A. Bourguignon < A. Brice < A. Brouard

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 30.
[0-20] [0 - 20][0 - 30][20-29][20-40]

Ident.	Authors (with country if any)	Title
000007 (1999)	N. Abbas [France] ; 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 ; Yves Agid [France] ; 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.
000009 (1999)	N. Sabbagh [France] ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Yves Agid [France] ; F. Broly	CYP2D6 polymorphism and Parkinson's disease susceptibility.
000054 (1999)	B S Harhangi [Pays-Bas] ; 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.
000059 (1999)	D. Brassat [France] ; A. Durr ; Yves Agid [France] ; A. Brice	[Genetics of Parkinson disease].
000097 (2000)	W J Gu [France] ; N. Abbas ; M Z Lagunes ; A. Parent ; L. Pradier ; G A Bohme ; Yves Agid [France] ; E C Hirsch ; R. Raisman-Vozari ; A. Brice	Cloning of rat parkin cDNA and distribution of parkin in rat brain.
000173 (2000)	C B Lücking [France] ; A. Brice	Alpha-synuclein and Parkinson's disease.
000298 (2002)	E. Lohmann [France] ; A. Durr ; A. Brice	[Current data on the genetic of Parkinson disease].
000448 (2004)	P. Ibá Ez [France] ; E. Lohmann ; P. Pollak ; F. Durif ; C. Tranchant ; Yves Agid [France] ; A. Dürr ; A. Brice	Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease.
000469 (????)	P. Ibá Ez [France] ; A-M Bonnet ; B. Débarges ; E. Lohmann ; F. Tison ; P. Pollak ; Yves Agid ; A. Dürr ; A. Brice	Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease.
000485 (2004)	M. Martinez ; A. Brice ; J. Vaughan ; A. Zimprich ; M. Breteler ; G. Meco ; A. Filla ; M. Farrer ; C. Betard ; J. Hardy ; G. De Michele ; V. Bonifati ; B. Oostra ; T. Gasser ; N. Wood ; A. Durr ; F. The	Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease
000586 (2006)	M. Sharma ; J C Mueller ; A. Zimprich ; P. Lichtner ; A. Hofer ; P. Leitner ; S. Maass ; D. Berg ; A. Dürr ; V. Bonifati ; G. De Michele ; B. Oostra ; A. Brice ; N W Wood ; B. Muller-Myhsok ; T. Gasser	The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations
000738 (2007)	P. Charles [France] ; A. Camuzat ; N. Benammar ; F. Sellal ; A. Destée ; A-M Bonnet ; S. Lesage ; I. Le Ber ; G. Stevanin ; A. Dürr ; A. Brice	Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
000762 (2008)	S. Lesage ; E. Lohmann ; F. Tison ; F. Durif ; A. Dürr ; A. Brice	Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls.
000924 (2008)	S. Lesage [France] ; S. Belarbi ; A. Troiano ; C. Condroyer ; N. Hecham ; P. Pollak ; E. Lohman ; T. Benhassine ; F. Ysmail-Dahlouk ; A. Dürr ; M. Tazir ; A. Brice	Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?
000926 (2009)	E. Lohmann ; S. Thobois ; S. Lesage ; E. Broussolle ; S Tezenas Du Montcel ; M J. Ribeiro ; P. Remy ; A. Pelissolo ; B. Dubois ; L. Mallet ; P. Pollak ; Yves Agid [France] ; A. Brice	A multidisciplinary study of patients with early-onset PD with and without parkin mutations
000C18 (2010)	A R Troiano [France] ; A. Elbaz ; E. Lohmann ; S. Belarbi ; M. Vidailhet ; A-M Bonnet ; S. Lesage ; P. Pollak ; C. Cazeneuve ; M. Borg ; J. Feingold ; A. Dürr ; M. Tazir ; A. Brice	Low disease risk in relatives of north african lrrk2 Parkinson disease patients.
000C70 (2011)	S. Lesage [France] ; C. Condroyer ; N. Hecham ; M. Anheim ; S. Belarbi ; E. Lohman ; F. Viallet ; P. Pollak ; M. Abada ; A. Dürr ; M. Tazir ; A. Brice	Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa.
000D36 (1990)	M. Ruberg [France] ; W. Mayo ; A. Brice ; C. Duyckaerts ; J J Hauw ; H. Simon ; M. Lemoal ; Yves Agid [France]	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.
000E38 (2012)	M. Anheim [France] ; A. Elbaz ; S. Lesage ; A. Durr ; C. Condroyer ; F. Viallet ; P. Pollak ; B. Bonaïti ; C. Bonaïti-Pellié ; A. Brice	Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers.
000E95 (2012)	S. Lesage [France] ; C. Condroyer ; S. Klebe ; A. Honoré ; F. Tison ; C. Brefel-Courbon ; A. Dürr ; A. Brice	Identification of VPS35 mutations replicated in French families with Parkinson disease.
001231 (2014)	C A Gautier [France] ; O. Corti [France] ; A. Brice [France]	Mitochondrial dysfunctions in Parkinson's disease.

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