(Q39030130)

8 September 2017

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study (English)

1 reference

8 September 2017

1 reference

parkinsonian syndrome

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8

Nobutaka Hattori

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8 September 2017

9

Yoshikuni Mizuno

1 reference

8 September 2017

7

Mongi Ben Hamida

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8 September 2017

Neziha Gouider-Khouja

1

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8 September 2017

Abdelmajid Larnaout

2

1 reference

8 September 2017

Rim Amouri

3

1 reference

8 September 2017

Sana Sfar

4

1 reference

8 September 2017

Samir Belal

5

1 reference

8 September 2017

Christiane Ben Hamida

6

1 reference

8 September 2017

Fayçal Hentati

10

1 reference

8 September 2017

1 June 2003

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8 September 2017

5

1 reference

Parkinsonism and Related Disorders

inferred from page(s)

published in

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8 September 2017

9

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8 September 2017

5

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8 September 2017

247-251

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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

8 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

1 reference

7 January 2021

Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individuals

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Familial juvenile parkinsonism: clinical and pathologic study in a family.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Clinical, pathologic and genetic studies on autosomal recessive early-onset parkinsonism with diurnal fluctuation

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Clinical and genetic study of familial Parkinson's disease in Tunisia

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Parkinsonism: onset, progression, and mortality

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Association between early-onset Parkinson's disease and mutations in the parkin gene

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Anatomy, pigmentation, ventral and dorsal subpopulations of the substantia nigra, and differential cell death in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Dominantly inherited, early-onset parkinsonism: neuropathology of a new form

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Western Nebraska family (family D) with autosomal dominant parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Dopa-responsive dystonia: pathological and biochemical observations in a case.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2803%2900016-6

7 January 2021

10.1016/S1353-8020(03)00016-6

Identifiers

DOI

1 reference

8 September 2017

1 reference