Literature DB >> 4699429

Fetal movements and Werdnig-Hoffmann disease.

J H Pearn.   

Abstract

Entities:  

Mesh:

Year:  1973        PMID: 4699429     DOI: 10.1016/0022-510x(73)90132-9

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


× No keyword cloud information.
  5 in total

1.  An investigative journalist looks at medical ethics.

Authors:  D Campbell
Journal:  BMJ       Date:  1989-04-29

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.  Congenital myotonic dystrophy in Britain. I. Clinical aspects.

Authors:  P S Harper
Journal:  Arch Dis Child       Date:  1975-07       Impact factor: 3.791

4.  Genetic studies of acute infantile spinal muscular atrophy (SMA type I). An analysis of sex ratios, segregation ratios, and sex influence.

Authors:  J Pearn
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

5.  A case of congenital bilateral absence of elbow flexor muscles: review of differential diagnosis and treatment.

Authors:  David T Netscher; Oluseyi Aliu; Saleh Samra; Eric Lewis
Journal:  Hand (N Y)       Date:  2007-10-09
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.