Literature DB >> 13810211

Serum enzymes and genetic carriers in muscular dystrophy.

C S CHUNG, N E MORTON, H A PETERS.   

Abstract

Entities:  

Keywords:  ENZYMES/blood; MUSCULAR DYSTROPHY

Mesh:

Substances:

Year:  1960        PMID: 13810211      PMCID: PMC1932054     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  23 in total

1.  Glycogenolytic enzymes in human progressive muscular dystrophy.

Authors:  G SCHAPIRA; J C DREYFUS; F SCHAPIRA; J KRUH
Journal:  Am J Phys Med       Date:  1955-02

2.  Genetic tests under incomplete ascertainment.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1959-03       Impact factor: 11.025

3.  Discrimination of genetic entities in muscular dystrophy.

Authors:  C S CHUNG; N E MORTON
Journal:  Am J Hum Genet       Date:  1959-12       Impact factor: 11.025

4.  Glutamic oxalacetic transaminase activity in the serum in muscular dystrophy and other neuromuscular disorders in childhood.

Authors:  E G MURPHY; M M CHERNIAK
Journal:  Pediatrics       Date:  1958-12       Impact factor: 7.124

5.  [Not Available].

Authors:  J C DREYFUS; G SCHAPIRA
Journal:  C R Seances Soc Biol Fil       Date:  1955-11

6.  Gradients of functional ability of importance in rehabilitation of patients with progressive muscular and neuromuscular diseases.

Authors:  C A SWINYARD; G G DEAVER; L GREENSPAN
Journal:  Arch Phys Med Rehabil       Date:  1957-09       Impact factor: 3.966

7.  The clinical significance of serum aldolase.

Authors:  J A SIBLEY; G A FLEISHER
Journal:  Proc Staff Meet Mayo Clin       Date:  1954-11-10

8.  The quantitative histochemistry of brain. II. Enzyme measurements.

Authors:  O H LOWRY; N R ROBERTS; M L WU; W S HIXON; E J CRAWFORD
Journal:  J Biol Chem       Date:  1954-03       Impact factor: 5.157

9.  [Determination and properties of the serumaldolase].

Authors:  F BRUNS
Journal:  Biochem Z       Date:  1954

10.  Serum enzymes; variations of activity in disease of muscle.

Authors:  L P WHITE
Journal:  Calif Med       Date:  1959-01
View more
  22 in total

1.  SERUM ENZYME STUDIES IN MUSCLE DISEASE. III. SERUM CREATINE KINASE ACTIVITY IN RELATIVES OF PATIENTS WITH THE DUCHENNE TYPE OF MUSCULAR DYSTROPHY.

Authors:  J M PEARCE; R J PENNINGTON; J N WALTON
Journal:  J Neurol Neurosurg Psychiatry       Date:  1964-06       Impact factor: 10.154

2.  SERUM ENZYME STUDIES IN MUSCLE DISEASE. I. VARIATIONS IN SERUM CREATINE KINASE ACTIVITY IN NORMAL INDIVIDUALS.

Authors:  J M PEARCE; R J PENNINGTON; J N WALTON
Journal:  J Neurol Neurosurg Psychiatry       Date:  1964-02       Impact factor: 10.154

3.  CREATINE KINASE LEVELS IN WOMEN WHO CARRY GENES FOR THREE TYPES OF MUSCULAR DYSTROPHY.

Authors:  K M WILSON; K A EVANS; C O CARTER
Journal:  Br Med J       Date:  1965-03-20

4.  Aldolase activity in the plasma or serum of normal children and families with muscular dystrophy.

Authors:  B E CLAYTON; K M WILSON; C O CARTER
Journal:  Arch Dis Child       Date:  1963-06       Impact factor: 3.791

5.  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

6.  X-chromosome mosaicism in females with muscular dystrophy.

Authors:  C M PEARSON; W M FOWLER; S W WRIGHT
Journal:  Proc Natl Acad Sci U S A       Date:  1963-07       Impact factor: 11.205

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

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

8.  The identification of carriers in Duchenne muscular dystrophy.

Authors:  G MONCKTON; B LUDVIGSEN
Journal:  Can Med Assoc J       Date:  1963-08-24       Impact factor: 8.262

9.  [Biochemistry of progressive muscular dystrophy].

Authors:  J C DREYFUS; G SCHAPIRA
Journal:  Klin Wochenschr       Date:  1962-04-15

10.  Serum enzymes in carriers of muscular dystrophy.

Authors:  B P HUGHES
Journal:  Br Med J       Date:  1962-10-13
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.