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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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2
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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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
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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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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
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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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5
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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6
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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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
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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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8
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years
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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

Namekawa, M ; Ribai, P ; Nelson, I ; Forlani, S ; Fellmann, F ; Goizet, C ; Depienne, C ; Stevanin, G ; Ruberg, M ; Dürr, A ; Brice, A

Neurology, 2006-01, Vol.66 (1), p.112-114 [Periódico revisado por pares]

United States

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9
Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1
Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1
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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

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10
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?
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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

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