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Neuromuscular Disorders : NMD
|
March 1, 1994
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy
K Matsumura, F M Tomé, H Collin, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 1, 2007
[Early detection of myocardial disease in young patients with Becker's muscular dystrophy asymptomatic from the cardiac point of view: value of myocardial doppler tissue imaging]
C Meune, K Wahbi, H M Bécane, et al.
Croatian Medical Journal
|
November 7, 2000
Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy
N Canki-Klain, D Récan, D Milicić, et al.
Nature Genetics
|
June 1, 1995
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
F Piccolo, S L Roberds, M Jeanpierre, et al.
Neuropediatrics
|
February 1, 1996
Neurosensory hearing loss in secondary adhalinopathy
K Oexle, R Herrmann, C Dodé, et al.
Journal of Medical Genetics
|
April 1, 1994
Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa
F el Kerch, A Sefiani, K Azibi, et al.
Human Genetics
|
May 1, 1994
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter
F Tihy, N Vogt, D Recan, et al.
The Journal of Clinical Investigation
|
February 1, 1992
Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?
D Récan, P Chafey, F Leturcq, et al.
The Journal of Clinical Investigation
|
January 1, 1994
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin
K Matsumura, A H Burghes, M Mora, et al.
Medicina Clinica
|
July 1, 1998
[Muscular dystrophy due to a mutation in the gene of alpha-sarcoglycan subunit of dystrophin associated protein complex]
M Urtasun, J J Poza, P Gallano, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 50) with videos related to
Sort By:
Page
of 5
Neuromuscular Disorders : NMD
|
March 1, 1994
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy
K Matsumura, F M Tomé, H Collin, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 1, 2007
[Early detection of myocardial disease in young patients with Becker's muscular dystrophy asymptomatic from the cardiac point of view: value of myocardial doppler tissue imaging]
C Meune, K Wahbi, H M Bécane, et al.
Croatian Medical Journal
|
November 7, 2000
Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy
N Canki-Klain, D Récan, D Milicić, et al.
Nature Genetics
|
June 1, 1995
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
F Piccolo, S L Roberds, M Jeanpierre, et al.
Neuropediatrics
|
February 1, 1996
Neurosensory hearing loss in secondary adhalinopathy
K Oexle, R Herrmann, C Dodé, et al.
Journal of Medical Genetics
|
April 1, 1994
Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa
F el Kerch, A Sefiani, K Azibi, et al.
Human Genetics
|
May 1, 1994
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter
F Tihy, N Vogt, D Recan, et al.
The Journal of Clinical Investigation
|
February 1, 1992
Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?
D Récan, P Chafey, F Leturcq, et al.
The Journal of Clinical Investigation
|
January 1, 1994
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin
K Matsumura, A H Burghes, M Mora, et al.
Medicina Clinica
|
July 1, 1998
[Muscular dystrophy due to a mutation in the gene of alpha-sarcoglycan subunit of dystrophin associated protein complex]
M Urtasun, J J Poza, P Gallano, et al.
Page
of 5