Literature DB >> 14258512

[CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. 3. RECESSIVE X-CHROMOSOMAL MUSCULAR DYSTROPHY WITH RELATIVELY BENIGN COURSE].

H W ROTTHAUWE, S KOWALEWSKI.   

Abstract

Entities:  

Keywords:  ADOLESCENCE; ALANINE AMINOTRANSFERASE; ALDOLASE; ASPARTATE AMINOTRANSFERASE; BLOOD CHEMICAL ANALYSIS; CHILD; CHROMOSOMES; CREATINE KINASE; ENZYME TESTS; LACTATE DEHYDROGENASE; MUSCULAR DYSTROPHY

Mesh：

Substances：

Year:  1965        PMID： 14258512     DOI： 10.1007/BF01484508

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN： 0023-2173


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  12 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.  [Progressive muscular dystrophy. III. Serum enzymes in muscular dystrophy in childhood].

Authors:  U AEBI; R RICHTERICH; H STILLHART; J P COLOMBO; E ROSSI
Journal:  Helv Paediatr Acta       Date:  1961-12

3.  Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance.

Authors:  V DUBOWITZ
Journal:  Brain       Date:  1960-09       Impact factor: 13.501

4.  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

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.  Formal genetics of muscular dystrophy.

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

7.  [A new x-chromosomal muscular dystrophy].

Authors:  P E BECKER; F KIENER
Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr       Date:  1955

8.  On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies.

Authors:  J N WALTON; R R RACE; U PHILIP
Journal:  Ann Hum Genet       Date:  1955-08       Impact factor: 1.670

9.  [Estimation of mutation rate in muscular dystrophy].

Authors:  P E BECKER; F LENZ
Journal:  Z Mensch Vererb Konstitutionsl       Date:  1955

10.  On the classification, natural history and treatment of the myopathies.

Authors:  J N WALTON; F J NATTRASS
Journal:  Brain       Date:  1954       Impact factor: 13.501
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  5 in total

Review 1.  [New data on the genetics and classification of muscular dystrophies].

Authors:  P E Becker
Journal:  Humangenetik       Date:  1972

2.  [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

3.  [Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy].

Authors:  H Radu; K Stenzel
Journal:  Dtsch Z Nervenheilkd       Date:  1969

4.  [A benign recessiv X-chromosomal hereditary muscular dystrophy. II. Examinations of female carriers].

Authors:  H W Rotthauwe; S Kowalewski
Journal:  Humangenetik       Date:  1966

5.  [Enzyme activity determination in progressive muscular dystrophy. IV. Serum enzymatic kinetics in the preclinical stage of the Duchenne type during the 1st 2 years of life].

Authors:  H Heyck; G Laudahn; P M Carsten
Journal:  Klin Wochenschr       Date:  1966-06-15
  5 in total

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