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La maladie de Parkinson en France (serveur d'exploration) - Curation (PubMed)

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List of bibliographic references

Number of relevant bibliographic references: 15.
Ident.Authors (with country if any)Title
000400 (2015) Yolaine Ollivier [France] ; Armelle Magot [France] ; Philippe Latour [France] ; Julie Perrier [France] ; Sandra Mercier [France] ; Thierry Maisonobe [France] ; Yann Péréon [France]Clinical and electrophysiological features in a French family presenting with seipinopathy.
000643 (2013) Wassilios G. Meissner [France] ; Marie Fernet ; Jérôme Couturier ; Janet Hall ; Anthony Laugé ; Patrick Henry ; Dominique Stoppa-Lyonnet ; François TisonIsolated generalized dystonia in biallelic missense mutations of the ATM gene.
000715 (2013) Suzanne Lesage [France] ; Mathieu Anheim ; Franck Letournel ; Luc Bousset ; Aurélie Honoré ; Nelly Rozas ; Laura Pieri ; Karine Madiona ; Alexandra Dürr ; Ronald Melki ; Christophe Verny ; Alexis BriceG51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome.
000800 (2012) Suzanne Lesage [France] ; Christel Condroyer ; Stephan Klebe ; Ebba Lohmann ; Franck Durif ; Philippe Damier ; François Tison ; Mathieu Anheim ; Aurélie Honoré ; François Viallet ; Anne-Marie Bonnet ; Anne-Marie Ouvrard-Hernandez ; Marie Vidailhet ; Alexandra Durr ; Alexis BriceEIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?
000A42 (2010) Suzanne Lesage [France] ; Christel Condroyer ; Ebba Lohman ; André Troiano ; François Tison ; François Viallet ; Philippe Damier ; Christine Tranchant ; Marie Vidhaillet ; Anne-Marie Ouvrard-Hernandez ; Alexandra Dürr ; Alexis BriceFollow-up study of the GIGYF2 gene in French families with Parkinson's disease.
000B54 (2009) Ebba Lohmann [France] ; Laurence Leclere ; Francesca De Anna ; Suzanne Lesage ; Bruno Dubois ; Yves Agid ; Alexandra Dürr ; Alexis BriceA clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations.
000D78 (2007) Suzanne Lesage [France] ; Laurence Leclere ; Ebba Lohmann ; Michel Borg ; Merle Ruberg ; Alexandra Dürr ; Alexis BriceFrequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease.
000E04 (2006) Anne-Louise Leutenegger [France] ; Mustafa A M. Salih ; Pablo Ibá Ez ; Maowia M. Mukhtar ; Suzanne Lesage ; Ali Arabi ; Ebba Lohmann ; Alexandra Dürr ; Ammar E M. Ahmed ; Alexis BriceJuvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1.
000E83 (2005) Suzanne Lesage ; Pablo Ibanez ; Ebba Lohmann ; Pierre Pollak ; François Tison ; Myriem Tazir ; Anne-Louise Leutenegger ; Joao Guimaraes ; Anne-Marie Bonnet ; Yves Agid ; Alexandra Dürr ; Alexis BriceG2019S LRRK2 mutation in French and North African families with Parkinson's disease.
000E97 (2005) Maria Martinez [France] ; Alexis Brice ; Jenny R. Vaughan ; Alexander Zimprich ; Monique M B. Breteler ; Giuseppe Meco ; Alessandro Filla ; Matthew J. Farrer ; Christine Bétard ; Andrew Singleton ; John Hardy ; Giuseppe De Michele ; Vincenzo Bonifati ; Ben A. Oostra ; Thomas Gasser ; Nick W. Wood ; Alexandra DürrApolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease.
001317 (1999) S. Schraen-Maschke [France] ; S. Brique ; M C Chartier-Harlin ; E. Brique ; A. Destée ; B. SablonnièreAnalysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.
001367 (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 ; Y. Agid ; A. BriceA 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.
001368 (1999) S S Mirra [États-Unis] ; J R Murrell ; M. Gearing ; M G Spillantini ; M. Goedert ; R A Crowther ; A I Levey ; R. Jones ; J. Green ; J M Shoffner ; B H Wainer ; M L Schmidt ; J Q Trojanowski ; B. GhettiTau pathology in a family with dementia and a P301L mutation in tau.
001375 (1999) N. Sabbagh [France] ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Y. Agid ; F. BrolyCYP2D6 polymorphism and Parkinson's disease susceptibility.
001489 (1997) V. Planté-Bordeneuve [France] ; D. Taussig ; F. Thomas ; G. Said ; N W Wood ; C D Marsden ; A E HardingEvaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele.

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