Literature DB >> 13636473

Serum aldolase in muscle disease.

R A THOMPSON, P J VIGNOS.   

Abstract

Entities:  

Keywords:  DESMOLASES/in blood; MUSCLES/diseases; NERVOUS SYSTEM/diseases

Mesh：

Substances：

Year:  1959        PMID： 13636473     DOI： 10.1001/archinte.1959.00270040037004

Source DB:  PubMed          Journal:  AMA Arch Intern Med        ISSN： 0888-2479


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  16 in total

1.  SERUM ENZYME STUDIES IN MUSCLE DISEASE. II. SERUM CREATINE KINASE ACTIVITY IN MUSCULAR DYSTROPHY AND IN OTHER MYOPATHIC AND NEUROPATHIC DISORDERS.

Authors:  J M PEARCE; R J PENNINGTON; J N WALTON
Journal:  J Neurol Neurosurg Psychiatry       Date:  1964-04       Impact factor: 10.154

2.  [CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. I. SERUM ENZYMES IN PROGRESSIVE MUSCULAR DYSTROPHY (TYPE I, II, IIIA)].

Authors:  H W ROTTHAUWE; S KOWALEWSKI
Journal:  Klin Wochenschr       Date:  1965-02-01

3.  Sources of error in the biochemical diagnosis of muscular dystrophy.

Authors:  W A THOMSON
Journal:  J Neurol Neurosurg Psychiatry       Date:  1962-08       Impact factor: 10.154

4.  [Enzyme activity determinations in healthy human musculature and in myopathies. II. Enzyme activity changes in muscle in progressive muscular dystrophy].

Authors:  H HEYCK; G LAUDAHN; C J LUDERS
Journal:  Klin Wochenschr       Date:  1963-05-15

5.  Serum enzyme changes in muscle disease and their relation to tissue change.

Authors:  B P HUGHES
Journal:  Proc R Soc Med       Date:  1963-03

6.  [Progressive muscular dystrophy. I. The heterogenicity of serum lactic dehydrgenase].

Authors:  R RICHTERICH; E GAUTIER; W EGLI; K ZUPPINGER; E ROSSI
Journal:  Klin Wochenschr       Date:  1961-04-01

7.  Serum enzyme activity in muscular dystrophy.

Authors:  W H THOMSON; P LEYBURN; J N WALTON
Journal:  Br Med J       Date:  1960-10-29

8.  Myopathy in a 20-year-old female patient with D4ST-1 deficient Ehlers-Danlos syndrome due to a homozygous CHST14 mutation.

Authors:  N C Voermans; M Kempers; M Lammens; N van Alfen; M C Janssen; C Bönnemann; B G van Engelen; B C Hamel
Journal:  Am J Med Genet A       Date:  2012-03-09       Impact factor: 2.802

9.  Progressive Muscular Dystrophy. V. The Identification of the Carrier State in the Duchenne Type by Serum Creatine Kinase Determination.

Authors:  R Richterich; S Rosin; U Aebi; E Rossi
Journal:  Am J Hum Genet       Date:  1963-06       Impact factor: 11.025

10.  Some Biochemical Aspects of the Myopathies.

Authors:  B P Hughes
Journal:  Postgrad Med J       Date:  1965-06       Impact factor: 2.401
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