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Journal of the Neurological Sciences
|
March 17, 2015
Adult onset limb-girdle muscular dystrophy - a recessive titinopathy masquerading as myositis
Ron Dabby, Menachem Sadeh, David Hilton-Jones, et al.
Neuromuscular Disorders : NMD
|
June 24, 2006
Myotilinopathy in a family with late onset myopathy
Isabelle Pénisson-Besnier, Kati Talvinen, Catherine Dumez, et al.
Neuromuscular Disorders : NMD
|
March 24, 2004
Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3)
Henna Haravuori, H Annika Siitonen, Ibrahim Mahjneh, et al.
Communications Biology
|
April 10, 2024
Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions
Huahua Zhong, Veronica Sian, Mridul Johari, et al.
The Journal of Biological Chemistry
|
July 17, 2010
Interactions with M-band titin and calpain 3 link myospryn (CMYA5) to tibial and limb-girdle muscular dystrophies
Jaakko Sarparanta, Gaëlle Blandin, Karine Charton, et al.
Brain : a Journal of Neurology
|
May 26, 2007
Distal myopathy caused by homozygous missense mutations in the nebulin gene
Carina Wallgren-Pettersson, Vilma-Lotta Lehtokari, Hannu Kalimo, et al.
Journal of Muscle Research and Cell Motility
|
October 9, 2025
Optimizing 2D in vitro differentiation conditions for C2C12 murine myoblasts on gelatin hydrogel
Veronica Sian, Per Harald Jonson, Anna Vainio, et al.
Neuromuscular Disorders : NMD
|
March 8, 2011
Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus
Peter Hackman, Satu Sandell, Jaakko Sarparanta, et al.
European Journal of Human Genetics : EJHG
|
March 3, 2011
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland
Tiina Suominen, Linda L Bachinski, Satu Auvinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
November 23, 2006
[Not Available]
Olayinka Raheem, Tiina Suominen, Peter Hackman, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 82) with videos related to
Sort By:
Page
of 9
Journal of the Neurological Sciences
|
March 17, 2015
Adult onset limb-girdle muscular dystrophy - a recessive titinopathy masquerading as myositis
Ron Dabby, Menachem Sadeh, David Hilton-Jones, et al.
Neuromuscular Disorders : NMD
|
June 24, 2006
Myotilinopathy in a family with late onset myopathy
Isabelle Pénisson-Besnier, Kati Talvinen, Catherine Dumez, et al.
Neuromuscular Disorders : NMD
|
March 24, 2004
Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3)
Henna Haravuori, H Annika Siitonen, Ibrahim Mahjneh, et al.
Communications Biology
|
April 10, 2024
Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions
Huahua Zhong, Veronica Sian, Mridul Johari, et al.
The Journal of Biological Chemistry
|
July 17, 2010
Interactions with M-band titin and calpain 3 link myospryn (CMYA5) to tibial and limb-girdle muscular dystrophies
Jaakko Sarparanta, Gaëlle Blandin, Karine Charton, et al.
Brain : a Journal of Neurology
|
May 26, 2007
Distal myopathy caused by homozygous missense mutations in the nebulin gene
Carina Wallgren-Pettersson, Vilma-Lotta Lehtokari, Hannu Kalimo, et al.
Journal of Muscle Research and Cell Motility
|
October 9, 2025
Optimizing 2D in vitro differentiation conditions for C2C12 murine myoblasts on gelatin hydrogel
Veronica Sian, Per Harald Jonson, Anna Vainio, et al.
Neuromuscular Disorders : NMD
|
March 8, 2011
Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus
Peter Hackman, Satu Sandell, Jaakko Sarparanta, et al.
European Journal of Human Genetics : EJHG
|
March 3, 2011
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland
Tiina Suominen, Linda L Bachinski, Satu Auvinen, et al.
Duodecim; Laaketieteellinen Aikakauskirja
|
November 23, 2006
[Not Available]
Olayinka Raheem, Tiina Suominen, Peter Hackman, et al.
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of 9