2014 Apr 11. Indian J Hematol Blood Transfus. 2015. PMID: 25548458 Free PMC 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: yildirim r. 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
YIPF5 mutations cause neonatal diabetes and microcephaly through endoplasmic reticulum stress.
De Franco E, Lytrivi M, Ibrahim H, Montaser H, Wakeling MN, Fantuzzi F, Patel K, Demarez C, Cai Y, Igoillo-Esteve M, Cosentino C, Lithovius V, Vihinen H, Jokitalo E, Laver TW, Johnson MB, Sawatani T, Shakeri H, Pachera N, Haliloglu B, Ozbek MN, Unal E, Yıldırım R, Godbole T, Yildiz M, Aydin B, Bilheu A, Suzuki I, Flanagan SE, Vanderhaeghen P, Senée V, Julier C, Marchetti P, Eizirik DL, Ellard S, Saarimäki-Vire J, Otonkoski T, Cnop M, Hattersley AT. De Franco E, et al. Among authors: yildirim r. J Clin Invest. 2020 Dec 1;130(12):6338-6353. doi: 10.1172/JCI141455. J Clin Invest. 2020. PMID: 33164986 Free PMC article.
29 results