A. Braun < A. Brice < A. Bronisz

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 31.
[20-40] [0 - 20][0 - 31]

Ident.	Authors (with country if any)	Title
001331 (2000)	W J Gu ; N. Abbas ; M Z Lagunes ; A. Parent ; L. Pradier ; G A Bohme ; Y. Agid ; E C Hirsch ; R. Raisman-Vozari ; A. Brice	Cloning of rat parkin cDNA and distribution of parkin in rat brain.
001387 (1999)	D. Brassat ; A. Durr ; Y. Agid ; A. Brice	[Genetics of Parkinson disease].
001389 (1999)	B S Harhangi ; M J Farrer ; S. Lincoln ; V. Bonifati ; G. Meco ; G. De Michele ; A. Brice ; A. Dürr ; M. Martinez ; T. Gasser ; B. Bereznai ; J R Vaughan ; N W Wood ; J. Hardy ; B A Oostra ; M M Breteler	The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease.
001408 (1999)	N. Abbas ; C B Lücking ; S. Ricard ; A. Dürr ; V. Bonifati ; G. De Michele ; S. Bouley ; J R Vaughan ; T. Gasser ; R. Marconi ; E. Broussolle ; C. Brefel-Courbon ; B S Harhangi ; B A Oostra ; E. Fabrizio ; G A Böhme ; L. Pradier ; N W Wood ; A. Filla ; G. Meco ; P. Denefle ; Y. Agid ; A. Brice	A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
001416 (1999)	N. Sabbagh ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Y. Agid ; F. Broly	CYP2D6 polymorphism and Parkinson's disease susceptibility.
001452 (1998)	A. Brice	[Parkinson disease: monogenic forms and genetic susceptibility factors].
001456 (1998)	C. Dumanchin ; A. Camuzat ; D. Campion ; P. Verpillat ; D. Hannequin ; B. Dubois ; P. Saugier-Veber ; C. Martin ; C. Penet ; F. Charbonnier ; Y. Agid ; T. Frebourg ; A. Brice	Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.
001462 (1998)	J. Tassin ; A. Dürr ; T. De Broucker ; N. Abbas ; V. Bonifati ; G. De Michele ; A M Bonnet ; E. Broussolle ; P. Pollak ; M. Vidailhet ; M. De Mari ; R. Marconi ; S. Medjbeur ; A. Filla ; G. Meco ; Y. Agid ; A. Brice	Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
001533 (1997)	M. Ruberg ; B. Brugg ; A. Prigent ; E. Hirsch ; A. Brice ; Y. Agid	Is differential regulation of mitochondrial transcripts in Parkinson's disease related to apoptosis?
001570 (1996)	A. Dürr ; A. Brice	Genetics of movement disorders.
001829 (1990)	M. Ruberg ; W. Mayo ; A. Brice ; C. Duyckaerts ; J J Hauw ; H. Simon ; M. Lemoal ; Y. Agid	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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