Literature DB >> 13532688

Cerebral lesions in arthrogryposis multiplex congenita.

J I EK.   

Abstract

Entities:  

Keywords:  BRAIN/diseases; JOINTS/abnormalities

Mesh：

Year:  1958        PMID： 13532688     DOI： 10.1111/j.1651-2227.1958.tb07887.x

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN： 0365-1436            Impact factor:   2.299


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  6 in total

1.  A case of arthrogryposis multiplex congenita with lesions in the nervous system.

Authors:  M FOWLER
Journal:  Arch Dis Child       Date:  1959-12       Impact factor: 3.791

2.  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

3.  [The arthrogrypotic syndrome].

Authors:  H Radu; K Stenzel; M Bene; Z Török; S Migea; L Bordeianu; A Osvath
Journal:  Dtsch Z Nervenheilkd       Date:  1968

4.  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

5.  [Significance of dermatoglyphics and skin grooves in the diagnosis of arthromyogryposis multiplex congenita].

Authors:  W Hirsch; D Tönnis
Journal:  Arch Orthop Unfallchir       Date:  1971

6.  The syndrome of multiple ankyloses and facial anomalies. A neuropathologic analysis.

Authors:  R S Williams; L B Holmes
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088
  6 in total

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