Prenatal treatment of ornithine transcarbamylase deficiency-Reference-Cited by-同舟云学术

Prenatal treatment of ornithine transcarbamylase deficiency

Published:2018-03 Issue:3 Volume:123 Page:297-300
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Wilnai Yael,Blumenfeld Yair J.,Cusmano Kristina,Hintz Susan R.,Alcorn Deborah,Benitz William E.,Berquist William E.,Bernstein Jonathan A.,Castillo Ricardo O.,Concepcion Waldo,Cowan Tina M.,Cox Kenneth L.,Lyell Deirdre J.,Esquivel Carlos O.,Homeyer Margaret,Hudgins Louanne,Hurwitz Melissa,Palma Jonathan P.,Schelley Susan,Akula Vishnu Priya,Summar Marshall L.,Enns Gregory M.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference26 articles.

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2. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency;Batshaw;J. Pediatr.,1986

3. Alternative pathway therapy for urea cycle disorders: twenty years later;Batshaw;J. Pediatr.,2001

4. New pathways of nitrogen excretion in inborn errors of urea synthesis;Brusilow;Lancet II,1979

5. Early orthotopic liver transplantation in urea cycle defects: follow up of a developmental outcome study;Campeau;Mol. Genet. Metab.,2010

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