Hepatic Manifestations of Urea Cycle Disorders-Reference-Cited by-同舟云学术

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Hepatic Manifestations of Urea Cycle Disorders

Published:2021-09 Issue:4 Volume:18 Page:198-203
ISSN:2046-2484
Container-title:Clinical Liver Disease
language:en
Short-container-title:Clinical Liver Disease

Author:

Strong Alanna¹²,Gold Jessica¹,Gold Nina B.³⁴,Yudkoff Marc¹⁵

Affiliation:

1. Division of Human Genetics Children's Hospital of Philadelphia Philadelphia PA

2. The Center for Applied Genomics Children's Hospital of Philadelphia Philadelphia PA

3. Division of Medical Genetics and Metabolism Massachusetts General Hospital Boston MA

4. Department of Pediatrics Harvard Medical School Boston MA

5. Department of Pediatrics Perelman School of Medicine University of Pennsylvania Philadelphia PA

Publisher

Wiley

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cld.1115

Reference11 articles.

1. Impact of Diagnosis and Therapy on Cognitive Function in Urea Cycle Disorders

2. The incidence of urea cycle disorders

3. Genotype–Phenotype Correlations in Ornithine Transcarbamylase Deficiency: A Mutation Update

4. Hypocitrullinemia in expanded newborn screening by LC–MS/MS is not a reliable marker for ornithine transcarbamylase deficiency

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1. Building a Better Microbiome: Advances in Microbiome Engineering for Human Health;Human Microbiome;2024

2. Case 30-2023: A 50-Year-Old Woman with Confusion;New England Journal of Medicine;2023-09-28

3. N-carbamylglutamate, a promising functional feed additive in swine production: A review;Animal Feed Science and Technology;2023-09

4. Diagnostic and Management Issues in Patients with Late-Onset Ornithine Transcarbamylase Deficiency;Children;2023-08-09

5. Early allograft dysfunction in a pediatric liver allograft with an occult pathogenic mutation in the urea cycle;American Journal of Transplantation;2023-05

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