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Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers
Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers
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Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers

ANHEIM, M ; ELBAZ, A ; LESAGE, S ; DURR, A ; CONDROYER, C ; VIALLET, F ; POLLAK, P ; BONAÏTI, B ; BONAÏTI-PELLIE, C ; BRICE, A

Neurology, 2012-02, Vol.78 (6), p.417-420 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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

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3
Age-related differences in the neural basis of the subjective vividness of memories: evidence from multivoxel pattern classification
Age-related differences in the neural basis of the subjective vividness of memories: evidence from multivoxel pattern classification
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Age-related differences in the neural basis of the subjective vividness of memories: evidence from multivoxel pattern classification

Johnson, Marcia K. ; Kuhl, Brice A. ; Mitchell, Karen J. ; Ankudowich, Elizabeth ; Durbin, Kelly A.

Cognitive, affective, & behavioral neuroscience, 2015-09, Vol.15 (3), p.644-661 [Periódico revisado por pares]

New York: Springer US

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4
IDENTIFICATION OF VPS35 MUTATIONS REPLICATED IN FRENCH FAMILIES WITH PARKINSON DISEASE
IDENTIFICATION OF VPS35 MUTATIONS REPLICATED IN FRENCH FAMILIES WITH PARKINSON DISEASE
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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

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5
A novel DCC mutation and genetic heterogeneity in congenital mirror movements
A novel DCC mutation and genetic heterogeneity in congenital mirror movements
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A novel DCC mutation and genetic heterogeneity in congenital mirror movements

Depienne, C ; Cincotta, M ; Billot, S ; Bouteiller, D ; Groppa, S ; Brochard, V ; Flamand, C ; Hubsch, C ; Meunier, S ; Giovannelli, F ; Klebe, S ; Corvol, J C ; Vidailhet, M ; Brice, A ; Roze, E

Neurology, 2011-01, Vol.76 (3), p.260-264 [Periódico revisado por pares]

United States

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6
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
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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

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7
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
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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

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8
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
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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

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9
Myoclonus-dystonia : Clinical and electrophysiologic pattern related to SGCE mutations
Myoclonus-dystonia : Clinical and electrophysiologic pattern related to SGCE mutations
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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

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10
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
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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

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