Literature DB >> 14824970

Hallervorden-Spatz disease and dystonia.

M G NETSKY, D SPIRO, H M ZIMMERMAN.   

Abstract

Entities:  

Keywords:  DYSTONIA MUSCULORUM DEFORMANS; EXTRAPYRAMIDAL TRACT

Mesh:

Year:  1951        PMID: 14824970     DOI: 10.1097/00005072-195104000-00002

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


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  8 in total

1.  Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life.

Authors:  L Angelini; N Nardocci; V Rumi; C Zorzi; L Strada; M Savoiardo
Journal:  J Neurol       Date:  1992-10       Impact factor: 4.849

2.  [HALLERVORDEN-SPATZ DISEASE. DISCUSSION OF THE PATHOLOGIC-ANATOMIC FINDINGS BASED ON A CASE PERSONALLY CONFIRMED BY AUTOPSY].

Authors:  A BISCHOFF; F REGLI
Journal:  Arch Psychiatr Nervenkr       Date:  1963-12-03

3.  [Hallervorden-Spatz' disease].

Authors:  K SCHARENBERG; R DE JONG
Journal:  Dtsch Z Nervenheilkd       Date:  1952-08

4.  [A contribution concerning the infantile neuro-axonal dystrophy. Comparison to Hallervorden-Spatz disease regarding histopathologic findings and clinical symptoms].

Authors:  E Richter
Journal:  Z Neurol       Date:  1972

5.  [Spinocerebellar atrophy and cerebellar calcification in a case of central neurofibromatosis (author's transl)].

Authors:  P Pilz
Journal:  Acta Neuropathol       Date:  1977-04-29       Impact factor: 17.088

6.  Hallervorden Spatz disease. Its pathogenesis and place among the axonal dystrophies.

Authors:  O W Sacks; M J Aguilar; W J Borwn
Journal:  Acta Neuropathol       Date:  1966-03-04       Impact factor: 17.088

7.  Basal ganglia calcification. Characteristics of CT scans and clinical findings.

Authors:  A E Adams
Journal:  Neurosurg Rev       Date:  1980       Impact factor: 3.042

8.  Unusual late-onset type of hallervorden-Spatz disease. Clinico-pathological study of a case presenting as parkinsonism.

Authors:  K Jellinger; E Neumayer
Journal:  Z Neurol       Date:  1972
  8 in total

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