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Molecular Microbiology
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April 9, 2005
Enteropathogenic Escherichia coli EspG disrupts microtubules and in conjunction with Orf3 enhances perturbation of the tight junction barrier
Farol L Tomson, V K Viswanathan, Kristen J Kanack, et al.
Neuromuscular Disorders : NMD
|
October 20, 2009
Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutations
U Schara, N Barisic, M Deschauer, et al.
Neurobiology of Aging
|
November 11, 2005
Effects of age on feeding behavior and chemosensory processing in the pond snail, Lymnaea stagnalis
M Arundell, B A Patel, V Straub, et al.
Molecular Cell
|
July 14, 1998
Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer
K H Holt, L E Lim, V Straub, et al.
Neuropediatrics
|
June 1, 1995
Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy
T Voit, C A Sewry, K Meyer, et al.
European Journal of Neurology
|
June 20, 2020
Adult-onset very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD)
F Fatehi, A A Okhovat, Y Nilipour, et al.
Neurology
|
April 2, 2008
A refined diagnostic algorithm for Bethlem myopathy
D Hicks, A K Lampe, R Barresi, et al.
Neuromuscular Disorders : NMD
|
April 9, 2008
Late onset in dysferlinopathy widens the clinical spectrum
L Klinge, A F Dean, W Kress, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
May 19, 2011
Pharmacological inhibition of Kv1.3 fails to modulate insulin sensitivity in diabetic mice or human insulin-sensitive tissues
Stephen V Straub, Sylvie M Perez, Beijing Tan, et al.
Neurology
|
April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene
H Haravuori, A Vihola, V Straub, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 92) with videos related to
Sort By:
Page
of 10
Molecular Microbiology
|
April 9, 2005
Enteropathogenic Escherichia coli EspG disrupts microtubules and in conjunction with Orf3 enhances perturbation of the tight junction barrier
Farol L Tomson, V K Viswanathan, Kristen J Kanack, et al.
Neuromuscular Disorders : NMD
|
October 20, 2009
Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutations
U Schara, N Barisic, M Deschauer, et al.
Neurobiology of Aging
|
November 11, 2005
Effects of age on feeding behavior and chemosensory processing in the pond snail, Lymnaea stagnalis
M Arundell, B A Patel, V Straub, et al.
Molecular Cell
|
July 14, 1998
Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer
K H Holt, L E Lim, V Straub, et al.
Neuropediatrics
|
June 1, 1995
Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy
T Voit, C A Sewry, K Meyer, et al.
European Journal of Neurology
|
June 20, 2020
Adult-onset very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD)
F Fatehi, A A Okhovat, Y Nilipour, et al.
Neurology
|
April 2, 2008
A refined diagnostic algorithm for Bethlem myopathy
D Hicks, A K Lampe, R Barresi, et al.
Neuromuscular Disorders : NMD
|
April 9, 2008
Late onset in dysferlinopathy widens the clinical spectrum
L Klinge, A F Dean, W Kress, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
May 19, 2011
Pharmacological inhibition of Kv1.3 fails to modulate insulin sensitivity in diabetic mice or human insulin-sensitive tissues
Stephen V Straub, Sylvie M Perez, Beijing Tan, et al.
Neurology
|
April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene
H Haravuori, A Vihola, V Straub, et al.
Page
of 10