Acute and Chronic-Intermittent Isovaleric Acidemia: Diagnosis and Glycine Therapy
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.1988.tb02535.x/fullpdf
Reference31 articles.
1. Isovaleric acidemia: a new genetic defect of leucine metabolism.
2. NEONATAL DEATH ASSOCIATED WITH ISOVALERICACIDÆMIA
3. Neonatal Isovaleric Acidemia Associated with Hyperammonemia
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2. Dietary practices in isovaleric acidemia: A European survey;Molecular Genetics and Metabolism Reports;2017-09
3. Organic Acidemias and Disorders of Fatty Acid Oxidation;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
4. Isovaleric acidemia: New aspects of genetic and phenotypic heterogeneity;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2006
5. Effect of Carnitine Administration on Glycine Metabolism in Patients with Isovaleric Acidemia: Significance of Acetylcarnitine Determination to Estimate the Proper Carnitine Dose.;The Tohoku Journal of Experimental Medicine;1996
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