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Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias
Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias
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Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias

Matilla-Dueñas, A. ; Ashizawa, T. ; Brice, A. ; Magri, S. ; McFarland, K. N. ; Pandolfo, M. ; Pulst, S. M. ; Riess, O. ; Rubinsztein, D. C. ; Schmidt, J. ; Schmidt, T. ; Scoles, D. R. ; Stevanin, G. ; Taroni, F. ; Underwood, B. R. ; Sánchez, I.

Cerebellum (London, England), 2014-04, Vol.13 (2), p.269-302 [Periódico revisado por pares]

Boston: Springer US

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2
Urinary LRRK2 phosphorylation predicts parkinsonian phenotypes in G2019S LRRK2 carriers
Urinary LRRK2 phosphorylation predicts parkinsonian phenotypes in G2019S LRRK2 carriers
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Urinary LRRK2 phosphorylation predicts parkinsonian phenotypes in G2019S LRRK2 carriers

Fraser, Kyle B ; Moehle, Mark S ; Alcalay, Roy N ; West, Andrew B

Neurology, 2016-03, Vol.86 (11), p.994-999 [Periódico revisado por pares]

United States: American Academy of Neurology

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3
Proteomic analysis of parkin knockout mice: alterations in energy metabolism, protein handling and synaptic function
Proteomic analysis of parkin knockout mice: alterations in energy metabolism, protein handling and synaptic function
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Proteomic analysis of parkin knockout mice: alterations in energy metabolism, protein handling and synaptic function

Periquet, Magali ; Corti, Olga ; Jacquier, Sandrine ; Brice, Alexis

Journal of neurochemistry, 2005-12, Vol.95 (5), p.1259-1276 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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4
Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia
Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia
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Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia

Rinaldi, Carlo ; Schmidt, Thomas ; Situ, Alan J ; Johnson, Janel O ; Lee, Philip R ; Chen, Ke-lian ; Bott, Laura C ; Fadó, Rut ; Harmison, George H ; Parodi, Sara ; Grunseich, Christopher ; Renvoisé, Benoît ; Biesecker, Leslie G ; De Michele, Giuseppe ; Santorelli, Filippo M ; Filla, Alessandro ; Stevanin, Giovanni ; Dürr, Alexandra ; Brice, Alexis ; Casals, Núria ; Traynor, Bryan J ; Blackstone, Craig ; Ulmer, Tobias S ; Fischbeck, Kenneth H

JAMA neurology, 2015-05, Vol.72 (5), p.561-570 [Periódico revisado por pares]

United States: American Medical Association

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5
Ultrastructural localization of parkin in the rat brainstem, thalamus and basal ganglia
Ultrastructural localization of parkin in the rat brainstem, thalamus and basal ganglia
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Ultrastructural localization of parkin in the rat brainstem, thalamus and basal ganglia

Mouatt-Prigent, A ; Muriel, M-P ; Gu, W-J ; El Hachimi, K H ; Lücking, C B ; Brice, A ; Hirsch, E C

Journal of Neural Transmission, 2004-10, Vol.111 (10-11), p.1209-1218 [Periódico revisado por pares]

Austria: Springer Nature B.V

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6
Age-related loss of orexin/hypocretin neurons
Age-related loss of orexin/hypocretin neurons
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Age-related loss of orexin/hypocretin neurons

Kessler, B.A ; Stanley, E.M ; Frederick-Duus, D ; Fadel, J

Neuroscience, 2011-03, Vol.178, p.82-88 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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7
Complete sequence of a cDNA encoding an active rat choline acetyltransferase: A tool to investigate the plasticity of cholinergic phenotype expression
Complete sequence of a cDNA encoding an active rat choline acetyltransferase: A tool to investigate the plasticity of cholinergic phenotype expression
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Complete sequence of a cDNA encoding an active rat choline acetyltransferase: A tool to investigate the plasticity of cholinergic phenotype expression

Brice, A. ; Berrard, S. ; Raynaud, B. ; Ansieau, S. ; Coppola, T. ; Weber, M. J. ; Mallet, J.

Journal of neuroscience research, 1989-07, Vol.23 (3), p.266-273 [Periódico revisado por pares]

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

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8
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5
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CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5

Goizet, Cyril ; Boukhris, Amir ; Durr, Alexandra ; Beetz, Christian ; Truchetto, Jeremy ; Tesson, Christelle ; Tsaousidou, Maria ; Forlani, Sylvie ; Guyant-Maréchal, Lucie ; Fontaine, Bertrand ; Guimarães, João ; Isidor, Bertrand ; Chazouillères, Olivier ; Wendum, Dominique ; Grid, Djamel ; Chevy, Françoise ; Chinnery, Patrick F. ; Coutinho, Paula ; Azulay, Jean-Philippe ; Feki, Imed ; Mochel, Fanny ; Wolf, Claude ; Mhiri, Chokri ; Crosby, Andrew ; Brice, Alexis ; Stevanin, Giovanni

Brain (London, England : 1878), 2009-06, Vol.132 (6), p.1589-1600 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
Monogenic idiopathic epilepsies
Monogenic idiopathic epilepsies
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Monogenic idiopathic epilepsies

Gourfinkel-An, Isabelle ; Baulac, Stéphanie ; Nabbout, Rima ; Ruberg, Merle ; Baulac, Michel ; Brice, Alexis ; LeGuern, Eric

Lancet neurology, 2004-04, Vol.3 (4), p.209-218 [Periódico revisado por pares]

England: Elsevier Ltd

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10
Neurotoxic Calcium Transfer from Endoplasmic Reticulum to Mitochondria Is Regulated by Cyclin-Dependent Kinase 5-Dependent Phosphorylation of Tau
Neurotoxic Calcium Transfer from Endoplasmic Reticulum to Mitochondria Is Regulated by Cyclin-Dependent Kinase 5-Dependent Phosphorylation of Tau
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Neurotoxic Calcium Transfer from Endoplasmic Reticulum to Mitochondria Is Regulated by Cyclin-Dependent Kinase 5-Dependent Phosphorylation of Tau

Darios, Frederic ; Muriel, Marie-Paule ; Khondiker, Myriam Escobar ; Brice, Alexis ; Ruberg, Merle

The Journal of neuroscience, 2005-04, Vol.25 (16), p.4159-4168 [Periódico revisado por pares]

United States: Soc Neuroscience

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