Literature DB >> 14248444

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

K M WILSON, K A EVANS, C O CARTER.   

Abstract

Entities:  

Keywords:  CREATINE KINASE; ENZYME TESTS; EXERTION; GENES; GENETICS, HUMAN; MUSCULAR DYSTROPHY; WOMEN

Mesh:

Substances:

Year:  1965        PMID: 14248444      PMCID: PMC2166169          DOI: 10.1136/bmj.1.5437.750

Source DB:  PubMed          Journal:  Br Med J        ISSN: 0007-1447


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  7 in total

1.  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

2.  [Technique for the determination of creatine phosphokinase in blood].

Authors:  J C DREYFUS; G SCHAPIRA
Journal:  Rev Fr Etud Clin Biol       Date:  1961 Aug-Sep

3.  An investigation of the carrier state in the Duchenne type muscular dystrophy.

Authors:  P LEYBURN; W H THOMSON; J N WALTON
Journal:  Ann Hum Genet       Date:  1961-05       Impact factor: 1.670

4.  Serum enzymes and genetic carriers in muscular dystrophy.

Authors:  C S CHUNG; N E MORTON; H A PETERS
Journal:  Am J Hum Genet       Date:  1960-03       Impact factor: 11.025

5.  Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance.

Authors:  H BLYTH; R J PUGH
Journal:  Ann Hum Genet       Date:  1959-04       Impact factor: 1.670

6.  Serum enzymes in carriers of muscular dystrophy.

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

7.  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

  7 in total
  26 in total

1.  The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.

Authors:  R Skinner; A E Emery; A J Anderson; C Foxall
Journal:  J Med Genet       Date:  1975-06       Impact factor: 6.318

2.  Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio.

Authors:  A Westwood; D N Raine
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

3.  Useful probability considerations in genetics: the goat problem with tigers and other applications of Bayes' theorem.

Authors:  Konrad Oexle
Journal:  Eur J Pediatr       Date:  2006-02-07       Impact factor: 3.183

4.  Some Biochemical Aspects of the Myopathies.

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

5.  Genetic counselling and the physician.

Authors:  F C Fraser
Journal:  Can Med Assoc J       Date:  1968-11-16       Impact factor: 8.262

6.  [Creatine phosphokinase activity in serum of carriers of progressive muscular dystrophy of Duchenne type].

Authors:  W Barthelmai; G Dikbas; S Wüllner
Journal:  Humangenetik       Date:  1969-10

7.  [Diagnosis of female carriers of Duchenne's progressive muscular dystrophy using discriminative analysis of various serum enzyme activities].

Authors:  C M Büsing; H Heyck; G Laudahn
Journal:  Klin Wochenschr       Date:  1969-10-15

8.  Use of creatine kinase for detecting severe X-linked muscular dystrophy carriers.

Authors:  N R Dennis; K Evans; B Clayton; C O Carter
Journal:  Br Med J       Date:  1976-09-04

9.  Quantitative electromyography in the detection of the carriers in Duchenne type muscular dystrophy.

Authors:  G Valli; G Scarlato; M Contartese
Journal:  J Neurol       Date:  1976-04-23       Impact factor: 4.849

10.  Serum creatine kinase levels in pubertal, mature, pregnant, and postmenopausal women.

Authors:  S Bundey; J M Crawley; J H Edwards; R A Westhead
Journal:  J Med Genet       Date:  1979-04       Impact factor: 6.318

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