Literature DB >> 5215287

The clinical diagnosis of McArdle's disease. Identification of another family with deficiency of muscle phosphorylase.

L P Rowland, R E Lovelace, D L Schotland, S Araki, P Carmel.   

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Year:  1966        PMID： 5215287     DOI： 10.1212/wnl.16.1.93

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  4 in total

Review 1.  Metabolic myopathy.

Authors:  P K Thomas
Journal:  Postgrad Med J       Date:  1967-02       Impact factor: 2.401

2.  Contracture of phosphorylase deficient muscle.

Authors:  R Gruener; B McArdle; B E Ryman; R O Weller
Journal:  J Neurol Neurosurg Psychiatry       Date:  1968-06       Impact factor: 10.154

3.  Chronic fatigue and myalgia syndrome: mitochondrial and glycolytic studies in skeletal muscle.

Authors:  E Byrne; I Trounce
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-06       Impact factor: 10.154

4.  Myophosphorylase deficiency (McArdle's disease) in two interrelated families.

Authors:  P Cochrane; R R Hughes; P H Buxton; R A Yorke
Journal:  J Neurol Neurosurg Psychiatry       Date:  1973-04       Impact factor: 10.154
  4 in total

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