Argininemia as a cause of severe chronic stunting and partial growth hormone deficiency (PGHD)
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference25 articles.
1. Estimated frequency of urea cycle enzymopathies in Japan;Nagata;Am J Med Genet,2010
2. Inherited metabolic disorders and stroke part 2: homocystinuria, organic acidurias, and urea cycle disorders;Testai;Arch Neurol,2010
3. Hyperargininemia due to liver arginase deficiency;Crombez;Mol Genet Metab,2005
4. Clinical, biochemical, and molecular spectrum of hyper-argininemia due to arginase I deficiency;Scaglia;Am J Med Genet C Semin Med Genet,2006
5. Argininemia presenting with progressive spastic diplegia;Lee;Pediatr Neurol,2011
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1. Argininemia: Pathophysiology and Novel Methods for Evaluation of the Disease;Applied Sciences;2024-02-18
2. Epidemiology, methods of diagnosis, and clinical management of patients with arginase 1 deficiency (ARG1-D): A systematic review;Molecular Genetics and Metabolism;2022-09
3. Natural history of arginase 1 deficiency and the unmet needs of patients: A systematic review of case reports;JIMD Reports;2022-03-25
4. A novel compound heterozygous mutation in the arginase-1 gene identified in a Chinese patient with argininemia;Medicine;2020-08-07
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