skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: assunto: Middle Aged remover assunto: Neurosciences & Neurology remover Neurology remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Inflammatory profile discriminates clinical subtypes in LRRK2‐associated Parkinson's disease
Inflammatory profile discriminates clinical subtypes in LRRK2‐associated Parkinson's disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Inflammatory profile discriminates clinical subtypes in LRRK2‐associated Parkinson's disease

Brockmann, K. ; Schulte, C. ; Schneiderhan‐Marra, N. ; Apel, A. ; Pont‐Sunyer, C. ; Vilas, D. ; Ruiz‐Martinez, J. ; Langkamp, M. ; Corvol, J.‐C. ; Cormier, F. ; Knorpp, T. ; Joos, T. O. ; Bernard, A. ; Gasser, T. ; Marras, C. ; Schüle, B. ; Aasly, J. O. ; Foroud, T. ; Marti‐Masso, J. F. ; Brice, A. ; Tolosa, E. ; Berg, D. ; Maetzler, W.

European journal of neurology, 2017-02, Vol.24 (2), p.427-e6 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
2
IDENTIFICATION OF VPS35 MUTATIONS REPLICATED IN FRENCH FAMILIES WITH PARKINSON DISEASE
IDENTIFICATION OF VPS35 MUTATIONS REPLICATED IN FRENCH FAMILIES WITH PARKINSON DISEASE
Material Type:
Artigo 		Adicionar ao Meu Espaço

IDENTIFICATION OF VPS35 MUTATIONS REPLICATED IN FRENCH FAMILIES WITH PARKINSON DISEASE

LESAGE, S ; CONDROYER, C ; KLEBE, S ; HONORE, A ; TISON, F ; BREFEL-COURBON, C ; DIIRR, A ; BRICE, A

Neurology, 2012-05, Vol.78 (18), p.1449-1450 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
3
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

LE BER, I ; CAMUZAT, A ; HEATH, S ; CAMU, W ; MARTINAUD, O ; LACOMBLEZ, L ; VERCELLETTO, M ; SALACHAS, F ; SELLAL, F ; DIDIC, M ; THOMAS-ANTERION, C ; PUEL, M ; BERGER, E ; MICHEL, B.-F ; BESSE, C ; DUYCKAERTS, C ; MEININGER, V ; CAMPION, D ; DUBOIS, B ; BRICE, A ; HANNEQUIN, D ; LAQUERRIERE, A ; GOLFIER, V ; SEILHEAN, D ; VIENNET, G ; COURATIER, P ; VERPILLAT, P

Neurology, 2009-05, Vol.72 (19), p.1669-1676 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
4
A multidisciplinary study of patients with early-onset PD with and without parkin mutations
A multidisciplinary study of patients with early-onset PD with and without parkin mutations
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

LOHMANN, E ; THOBOIS, S ; POLLAK, P ; AGID, Y ; BRICE, A ; LESAGE, S ; BROUSSOLLE, E ; TEZENAS DU MONTCEL, S ; RIBEIRO, M.-J ; REMY, P ; PELISSOLO, A ; DUBOIS, B ; MALLET, L

Neurology, 2009-01, Vol.72 (2), p.110-116 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
5
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
Material Type:
Artigo 		Adicionar ao Meu Espaço

Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?

CHARLES, P ; CAMUZAT, A ; BRICE, A ; BENAMMAR, N ; SELLAI, F ; DESTEE, A ; BONNET, A.-M ; LESAGE, S ; LE BER, I ; STEVANIN, G ; DURR, A

Neurology, 2007-11, Vol.69 (21), p.1970-1975 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
6
Myoclonus-dystonia : Clinical and electrophysiologic pattern related to SGCE mutations
Myoclonus-dystonia : Clinical and electrophysiologic pattern related to SGCE mutations
Material Type:
Artigo 		Adicionar ao Meu Espaço

Myoclonus-dystonia : Clinical and electrophysiologic pattern related to SGCE mutations

ROZE, E ; APARTIS, E ; ANDRE-OBADIA, N ; MALTETE, D ; ECHANIZ-LAGUNA, A ; PEREON, Y ; BEAUGENDRE, Y ; DUPONT, S ; DE GRESLAN, T ; JEDYNAK, C. P ; PONSOT, G ; DUSSAULE, J. C ; CLOT, F ; BRICE, A ; DÜRR, A ; VIDAILHET, M ; DORISON, N ; THOBOIS, S ; GUYANT-MARECHAL, L ; TRANCHANT, C ; DAMIER, P ; DOUMMAR, D ; BAHI-BUISSON, N

Neurology, 2008-03, Vol.70 (13), p.1010-1016 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
7
MUTATIONS IN THE GLUCOCEREBROSIDASE GENE CONFER A RISK FOR PARKINSON DISEASE IN NORTH AFRICA
MUTATIONS IN THE GLUCOCEREBROSIDASE GENE CONFER A RISK FOR PARKINSON DISEASE IN NORTH AFRICA
Material Type:
Artigo 		Adicionar ao Meu Espaço

MUTATIONS IN THE GLUCOCEREBROSIDASE GENE CONFER A RISK FOR PARKINSON DISEASE IN NORTH AFRICA

LESAGE, S ; CONDROYER, C ; TAZIR, M ; BRICE, A ; HECHAM, N ; ANHEIM, M ; BELARBI, S ; LOHMAN, E ; VIALLET, F ; POLLAK, P ; ABADA, M ; DÜRR, A

Neurology, 2011-01, Vol.76 (3), p.301-303 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
8
Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1
Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1
Material Type:
Artigo 		Adicionar ao Meu Espaço

Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1

LE BER, I ; DUBOURG, O ; BENOIST, J.-F ; JARDEL, C ; MOCHEL, F ; KOENIG, M ; BRICE, A ; LOMBES, A ; DÜRR, A

Neurology, 2007-01, Vol.68 (4), p.295-297 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
9
IS THE COMMON LRRK2 G2019S MUTATION RELATED TO DYSKINESIAS IN NORTH AFRICAN PARKINSON DISEASE?
IS THE COMMON LRRK2 G2019S MUTATION RELATED TO DYSKINESIAS IN NORTH AFRICAN PARKINSON DISEASE?
Material Type:
Artigo 		Adicionar ao Meu Espaço

IS THE COMMON LRRK2 G2019S MUTATION RELATED TO DYSKINESIAS IN NORTH AFRICAN PARKINSON DISEASE?

LESAGE, S ; BELARBI, S ; TAZIR, M ; BRICE, A ; TROIANO, A ; CONDROYER, C ; HECHAM, N ; POLLAK, P ; LOHMAN, E ; BENHASSINE, T ; YSMAIL-DAHLOUK, F ; DÜRR, A

Neurology, 2008-11, Vol.71 (19), p.1550-1552 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
10
Predominant dystonia with marked cerebellar atrophy : A rare phenotype in familial dystonia
Predominant dystonia with marked cerebellar atrophy : A rare phenotype in familial dystonia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Predominant dystonia with marked cerebellar atrophy : A rare phenotype in familial dystonia

LE BER, I ; CLOT, F ; BRICE, A ; DÜRR, A ; VERCUEIL, L ; CAMUZAT, A ; VIEMONT, M ; BENAMAR, N ; DE LIEGE, P ; OUVRARD-HERNANDEZ, A.-M ; POLLAK, P ; STEVANIN, G

Neurology, 2006-11, Vol.67 (10), p.1769-1773 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Revistas revisadas por pares (136)

Data de Publicação 

De até
Refinar
  1. Antes de1999  (12)
  2. 1999Até2004  (33)
  3. 2005Até2010  (40)
  4. 2011Até2017  (57)
  5. Após 2017  (8)
  6. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.