Literature DB >> 5801822

Heritable spinal muscular atrophies.

H Zellweger, H J Schneider, D R Schuldt, W Mergner.   

Abstract

Entities:  

Mesh：

Year:  1969        PMID： 5801822

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN： 0018-022X


× No keyword cloud information.
  7 in total

1.  Anterior horn cell disease associated with pontocerebellar hypoplasia in infants.

Authors:  F Goutières; J Aicardi; E Farkas
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-04       Impact factor: 10.154

2.  Chronic generalized spinal muscular atrophy of infancy and childhood. Arrested Werdnig-Hoffman disease.

Authors:  J H Pearn; J Wilson
Journal:  Arch Dis Child       Date:  1973-10       Impact factor: 3.791

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

Authors:  H Zellweger; E Hanhart; H J Schneider
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

4.  Genetics of childhood spinal muscular atrophy.

Authors:  E J Winsor; E G Murphy; M W Thompson; T E Reed
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

5.  Genetic investigations on chronic forms of infantile and juvenile spinal muscular atrophy.

Authors:  I Hausmanowa-Petrusewicz; J Zaremba; J Borkowska; J Prot
Journal:  J Neurol       Date:  1976-10-04       Impact factor: 4.849

Review 6.  The nosology of the spinal muscular atrophies.

Authors:  A E Emery
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

7.  Chronic spinal muscular atrophy of facioscapulohumeral type.

Authors:  T Furukawa; Y Toyokura
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.