Urinary Succinylacetone Analysis by Gas Chromatography-Mass Spectrometry (GC-MS)
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4939-3182-8_30
Reference11 articles.
1. de Laet C, Dionisi-Vici C, Leonard JV, McKiernan P, Mitchell G, Monti L, de Baulny HO, Pintos-Morell G, Spiekerkotter U (2013) Recommendations for the management of tyrosinaemia type 1. Orphanet J Rare Dis 8:8
2. Barnby E (2014) Tyrosinemia type 1: an overview of nursing care. Pediatr Nurs 40:61–68, 90
3. Lindblad B, Lindstedt S, Steen G (1977) Enzymic defects in hereditary tyrosinemia. Proc Natl Acad Sci U S A 74:4641–4645
4. Santra S, Baumann U (2008) Experience of nitisinone for the pharmacological treatment of hereditary tyrosinaemia type 1. Expert Opin Pharmacother 9:1229–1236
5. Sassa S, Kappas A (1983) Hereditary tyrosinemia and the heme biosynthetic pathway. Profound inhibition of delta-aminolevulinic acid dehydratase activity by succinylacetone. J Clin Invest 71:625–634
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1. Identification and Characterization of Novel Variants of Fumarylacetoacetate Hydrolase (FAH) Gene in Clinically Suspected Patients of Tyrosinemia Type 1: Tertiary Care Centre Study of North India;Indian Journal of Clinical Biochemistry;2024-06-05
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