V Allamand
Overview
Explore the profile of V Allamand including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
33
Citations
921
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Saunier M, Bonnemann C, Durbeej M, Allamand V
Neuromuscul Disord
. 2016 Mar;
26(3):252-9.
PMID: 26948708
No abstract available.
2.
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution
Deconinck N, Richard P, Allamand V, Behin A, Laforet P, Ferreiro A, et al.
J Neurol Neurosurg Psychiatry
. 2014 Dec;
86(12):1337-46.
PMID: 25535305
Objective: Mutations in one of the 3 genes encoding collagen VI (COLVI) are responsible for a group of heterogeneous phenotypes of which Bethlem myopathy (BM) represents the milder end of...
3.
Quijano-Roy S, Khirani S, Colella M, Ramirez A, Aloui S, Wehbi S, et al.
Neuromuscul Disord
. 2013 Dec;
24(2):125-33.
PMID: 24314752
Collagen VI-related myopathies are hereditary disorders causing progressive restrictive respiratory insufficiency. Specific diaphragm involvement has been suggested by a drop in supine volumes. This pilot study aimed at characterizing the...
4.
Deconinck N, Dion E, Ben Yaou R, Ferreiro A, Eymard B, Brinas L, et al.
Neuromuscul Disord
. 2010 Jun;
20(8):517-23.
PMID: 20576434
Bethlem myopathy and Ullrich congenital muscular dystrophy are part of the heterogeneous group of collagen VI-related muscle disorders. They are caused by mutations in collagen VI (ColVI) genes (COL6A1, COL6A2,...
5.
Hicks D, Lampe A, Laval S, Allamand V, Jimenez-Mallebrera C, Walter M, et al.
Brain
. 2008 Nov;
132(Pt 1):147-55.
PMID: 19015158
Mutations in COL6A1, COL6A2 and COL6A3, the genes which encode the extra-cellular matrix component collagen VI, lead to Bethlem myopathy and Ullrich congenital muscular dystrophy (UCMD). Although the Col6a1(-/-) null...
6.
Rederstorff M, Allamand V, Guicheney P, Gartioux C, Richard P, Chaigne D, et al.
Nucleic Acids Res
. 2007 Nov;
36(1):237-44.
PMID: 18025044
Premature termination of translation due to nonsense mutations is a frequent cause of inherited diseases. Therefore, many efforts were invested in the development of strategies or compounds to selectively suppress...
7.
Demir E, Ferreiro A, Sabatelli P, Allamand V, Makri S, Echenne B, et al.
Neuropediatrics
. 2004 May;
35(2):103-12.
PMID: 15127309
Ullrich's congenital muscular dystrophy (UCMD) is an autosomal recessive myopathy characterised by neonatal muscle weakness, proximal joint contractures and distal hyperlaxity. Mutations in the COL6A1, COL6A2 (21 q22.3) and COL6A3...
8.
Bidou L, Hatin I, Perez N, Allamand V, Panthier J, Rousset J
Gene Ther
. 2004 Feb;
11(7):619-27.
PMID: 14973546
The suppression levels induced by gentamicin on premature stop codons, caused by primary nonsense mutations found in muscular dystrophy patients, were assessed using a very sensitive dual reporter gene assay....
9.
Straub V, Donahue K, Allamand V, Davisson R, Kim Y, Campbell K
Magn Reson Med
. 2000 Oct;
44(4):655-9.
PMID: 11025524
Membrane lesions play an early role in the pathogenesis of muscular dystrophy. Using a new albumin-targeted contrast agent (MS-325), sarcolemmal integrity of two animal models for muscular dystrophy was studied...
10.
Allamand V, Campbell K
Hum Mol Genet
. 2000 Sep;
9(16):2459-67.
PMID: 11005802
Since the identification of dystrophin as the causative factor in Duchenne muscular dystrophy, an increasing amount of information on the molecular basis of muscular dystrophies has facilitated the division of...