Ident. | Authors (with country if any) | Title |
---|
000114 |
Suzanne Lesage [France] ; Isabelle Le Ber [France] ; Christel Condroyer [France] ; Emmanuel Broussolle [France] ; Audrey Gabelle [France] ; Stéphane Thobois [France] ; Florence Pasquier [France] ; Karl Mondon [France] ; Patrick A. Dion [Canada] ; Daniel Rochefort [Canada] ; Guy A. Rouleau [Canada] ; Alexandra Dürr [France] ; Alexis Brice [France] | C9orf72 repeat expansions are a rare genetic cause of parkinsonism |
000329 |
Suzanne Lesage [France] ; Mathieu Anheim [France] ; Christel Condroyer [France] ; Pierre Pollak [France] ; Franck Durif [France] ; Céline Dupuits [France] ; François Viallet [France] ; Ebba Lohmann [France] ; Jean-Christophe Corvol [France] ; Aurélie Honore [France] ; Sophie Rivaud [France] ; Marie Vidailhet [France] ; Alexandra Dürr [France] ; Alexis Brice [France] | Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease |
000469 |
Suzanne Lesage [France] ; Etienne Patin [France] ; Christel Condroyer [France] ; Anne-Louise Leutenegger [France] ; Ebba Lohmann [France] ; Nir Giladi [Israël] ; Anat Bar-Shira [Israël] ; Soraya Belarbi [Algérie] ; Nassima Hecham [Algérie] ; Pierre Pollak [France] ; Anne-Marie Ouvrard-Hernandez [France] ; Soraya Bardien [Afrique du Sud] ; Jonathan Carr [Afrique du Sud] ; Traki Benhassine [Algérie] ; Hiroyuki Tomiyama [Japon] ; Caroline Pirkevi [Turquie] ; Tarik Hamadouche [Algérie] ; Cécile Cazeneuve [France] ; A. Nazli Basak [Turquie] ; Nobutaka Hattori [Japon] ; Alexandra Dürr [France] ; Meriem Tazir [Algérie] ; Avi Orr-Urtreger [Israël] ; Lluis Quintana-Murci [France] ; Alexis Brice [France] | Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans |
000571 |
Pablo Ibanez [France, Royaume-Uni] ; LESAGE [France] ; Sabine Janin [France] ; Ebba Lohmann [France] ; Frank Durif [France] ; Alain Destée [France] ; Anne-Marie Bonnet [France] ; Christine Brefel-Courbon [France] ; Simon Heath [France] ; Diana Zelenika [France] ; Yves Agid [France] ; Alexandra Dürr [France] ; Alexis Brice [France] | α-Synuclein Gene Rearrangements in Dominantly Inherited Parkinsonism : Frequency, Phenotype, and Mechanisms |
000583 |
Nadège Limousin [France] ; Eric Konofal [France] ; Elias Karroum [France] ; Ebba Lohmann [France] ; Ioannis Theodorou [France] ; Alexandra Dürr [France] ; Isabelle Amulf [France] | Restless Legs Syndrome, Rapid Eye Movement Sleep Behavior Disorder, and Hypersomnia in Patients with Two Parkin Mutations |
000713 |
Agnès Camuzat [France] ; Marc Romana [France] ; Alexandra Dürr [France] ; Josué Feingold [France] ; Alexis Brice [France] ; Merle Ruberg [France] ; Annie Lannuzel [France] | The PSP-Associated MAPT H1 Subhaplotype in Guadeloupean Atypical Parkinsonism |
000738 |
Corinne Lautier [États-Unis, France] ; Stefano Goldwurm [Italie] ; Alexandra Dürr [France] ; Barbara Giovannone [États-Unis] ; William G. Tsiaras [États-Unis] ; Gianni Pezzoli [Italie] ; Alexis Brice [France] ; Robert J. Smith [États-Unis] | Mutations in the GIGYF2 (TNRC15) Gene at the PARK11 Locus in Familial Parkinson Disease |
000847 |
Michael Schüpbach [France] ; Ebba Lohmann [France] ; Mathieu Anheim [France] ; Suzanne Lesage [France] ; Virginie Czernecki [France] ; Sadek Yaici [France] ; Yulia Worbe [France] ; Perrine Charles [France] ; Marie-Laure Welter [France] ; Pierre Pollak [France] ; Alexandra Dürr [France] ; Yves Agid [France] ; Alexis Brice [France] | Subthalamic nucleus stimulation is efficacious in patients with parkinsonism and LRRK2 mutations |
000884 |
Suzanne Lesage [France] ; Sabine Janin [France] ; Ebba Lohmann [France] ; Anne-Louise Leutenegger [France] ; Laurence Leclere [France] ; Francois Viallet [France] ; Pierre Pollak [France] ; Franck Durif [France] ; Stephane Thobois [France] ; Valérie Layet [France] ; Marie Vidailhet [France] ; Yves Agid [France] ; Alexandra Dürr [France] ; Alexis Brice [France] | LRRK2 exon 41 mutations in sporadic parkinson disease in europeans |
000948 |
Suzanne Lesage [France] ; Alexandra Dürr [France] ; Alexis Brice [France] | LRRK2, gène majeur de la maladie de parkinson dans les pays du Maghreb |
000995 |
Pablo Ibanez [France] ; Suzanne Lesage [France] ; Ebba Lohmann [France] ; Stéphane Thobois [France] ; Giuseppe De Michele [Italie] ; Michel Borg [France] ; Yves Agid [France] ; Alexandra Dürr [France] ; Alexis Brice [France] | Mutational analysis of the PINK I gene in early-onset parkinsonism in Europe and North Africa |
000A00 |
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 |
000B54 |
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. Fatter [États-Unis] ; Christine Betard [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 |
000D31 |
Stéphane Thobois [France] ; Maria-Joao Ribeiro [France] ; Ebba Lohmann [France] ; Alexandra Dürr [France] ; Pierre Pollak [France] ; Olivier Rascol [France] ; Stéphane Guillouet [France] ; Elizabeth Chapoy [France] ; Nicolas Costes [France] ; Yves Agid [France] ; Philippe Remy [France] ; Alexis Brice [France] ; Emmanuel Broussolle [France] | Young-onset Parkinson disease with and without parkin gene mutations: A fluorodopa F 18 positron emission tomography study |
000D65 |
Thomas Gasser [Allemagne] ; Susan Bressman [États-Unis] ; Alexandra Dürr [France] ; Joseph Higgins [États-Unis] ; Thomas Klockgether [Allemagne] ; Richard H. Myers [États-Unis] | Molecular diagnosis of inherited movement disorders. Movement disorders Society Task Force on Molecular Diagnosis |
000D96 |
Christoph-Burkhard Lücking [France] ; Véronique Chesneau [France] ; Ebba Lohmann [France] ; Patrice Verpillat [France] ; Cyprien Dulac [France] ; Anne-Marie Bonnet [France] ; Francesca Gasparini [France] ; Yves Agid [France] ; Alexandra Dürr [France] ; Alexis Brice [France] | Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease |
000F07 |
Enza Maria Valente [Italie, Royaume-Uni] ; Francesco Brancati [Italie] ; Alessandro Ferraris [Italie] ; Elizabeth A. Graham [Royaume-Uni] ; Mary B. Davis [Royaume-Uni] ; Monique M. B. Breteler [Pays-Bas] ; Thomas Gasser [Allemagne] ; Vincenzo Bonifati [Italie] ; Anna Rita Bentivoglio [Italie] ; Giuseppe De Michele [Italie] ; Alexandra Dürr [France] ; Pietro Cortelli [Italie] ; Dietmar Wassilowsky [Allemagne] ; Biswadjiet S. Harhangi [Pays-Bas] ; Nina Rawal [France] ; Viviana Caputo [Italie] ; Alessandro Filla [Italie] ; Giuseppe Meco [Italie] ; Ben A. Oostra [Pays-Bas] ; Alexis Brice [France] ; Alberto Albanese [Italie] ; Bruno Dallapiccola [Italie] ; Nicholas W. Wood [Royaume-Uni] | PARK6-linked parkinsonism occurs in several European families |
000F40 |
Nina Rawal [France] ; Magali Periquet [France] ; Alexandra Dürr [France] ; Giuseppe De Michele [Italie] ; Vincenzo Bonifati [Italie] ; Helio A. Teive [Brésil] ; Salmo Raskin [Brésil] ; Joao Guimaraes [Portugal] ; Yves Agid [France] ; Alexis Brice [France] | Exclusion of the Nurr1 gene in autosomal recessive Parkinson's disease |
000F60 |
Andrew West [États-Unis] ; Magali Periquet [France] ; Sarah Lincoln [États-Unis] ; Christoph B. Lücking [France, Allemagne] ; David Nicholl [Royaume-Uni] ; Vincenzo Bonifati [Italie] ; Nina Rawal [France] ; Thomas Gasser [Allemagne] ; Ebba Lohmann [France] ; Jean-Francois Deleuze [France] ; Demetrius Maraganore [États-Unis] ; Allan Levey [États-Unis] ; Nick Wood [Royaume-Uni] ; Alexandra Dürr [France] ; John Hardy [États-Unis] ; Alexis Brice [France] ; Matt Farrer [États-Unis] | Complex relationship between Parkin mutations and Parkinson disease |
000F70 |
Claire Borie [France] ; Francesca Gasparini [France] ; Patrice Verpillat [France] ; Anne-Marie Bonnet [France] ; Yves Agid [France] ; Gilles Hetet [France] ; Alexis Brice [France] ; Alexandra Dürr [France] ; Bernard Grandchamp [France] | Association study between iron-related genes polymorphisms and Parkinson's disease |
001040 |
Magali Periquet [France] ; Christoph B. Lücking [France] ; Jenny R. Vaughan [Royaume-Uni] ; Vincenzo Bonifati [Italie] ; Alexandra Dürr [France] ; Giuseppe De Michele [Italie] ; Martin W. Horstink [Pays-Bas] ; Matt Farrer [États-Unis] ; Sergei N. Illarioshkin [France] ; Pierre Pollak [France] ; Michel Borg [France] ; Christine Brefel-Courbon [Pays-Bas] ; Patrice Denefle [Allemagne] ; Giuseppe Meco [Italie] ; Thomas Gasser ; Monique M. B. Breteler ; Nick W. Wood [Royaume-Uni] ; Yves Agid [France] ; Alexis Brice [France] | Origin of the mutations in the parkin gene in Europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects |
001144 |
Alexandra Dürr [France] ; Christoph Lücking [France] ; Alexis Brice [France] | La maladie de Parkinson due aux mutations de la parkine |