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Neurology
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February 28, 2002
Three novel COLQ mutations and variation of phenotypic expressivity due to G240X
Y A Shapira, M E Sadeh, M P Bergtraum, et al.
Nature Neuroscience
|
April 9, 1999
Acetylcholine receptor M3 domain: stereochemical and volume contributions to channel gating
H L Wang, M Milone, K Ohno, et al.
Neurology
|
July 13, 2005
Congenital endplate acetylcholinesterase deficiency responsive to ephedrine
M Bestue-Cardiel, A Sáenz de Cabezón-Alvarez, J L Capablo-Liesa, et al.
Cell
|
June 17, 1994
Dihydropyridine receptor mutations cause hypokalemic periodic paralysis
L J Ptácek, R Tawil, R C Griggs, et al.
The Journal of General Physiology
|
August 30, 2000
Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndrome
H L Wang, K Ohno, M Milone, et al.
Neuron
|
April 16, 1998
Mode switching kinetics produced by a naturally occurring mutation in the cytoplasmic loop of the human acetylcholine receptor epsilon subunit
M Milone, H L Wang, K Ohno, et al.
Annals of Neurology
|
February 9, 2000
The spectrum of mutations causing end-plate acetylcholinesterase deficiency
K Ohno, A G Engel, J M Brengman, et al.
Medicine
|
February 18, 1998
Retinocochleocerebral vasculopathy
G W Petty, A G Engel, B R Younge, et al.
Brain : a Journal of Neurology
|
June 1, 1993
Congenital endplate acetylcholinesterase deficiency
D O Hutchinson, T J Walls, S Nakano, et al.
Human Molecular Genetics
|
September 1, 1996
New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome
A G Engel, K Ohno, M Milone, et al.
Page
of 25
Search research articles
Search
Showing results (231-240 of 242) with videos related to
Sort By:
Page
of 25
Neurology
|
February 28, 2002
Three novel COLQ mutations and variation of phenotypic expressivity due to G240X
Y A Shapira, M E Sadeh, M P Bergtraum, et al.
Nature Neuroscience
|
April 9, 1999
Acetylcholine receptor M3 domain: stereochemical and volume contributions to channel gating
H L Wang, M Milone, K Ohno, et al.
Neurology
|
July 13, 2005
Congenital endplate acetylcholinesterase deficiency responsive to ephedrine
M Bestue-Cardiel, A Sáenz de Cabezón-Alvarez, J L Capablo-Liesa, et al.
Cell
|
June 17, 1994
Dihydropyridine receptor mutations cause hypokalemic periodic paralysis
L J Ptácek, R Tawil, R C Griggs, et al.
The Journal of General Physiology
|
August 30, 2000
Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndrome
H L Wang, K Ohno, M Milone, et al.
Neuron
|
April 16, 1998
Mode switching kinetics produced by a naturally occurring mutation in the cytoplasmic loop of the human acetylcholine receptor epsilon subunit
M Milone, H L Wang, K Ohno, et al.
Annals of Neurology
|
February 9, 2000
The spectrum of mutations causing end-plate acetylcholinesterase deficiency
K Ohno, A G Engel, J M Brengman, et al.
Medicine
|
February 18, 1998
Retinocochleocerebral vasculopathy
G W Petty, A G Engel, B R Younge, et al.
Brain : a Journal of Neurology
|
June 1, 1993
Congenital endplate acetylcholinesterase deficiency
D O Hutchinson, T J Walls, S Nakano, et al.
Human Molecular Genetics
|
September 1, 1996
New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome
A G Engel, K Ohno, M Milone, et al.
Page
of 25