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La maladie de Parkinson en France (serveur d'exploration) - Exploration (Accueil)

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Family Conflict (psychology) < Family Health < Family Practice  Facettes :

List of bibliographic references indexed by Family Health

Number of relevant bibliographic references: 15.
Ident.Authors (with country if any)Title
000687 (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.
000E66 (2013) Wassilios G. Meissner [France] ; Marie Fernet [France] ; Jérôme Couturier [France] ; Janet Hall [France] ; Anthony Laugé [France] ; Patrick Henry [France] ; Dominique Stoppa-Lyonnet [France] ; François Tison [France]Isolated generalized dystonia in biallelic missense mutations of the ATM gene
000E76 (2013) Suzanne Lesage [France] ; Mathieu Anheim [France] ; Franck Letournel ; Luc Bousset ; Aurélie Honoré [France] ; Nelly Rozas [France] ; Laura Pieri ; Karine Madiona ; Alexandra Dürr [France] ; Ronald Melki ; Christophe Verny [France] ; Alexis Brice [France]G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome
001147 (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?
001A30 (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.
001F64 (2009) Ebba Lohmann [France] ; Laurence Leclere ; Francesca De Anna ; Suzanne Lesage ; Bruno Dubois ; Yves Agid [France] ; Alexandra Dürr ; Alexis BriceA clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations.
002624 (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.
002B15 (2006) Anne-Louise Leutenegger [France] ; Mustafa A. M. Salih [Arabie saoudite] ; Pablo Ibanez [France] ; Maowia M. Mukhtar [Soudan] ; Suzanne Lesage [France] ; All Arabi [Soudan] ; Ebba Lohmann [France] ; Alexandra Dürr [France] ; Ammar E. M. Ahmed [Soudan] ; Alexis Brice [France]Juvenile-onset parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1
002C87 (2005) Maria Martinez [France] ; Alexis Brice [France] ; Jenny R. Vaughan [Royaume-Uni] ; Alexander Zimprich [Allemagne] ; Monique M. B. Breteler [Pays-Bas] ; Giuseppe Meco [Italie] ; Alessandro Filla [Italie] ; Matthew J. Farrer [États-Unis] ; Christine Bétard [France] ; Andrew Singleton [États-Unis] ; John Hardy [États-Unis] ; Giuseppe De Michele [Italie] ; Vincenzo Bonifati [Italie] ; Ben A. Oostra [Pays-Bas] ; Thomas Gasser [Allemagne] ; Nick W. Wood [Royaume-Uni] ; Alexandra Dürr [France]Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease
002D69 (2005) Suzanne Lesage [France] ; Pablo Ibanez [France] ; Ebba Lohmann [France] ; Pierre Pollak [France] ; Francois Tison [France] ; Myriem Tazir [Algérie] ; Anne-Louise Leutenegger [France] ; Joao Guimaraes [Portugal] ; Anne-Marie Bonnet [France] ; Yves Agid [France] ; Alexandra Durr [France] ; Alexis Brice [France]G2019S LRRK2 mutation in French and North African families with Parkinson's disease
003C35 (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.
003D14 (1999) Nacer Abbas [France] ; Christoph B. Lücking [France] ; Sylvain Ricard [France] ; Alexandra Dürr [France] ; Vincenzo Bonifati [Italie] ; Giuseppe De Michele [Italie] ; Sandrine Bouley [France] ; Jenny R. Vaughan [Royaume-Uni] ; Thomas Gasser [Allemagne] ; Roberto Marconi [Italie] ; Emmanuel Broussolle [France] ; Christine Brefel-Courbon [France] ; Biswadjiet S. Harhangi [Pays-Bas] ; Ben A. Oostra [Pays-Bas] ; Edito Fabrizio [Italie] ; Georg A. Böhme [France] ; Laurent Pradier [France] ; Nick W. Wood [Royaume-Uni] ; Alessandro Filla [Italie] ; Giuseppe Meco [Italie] ; Patrice Denefle [France] ; Yves Agid [France] ; Alexis Brice [France]A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe
003F25 (1999) N. Sabbagh [France] ; A. Brice [France] ; D. Marez [France] ; A. Dürr [France] ; M. Legrand [France] ; J.-M. Lo Guidice [France] ; A. Destee [France] ; Yves Agid [France] ; F. Broly [France]CYP2D6 polymorphism and Parkinson's disease susceptibility
003F28 (1999) S. Schraen-Maschke [France] ; S. Brique [France] ; M.-C. Chartier-Harlin [France] ; E. Brique [France] ; A. Destee [France] ; B. Sablonniere [France]Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation
004440 (1997) V. Plante-Bordeneuve [France] ; D. Taussig [France] ; F. Thomas [France] ; G. Said [France] ; N. W. Wood [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] ; A. E. Harding [Royaume-Uni]Evaluation 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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