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Neuromuscular Disorders : NMD
|
July 17, 1999
A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21
F Xiang, P Nicolao, F Chapon, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
April 30, 1999
Levels of transforming growth factor alpha (TGF-alpha) in human cerebrospinal fluid
G B Van Setten, L Edström, H Stibler, et al.
Neuromuscular Disorders : NMD
|
January 1, 1994
Distribution of muscle degeneration in Welander distal myopathy--a magnetic resonance imaging and muscle biopsy study
G Ahlberg, F Jakobsson, A Fransson, et al.
Lakartidningen
|
February 15, 1989
[Diseases of the motor system--a review]
L Edström, S Conradi, K G Henriksson, et al.
Human Molecular Genetics
|
September 1, 1993
Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy
M Anvret, G Ahlberg, U Grandell, et al.
Journal of the Neurological Sciences
|
August 1, 1980
The distribution of intermediate filament protein (skeletin) in normal and diseased human skeletal muscle--an immunohistochemical and electron-microscopic study
L E Thornell, L Edström, A Eriksson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1989
Motoneuron firing and isomyosin type of muscle fibres in prior polio
K Borg, J Borg, G Dhoot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 1, 1987
Muscle biopsy findings, conduction velocity and refractory period of single motor nerve fibres in schizophrenia
J Borg, L Edström, L Bjerkenstedt, et al.
Annals of the New York Academy of Sciences
|
May 25, 1995
Motoneuron and muscle fiber properties of remaining motor units in weak tibialis anterior muscles in prior polio
J Borg, K Borg, L Edström, et al.
Human Genetics
|
January 1, 1990
A normal male with an inherited deletion of one exon within the DMD gene
M Nordenskjöld, L Nicholson, L Edström, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 101) with videos related to
Sort By:
Page
of 11
Neuromuscular Disorders : NMD
|
July 17, 1999
A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21
F Xiang, P Nicolao, F Chapon, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
April 30, 1999
Levels of transforming growth factor alpha (TGF-alpha) in human cerebrospinal fluid
G B Van Setten, L Edström, H Stibler, et al.
Neuromuscular Disorders : NMD
|
January 1, 1994
Distribution of muscle degeneration in Welander distal myopathy--a magnetic resonance imaging and muscle biopsy study
G Ahlberg, F Jakobsson, A Fransson, et al.
Lakartidningen
|
February 15, 1989
[Diseases of the motor system--a review]
L Edström, S Conradi, K G Henriksson, et al.
Human Molecular Genetics
|
September 1, 1993
Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy
M Anvret, G Ahlberg, U Grandell, et al.
Journal of the Neurological Sciences
|
August 1, 1980
The distribution of intermediate filament protein (skeletin) in normal and diseased human skeletal muscle--an immunohistochemical and electron-microscopic study
L E Thornell, L Edström, A Eriksson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1989
Motoneuron firing and isomyosin type of muscle fibres in prior polio
K Borg, J Borg, G Dhoot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 1, 1987
Muscle biopsy findings, conduction velocity and refractory period of single motor nerve fibres in schizophrenia
J Borg, L Edström, L Bjerkenstedt, et al.
Annals of the New York Academy of Sciences
|
May 25, 1995
Motoneuron and muscle fiber properties of remaining motor units in weak tibialis anterior muscles in prior polio
J Borg, K Borg, L Edström, et al.
Human Genetics
|
January 1, 1990
A normal male with an inherited deletion of one exon within the DMD gene
M Nordenskjöld, L Nicholson, L Edström, et al.
Page
of 11