Literature DB >> 5491443

Arthrogryposis multiplex congenita: twenty-three cases in an Arab kindred.

E Lebenthal, S B Shochet, A Adam, M Seelenfreund, A Fried, T Najenson, U Sandbank, Y Matoth.   

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Year:  1970        PMID： 5491443

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  9 in total

1.  Anesthesia for arthrogryposis multiplex congenita--report of 12 cases.

Authors:  Y Oda; H Yukioka; M Fujimori
Journal:  J Anesth       Date:  1990-07       Impact factor: 2.078

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.  Anaesthesia in arthrogryposis multiplex congenita: case report.

Authors:  G S Oberoi; H L Kaul; I S Gill; R K Batra
Journal:  Can J Anaesth       Date:  1987-05       Impact factor: 5.063

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.  [Electromyographical and histological changes in arthrogryposis (author's transl)].

Authors:  L Kullmann; E Szijj
Journal:  Arch Orthop Unfallchir       Date:  1973

6.  A zebrafish model of lethal congenital contracture syndrome 1 reveals Gle1 function in spinal neural precursor survival and motor axon arborization.

Authors:  Li-En Jao; Bruce Appel; Susan R Wente
Journal:  Development       Date:  2012-02-22       Impact factor: 6.868

7.  Ultrastructural abnormalities of muscle and neuromuscular junction differentiation in a bovine congenital neuromuscular disease.

Authors:  R G Russell; F T Oteruelo
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

8.  Arthrogryposis-like signs in trisomy 18.

Authors:  J C Lambert; M Ferrari; M Donzeau; N Ayraud; W Chiaramello; R Mariani
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Bi-allelic loss of ERGIC1 causes relatively mild arthrogryposis.

Authors:  Caterina Marconi; Laure Lemmens; Frédéric Masclaux; Francesca Mattioli; Joël Fluss; Philippe Extermann; Purificacion Mendez; Russia Ha-Vinh Leuchter; Elissavet Stathaki; Sacha Laurent; Eva Hammar; Anne Vannier; Konstantinos Varvagiannis; Michel Guipponi; Frédérique Sloan-Bena; Jean-Louis Blouin; Marc Abramowicz; Siv Fokstuen
Journal:  Clin Genet       Date:  2021-06-14       Impact factor: 4.438
  9 in total

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