Literature DB >> 6262513

Arachnodactyly with unusual neuromyopathic and skeletal abnormalities.

I G Barrison, D A Isenberg, S P Kane.   

Abstract

Entities:  

Mesh：

Year:  1980        PMID： 6262513      PMCID： PMC1440058          DOI： 10.1177/014107688007300116

Source DB:  PubMed          Journal:  J R Soc Med        ISSN： 0141-0768            Impact factor:   18.000


× No keyword cloud information.
  11 in total

1.  Skeletal syndromes associated with arachnodactyly.

Authors:  J G PARISH
Journal:  Proc R Soc Med       Date:  1960-07

2.  Skeletal abnormalities in homocystinuria.

Authors:  D P Brenton
Journal:  Postgrad Med J       Date:  1977-08       Impact factor: 2.401

3.  Myopathy associated with Marfan's syndrome. Fine structural and histochemical observations.

Authors:  H H Goebel; J Muller; W DeMyer
Journal:  Neurology       Date:  1973-12       Impact factor: 9.910

4.  Nemaline myopathy.

Authors:  P Hudgson; D Gardner-Medwin; J J Fulthorpe; J N Walton
Journal:  Neurology       Date:  1967-12       Impact factor: 9.910

5.  Camptodactyly: occurrence in two new genetic syndromes and its relationship to other syndromes.

Authors:  R M Goodman; M B Katznelson; E Manor
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

6.  Fronto-metaphyseal dysplasia. A progressive disease of bone and connective tissue.

Authors:  D M Danks; V Mayne; R K Hall; M C McKinnon
Journal:  Am J Dis Child       Date:  1972-03

7.  The marfanoid hypermobility syndrome.

Authors:  B A Walker; P H Beighton; J L Murdoch
Journal:  Ann Intern Med       Date:  1969-08       Impact factor: 25.391

8.  Congenital contractural arachnodactyly. A heritable disorder of connective tissue.

Authors:  R K Beals; F Hecht
Journal:  J Bone Joint Surg Am       Date:  1971-07       Impact factor: 5.284

9.  A new generalized connective tissue syndrome.

Authors:  P M Marden; W A Walker
Journal:  Am J Dis Child       Date:  1966-09

10.  Marfan's syndrome (arachnodactyly) with arthrogryposis (amyoplasia congenita).

Authors:  R REEVE; H K SILVER; P FERRIER
Journal:  AMA J Dis Child       Date:  1960-01
View more
  2 in total

1.  Muscle fibrillin deficiency in Marfan's syndrome myopathy.

Authors:  W M H Behan; C Longman; R K H Petty; P Comeglio; A H Child; M Boxer; P Foskett; D G F Harriman
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-05       Impact factor: 10.154

Review 2.  The association of hereditary neuropathies and heritable skeletal disorders.

Authors:  A K Chattopadhyay; R H Kandler; B Sharrack
Journal:  Postgrad Med J       Date:  1995-04       Impact factor: 2.401
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.