Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin | Zendy

Benoît Marin | Zendy; Giancarlo Logroscino | Zendy; Farid Boumédiène | Zendy; Anaïs Labrunie | Zendy; Philippe Couratier | Zendy; MarieClaude Babron | Zendy; Anne-Louise Leutenegger | Zendy; PierreMarie Preux | Zendy; Ettore Beghi | Zendy

Open Access

Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin

Author(s) -

Benoît Marin,

Giancarlo Logroscino,

Farid Boumédiène,

Anaïs Labrunie,

Philippe Couratier,

MarieClaude Babron,

Anne-Louise Leutenegger,

PierreMarie Preux,

Ettore Beghi

Publication year - 2015

Publication title -

european journal of epidemiology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 3.825

H-Index - 111

eISSN - 1573-7284

pISSN - 0393-2990

DOI - 10.1007/s10654-015-0090-x

Subject(s) - amyotrophic lateral sclerosis , medicine , population , disease , epidemiology , age of onset , phenotype , demography , pathology , genetics , biology , environmental health , sociology , gene

To review how the phenotype and outcome of amyotrophic lateral sclerosis (ALS) change with variations in population ancestral origin (PAO). Knowledge of how PAO modifies ALS phenotype may provide important insight into the risk factors and pathogenic mechanisms of the disease.

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