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Neuromuscular Disorders : NMD
|
April 20, 2006
Predictors of severe chest infections in pediatric neuromuscular disorders
C Dohna-Schwake, R Ragette, H Teschler, et al.
European Journal of Pediatrics
|
October 1, 1993
Demonstration of Borrelia burgdorferi infection in a child with Guillain-Barré syndrome
G Horneff, H I Huppertz, K Müller, et al.
European Journal of Pediatrics
|
February 1, 1992
Somatic mosaicism for a deletion of the dystrophin gene in a carrier of Becker muscular dystrophy
T Voit, E Neuen-Jacob, V Mahler, et al.
Pediatric Neurology
|
July 1, 1993
Pallister-Killian syndrome in older children and adolescents
G Horneff, F Majewski, B Hildebrand, et al.
Journal of the Neurological Sciences
|
February 1, 1989
Distribution of dystrophin, nebulin and Ricinus communis I (RCA-I)-binding glycoprotein in tissues of normal and mdx mice
T Voit, K Patel, M J Dunn, et al.
American Journal of Medical Genetics
|
December 5, 2000
Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: specific entity or variant of a described condition?
G Göhlich-Ratmann, A Lackner, J Schaper, et al.
Neurology
|
October 10, 2001
Sleep-disordered breathing and respiratory failure in acid maltase deficiency
U Mellies, R Ragette, C Schwake, et al.
Neuromuscular Disorders : NMD
|
June 3, 1998
HMSNL in a 13-year-old Bulgarian girl
M Baethmann, G Göhlich-Ratmann, J M Schröder, et al.
European Journal of Pediatrics
|
November 1, 1996
Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry
R Herrmann, V Straub, K Meyer, et al.
Journal of the Neurological Sciences
|
November 1, 1988
Dystrophin and nebulin in the muscular dystrophies
K Patel, T Voit, M J Dunn, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 143) with videos related to
Sort By:
Page
of 15
Neuromuscular Disorders : NMD
|
April 20, 2006
Predictors of severe chest infections in pediatric neuromuscular disorders
C Dohna-Schwake, R Ragette, H Teschler, et al.
European Journal of Pediatrics
|
October 1, 1993
Demonstration of Borrelia burgdorferi infection in a child with Guillain-Barré syndrome
G Horneff, H I Huppertz, K Müller, et al.
European Journal of Pediatrics
|
February 1, 1992
Somatic mosaicism for a deletion of the dystrophin gene in a carrier of Becker muscular dystrophy
T Voit, E Neuen-Jacob, V Mahler, et al.
Pediatric Neurology
|
July 1, 1993
Pallister-Killian syndrome in older children and adolescents
G Horneff, F Majewski, B Hildebrand, et al.
Journal of the Neurological Sciences
|
February 1, 1989
Distribution of dystrophin, nebulin and Ricinus communis I (RCA-I)-binding glycoprotein in tissues of normal and mdx mice
T Voit, K Patel, M J Dunn, et al.
American Journal of Medical Genetics
|
December 5, 2000
Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: specific entity or variant of a described condition?
G Göhlich-Ratmann, A Lackner, J Schaper, et al.
Neurology
|
October 10, 2001
Sleep-disordered breathing and respiratory failure in acid maltase deficiency
U Mellies, R Ragette, C Schwake, et al.
Neuromuscular Disorders : NMD
|
June 3, 1998
HMSNL in a 13-year-old Bulgarian girl
M Baethmann, G Göhlich-Ratmann, J M Schröder, et al.
European Journal of Pediatrics
|
November 1, 1996
Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry
R Herrmann, V Straub, K Meyer, et al.
Journal of the Neurological Sciences
|
November 1, 1988
Dystrophin and nebulin in the muscular dystrophies
K Patel, T Voit, M J Dunn, et al.
Page
of 15