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Human Mutation
|
February 6, 1998
A small in-frame deletion within the protease domain of muscle-specific calpain, p94 causes early-onset limb-girdle muscular dystrophy 2A
K Häffner, A Speer, C Hübner, et al.
Thorax
|
August 1, 2002
Patterns and predictors of sleep disordered breathing in primary myopathies
R Ragette, U Mellies, C Schwake, et al.
European Journal of Pediatrics
|
September 1, 1986
Hearing loss in facioscapulohumeral dystrophy
T Voit, A Lamprecht, H G Lenard, et al.
Neuropediatrics
|
August 1, 1987
Damage of thalamus and basal ganglia in asphyxiated full-term neonates
T Voit, P Lemburg, E Neuen, et al.
Journal of Inherited Metabolic Disease
|
September 10, 2005
Fumarase deficiency presenting with periventricular cysts
J Loeffen, R Smeets, T Voit, et al.
The Journal of Cell Biology
|
December 1, 1992
Direct visualization of the dystrophin network on skeletal muscle fiber membrane
V Straub, R E Bittner, J J Léger, et al.
Journal of the Neurological Sciences
|
April 1, 1988
Binding of Ricinus communis I lectin to developing dystrophic muscle in human fetus
T Voit, C A Sewry, M J Dunn, et al.
Neuromuscular Disorders : NMD
|
November 5, 1997
Changes of laminin beta 2 chain expression in congenital muscular dystrophy
R D Cohn, R Herrmann, U M Wewer, et al.
Muscle & Nerve
|
January 20, 2000
Focal myopathy induced by chronic heroin injection is reversible
M Weber, H C Diener, T Voit, et al.
Lancet (London, England)
|
January 11, 1997
Hepatoblastoma in a 2-year-old child of a liver-transplanted mother
C Roll, H J Luboldt, A Winter, et al.
Page
of 15
Search research articles
Search
Showing results (31-40 of 143) with videos related to
Sort By:
Page
of 15
Human Mutation
|
February 6, 1998
A small in-frame deletion within the protease domain of muscle-specific calpain, p94 causes early-onset limb-girdle muscular dystrophy 2A
K Häffner, A Speer, C Hübner, et al.
Thorax
|
August 1, 2002
Patterns and predictors of sleep disordered breathing in primary myopathies
R Ragette, U Mellies, C Schwake, et al.
European Journal of Pediatrics
|
September 1, 1986
Hearing loss in facioscapulohumeral dystrophy
T Voit, A Lamprecht, H G Lenard, et al.
Neuropediatrics
|
August 1, 1987
Damage of thalamus and basal ganglia in asphyxiated full-term neonates
T Voit, P Lemburg, E Neuen, et al.
Journal of Inherited Metabolic Disease
|
September 10, 2005
Fumarase deficiency presenting with periventricular cysts
J Loeffen, R Smeets, T Voit, et al.
The Journal of Cell Biology
|
December 1, 1992
Direct visualization of the dystrophin network on skeletal muscle fiber membrane
V Straub, R E Bittner, J J Léger, et al.
Journal of the Neurological Sciences
|
April 1, 1988
Binding of Ricinus communis I lectin to developing dystrophic muscle in human fetus
T Voit, C A Sewry, M J Dunn, et al.
Neuromuscular Disorders : NMD
|
November 5, 1997
Changes of laminin beta 2 chain expression in congenital muscular dystrophy
R D Cohn, R Herrmann, U M Wewer, et al.
Muscle & Nerve
|
January 20, 2000
Focal myopathy induced by chronic heroin injection is reversible
M Weber, H C Diener, T Voit, et al.
Lancet (London, England)
|
January 11, 1997
Hepatoblastoma in a 2-year-old child of a liver-transplanted mother
C Roll, H J Luboldt, A Winter, et al.
Page
of 15