Literature DB >> 5235736

McArdle's syndrome (myophosphorylase deficiency). A study of a family.

R H Salter, D G Adamson, G W Pearce.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1967        PMID： 5235736

Source DB:  PubMed          Journal:  Q J Med        ISSN： 0033-5622


× No keyword cloud information.
  6 in total

1.  Steroid myopathy complicating McArdle's disease.

Authors:  F L Mastaglia; J P McCollum; P F Larson; P Hudgson
Journal:  J Neurol Neurosurg Psychiatry       Date:  1970-02       Impact factor: 10.154

2.  Acute renal failure complicating McArdle's syndrome.

Authors:  P M Ford; A A Manugian; W R Weir
Journal:  Postgrad Med J       Date:  1973-12       Impact factor: 2.401

3.  McArdle's syndrome.

Authors: 
Journal:  Br Med J       Date:  1968-06-15

Review 4.  The glycogen storage diseases.

Authors:  B E Ryman
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

5.  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

6.  McArdle's syndrome. Fine structural changes in muscle.

Authors:  A Korényi-Both; B H Smith; J K Baruah
Journal:  Acta Neuropathol       Date:  1977-09-26       Impact factor: 17.088
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.