Alpha 2.0
Login Register
» Authors » L Viollet

L Viollet

Explore the profile of L Viollet including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 17
Citations 1905
Followers 0
Related Specialties
Genetics
Neurology
Cell Biology
Top 10 Co-Authors
A Munnich
S Lefebvre
J Melki
O Clermont
P Burlet
L Burglen
M Fardeau
J Estaquier
V Monceaux
N B Romero
Published In
Neurology
Genomics
J Virol
Cell
Am J Med Genet
Affiliations
Soon will be listed here.
Recent Articles
1.
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7
Ben Ammar A, Petit F, Alexandri N, Gaudon K, Bauche S, Rouche A, et al.
J Neurol . 2009 Dec; 257(5):754-66. PMID: 20012313
Congenital myasthenic syndromes (CMSs) are a heterogeneous group of diseases caused by genetic defects affecting neuromuscular transmission. Mutations of DOK7 have recently been described in recessive forms of CMS. Dok-7...
2.
Early divergence in lymphoid tissue apoptosis between pathogenic and nonpathogenic simian immunodeficiency virus infections of nonhuman primates
Cumont M, Diop O, Vaslin B, Elbim C, Viollet L, Monceaux V, et al.
J Virol . 2007 Nov; 82(3):1175-84. PMID: 18032487
The events that contribute to the progression to AIDS during the acute phase of a primate lentiviral infection are still poorly understood. In this study, we used pathogenic and nonpathogenic...
3.
CD4+ CCR5+ T-cell dynamics during simian immunodeficiency virus infection of Chinese rhesus macaques
Monceaux V, Viollet L, Petit F, Cumont M, Kaufmann G, Aubertin A, et al.
J Virol . 2007 Sep; 81(24):13865-75. PMID: 17898067
Simian immunodeficiency virus (SIV) infection of rhesus macaques (RMs) provides a reliable model to study the relationship between lentivirus replication, cellular immune responses, and CD4+ T-cell dynamics. Here we investigated,...
4.
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation
Yanagisawa A, Bouchet C, van den Bergh P, Cuisset J, Viollet L, Leturcq F, et al.
Neurology . 2007 Jul; 69(12):1254-60. PMID: 17634419
Background: Dystroglycanopathies are a group of congenital muscular dystrophies (CMDs) with autosomal recessive inheritance, often associated with CNS and ocular involvement. They are characterized by the abnormal glycosylation of alpha-dystroglycan,...
5.
TGF-beta in intestinal lymphoid organs contributes to the death of armed effector CD8 T cells and is associated with the absence of virus containment in rhesus macaques infected with the simian immunodeficiency virus
Cumont M, Monceaux V, Viollet L, Lay S, Parker R, Hurtrel B, et al.
Cell Death Differ . 2007 Jul; 14(10):1747-58. PMID: 17612589
SIV-infected macaques exhibit distinct rates of progression to AIDS and despite significant increases in CD8+ T cells, immune cells fail to control and eradicate SIV in vivo. Here, we investigated...
6.
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 gene
Fischer D, Herasse M, Ferreiro A, Barragan-Campos H, Chiras J, Viollet L, et al.
Neurology . 2006 Dec; 67(12):2217-20. PMID: 17190947
Objective: To characterize the muscle involvement of patients with central core disease (CCD) caused by mutations in the ryanodine receptor 1 gene (RYR1) and to compare these findings with those...
7.
A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36
Maystadt I, Zarhrate M, Leclair-Richard D, Estournet B, Barois A, Renault F, et al.
Neurology . 2006 May; 67(1):120-4. PMID: 16728649
Objective: To describe the clinical features of a novel variant of autosomal recessive lower motor neuron disease (LMND) with childhood onset and to map the disease-causing gene. Methods: The authors...
8.
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locus
Romero N, Herasse M, Monnier N, Leroy J, Fischer D, Ferreiro A, et al.
Acta Myol . 2006 Mar; 24(2):70-3. PMID: 16550918
We analysed the clinical, histochemical, ultrastructural and genetic data of patients affected by central core disease (CCD) studied during the last 20 years. From a total series of 86 CCD-families,...
9.
Allelic heterogeneity of SMARD1 at the IGHMBP2 locus
Maystadt I, Zarhrate M, Landrieu P, Boespflug-Tanguy O, Sukno S, Collignon P, et al.
Hum Mutat . 2004 Apr; 23(5):525-6. PMID: 15108294
Spinal Muscular Atrophy with Respiratory Distress (SMARD) is an autosomal recessive disorder characterized by neurogenic muscular atrophy due to progressive anterior horn cell degeneration and early life-threatening respiratory failure ascribed...
10.
New autosomal recessive cerebellar ataxia disorder in a large inbred Lebanese family
Megarbane A, Delague V, Ruchoux M, Rizkallah E, Maurage C, Viollet L, et al.
Am J Med Genet . 2001 Jun; 101(2):135-41. PMID: 11391656
A large inbred Lebanese pedigree with congenital spastic ataxia, microcephaly, optic atrophy, short stature, speech defect, abnormal osmiophilic pattern of skin vessels, cerebellar atrophy, and severe mental retardation transmitted as...