Literature DB >> 4176659

Arthrogryposis multiplex congenita. Report of two cases of a radicular type with familial incidence.

C E Peña, F Miller, G N Budzilovich, I Feigin.   

Abstract

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Year:  1968        PMID： 4176659     DOI： 10.1212/wnl.18.9.926

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  4 in total

1.  A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.

Authors:  M Shohat; R Lotan; N Magal; T Shohat; N Fischel-Ghodsian; J I Rotter; L Jaber
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

2.  Arthrogryposis multiplex congenita: neurogenic type with autosomal recessive inheritance.

Authors:  A Rosenmann; I Arad
Journal:  J Med Genet       Date:  1974-03       Impact factor: 6.318

3.  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

4.  Werdnig-Hoffmann disease: proposal of a pathogenetic mechanism.

Authors:  S M Chou; I Nonaka
Journal:  Acta Neuropathol       Date:  1978-01-19       Impact factor: 17.088
  4 in total

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