Alexis Brice

发表

Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion

Y. Agid, A. Brice, R. Gouider, 1995, Neurology.

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.

Y. Agid, J. Melki, A. Dürr, 1994, Human molecular genetics.

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.

G. Gyapay, J. Weissenbach, D. Le Paslier, 1995, American journal of human genetics.

SMN gene analysis of the spinal form of Charcot-Marie-Tooth disease.

J. Melki, A. Brice, J. Pouget, 1997, Journal of medical genetics.

A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease.

A. Mégarbané, A. Brice, D. Sherman, 2001, Human molecular genetics.

Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormality

A. Dürr, C. Depienne, A. Brice, 2013, European journal of neurology.

Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease

A Dürr, Y Agid, Y. Agid, 2004, The Lancet.

Frequency of the DYT1 mutation in primary torsion dystonia without family history.

Y. Agid, M. Vidailhet, A. Dürr, 2000, Archives of neurology.

DYT1 mutation in French families with idiopathic torsion dystonia.

Y. Agid, M. Vidailhet, A. Durr, 1999, Brain : a journal of neurology.

Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.

Í. Lopes-Cendes, S. Tsuji, A. Brice, 2001, American journal of human genetics.

Correlation between left ventricular hypertrophy and GAA trinucleotide repeat length in Friedreich's ataxia.

M. Komajda, M. Koenig, A. Dürr, 1997, Circulation.

No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.

Miguel Ángel Martínez, Y. Agid, B. Dubois, 1996, Journal of medical genetics.

Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease

Y. Agid, P. Pollak, A. Dürr, 2004, Neurology.

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.

D. Hernandez, M. Nalls, A. Singleton, 2013, Human molecular genetics.

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus

Y. Agid, G. Stevanin, M. Hamida, 1994, Neurology.

Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.

Y. Agid, A. Brice, N. Birouk, 1996, American journal of human genetics.

Neurophysiological evidence of corticospinal tract abnormality in patients with Parkin mutations

A. Brice, L. Santoro, G. De Michele, 2006, Journal of Neurology.

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.

J. Weissenbach, J. Burgunder, J. Prud'homme, 2000, Human molecular genetics.

SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum

A. Durr, J. Melki, S. Hanein, 2009, Neurology.