Parkinson's disease in Arabs: a systematic review. - Wikidata - wikimedia - TriplyDB

Parkinson's disease in Arabs: a systematic review.

Parkinson's disease in Arabs: a systematic review.

http://www.wikidata.org/entity/Q37149360

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Parkinson disease male-to-female ratios increase with age: French nationwide study and meta-analysis.Asian perspectives on the recognition and management of levodopa 'wearing-off' in Parkinson's disease.The VPS35 gene and Parkinson's disease.Construction of standardized Arabic questionnaires for screening neurological disorders (dementia, stroke, epilepsy, movement disorders, muscle and neuromuscular junction disorders).MDPD: an integrated genetic information resource for Parkinson's disease.Dementia in Eastern Mediterranean countries: A systematic review.Variable PARK2 Mutations Cause Early-Onset Parkinson's Disease in a Small Restricted Population.Non-Motor Symptoms as Predictors of Quality of Life in Egyptian Patients With Parkinson's Disease: A Cross-Sectional Study Using a Culturally Adapted 39-Item Parkinson's Disease Questionnaire.K-variant BCHE and pesticide exposure: Gene-environment interactions in a case-control study of Parkinson's disease in Egypt

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P2860

Parkinson's disease in Arabs: a systematic review.

http://www.wikidata.org/entity/Q37149360

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on July 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Parkinson's disease in Arabs: a systematic review.

@en

Parkinson's disease in Arabs: a systematic review.

@nl

type

label

Parkinson's disease in Arabs: a systematic review.

@en

Parkinson's disease in Arabs: a systematic review.

@nl

prefLabel

Parkinson's disease in Arabs: a systematic review.

@en

Parkinson's disease in Arabs: a systematic review.

@nl

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Movement Disorders

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Parkinson's disease in Arabs: a systematic review.

@en

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Donald G Grosset

http://www.w3.org/2001/XMLSchema#string

Hani T S Benamer

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Khurram A Siddiqui

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Rajith de Silva

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P2860

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

Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

Neurological disorders in Nigerian Africans: a community-based study.

Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region

Kufor Rakeb disease: autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia.

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

Parkinson's disease in Africa: A systematic review of epidemiologic and genetic studies.

Epidemiology of Parkinson's disease in Benghazi, North-East Libya.

Prevalence study of neurologic disorders in Kelibia (Tunisia).

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1205-1210

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scholarly article

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10.1002/MDS.22041

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9

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Parkinson's disease