Mitochondrial myopathy and familial thiamine deficiency.
about
Thiamin uptake by the human-derived renal epithelial (HEK-293) cells: cellular and molecular mechanismsCan long-term thiamine treatment improve the clinical outcomes of myotonic dystrophy type 1?Treatment of central nervous system manifestations in mitochondrial disorders.Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.Therapies for mitochondrial diseases and current clinical trials.
P2860
Mitochondrial myopathy and familial thiamine deficiency.
description
2000 nî lūn-bûn
@nan
2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Mitochondrial myopathy and familial thiamine deficiency.
@ast
Mitochondrial myopathy and familial thiamine deficiency.
@en
type
label
Mitochondrial myopathy and familial thiamine deficiency.
@ast
Mitochondrial myopathy and familial thiamine deficiency.
@en
prefLabel
Mitochondrial myopathy and familial thiamine deficiency.
@ast
Mitochondrial myopathy and familial thiamine deficiency.
@en
P2093
P2860
P1433
P1476
Mitochondrial myopathy and familial thiamine deficiency.
@en
P2093
P2860
P304
P356
10.1002/1097-4598(200007)23:7<1069::AID-MUS9>3.0.CO;2-0
P577
2000-07-01T00:00:00Z