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1

Implication du gène GBA dans la maladie de Parkinson en Tunisie : fréquence et caractéristique clinique

Romdhan, Sawssan Ben, Nouha, Bouzid, Salma, Sakka, Alexis, Brice, Dammak, Mariem, Suzanne, Lesage, Mhiri, Chokri

Journal:

Revue Neurologique

Year:

2019

Language:

french

File:

PDF, 299 KB

french, 2019

2

Recurrent polyradiculoneuropathy with the 17p11.2 deletion

Nadine Le Forestier, Eric LeGuern, Philippe Coullin, Nazha Birouk, Thierry Maisonobe, Alexis Brice, Jean Marc Léger, Pierre Bouche

Journal:

Year:

1997

Language:

english

File:

PDF, 24 KB

english, 1997

3

Polyneuropathy in autosomal dominant cerebellar ataxias: Phenotype–genotype correlation

Nathalie Kubis, Alexandra Dürr, Michel Gugenheim, Hervé Chneiweiss, Pilar Mazzetti, Alexis Brice, Pierre Bouche

Journal:

Year:

1999

Language:

english

File:

PDF, 101 KB

english, 1999

4

The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q

H. Z. Ring, H. Chang, Angèle Guilbot, Alexis Brice, Eric LeGuern, Uta Francke

Journal:

Year:

1999

Language:

english

File:

PDF, 228 KB

english, 1999

5

A de novoSPASTmutation leading to somatic mosaicism is associated with a later age at onset in HSP

Christel Depienne, Estelle Fedirko, Jean-Marc Faucheux, Sylvie Forlani, Bernard Bricka, Cyril Goizet, Sylvie Lesourd, Giovanni Stevanin, Merle Ruberg, Alexandra Durr, Alexis Brice

Journal:

Year:

2007

Language:

english

File:

PDF, 186 KB

english, 2007

6

Genetic association between alpha 2-macroglobulin gene and Alzheimer's disease in the French population

Patrice Verpillat, Sandrine Bouley, Didier Hannequin, Serge Belliard, Michele Puel, Dominique Campion, Francoise Clerget-Darpoux, Alexis Brice

Journal:

Neurobiology of Aging

Year:

2000

Language:

english

File:

PDF, 177 KB

english, 2000

7

The spectrum ofKIAA0196variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8

Jahic, Amir, Khundadze, Mukhran, Jaenisch, Nadine, Schüle, Rebecca, Klimpe, Sven, Klebe, Stephan, Frahm, Christiane, Kassubek, Jan, Stevanin, Giovanni, Schöls, Ludger, Brice, Alexis, Hübner, Christian

Journal:

Orphanet Journal of Rare Diseases

Year:

2015

Language:

english

File:

PDF, 1.58 MB

english, 2015

8

Implication of the Immune System in Alzheimer's Disease: Evidence from Genome-Wide Pathway Analysis

Lambert, Jean-Charles, Grenier-Boley, Benjamin, Chouraki, Vincent, Heath, Simon, Zelenika, Diana, Fievet, Nathalie, Hannequin, Didier, Pasquier, Florence, Hanon, Olivier, Brice, Alexis, Epelbaum, Jacq

Journal:

Journal of Alzheimer's Disease

Year:

2010

Language:

english

File:

PDF, 445 KB

english, 2010

9

Maneuvering in Poor Visibility: How Firms Play the Ecosystem Game when Uncertainty is High

Dattée, Brice, Alexy, Oliver, Autio, Erkko

Journal:

The Academy of Management Journal

Year:

2017

Language:

english

File:

PDF, 1.54 MB

english, 2017

10

Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry

Lee, Annie J., Wang, Yuanjia, Alcalay, Roy N., Mejia-Santana, Helen, Saunders-Pullman, Rachel, Bressman, Susan, Corvol, Jean-Christophe, Brice, Alexis, Lesage, Suzanne, Mangone, Graziella, Tolosa, Edu

Journal:

Movement Disorders

Year:

2017

Language:

english

File:

PDF, 262 KB

english, 2017

11

The relationship between the abundance of the Nigeria-Cameroon chimpanzee (Pan troglodytes ellioti) and its habitat: a conservation concern in Mbam-Djerem National Park, Cameroon

Kamgang, Serge Alexis, Bobo, Kadiri Serge, Maisels, Fiona, Ambahe, Ruffin Dupleix Delarue, Ambassa Ongono, Désiré Edgar, Gonder, Mary Katherine, Johnson, Paul, Marino, Jorgelina, Sinsin, Brice

Journal:

Year:

2018

Language:

english

File:

PDF, 1.90 MB

english, 2018

12

Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease

Smaili, Imane, Tesson, Christelle, Regragui, Wafa, Bertrand, HÃ©lÃ¨ne, Rahmani, Mounia, Bouslam, Naima, Benomar, Ali, Brice, Alexis, Lesage, Suzanne, Bouhouche, Ahmed

Journal:

Journal of Molecular Neuroscience

Year:

2020

File:

PDF, 825 KB

2020

13

Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph disease

Géraldine Cancel, Isabelle Gourfinkel-An, Giovanni Stevanin, Olivier Didierjean, Nacer Abbas, Etienne Hirsch, Yves Agid, Alexis Brice

Journal:

Year:

1998

Language:

english

File:

PDF, 159 KB

english, 1998

14

Edg-2 in myelin-forming cells: Isoforms, genomic mapping, and exclusion in Charcot-Marie-Tooth disease

Julien Allard, Sonia Barron, Suzanne Trottier, Pascale Cervera, Catherine Daumas-Duport, Eric Leguern, Alexis Brice, Jean-Charles Schwartz, Pierre Sokoloff

Journal:

Year:

1999

Language:

english

File:

PDF, 186 KB

english, 1999

15

Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness

Odile Dubourg, Choukri Barhoumi, Hamid Azzedine, Nazha Birouk, Alexis Brice, Pierre Bouche, Eric Leguern

Journal:

Year:

2000

Language:

english

File:

PDF, 269 KB

english, 2000

16

D2 dopamine receptor gene in myoclonic dystonia and essential myoclonus

Alexandra Dürr, Johann Tassin, Marie Vidailhet, Franck Durif, Pierre Jedynak, Yves Agid, Alexis Brice

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 176 KB

english, 2000

17

α2-Macroglobulin gene and Alzheimer's disease: Confirmation of association by haplotypes analyses

Patrice Verpillat, Sandrine Bouley, Didier Hannequin, Serge Belliard, Michèle Puel, Catherine Thomas-Anterion, Bruno Dubois, Yves Agid, Dominique Campion, Françoise Clerget-Darpoux, Alexis Brice

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 154 KB

english, 2000

18

CYP2D6 Polymorphism and Parkinson's disease susceptibility

Nada Sabbagh, Alexis Brice, Delphine Marez, Alexandra Dürr, Maryline Legrand, Jean-Marc Lo Guidice, Alain Destée, Yves Agid, Franck Broly

Journal:

Movement Disorders

Year:

1999

Language:

english

File:

PDF, 49 KB

english, 1999

19

Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan

Sergei N. Illarioshkin, Irina A. Ivanova-Smolenskaya, Rahmatullo A. Rahmonov, Elena D. Markova, Giovanni Stevanin, Alexis Brice

Journal:

Movement Disorders

Year:

2000

Language:

english

File:

PDF, 475 KB

english, 2000

20

Allelic association at the D14S43 locus in early onset Alzheimer's disease

Alexis Brice, Sandrine Tardieu, Dominique Campion, Eric Le Guern, Maria Martinez, Alexandre Carpentier, Christiane Penet, Bruno Dubois, Michel Bellis, Jacques Mallet, Didier Hannequin, Françoise Clerg

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 334 KB

english, 1995

21

SCA2 is not a major locus for ADCA type I in French families

Géraldine Cancel, Giovanni Stevanin, Alexandra Dürr, Hervé Chneiweiss, Christiane Penet, Yolaine Pothin, Yves Agid, Dr. Alexis Brice

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 357 KB

english, 1995

22

Evidence for apolipoprotein E ϵ4 association in early-onset Alzheimer's patients with late-onset relatives

Jordi Pérez-Tur, Dominique Campion, Maria Martinez, Alexis Brice, Sandrine Tardieu, Didier Hannequin, Yves Agid, André Delacourte, Françoise Clerget-Darpoux, Dr. Marie-Christine Chartier-Harlin

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 447 KB

english, 1995

23

Rapid detection of 17p11.2 rearrangements by FISH without cell culture (direct FISH, DFISH): A prospective study of 130 patients with inherited peripheral neuropathies

Nicole Ravisé, Odile Dubourg, Sandrine Tardieu, Françoise Aurias, Monique Mercadiel, Philippe Coullin, Merle Ruberg, Martin Catala, Sylvie Lesourd, Alexis Brice, Eric LeGuern

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 135 KB

english, 2003

24

Detection of genomic rearrangements by DHPLC: A prospective study of 90 patients with inherited peripheral neuropathies associated with 17p11.2 rearrangements

Mourad Naïmi, Sandrine Tardieu, Christel Depienne, Merle Ruberg, Alexis Brice, Odile Dubourg, Eric LeGuern

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 125 KB

english, 2005

25

Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease

Maria Martinez, 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

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2005

Language:

english

File:

PDF, 51 KB

english, 2005

26

Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: Large-scale collaborative study

Evangelos Evangelou, Demetrius M. Maraganore, Grazia Annesi, Laura Brighina, Alexis Brice, Alexis Elbaz, Carlo Ferrarese, Georgios M. Hadjigeorgiou, Rejko Krueger, Jean-Charles Lambert, Suzanne Lesage

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2010

Language:

english

File:

PDF, 150 KB

english, 2010

27

Spinocerebellar ataxia type 10 in the French population

Hiroto Fujigasaki, Sandrine Tardieu, Agnès Camuzat, Giovanni Stevanin, Eric LeGuern, Tohru Matsuura, Tetsuo Ashizawa, Alexandra Dürr, Alexis Brice

Journal:

Annals of Neurology

Year:

2002

Language:

english

File:

PDF, 214 KB

english, 2002

28

Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31

Stéphanie Baulac, Fabienne Picard, Alexandra Herman, Josué Feingold, Emmanuelle Genin, Edouard Hirsch, Jean-François Prud'Homme, Michel Baulac, Alexis Brice, Eric LeGuern

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 208 KB

english, 2001

29

Is the Saitohin gene involved in neurodegenerative diseases?

Patrice Verpillat, Sylvain Ricard, Didier Hannequin, Bruno Dubois, Jacqueline Bou, Agnès Camuzat, Laurent Pradier, Thierry Frebourg, Alexis Brice, Françoise Clerget-Darpoux, Jean-François Deleuze, Dom

Journal:

Annals of Neurology

Year:

2002

Language:

english

File:

PDF, 69 KB

english, 2002

30

Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p

Giovanni Stevanin, Naima Bouslam, Stéphane Thobois, Hamid Azzedine, Lucas Ravaux, Anne Boland, Martin Schalling, Emmanuel Broussolle, Alexandra Dürr, Alexis Brice

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 288 KB

english, 2004

31

Parkin and Parkinson's: More than homonymy?

Olga Corti, Alexis Brice

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 106 KB

english, 2001

32

Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)

Naima Bouslam, Ali Benomar, Hamid Azzedine, Ahmed Bouhouche, Michito Namekawa, Stephan Klebe, Céline Charon, Alexandra Durr, Merle Ruberg, Alexis Brice, Mohamed Yahyaoui, Giovanni Stevanin

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 210 KB

english, 2005

33

Age at onset variance analysis in spinocerebellar ataxias: A study in a Dutch–French cohort

Bart P. C. van de Warrenburg, Harrie Hendriks, Alexandra Dürr, Martin C. A. van Zuijlen, Giovanni Stevanin, Agnès Camuzat, Richard J. Sinke, Alexis Brice, Berry P. H. Kremer

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 105 KB

english, 2005

34

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

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 Brice

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 79 KB

english, 2005

35

Ultrastructural PMP22 expression in inherited demyelinating neuropathies

Dr Jean-Michel Vallat, Philippe Sindou, Pierre-Marie Preux, Fransois Tabaraud, André-Michel Milor, Philippe Couratier, Eric Leguern, Alexis Brice

Journal:

Annals of Neurology

Year:

1996

Language:

english

File:

PDF, 485 KB

english, 1996

36

Differential distribution of the normal and mutated forms of huntingtin in the human brain

Isabelle Gourfinkel-An, Géraldine Cancel, Yvon Trottier, Didier Devys, Laszlo Tora, Yves Lutz, Georges Imbert, Frédéric Saudou, Giovanni Stevanin, Yves Agid, Alexis Brice, Jean-Louis Mandel, Dr. Etien

Journal:

Annals of Neurology

Year:

1997

Language:

english

File:

PDF, 873 KB

english, 1997

37

Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I

Dr Sophie Rivaud-Pechoux, Alexandra Dürr, Bertrand Gaymard, Géaraldine Cancel, Christoph J. Ploner, Yves Agid, Alexis Brice, Charles Pierrot-Deseilligny

Journal:

Annals of Neurology

Year:

1998

Language:

english

File:

PDF, 565 KB

english, 1998

38

From Genes to Proteins in Mendelian Parkinson's Disease: An Overview

Caroline Pirkevi, Suzanne Lesage, Alexis Brice, A. Nazli Başak

Journal:

The Anatomical Record Advances in Integrative Anatomy and Evolutionary Biology

Year:

2009

Language:

english

File:

PDF, 115 KB

english, 2009

39

Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism

Suzanne Lesage, Periquet Magali, Ebba Lohmann, Lucette Lacomblez, Helio Teive, Sabine Janin, Pierre-Yves Cousin, Alexandra Dürr, Alexis Brice

Journal:

Year:

2007

Language:

english

File:

PDF, 210 KB

english, 2007

40

Partial deletion of the MAPT gene: A novel mechanism of FTDP-17

Anne Rovelet-Lecrux, Magalie Lecourtois, Catherine Thomas-Anterion, Isabelle Le Ber, Alexis Brice, Thierry Frebourg, Didier Hannequin, Dominique Campion

Journal:

Year:

2009

Language:

english

File:

PDF, 338 KB

english, 2009

41

KCNC3: phenotype, mutations, channel biophysics—a study of 260 familial ataxia patients

Karla P. Figueroa, Natali A. Minassian, Giovanni Stevanin, Michael Waters, Vartan Garibyan, Sylvie Forlani, Adam Strzelczyk, Katrin Bürk, Alexis Brice, Alexandra Dürr, Diane M. Papazian, Stefan M. Pul

Journal:

Year:

2010

Language:

english

File:

PDF, 180 KB

english, 2010

42

The (−16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients

Claudia Cagnoli, Alessandro Brussino, Eleonora Di Gregorio, Alfredo Brusco, Giovanni Stevanin, Alexandra Durr, Alexis Brice

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 47 KB

english, 2007

43

Spastic paraplegia 15: Linkage and clinical description of three Tunisian families

Amir Boukhris, Imed Feki, Elodie Denis, Mohamed Imed Miladi, Alexis Brice, Chokri Mhiri, Giovanni Stevanin

Journal:

Movement Disorders

Year:

2008

Language:

english

File:

PDF, 206 KB

english, 2008

44

Are parkin patients particularly suited for deep-brain stimulation?

Ebba Lohmann, Marie-Laure Welter, Valérie Fraix, Paul Krack, Suzanne Lesage, Sophie Laine, Marie-Laure Tanguy, Jean-Luc Houeto, Valérie Mesnage, Pierre Pollak, Alexandra Durr, Yves Agid, Alexis Brice

Journal:

Movement Disorders

Year:

2008

Language:

english

File:

PDF, 64 KB

english, 2008

45

Huntington's disease-like 2 in Brazil—Report of 4 patients

Guilherme G. Riccioppo Rodrigues, Ruth H. Walker, Alexis Brice, Cécile Cazeneuve, Odile Russaouen, Helio A.G. Teive, Renato Puppi Munhoz, Nilson Becker, Salmo Raskin, Lineu Cesar Werneck, Wilson Marqu

Journal:

Movement Disorders

Year:

2008

Language:

english

File:

PDF, 225 KB

english, 2008

46

The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical Parkinsonism

Agnès Camuzat, Marc Romana, Alexandra Dürr, Josué Feingold, Alexis Brice, Merle Ruberg, Annie Lannuzel

Journal:

Movement Disorders

Year:

2008

Language:

english

File:

PDF, 177 KB

english, 2008

47

Infantile hypokinetic-hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene

Diane Doummar, Fabienne Clot, Marie Vidailhet, Alexandra Afenjar, Alexandra Durr, Alexis Brice, Cyril Mignot, Agnès Guet, Thierry Billette de Villemeur, Diana Rodriguez

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 302 KB

english, 2009

48

Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations

Salima Assami, Hamid Azzedine, Sonia Nouioua, Emeline Mundwiller, Soulaiman Mahoui, Samira Makri, Meriam Djemai, Djamel Grid, Alexis Brice, Tarik Hamadouche, Giovanni Stevanin, Meriem Tazir

Journal:

Movement Disorders

Year:

2011

Language:

english

File:

PDF, 486 KB

english, 2011

49

Annual change in Friedreich's ataxia evaluated by the Scale for the Assessment and Rating of Ataxia (SARA) is independent of disease severity

Cecilia Marelli, Julie Figoni, Perrine Charles, Mathieu Anheim, Maya Tchikviladze, Carlo-Maria Vincitorio, Sophie Tezenas du Montcel, Alexis Brice, Jean Louis Golmard, Alexandra Dürr

Journal:

Movement Disorders

Year:

2012

Language:

english

File:

PDF, 1006 KB

english, 2012

50

The normal parkin sequence

Yong Ren, Xiaojun Liu, Suzanne Lesage, Miao Cai, Jiali Pu, Baorong Zhang, Alexis Brice, Jian Feng

Journal:

Movement Disorders

Year:

2012

Language:

english

File:

PDF, 1.01 MB

english, 2012