L Brenguier
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Explore the profile of L Brenguier including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
372
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Recent Articles
1.
Dincer P, Leturcq F, Richard I, Piccolo F, Yalnizoglu D, De Toma C, et al.
Ann Neurol
. 1997 Aug;
42(2):222-9.
PMID: 9266733
Autosomal recessive limb girdle muscular dystrophy (LGMD2) is a clinically and genetically heterogenous group of diseases involving at least six different loci. Five genes have already been identified: calpain-3 at...
2.
Richard I, Brenguier L, Dincer P, Roudaut C, BADY B, Burgunder J, et al.
Am J Hum Genet
. 1997 May;
60(5):1128-38.
PMID: 9150160
Limb-girdle muscular dystrophies (LGMDs) are a group of neuromuscular diseases presenting great clinical heterogeneity. Mutations in CANP3, the gene encoding muscle-specific calpain, were used to identify this gene as the...
3.
Beckmann J, Richard I, Broux O, Fougerousse F, Allamand V, Chiannilkulchai N, et al.
Neuromuscul Disord
. 1996 Dec;
6(6):455-62.
PMID: 9027855
The autosomal recessive forms of limb-girdle muscular dystrophies are encoded by at least five distinct genes. The work performed towards the identification of two of these is summarized in this...
4.
Allamand V, Broux O, Richard I, Fougerousse F, Chiannilkulchai N, Bourg N, et al.
Am J Hum Genet
. 1995 Jun;
56(6):1417-30.
PMID: 7762565
A gene for a recessive form of limb-girdle muscular dystrophy (LGMD2A) has been localized to chromosome 15. A physical map of the 7-cM candidate 15q15.1-q21.1 region has been constructed by...
5.
Richard I, Broux O, Allamand V, Fougerousse F, Chiannilkulchai N, Bourg N, et al.
Cell
. 1995 Apr;
81(1):27-40.
PMID: 7720071
Limb-girdle muscular dystrophies (LGMDs) are a group of inherited diseases whose genetic etiology has yet to be elucidated. The autosomal recessive forms (LGMD2) constitute a genetically heterogeneous group with LGMD2A...
6.
Richard I, Broux O, Chiannilkulchai N, Fougerousse F, Allamand V, Bourg N, et al.
Genomics
. 1994 Oct;
23(3):619-27.
PMID: 7851890
One hundred forty-nine chromosome 15 loci were mapped by PCR with respect to chromosome breakpoints in three somatic cell hybrids retaining total or part of chromosome 15 and to a...
7.
de Souza A, Allamand V, Richard I, Brenguier L, Beckmann J
Hum Mol Genet
. 1994 Feb;
3(2):382.
PMID: 8004117
No abstract available.
8.
Allamand V, de Souza A, Richard I, Brenguier L, Beckmann J
Hum Mol Genet
. 1994 Feb;
3(2):382.
PMID: 8004116
No abstract available.
9.
de Souza A, Allamand V, Richard I, Brenguier L, Beckmann J
Hum Mol Genet
. 1994 Feb;
3(2):381.
PMID: 8004115
No abstract available.
10.
Fougerousse F, Broux O, Richard I, Allamand V, de Souza A, Bourg N, et al.
Hum Mol Genet
. 1994 Feb;
3(2):285-93.
PMID: 8004096
A gene responsible for an autosomal recessive form of limb girdle muscular dystrophy (LGMD2, MIM number 253600) has been localized on chromosome 15. After genotyping additional markers of this chromosome,...