Literature DB >> 5576061

[Biochemical, histological and clinical findings in a four-year-old female carrier of benign X-linked muscular dystrophy (Becker type)].

H Moser.   

Abstract

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Year:  1971        PMID： 5576061     DOI： 10.1007/bf00278661

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  19 in total

1.  MUSCLE LACTATE DEHYDROGENASE PATTERNS IN TWO TYPES OF X-LINKED MUSCULAR DYSTROPHY.

Authors:  C M PEARSON; N C KAR; J B PETER; T L MUNSAT
Journal:  Am J Med       Date:  1965-07       Impact factor: 4.965

2.  [PROGRESSIVE MUSCULAR DYSTROPHY. VI. INCIDENCE, CLINICAL ASPECTS AND GENETICS OF THE DUCHENNE TYPE].

Authors:  H MOSER; U WIESMANN; R RICHTERICH; E ROSSI
Journal:  Schweiz Med Wochenschr       Date:  1964-11-14

3.  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

4.  Survival in x-chromosomal muscular dystrophy.

Authors:  F E DREIFUSS; G R HOGAN
Journal:  Neurology       Date:  1961-08       Impact factor: 9.910

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

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

6.  Benign sex-linked muscular dystrophy. Clinical and pathological features.

Authors:  O N Markand; R R North; A N D'Agostino; D D Daly
Journal:  Neurology       Date:  1969-07       Impact factor: 9.910

7.  X-linked pseudohypertrophic muscular dystrophy with a late onset and slow progression.

Authors:  C C Mabry; I E Roeckel; R L Munich; D Robertson
Journal:  N Engl J Med       Date:  1965-11-11       Impact factor: 91.245

8.  Carrier detection in sex-linked muscular dystrophy.

Authors:  A E Emery
Journal:  J Genet Hum       Date:  1965-12

9.  Unusual type of benign x-linked muscular dystrophy.

Authors:  A E Emery; F E Dreifuss
Journal:  J Neurol Neurosurg Psychiatry       Date:  1966-08       Impact factor: 10.154

10.  [Detection of healthy carriers of the myopathic trait in human myopathy].

Authors:  J Demos
Journal:  Ann Genet       Date:  1969-09
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  2 in total

1.  Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.

Authors:  G K Suthers; J I Manson; L M Stern; E A Haan; J C Mulley
Journal:  J Med Genet       Date:  1989-04       Impact factor: 6.318

2.  Dystrophin immunohistochemistry in a symptomatic carrier of Becker muscular dystrophy.

Authors:  K Haginoya; K Yamamoto; K Iinuma; T Yanagisawa; Y Ichinohasama; M Shimmoto; Y Suzuki; K Tada
Journal:  J Neurol       Date:  1991-10       Impact factor: 4.849
  2 in total

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