Literature DB >> 14259214

A FAMILY STUDY OF PHOSPHORYLASE DEFICIENCY IN MUSCLE.

R B TOBIN, W A COLEMAN.   

Abstract

Entities:  

Keywords:  ADOLESCENCE; BLOOD CHEMICAL ANALYSIS; CHILD; EXERTION; GENETICS, HUMAN; GLYCOGENOSIS; HYDROGEN-ION CONCENTRATION; LACTATES; MUSCULAR DISEASES; MYOGLOBINURIA; PHOSPHOTRANSFERASES; PYRUVATES

Mesh：

Substances：

Year:  1965        PMID： 14259214     DOI： 10.7326/0003-4819-62-2-313

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN： 0003-4819            Impact factor:   25.391


× No keyword cloud information.
  6 in total

1.  McArdle's syndrome: a review and a preliminary report of four further cases.

Authors:  R H Salter
Journal:  Postgrad Med J       Date:  1967-05       Impact factor: 2.401

2.  Endogenous prostaglandins as local regulators of blood flow in man: effect of indomethacin on reactive and functional hyperaemia.

Authors:  A Kilbom; A Wennmalm
Journal:  J Physiol       Date:  1976-05       Impact factor: 5.182

3.  McArdle's syndrome.

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

4.  Myoglobinuria and skeletal muscle phosphorylase deficiency: report of a case of McArdle's disease.

Authors:  J C Nixon; W K Hobbs; J Greenblatt
Journal:  Can Med Assoc J       Date:  1966-05-07       Impact factor: 8.262

5.  Normal pregnancy and successful delivery in myophosphorylase deficiency (McArdle's disease).

Authors:  P Cochrane; B Alderman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1973-04       Impact factor: 10.154

6.  [McArdle's syndrome (myopathy in muscle phosphorylase deficiency)].

Authors:  K Schimrigk; H G Mertens; K Ricker; J Führ; P Eyer; D Pette
Journal:  Klin Wochenschr       Date:  1967-01-01
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.