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A multidisciplinary study of patients with early-onset PD with and without parkin mutations

Author
LOHMANN, E1 2 3 ; THOBOIS, S4 ; POLLAK, P13 ; AGID, Y1 14 2 3 ; BRICE, A1 15 16 2 3 ; LESAGE, S1 3 ; BROUSSOLLE, E4 ; TEZENAS DU MONTCEL, S5 6 ; RIBEIRO, M.-J7 ; REMY, P8 ; PELISSOLO, A9 ; DUBOIS, B10 11 2 ; MALLET, L12
[1] INSERM UMR_S679 Neurologic & Therapeurique Expérimentale, Paris, France
[2] AP-HP Pitié-Salpêtrière Hospital, Department of the Nervous System Disorders, Paris, France
[3] UPMC Univ Paris 06 UMR_S679, Paris, France
[4] University of Lyon I and INSERM UMR 864 and The Pierre Werrheimer Neurological Hospital Department of Neurology, Lyon, France
[5] AP-HP Pitie-Salpetriere Hospital, Department of Public Health, Unit of de Biostatistics and Medical Information and Unit of Medical Research, Paris, France
[6] UPMC Univ Paris 06 EA3974 Modelisation in Clinical Research, Paris, France
[7] CEA 12BM, Service Hospitalier Frédéric Joliot, Orsay, France
[8] CEA 12BM, URA-CEA-CNRS 2210, Orsay, France
[9] CHU Henri Mondor AP-HP et Faculte de Médecine Paris 12, Créteil, France
[10] AP-HP Pitié-Salpetriere Hospital, Department of Psychiatry, Paris, France
[11] INSERM UMR 610 Neuroanatomie Fonctionnelle du Comportement et de ses Troubles, Paris, France
[12] AP-HP Pitié-Salpêtrière Hospital, Centre de Référence sur la Maladie de Pick, Paris, France
[13] Inserm Avenir Group IFR 70 Behaviour Emotion and Basal Ganglia, Center of Clinical Investigation, Paris, France
[14] Department of Clinical and Biological Neurosciences University Hospital of Grenoble, France
[15] AP-HP Pitié-Salpêtrière Hospital, Clinical Investigation Center, Paris, France
[16] AP-HP Pitié-Salpêtrière Hospital, Department of Genetics and Cyrogenetics, Paris, France
French Parkinson's Disease Genetics Study Group, France
Source

Neurology. 2009, Vol 72, Num 2, pp 110-116, 7 p ; ref : 23 ref

CODEN
NEURAI
ISSN
0028-3878
Scientific domain
Cognition; Neurology
Publisher
Lippincott Williams & Wilkins, Hagerstown, MD
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Homme Mutation Parkine Pathologie du système nerveux
Keyword (en)
Human Mutation Parkin Nervous system diseases
Keyword (es)
Hombre Mutación Parkin Sistema nervioso 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

Discipline
Neurology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
21051434

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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