(Q73807473)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Intrafamilial phenotypic variability of Hallervorden-Spätz syndrome in a Tunisian family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

Gouider-Khouja N

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Miladi N

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Belal S

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Hentati F

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 July 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

number of pages

5

1 reference

Parkinsonism and Related Disorders

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

175-179

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

Hallervorden-Spatz syndrome

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Hallervorden-Spatz syndrome: clinical and magnetic resonance imaging correlations

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

The nosology of Hallervorden-spatz disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Late-onset Hallervorden-Spatz disease presenting as familial parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Clinicopathologic correlation and pathogenesis of ocular and central nervous system manifestations in Hallervorden-Spatz syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Sea-blue histiocytes, lymphocytic cytosomes, movement disorder and 59Fe-uptake in basal ganglia: Hallervorden-Spatz disease or ceroid storage disease with abnormal isotope scan?

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Acanthocytosis, retinitis pigmentosa, and pallidal degeneration: a report of three patients, including the second reported case with hypoprebetalipoproteinemia (HARP syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Late onset parkinsonian syndrome in Hallervorden-Spatz disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Computed tomography in Hallervorden-Spatz disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Clinical NMR imaging of the brain in children: normal and neurologic disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

Magnetic resonance imaging in pathologically proven Hallervorden-Spatz disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2899%2900060-7

7 January 2021

10.1016/S1353-8020(99)00060-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10817958%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference