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Choline acetyltransferase activity and [ 3H]vesamicol binding in the temporal cortex of patients with Alzheimer's disease, Parkinson's disease, and rats with basal forebrain lesions
Choline acetyltransferase activity and [ 3H]vesamicol binding in the temporal cortex of patients with Alzheimer's disease, Parkinson's disease, and rats with basal forebrain lesions
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Choline acetyltransferase activity and [ 3H]vesamicol binding in the temporal cortex of patients with Alzheimer's disease, Parkinson's disease, and rats with basal forebrain lesions

Ruberg, M. ; Mayo, W. ; Brice, A. ; Duyckaerts, C. ; Hauw, J.J ; Simon, H. ; LeMoal, M. ; Agid, Y.

Neuroscience, 1990, Vol.35 (2), p.327-333 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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2
Herpes simplex encephalitis: long term magnetic resonance imaging and neuropsychological profile
Herpes simplex encephalitis: long term magnetic resonance imaging and neuropsychological profile
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Herpes simplex encephalitis: long term magnetic resonance imaging and neuropsychological profile

Kapur, N ; Barker, S ; Burrows, E H ; Ellison, D ; Brice, J ; Illis, L S ; Scholey, K ; Colbourn, C ; Wilson, B ; Loates, M

Journal of neurology, neurosurgery and psychiatry, 1994-11, Vol.57 (11), p.1334-1342 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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3
Diagnosis of “sporadic” Huntington's disease
Diagnosis of “sporadic” Huntington's disease
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Diagnosis of “sporadic” Huntington's disease

Dürr, A. ; Dodé, C. ; Hahn, V. ; Pêcheux, C. ; Pillon, B. ; Feingold, J. ; Kaplan, J-C. ; Agid, Y. ; Brice, A.

Journal of the neurological sciences, 1995-03, Vol.129 (1), p.51-55 [Periódico revisado por pares]

Shannon: Elsevier B.V

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4
Spinocerebellar ataxia 3 and machado-joseph disease: Clinical, molecular, and neuropathological features
Spinocerebellar ataxia 3 and machado-joseph disease: Clinical, molecular, and neuropathological features
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Spinocerebellar ataxia 3 and machado-joseph disease: Clinical, molecular, and neuropathological features

Durr, Alexandra ; Stevanin, Giovanni ; Cancel, Geraldine ; Duyckaerts, Charles ; Abbas, Nacer ; Didierjean, Olivier ; Chneiweiss, Herve ; Benomar, Ali ; Lyon-Caen, Olivier ; Julien, Jean ; Serdaru, Michel ; Penet, Christiane ; Agid, Yves ; Brice, Alexis

Annals of neurology, 1996-04, Vol.39 (4), p.490-499 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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5
Ultrastructural PMP22 expression in inherited demyelinating neuropathies
Ultrastructural PMP22 expression in inherited demyelinating neuropathies
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Ultrastructural PMP22 expression in inherited demyelinating neuropathies

Vallat, Jean-Michel ; Sindou, Philippe ; Preux, Pierre-Marie ; Tabaraud, Fransois ; Milor, André-Michel ; Couratier, Philippe ; Leguern, Eric ; Brice, Alexis

Annals of neurology, 1996-06, Vol.39 (6), p.813-817 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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6
Long-Term Retention Deficits in Two Cases of Disproportionate Retrograde Amnesia
Long-Term Retention Deficits in Two Cases of Disproportionate Retrograde Amnesia
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Long-Term Retention Deficits in Two Cases of Disproportionate Retrograde Amnesia

Kapur, Narinder ; Scholey, Keith ; Moore, Elizabeth ; Barker, Simon ; Brice, Jason ; Thompson, Simon ; Shiel, Agnes ; Carn, Roland ; Abbott, Patricia ; Fleming, John

Journal of cognitive neuroscience, 1996-09, Vol.8 (5), p.416-434 [Periódico revisado por pares]

One Rogers Street, Cambridge, MA 02142-1209, USA: MIT Press

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7
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2
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Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2

Dürr, A. ; Davoine, C.-S. ; Paternotte, C. ; von Fellenberg, J. ; Cogilnicean, S. ; Coutinho, P. ; Lamy, C. ; Bourgeois, S. ; Prud'homme, J.-F. ; Penet, C. ; Mas, J.-L. ; Burgunder, J.-M. ; Hazan, J. ; Weissenbach, J. ; Brice, A. ; Fontaine, B.

Brain (London, England : 1878), 1996-10, Vol.119 (5), p.1487-1496 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease
Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease
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Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease

LEGUERN, E ; GOUIDER, R ; MABIN, D ; TARDIEU, S ; BIROUK, N ; PARENT, P ; BOUCHE, P ; BRICE, A

Annals of neurology, 1997, Vol.41 (1), p.104-108 [Periódico revisado por pares]

Hoboken: Willey-Liss

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9
Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus
Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus
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Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus

BÜRK, K ; STEVANIN, G ; DIDIERJEAN, O ; CANCEL, G ; TROTTIER, Y ; SKALEJ, M ; ABELE, M ; BRICE, A ; DICHGANS, J ; KLOCKGETHER, T

Journal of neurology, 1997-04, Vol.244 (4), p.256-261 [Periódico revisado por pares]

Berlin: Springer

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10
Is Differential Regulation of Mitochondrial Transcripts in Parkinson's Disease Related to Apoptosis?
Is Differential Regulation of Mitochondrial Transcripts in Parkinson's Disease Related to Apoptosis?
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Is Differential Regulation of Mitochondrial Transcripts in Parkinson's Disease Related to Apoptosis?

Ruberg, Merle ; Brugg, Bernard ; Prigent, Annick ; Hirsch, Etienne ; Brice, Alexis ; Agid, Yves

Journal of neurochemistry, 1997-05, Vol.68 (5), p.2098-2110 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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