Genetic burden of common variants in progressive and bout-onset multiple sclerosis
- Author
- SOROSINA, Melissa1 ; BRAMBILLA, Paola1 ; PATTI, Francesco8 ; MANCARDI, Gianluigi9 ; MANUNTA, Paolo10 ; GLORIOSO, Nicola11 ; GUERINI, Franca R12 ; BERGAMASCHI, Roberto13 ; PERLA, Franco14 ; MARTINELLI, Vittorio5 ; CUSI, Daniele4 ; LEONE, Maurizio2 ; CLARELLI, Ferdinando1 ; COMI, Giancarlo1 5 ; D'ALFONSO, Sandra2 3 ; MARTINELLI-BONESCHI, Filippo1 5 ; BARIZZONE, Nadia2 3 ; LUPOLI, Sara4 ; GUASCHINO, Clara1 5 ; OSICEANU, Ana Maria1 ; MOIOLA, Lucia1 5 ; GHEZZI, Angelo6 ; CONIGLIO, Gabriella7
[1] Laboratory of Genetics of Neurological Complex Disorders, Institute of Experimental Neurology (INSPE), Division of Neuroscience, San Raffaele Scientific Institute, Italy
[2] Interdisciplinary Research Center of Autoimmune Disease IRCAD, University of Eastern Piedmont, Italy
[3] Department of Health Sciences, University of Eastern Piedmont, Italy
[4] Department of Health Sciences, University of Milan and Genomics & Bioinformatics Unit, c/o Fondazione Filarete, Italy
[5] Department of Neurology, Institute of Experimental Neurology (INSPE), Division of Neuroscience, San Raffaele Scientific Institute, Italy
[6] Department of Neurology, S. Antonio Abate Hospital, Italy
[7] Department of Neurology, Madonna delle Grazie Hospital, Italy
[8] Department DANA, G.F. Ingrassia, Neurosciences Section, Multiple Sclerosis Center, PO G. Rodolico, Italy
[9] Department of Neuroscience, Ophthalmology and Genetics, University of Genova, Italy
[10] Division of Nephrology and Dialysis, San Raffaele Scientific Institute, Università Vita-Salute San Raffaele, Italy
[11] Hypertension and Related Diseases Centre-AOU, University of Sassari, Italy
[12] Don C. Gnocchi Foundation ONLUS, Italy
[13] Fondazione Istituto Neurologico C. Mondino IRCCS, Italy
[14] Department of Neurology, Mondovì Hospital, Italy - Source
Multiple sclerosis. 2014, Vol 20, Num 7, pp 802-811, 10 p ; ref : 30 ref
- Publisher
- Sage Publications, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- Multiple sclerosis genome-wide association study heritability primary progressive relapsing-remitting
- Keyword (fr)
- Génome Héritabilité Maladie dégénérative Pathologie du système nerveux Sclérose en plaques Variant génétique Maladie inflammatoire Pathologie du système nerveux central
- Keyword (en)
- Genome Heritability Degenerative disease Nervous system diseases Multiple sclerosis Genetic variant Inflammatory disease Central nervous system disease
- Keyword (es)
- Genoma Heredabilidad Enfermedad degenerativa Sistema nervioso patología Esclerosis en placa Variante genética Enfermedad inflamatoria Sistema nervosio central patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02Q Immunomodulators
- 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 Pharmacological treatments
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 28527985
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
10.1177/1352458513512707 
https://dx.doi.org/10.1177/1352458513512707
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