A child with chronic kidney disease and hepatic dysfunction: Answers-Reference-Cited by-同舟云学术

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A child with chronic kidney disease and hepatic dysfunction: Answers

Published:2023-03-29 Issue:10 Volume:38 Page:3277-3279
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Sethi Sidharth Kumar,Mohan Neelam,Rana Alka,Bagoria Gaurav,Soni Kritika,Sharma Vivek,Nair Aishwarya,Savita Savita,Bansal Shyam Bihari,Raina Rupesh

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology and Child Health

Link

https://link.springer.com/content/pdf/10.1007/s00467-023-05949-3.pdf

Reference10 articles.

1. Turnpenny PD, Ellard S (2012) Alagille syndrome: pathogenesis, diagnosis and management. Eur J Hum Genet 20:251–257

2. Li L, Krantz ID, Deng Y, Genin A, Banta AB, Collins CC, Qi M, Trask BJ, Kuo WL, Cochran J, Costa T, Pierpont ME, Rand EB, Piccoli DA, Hood L, Spinner NB (1997) Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. Nat Genet 16:243–251

3. Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, Piccoli DA, Meltzer PS, Spinner NB, Collins FS, Chandrasekharappa SC (1997) Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat Genet 16:235–242

4. Crosnier C, Driancourt C, Raynaud N, Dhorne-Pollet S, Pollet N, Bernard O, Hadchouel M, Meunier-Rotival M (1999) Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome. Gastroenterology 116:1141–1148

5. Saleh M, Kamath BM, Chitayat D (2016) Alagille syndrome: clinical perspectives. Appl Clin Genet 9:75–82

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1. Correction: A child with chronic kidney disease and hepatic dysfunction: Answers;Pediatric Nephrology;2023-07-05

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