Literature DB >> 572128

Becker's x-linked muscular dystrophy. Histological, enzyme-histochemical, and ultrastructural studies of two cases, originally reported by Becker.

H H Goebel, H Prange, F Gullotta, H Kiefer, M Z Jones.   

Abstract

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Year:  1979        PMID： 572128     DOI： 10.1007/bf00684807

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN： 0001-6322            Impact factor:   17.088


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  10 in total

1.  Two families of benign sex-linked recessive muscular dystrophy.

Authors:  P E BECKER
Journal:  Rev Can Biol       Date:  1962 Sep-Dec

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

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

3.  The spectrum of mild X-linked recessive muscular dystrophy.

Authors:  S P Ringel; J E Carroll; S C Schold
Journal:  Arch Neurol       Date:  1977-07

4.  Data on the distribution of fibre types in thirty-six human muscles. An autopsy study.

Authors:  M A Johnson; J Polgar; D Weightman; D Appleton
Journal:  J Neurol Sci       Date:  1973-01       Impact factor: 3.181

5.  Proximal neurogenic muscular atrophy in adolescence and adulthood with X-linked recessive inheritance. Kugelberg-Welander disease and its variant of late onset in one pedigree.

Authors:  H Tsukagoshi; H Shoji; T Furukawa
Journal:  Neurology       Date:  1970-12       Impact factor: 9.910

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.  Sex-linked form of Kugelberg-Welander syndrome.

Authors:  G W Paulson; L Liss; P J Sweeney
Journal:  Trans Am Neurol Assoc       Date:  1977

8.  [A benign X-chromosomal hereditary muscular dystrophy. I. Examinations of symptom-carriers].

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

9.  Becker-type muscular dystrophy.

Authors:  W G Bradley; M Z Jones; J M Mussini; P R Fawcett
Journal:  Muscle Nerve       Date:  1978 Mar-Apr       Impact factor: 3.217

10.  Anterior-horn cell degeneration and gross calf hypertrophy with adolescent onset. A new spinal muscular atrophy syndrome.

Authors:  J Pearn; P Hudgson
Journal:  Lancet       Date:  1978-05-20       Impact factor: 79.321
  10 in total
  7 in total

1.  Hearing loss in facioscapulohumeral dystrophy.

Authors:  T Voit; A Lamprecht; H G Lenard; H H Goebel
Journal:  Eur J Pediatr       Date:  1986-09       Impact factor: 3.183

2.  Fetal congenital lethal hypophosphatasia: histochemical absence of alkaline phosphatase activity in endothelial cells of intramuscular capillaries.

Authors:  H H Goebel; M Schlie; U Burck
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

3.  Ultrastructural studies on the neuromuscular junctions of Becker's muscular dystrophy.

Authors:  N Fukuhara; M Suzuki; T Tsubaki; S Kushiro; N Takasawa
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

4.  DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases.

Authors:  J C Defesche; M de Vissar; E Bakker; G Bouwsma; J J de Vijlder; P A Bolhuis
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

5.  Neuropathologic and morphometric studies in hereditary motor and sensory neuropathy type II with neurofilament accumulation.

Authors:  H H Goebel; P Vogel; M Gabriel
Journal:  Ital J Neurol Sci       Date:  1986-06

6.  Childhood neuromuscular disease with rimmed vacuoles.

Authors:  H H Goebel; S von Loh; J Gehler
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

7.  Myoadenylate deaminase deficiency.

Authors:  H H Goebel; A Bardosi; B Conrad; H D Kuhlendahl; S DiMauro; K W Rumpf
Journal:  Klin Wochenschr       Date:  1986-04-01
  7 in total

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