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Neuromuscular Disorders : NMD
|
January 1, 1991
Dystrophin abnormalities in polymyositis and dermatomyositis
C A Sewry, A Clerk, J Z Heckmatt, et al.
Lancet (London, England)
|
April 21, 1979
Antenatal diagnosis of Duchenne muscular dystrophy
A E Emery, D Burt, V Dubowitz, et al.
Lancet (London, England)
|
March 4, 1995
Prenatal diagnosis in congenital muscular dystrophy
F Muntoni, C Sewry, L Wilson, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
January 1, 1989
[Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin]
T Voit, K Patel, C A Sewry, et al.
Journal of the Neurological Sciences
|
April 1, 1991
Characterisation of dystrophin in carriers of Duchenne muscular dystrophy
A Clerk, E Rodillo, J Z Heckmatt, et al.
Human Genetics
|
December 1, 1986
A linkage study of Emery-Dreifuss muscular dystrophy
S Hodgson, E Boswinkel, C Cole, et al.
The Journal of Pediatrics
|
September 1, 1984
Correlation of neurologic assessment in the preterm newborn infant with outcome at 1 year
L M Dubowitz, V Dubowitz, P G Palmer, et al.
Human Genetics
|
March 1, 1987
DNA deletions in mild and severe Becker muscular dystrophy
K A Hart, S Hodgson, A Walker, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy
I Naom, M D'Alessandro, C A Sewry, et al.
Lancet (London, England)
|
January 7, 1989
Absence of dystrophin in Becker muscular dystrophy
K Patel, S Leevers, S Abbs, et al.
Page
of 35
Search research articles
Search
Showing results (281-290 of 349) with videos related to
Sort By:
Page
of 35
Neuromuscular Disorders : NMD
|
January 1, 1991
Dystrophin abnormalities in polymyositis and dermatomyositis
C A Sewry, A Clerk, J Z Heckmatt, et al.
Lancet (London, England)
|
April 21, 1979
Antenatal diagnosis of Duchenne muscular dystrophy
A E Emery, D Burt, V Dubowitz, et al.
Lancet (London, England)
|
March 4, 1995
Prenatal diagnosis in congenital muscular dystrophy
F Muntoni, C Sewry, L Wilson, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
January 1, 1989
[Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin]
T Voit, K Patel, C A Sewry, et al.
Journal of the Neurological Sciences
|
April 1, 1991
Characterisation of dystrophin in carriers of Duchenne muscular dystrophy
A Clerk, E Rodillo, J Z Heckmatt, et al.
Human Genetics
|
December 1, 1986
A linkage study of Emery-Dreifuss muscular dystrophy
S Hodgson, E Boswinkel, C Cole, et al.
The Journal of Pediatrics
|
September 1, 1984
Correlation of neurologic assessment in the preterm newborn infant with outcome at 1 year
L M Dubowitz, V Dubowitz, P G Palmer, et al.
Human Genetics
|
March 1, 1987
DNA deletions in mild and severe Becker muscular dystrophy
K A Hart, S Hodgson, A Walker, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy
I Naom, M D'Alessandro, C A Sewry, et al.
Lancet (London, England)
|
January 7, 1989
Absence of dystrophin in Becker muscular dystrophy
K Patel, S Leevers, S Abbs, et al.
Page
of 35