Search research articles
Contact Us
Filters
Showing results (1-10 of 11) with videos related to
Page
of 2
Sort By:
Cellular and Molecular Life Sciences : CMLS
|
May 4, 2005
Congenital muscular dystrophy: molecular and cellular aspects
C Jimenez-Mallebrera, S C Brown, C A Sewry, et al.
Neuropathology and Applied Neurobiology
|
October 19, 2004
Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions
S Torelli, S C Brown, C Jimenez-Mallebrera, et al.
Neuromuscular Disorders : NMD
|
January 24, 2007
A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locus
L Hartley, M Kinali, R Knight, et al.
Neuromuscular Disorders : NMD
|
November 15, 2011
Flow cytometry analysis: a quantitative method for collagen VI deficiency screening
J Kim, C Jimenez-Mallebrera, A R Foley, et al.
Neurology
|
July 1, 2009
Natural history of Ullrich congenital muscular dystrophy
A Nadeau, M Kinali, M Main, et al.
Journal of Neurology
|
January 13, 2016
KLHL40-related nemaline myopathy with a sustained, positive response to treatment with acetylcholinesterase inhibitors
D Natera-de Benito, A Nascimento, A Abicht, et al.
Neuromuscular Disorders : NMD
|
August 29, 2006
A comparative analysis of collagen VI production in muscle, skin and fibroblasts from 14 Ullrich congenital muscular dystrophy patients with dominant and recessive COL6A mutations
C Jimenez-Mallebrera, M A Maioli, J Kim, et al.
Brain : a Journal of Neurology
|
November 19, 2008
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue
D Hicks, A K Lampe, S H Laval, et al.
Journal of Neuroimmunology
|
August 19, 2008
Congenital myasthenic syndromes in childhood: diagnostic and management challenges
M Kinali, D Beeson, M C Pitt, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 24, 2008
Muscular dystrophies due to defective glycosylation of dystroglycan
F Muntoni, M Brockington, C Godfrey, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Cellular and Molecular Life Sciences : CMLS
|
May 4, 2005
Congenital muscular dystrophy: molecular and cellular aspects
C Jimenez-Mallebrera, S C Brown, C A Sewry, et al.
Neuropathology and Applied Neurobiology
|
October 19, 2004
Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions
S Torelli, S C Brown, C Jimenez-Mallebrera, et al.
Neuromuscular Disorders : NMD
|
January 24, 2007
A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locus
L Hartley, M Kinali, R Knight, et al.
Neuromuscular Disorders : NMD
|
November 15, 2011
Flow cytometry analysis: a quantitative method for collagen VI deficiency screening
J Kim, C Jimenez-Mallebrera, A R Foley, et al.
Neurology
|
July 1, 2009
Natural history of Ullrich congenital muscular dystrophy
A Nadeau, M Kinali, M Main, et al.
Journal of Neurology
|
January 13, 2016
KLHL40-related nemaline myopathy with a sustained, positive response to treatment with acetylcholinesterase inhibitors
D Natera-de Benito, A Nascimento, A Abicht, et al.
Neuromuscular Disorders : NMD
|
August 29, 2006
A comparative analysis of collagen VI production in muscle, skin and fibroblasts from 14 Ullrich congenital muscular dystrophy patients with dominant and recessive COL6A mutations
C Jimenez-Mallebrera, M A Maioli, J Kim, et al.
Brain : a Journal of Neurology
|
November 19, 2008
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue
D Hicks, A K Lampe, S H Laval, et al.
Journal of Neuroimmunology
|
August 19, 2008
Congenital myasthenic syndromes in childhood: diagnostic and management challenges
M Kinali, D Beeson, M C Pitt, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 24, 2008
Muscular dystrophies due to defective glycosylation of dystroglycan
F Muntoni, M Brockington, C Godfrey, et al.
Page
of 2