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Neuromuscular Disorders : NMD
|
April 14, 2024
Axial involvement as a prominent feature in SMPX-related distal myopathy
D Salman, C Bolano-Diaz, R Muni-Lofra, et al.
Human Molecular Genetics
|
May 23, 1998
mdx muscle pathology is independent of nNOS perturbation
R H Crosbie, V Straub, H Y Yun, et al.
The Journal of Cell Biology
|
April 6, 1999
Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex
R H Crosbie, C S Lebakken, K H Holt, et al.
Neuropediatrics
|
February 24, 1999
A novel form of familial congenital muscular dystrophy in two adolescents
M A Salih, M Al Rayess, S Cutshall, et al.
Neurology
|
January 19, 2011
Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patients
H Durmus, S H Laval, F Deymeer, 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.
British Journal of Pharmacology
|
January 20, 2016
Pharmacological characterization of the first in class clinical candidate PF-05190457: a selective ghrelin receptor competitive antagonist with inverse agonism that increases vagal afferent firing and glucose-dependent insulin secretion ex vivo
J Kong, J Chuddy, I A Stock, et al.
Cell
|
September 11, 1999
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy
R Coral-Vazquez, R D Cohn, S A Moore, et al.
Neuropediatrics
|
August 26, 2004
Congenital muscular dystrophy with short stature, proximal contractures and distal laxity
E Mercuri, A Lampe, V Straub, et al.
Neuromuscular Disorders : NMD
|
August 5, 2014
Psycho-organic symptoms as early manifestation of adult onset POMT1-related limb girdle muscular dystrophy
J Haberlova, Z Mitrović, K Zarković, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 92) with videos related to
Sort By:
Page
of 10
Neuromuscular Disorders : NMD
|
April 14, 2024
Axial involvement as a prominent feature in SMPX-related distal myopathy
D Salman, C Bolano-Diaz, R Muni-Lofra, et al.
Human Molecular Genetics
|
May 23, 1998
mdx muscle pathology is independent of nNOS perturbation
R H Crosbie, V Straub, H Y Yun, et al.
The Journal of Cell Biology
|
April 6, 1999
Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex
R H Crosbie, C S Lebakken, K H Holt, et al.
Neuropediatrics
|
February 24, 1999
A novel form of familial congenital muscular dystrophy in two adolescents
M A Salih, M Al Rayess, S Cutshall, et al.
Neurology
|
January 19, 2011
Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patients
H Durmus, S H Laval, F Deymeer, 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.
British Journal of Pharmacology
|
January 20, 2016
Pharmacological characterization of the first in class clinical candidate PF-05190457: a selective ghrelin receptor competitive antagonist with inverse agonism that increases vagal afferent firing and glucose-dependent insulin secretion ex vivo
J Kong, J Chuddy, I A Stock, et al.
Cell
|
September 11, 1999
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy
R Coral-Vazquez, R D Cohn, S A Moore, et al.
Neuropediatrics
|
August 26, 2004
Congenital muscular dystrophy with short stature, proximal contractures and distal laxity
E Mercuri, A Lampe, V Straub, et al.
Neuromuscular Disorders : NMD
|
August 5, 2014
Psycho-organic symptoms as early manifestation of adult onset POMT1-related limb girdle muscular dystrophy
J Haberlova, Z Mitrović, K Zarković, et al.
Page
of 10