Widespread expression of alpha-synuclein and tau immunoreactivity in Hallervorden-Spatz syndrome with protracted clinical course (Q34019790)

30 July 2017

1 reference

title

Widespread expression of alpha-synuclein and tau immunoreactivity in Hallervorden-Spatz syndrome with protracted clinical course (English)

1 reference

30 July 2017

1 reference

Saito Y

1

1 reference

30 July 2017

Kawai M

2

1 reference

30 July 2017

Inoue K

3

1 reference

30 July 2017

Sasaki R

4

1 reference

30 July 2017

Arai H

5

1 reference

30 July 2017

Nanba E

6

1 reference

30 July 2017

Kuzuhara S

7

1 reference

30 July 2017

Ihara Y

8

1 reference

30 July 2017

Kanazawa I

9

1 reference

30 July 2017

Murayama S

10

1 reference

30 July 2017

1 August 2000

1 reference

Journal of the Neurological Sciences

30 July 2017

1 reference

30 July 2017

177

1 reference

30 July 2017

1

1 reference

30 July 2017

48-59

1 reference

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.

30 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Hallervorden-Spatz syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Hallervorden-Spatz syndrome: clinical and magnetic resonance imaging correlations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Apolipoprotein E genotyping by one-stage PCR

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Lewy body in neurodegeneration with brain iron accumulation type 1 is immunoreactive for alpha-synuclein.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Clinical characteristics and nosological considerations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Ultrastructural observations, anatomical pathology and nosology.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Neuroaxonal dystrophy in young adults: a clinicopathological study of two unrelated cases.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Neuroaxonal dystrophy. A case of delayed onset and protracted course.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Atypical dopa responsive parkinsonism in a patient with megalencephaly, midbrain Lewy body disease, and some pathological features of Hallervorden-Spatz disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Adult onset Hallervorden-Spatz disease with neurofibrillary pathology. A discrete clinicopathological entity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Alzheimer neurofibrillary tangles in diseases other than senile and presenile dementia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Senile dementia with tangles (tangle predominant form of senile dementia).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Specific tau variants in the brains of patients with myotonic dystrophy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Neurofibrillary tangles in Niemann-Pick disease type C.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Mutational analysis of the tau gene in progressive supranuclear palsy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): report of the consortium on DLB international workshop

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

A neuropathological subset of Alzheimer's disease with concomitant Lewy body disease and spongiform change

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Neurofibrillary tangles and Lewy bodies in the locus ceruleus neurons of the aged brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Frequent coexistence of Lewy bodies and neurofibrillary tangles in the same neurons of patients with diffuse Lewy body disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Mineralization of the basal ganglia detected by CT in Hallervorden-Spatz syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Neuroaxonal dystrophy with neuromelanin deposition, neurofibrillary tangles, and neuronal loss. Light- and electron-microscopic changes in a 45-year-old woman with progressive psychomotor deterioration.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Late onset parkinsonian syndrome in Hallervorden-Spatz disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

The nosology of Hallervorden-spatz disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

Pathogenesis of pigment and spheroid formation in Hallervorden-Spatz syndrome and related disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900337-3

10.1016/S0022-510X(00)00337-3

7 January 2021

Identifiers

DOI

1 reference

30 July 2017

1 reference