Literature DB >> 4646546

A new genetic variant of the spinal muscular atrophies in infancy.

H Zellweger, E Hanhart, H J Schneider.   

Abstract

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Year:  1972        PMID： 4646546      PMCID： PMC1469055          DOI： 10.1136/jmg.9.4.401

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  8 in total

1.  [Late manifestations with protracted course in Werdnig-Hoffmann's spinal muscular atrophy (with familial aspects)].

Authors:  J K KIRCHHOF; K KUMRAL; S FADILOGLU
Journal:  Nervenarzt       Date:  1962-10       Impact factor: 1.214

2.  Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.

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

3.  Hereditary proximal spinal muscular atrophy, a clinical entity simulating progressive muscular dystrophy.

Authors:  G WOHLFART; J FEX; S ELIASSON
Journal:  Acta Psychiatr Neurol Scand       Date:  1955

4.  [Forty cases of Werdnig-Hoffmann disease with eleven anatomical examinations].

Authors:  S THIEFFRY; M ARTHUIS; E BARGETON
Journal:  Rev Neurol (Paris)       Date:  1955-10       Impact factor: 2.607

5.  An unusual inheritane pattern for spinal muscular atrophy.

Authors:  N R White; M E Blaw
Journal:  Dev Med Child Neurol       Date:  1971-10       Impact factor: 5.449

6.  A new genetic variant of spinal muscular atrophy.

Authors:  H Zellweger; H Schneider; D R Schuldt
Journal:  Neurology       Date:  1969-09       Impact factor: 9.910

7.  Heritable spinal muscular atrophies.

Authors:  H Zellweger; H J Schneider; D R Schuldt; W Mergner
Journal:  Helv Paediatr Acta       Date:  1969-02

8.  The genetic heterogeneity of spinal muscular atrophy (SMA).

Authors:  H Zellweger
Journal:  Birth Defects Orig Artic Ser       Date:  1971-02
  8 in total
  4 in total

1.  Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive syndrome?

Authors:  F C Fraser; T Gunn
Journal:  J Med Genet       Date:  1977-06       Impact factor: 6.318

2.  The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England.

Authors:  J H Pearn
Journal:  J Med Genet       Date:  1973-09       Impact factor: 6.318

3.  Nephrogenic diabetes insipidus and Werdnig-Hoffmann disease in a child: an unusual association.

Authors:  S Bernasconi; C Pezzani; P Balestrazzi; A Marbini
Journal:  J Med Genet       Date:  1978-06       Impact factor: 6.318

4.  Hereditary distal spinal muscular atrophy with vocal cord paralysis.

Authors:  I D Young; P S Harper
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-05       Impact factor: 10.154
  4 in total

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