Literature DB >> 4755211

Editorial: Diagnosis of childhood spinal muscular atrophy.

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Year:  1973        PMID: 4755211      PMCID: PMC1587093          DOI: 10.1136/bmj.4.5883.2

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


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  10 in total

1.  Infantile muscular atrophy.

Authors:  R K BYERS; B Q BANKER
Journal:  Arch Neurol       Date:  1961-08

2.  INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY.

Authors:  V DUBOWITZ
Journal:  Brain       Date:  1964-12       Impact factor: 13.501

3.  Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.

Authors:  E KUGELBERG; L WELANDER
Journal:  AMA Arch Neurol Psychiatry       Date:  1956-05

4.  Spinal muscular atrophy in childhood. Two clues to clinical diagnosis.

Authors:  A Moosa; V Dubowitz
Journal:  Arch Dis Child       Date:  1973-05       Impact factor: 3.791

5.  Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease.

Authors:  T L Munsat; R Woods; W Fowler; C M Pearson
Journal:  Brain       Date:  1969-03       Impact factor: 13.501

6.  The benign proximal spinal progressive muscular atrophies.

Authors:  H A Peters; J M Opitz; I Goto; H H Reese
Journal:  Acta Neurol Scand       Date:  1968       Impact factor: 3.209

7.  "Myopathic" changes in chronically denervated muscle.

Authors:  D B Drachman; S R Murphy; M P Nigam; J R Hills
Journal:  Arch Neurol       Date:  1967-01

8.  Benign spinal muscular atrophy arising in childhood and adolescence.

Authors:  D Gardner-Medwin; P Hudgson; J N Walton
Journal:  J Neurol Sci       Date:  1967 Jul-Aug       Impact factor: 3.181

9.  Microcephaly and mental subnormalitiy in chronic progressive spinal muscular atrophy of childhood.

Authors:  A J Spiro; M H Fogelson; A C Goldberg
Journal:  Dev Med Child Neurol       Date:  1967-10       Impact factor: 5.449

10.  Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease).

Authors:  K Fried; A E Emery
Journal:  Clin Genet       Date:  1971       Impact factor: 4.438

  10 in total

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