Literature DB >> 13427576

[Nosological position of so-called scapulo-peroneal syndrome].

D SEITZ.   

Abstract

Entities:  

Keywords:  MUSCLES/diseases

Mesh：

Year:  1957        PMID： 13427576

Source DB:  PubMed          Journal:  Dtsch Z Nervenheilkd        ISSN： 0367-004X


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  1 in total

1.  Myopathia distalis tarda hereditaria; 249 examined cases in 72 pedigrees.

Authors:  L WELANDER
Journal:  Acta Med Scand Suppl       Date:  1951
  1 in total
  10 in total

1.  [FAMILIAL SCAPULOPERONEAL MUSCULAR ATROPHY].

Authors:  H E KAESER
Journal:  Dtsch Z Nervenheilkd       Date:  1964-11-25

2.  [On the nosological role of the scapulo-peroneal syndrome].

Authors:  I HAUSMANOWA-PETRUSEWICZ; S ZIELINSKA
Journal:  Dtsch Z Nervenheilkd       Date:  1962

3.  [An unusual muscular affection manifested by extensive contractures; also a contribution on the differential diagnosis of primary muscle diseases].

Authors:  D SEITZ
Journal:  Dtsch Z Nervenheilkd       Date:  1958

4.  X-linked scapuloperoneal syndrome.

Authors:  P K Thomas; D B Calne; C F Elliott
Journal:  J Neurol Neurosurg Psychiatry       Date:  1972-04       Impact factor: 10.154

5.  [New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias].

Authors:  H W Rotthauwe; W Mortier; H Beyer
Journal:  Humangenetik       Date:  1972

6.  Neurogenic scapuloperoneal syndrome in childhood.

Authors:  R Mercelis; J Demeester; J J Martin
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-10       Impact factor: 10.154

7.  The differential diagnosis of scapuloperoneal amyotrophy.

Authors:  G Spalke; H Hökendorf; P von Roques
Journal:  J Neurol       Date:  1976-06-14       Impact factor: 4.849

8.  Scapuloperoneal syndrome with cardiomyopathy: report of a family with autosomal dominant inheritance and unusual features.

Authors:  A Chakrabarti; J M Pearce
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-12       Impact factor: 10.154

9.  Adult onset scapuloperoneal myopathy: diagnostic value of nerve morphometry and multiple muscle biopsies.

Authors:  W C Yee; A F Hahn; J J Gilbert
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-06       Impact factor: 10.154

10.  The course of a model cutaneous inflammation in the scapuloperoneal syndrome and in systemic neuromuscular diseases.

Authors:  K Urbánek; P jansa; L Steidl; D Jandová
Journal:  J Neurol       Date:  1974       Impact factor: 4.849
  10 in total

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