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Showing results (141-150 of 159) with videos related to

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Multiple Sclerosis and Related Disorders|December 19, 2024
MOG-IgG is rare in AQP4-IgG seronegative NMO phenotype in BrazilDenison Alves Pedrosa, Gustavo B P Fernandes, Natália Talim, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centersMariz Vainzof, Pascale Richard, Ralf Herrmann, et al.
Brain Pathology (Zurich, Switzerland)|August 12, 2008
A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severityCecilia Jimenez-Mallebrera, Silvia Torelli, Lucy Feng, et al.
Neurology|January 14, 2014
Distinction between MOG antibody-positive and AQP4 antibody-positive NMO spectrum disordersDouglas Kazutoshi Sato, Dagoberto Callegaro, Marco Aurelio Lana-Peixoto, et al.
Human Molecular Genetics|February 18, 2003
Worldwide distribution and broader clinical spectrum of muscle-eye-brain diseaseKiyomi Taniguchi, Kazuhiro Kobayashi, Kayoko Saito, et al.
Annals of Neurology|December 11, 2008
Brain involvement in muscular dystrophies with defective dystroglycan glycosylationEmma Clement, Eugenio Mercuri, Caroline Godfrey, et al.
The New England Journal of Medicine|March 11, 2011
A dystroglycan mutation associated with limb-girdle muscular dystrophyYuji Hara, Burcu Balci-Hayta, Takako Yoshida-Moriguchi, et al.
Human Molecular Genetics|September 15, 2018
Bi-allelic mutations in MYL1 cause a severe congenital myopathyGianina Ravenscroft, Irina T Zaharieva, Carlo A Bortolotti, et al.
Brain : a Journal of Neurology|December 21, 2010
Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiencyJohn P Kemp, Paul M Smith, Angela Pyle, et al.
Brain : a Journal of Neurology|September 20, 2007
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycanCaroline Godfrey, Emma Clement, Rachael Mein, et al.
Pageof 16

Showing results (141-150 of 159) with videos related to

Sort By:
Pageof 16
Multiple Sclerosis and Related Disorders|December 19, 2024
MOG-IgG is rare in AQP4-IgG seronegative NMO phenotype in BrazilDenison Alves Pedrosa, Gustavo B P Fernandes, Natália Talim, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centersMariz Vainzof, Pascale Richard, Ralf Herrmann, et al.
Brain Pathology (Zurich, Switzerland)|August 12, 2008
A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severityCecilia Jimenez-Mallebrera, Silvia Torelli, Lucy Feng, et al.
Neurology|January 14, 2014
Distinction between MOG antibody-positive and AQP4 antibody-positive NMO spectrum disordersDouglas Kazutoshi Sato, Dagoberto Callegaro, Marco Aurelio Lana-Peixoto, et al.
Human Molecular Genetics|February 18, 2003
Worldwide distribution and broader clinical spectrum of muscle-eye-brain diseaseKiyomi Taniguchi, Kazuhiro Kobayashi, Kayoko Saito, et al.
Annals of Neurology|December 11, 2008
Brain involvement in muscular dystrophies with defective dystroglycan glycosylationEmma Clement, Eugenio Mercuri, Caroline Godfrey, et al.
The New England Journal of Medicine|March 11, 2011
A dystroglycan mutation associated with limb-girdle muscular dystrophyYuji Hara, Burcu Balci-Hayta, Takako Yoshida-Moriguchi, et al.
Human Molecular Genetics|September 15, 2018
Bi-allelic mutations in MYL1 cause a severe congenital myopathyGianina Ravenscroft, Irina T Zaharieva, Carlo A Bortolotti, et al.
Brain : a Journal of Neurology|December 21, 2010
Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiencyJohn P Kemp, Paul M Smith, Angela Pyle, et al.
Brain : a Journal of Neurology|September 20, 2007
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycanCaroline Godfrey, Emma Clement, Rachael Mein, et al.
Pageof 16