A biochemical study of certain skeletal muscle constituents in human progressive muscular dystrophy.
about
Attempting to Compensate for Reduced Neuronal Nitric Oxide Synthase Protein with Nitrate Supplementation Cannot Overcome Metabolic Dysfunction but Rather Has Detrimental Effects in Dystrophin-Deficient mdx Muscle.Serum enzyme changes in muscle disease and their relation to tissue changeAlpha-hydroxybutyrate dehydrogenase activity in sex-linked muscular dystrophySome Biochemical Aspects of the Myopathies.Therapeutic strategies to address neuronal nitric oxide synthase deficiency and the loss of nitric oxide bioavailability in Duchenne Muscular Dystrophy.STUDIES OF MYOSIN IN HEREDITARY MUSCULAR DYSTROPHY IN MICE.Reduced cytosolic acidification during exercise suggests defective glycolytic activity in skeletal muscle of patients with Becker muscular dystrophy. An in vivo 31P magnetic resonance spectroscopy study.
P2860
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P2860
A biochemical study of certain skeletal muscle constituents in human progressive muscular dystrophy.
description
1959 nî lūn-bûn
@nan
1959年の論文
@ja
1959年論文
@yue
1959年論文
@zh-hant
1959年論文
@zh-hk
1959年論文
@zh-mo
1959年論文
@zh-tw
1959年论文
@wuu
1959年论文
@zh
1959年论文
@zh-cn
name
A biochemical study of certain ...... rogressive muscular dystrophy.
@en
type
label
A biochemical study of certain ...... rogressive muscular dystrophy.
@en
prefLabel
A biochemical study of certain ...... rogressive muscular dystrophy.
@en
P2860
P356
P1476
A biochemical study of certain ...... rogressive muscular dystrophy.
@en
P2093
LEFKOWITZ M
VIGNOS PJ Jr
P2860
P304
P356
10.1172/JCI103869
P407
P577
1959-06-01T00:00:00Z