Can selection of rapidly progressing patients shorten clinical trials in amyotrophic lateral sclerosis?
- Author
- DE CARVALHO, Mamede1 2 3 ; SWASH, Michael4 5
[1] Department of Neurology, Hospital de Santa Maria, Lisbon, Portugal
[2] Laboratory of Electromyography, Centro de Estudos Egas Moniz, Lisbon, Portugal
[3] Faculty of Medicine, Institute of Molecular Medicine, Lisbon, Portugal
[4] Institute of Neuroscience, Queen Mary School of Medicine and Dentistry, Queen Mary University of London, London, England, United Kingdom
[5] Department of Neurology, Royal London Hospital, United Kingdom - Source
Archives of neurology (Chicago). 2006, Vol 63, Num 4, pp 557-560, 4 p ; ref : 11 ref
- Publisher
- American Medical Association, Chicago, IL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Essai clinique Homme Sclérose latérale amyotrophique Système nerveux pathologie Maladie dégénérative Moelle épinière pathologie Système nerveux central pathologie
- Keyword (en)
- Clinical trial Human Amyotrophic lateral sclerosis Nervous system diseases Degenerative disease Spinal cord disease Central nervous system disease
- Keyword (es)
- Ensayo clínico Hombre Esclerosis lateral amiotrófica Sistema nervioso patología Enfermedad degenerativa Médula espinal patología Sistema nervosio central patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17F Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 17700393
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1001/archneur.63.4.557 
https://dx.doi.org/10.1001/archneur.63.4.557
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