Literature DB >> 4119022

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

K Jellinger, E Neumayer.   

Abstract

Entities:  

Mesh:

Year:  1972        PMID: 4119022     DOI: 10.1007/bf00316039

Source DB:  PubMed          Journal:  Z Neurol        ISSN: 0012-1037


× No keyword cloud information.
  18 in total

1.  Hallervorden-Spatz disease and dystonia.

Authors:  M G NETSKY; D SPIRO; H M ZIMMERMAN
Journal:  J Neuropathol Exp Neurol       Date:  1951-04       Impact factor: 3.685

2.  [Not Available].

Authors:  L VAN BOGAERT
Journal:  Monatsschr Psychiatr Neurol       Date:  1947

3.  Observations on the fine structure of the substantia nigra in the cat.

Authors:  E Rinvik; I Grofová
Journal:  Exp Brain Res       Date:  1970       Impact factor: 1.972

4.  [CNS lesions in olivo-ponto-cerebellar atrophies].

Authors:  K Jellinger; E Tarnowska-Dziduszko
Journal:  Z Neurol       Date:  1971

5.  [Parkinson's disease concurring with other diseases of the central nervous system].

Authors:  E Neumayer
Journal:  Z Neurol       Date:  1971

6.  Observations on the efficacy of L-dopa in progressive supranuclear palsy.

Authors:  H L Klawans; S P Ringel
Journal:  Eur Neurol       Date:  1971       Impact factor: 1.710

7.  Hallervorden-Spatz disease. Late infantile and adult types, report of two cases.

Authors:  B Rozdilsky; J N Cumings; A F Huston
Journal:  Acta Neuropathol       Date:  1968-01-02       Impact factor: 17.088

8.  [Late Hallervorden-Spatz disease with important reticular and cerebellar participation].

Authors:  E Evrard; J Hariga; J J Martin; M Reznik
Journal:  Psychiatr Neurol Neurochir       Date:  1968 May-Jun

9.  Neuroaxonal dystrophy in man: character and natural history.

Authors:  K Jellinger; A Jirásek
Journal:  Acta Neuropathol       Date:  1971       Impact factor: 17.088

10.  Clinico-pathological and histochemical studies of Hallervorden-Spatz disease with torsion dystonia with special reference to diagnostic criteria of the disease from the clinico-pathological viewpoint.

Authors:  N Yanagisawa; H Shiraki; M Minakawa; H Narabayashi
Journal:  Prog Brain Res       Date:  1966       Impact factor: 2.453

View more
  3 in total

1.  Pallido-nigro-luysial atrophy with massive appearance of corpora amylacea in the CNS.

Authors:  K Kosaka; M Matsushita; S Oyanagi; S Uchiyama; S Iwase
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

2.  Pallido-nigro-luysial atrophy associated with degeneration of the centrum medianum. A clinicopathologic and electron microscopic study.

Authors:  K Takahashi; R Nakashima; T Takao; H Nakamura
Journal:  Acta Neuropathol       Date:  1977-01-31       Impact factor: 17.088

3.  Late onset neurodegeneration with brain-iron accumulation presenting as parkinsonism.

Authors:  Robert Fekete
Journal:  Case Rep Neurol Med       Date:  2012-12-18
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.