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Volumn 13, Issue , 2013, Pages

Implementation of a population-based epidemiological rare disease registry: Study protocol of the amyotrophic lateral sclerosis (ALS) - registry Swabia

(64)  Nagel, Gabriele a   Ünal, Hatice a   Rosenbohm, Angela a   Ludolph, Albert C a   Rothenbacher, Dietrich a   Arnold, G b   Adam, T c   Neusch, C c   Bazner H d   Bortlein A d   Baier, H e   Behne, F e   Raape, J e   Rothmeier, J e   Beattie, J f   Peters, J f   Kaspar, A f   Bengel, D g   Bluthardt, M h   Schabet, M h   more..


Author keywords

Amyotrophic lateral sclerosis; Registry; Risk factors

Indexed keywords

AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; BLOOD SAMPLING; CLINICAL PROTOCOL; DISEASE REGISTRY; FEMALE; GERMANY; HUMAN; MAJOR CLINICAL STUDY; MALE; POPULATION BASED CASE CONTROL STUDY; PROSPECTIVE STUDY; RETROSPECTIVE STUDY;

EID: 84873730775     PISSN: None     EISSN: 14712377     Source Type: Journal    
DOI: 10.1186/1471-2377-13-22     Document Type: Article
Times cited : (30)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.