Hydroxymethylglutaryl CoA lyase deficiency: features resembling Reye syndrome.
about
Genetic complementation analysis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency in cultured fibroblasts.Organic acidurias: a review. Part 1.Inborn errors of amino acid and fatty acid metabolism with hypoglycemia as a major clinical manifestation.3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients.3-Hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a review.3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: report of five new patients.Reye's syndrome: current concepts.Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.Effect of Reye's syndrome serum on isolated chinchilla liver mitochondria.The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia.Molecular basis of 3-hydroxy-3-methylglutaric aciduria.[3-Hydroxy-3-methyl-glutaryl-CoA-lyase deficiency as coma etiology in the neonatal period: case report]The contribution of protein catabolism to metabolic decompensation in 3-hydroxy-3-methylglutaric aciduria.Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome.
P2860
Q35199982-B0795019-7AD0-4092-A38C-137C247E678DQ37254022-39AFE0B0-A0DC-4463-8E5A-8C4D72A26B0FQ38612836-D457EAA0-BD2B-4EB6-9400-43B157C3B45FQ39555050-B35AE9C0-94CE-4CEE-BAC7-A306013BD555Q39592562-FE2A6D2B-6942-4E87-A44A-1266D8ABD3A1Q39602156-8640A792-EFA4-4239-8F4D-7FBD21586AE8Q39754671-E44BC3E2-6D10-4DFD-8E9B-65219C414805Q40805245-F17446FC-ED74-413C-A68D-F841F8657322Q40919978-7621AB72-A1EF-401A-AA0E-35A31AF342A6Q42263321-175B44F1-A43C-4707-9D41-D32CEAF8D683Q44911924-65054534-868E-468E-A504-B05A53BF8DEDQ51567852-9248914F-942D-4268-BDFC-C6A6D713E61FQ51617108-C165E0FF-77AF-44B8-8EB8-E82A071BEBADQ51632103-43606410-55D1-43BE-822B-3056D92170DF
P2860
Hydroxymethylglutaryl CoA lyase deficiency: features resembling Reye syndrome.
description
1980 nî lūn-bûn
@nan
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
1980年论文
@zh
1980年论文
@zh-cn
name
Hydroxymethylglutaryl CoA lyase deficiency: features resembling Reye syndrome.
@en
type
label
Hydroxymethylglutaryl CoA lyase deficiency: features resembling Reye syndrome.
@en
prefLabel
Hydroxymethylglutaryl CoA lyase deficiency: features resembling Reye syndrome.
@en
P2093
P356
P1433
P1476
Hydroxymethylglutaryl CoA lyase deficiency: features resembling Reye syndrome.
@en
P2093
P304
P356
10.1212/WNL.30.7.714
P407
P433
P577
1980-07-01T00:00:00Z