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Genetic landscape of pediatric acute liver failure of indeterminate origin.
Hepatology. 2024 May 1;79(5):1075-1087. doi: 10.1097/HEP.0000000000000684. Epub 2023 Nov 16.
Hepatology. 2024.
PMID: 37976411
Free PMC article.
Diagnostic value of plasma lysosphingolipids levels in a Niemann-Pick disease type C patient with transient neonatal cholestasis.
Bulut FD, Bozbulut NE, Özalp Ö, Dalgiç B, Mungan NÖ, Koç Uçar H, Biberoğlu G.
Bulut FD, et al. Among authors: bozbulut ne.
J Pediatr Endocrinol Metab. 2022 Feb 2;35(5):681-685. doi: 10.1515/jpem-2021-0580. Print 2022 May 25.
J Pediatr Endocrinol Metab. 2022.
PMID: 35107903
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Obstructive jaundice and severe pancreatitis due to the foramen of Winslow hernia with multiple anomalies.
Bozbulut NE, Akdulum İ, Sarı S, Özen İO, Çavuşoğlu YH, Boyunağa Ö, Dalgıç A, Dalgıç B.
Bozbulut NE, et al.
Turk J Pediatr. 2020;62(1):152-155. doi: 10.24953/turkjped.2020.01.023.
Turk J Pediatr. 2020.
PMID: 32253883
Free article.
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Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patients.
Staufner C, Peters B, Wagner M, Alameer S, Barić I, Broué P, Bulut D, Church JA, Crushell E, Dalgıç B, Das AM, Dick A, Dikow N, Dionisi-Vici C, Distelmaier F, Bozbulut NE, Feillet F, Gonzales E, Hadzic N, Hauck F, Hegarty R, Hempel M, Herget T, Klein C, Konstantopoulou V, Kopajtich R, Kuster A, Laass MW, Lainka E, Larson-Nath C, Leibner A, Lurz E, Mayr JA, McKiernan P, Mention K, Moog U, Mungan NO, Riedhammer KM, Santer R, Palafoll IV, Vockley J, Westphal DS, Wiedemann A, Wortmann SB, Diwan GD, Russell RB, Prokisch H, Garbade SF, Kölker S, Hoffmann GF, Lenz D.
Staufner C, et al. Among authors: bozbulut ne.
Genet Med. 2020 Mar;22(3):610-621. doi: 10.1038/s41436-019-0698-4. Epub 2019 Nov 25.
Genet Med. 2020.
PMID: 31761904
Free article.
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