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A G Engel

Showing results (161-170 of 242) with videos related to

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Human Molecular Genetics|November 1, 1994
Human muscle glycogenosis due to phosphorylase kinase deficiency associated with a nonsense mutation in the muscle isoform of the alpha subunitM Wehner, P R Clemens, A G Engel, et al.
The Lancet. Neurology|April 22, 2015
Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatmentA G Engel, X-M Shen, D Selcen, et al.
Deutsche Medizinische Wochenschrift (1946)|April 4, 1980
[Carnitine deficiency myopathy (author's transl)]F Jerusalem, A G Engel, C Sengupta, et al.
Neurology|June 1, 1977
Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twinsM R Gomez, A G Engel, G Dewald, et al.
Neurology|August 1, 1981
Freeze-fracture electronmicroscopic analysis of plasma membranes of cultured muscle cells in Duchenne dystrophyM Osame, A G Engel, C J Rebouche, et al.
Annals of Neurology|October 1, 1988
Lambert-Eaton myasthenic syndrome IgG depletes presynaptic membrane active zone particles by antigenic modulationA Nagel, A G Engel, B Lang, et al.
Annals of Neurology|May 1, 1991
Eosinophilia myalgia syndrome: I. Immunocytochemical evidence for a T-cell-mediated immune effector responseA M Emslie-Smith, A G Engel, J Duffy, et al.
Journal of Medical Genetics|August 3, 2005
Spectrum of splicing errors caused by CHRNE mutations affecting introns and intron/exon boundariesK Ohno, A Tsujino, X-M Shen, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Frameshifting and splice-site mutations in the acetylcholine receptor epsilon subunit gene in three Turkish kinships with congenital myasthenic syndromesK Ohno, B Anlar, E Ozdirim, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1983
Passive transfer of Lambert-Eaton myasthenic syndrome with IgG from man to mouse depletes the presynaptic membrane active zonesH Fukunaga, A G Engel, B Lang, et al.
Pageof 25

Showing results (161-170 of 242) with videos related to

Sort By:
Pageof 25
Human Molecular Genetics|November 1, 1994
Human muscle glycogenosis due to phosphorylase kinase deficiency associated with a nonsense mutation in the muscle isoform of the alpha subunitM Wehner, P R Clemens, A G Engel, et al.
The Lancet. Neurology|April 22, 2015
Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatmentA G Engel, X-M Shen, D Selcen, et al.
Deutsche Medizinische Wochenschrift (1946)|April 4, 1980
[Carnitine deficiency myopathy (author's transl)]F Jerusalem, A G Engel, C Sengupta, et al.
Neurology|June 1, 1977
Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twinsM R Gomez, A G Engel, G Dewald, et al.
Neurology|August 1, 1981
Freeze-fracture electronmicroscopic analysis of plasma membranes of cultured muscle cells in Duchenne dystrophyM Osame, A G Engel, C J Rebouche, et al.
Annals of Neurology|October 1, 1988
Lambert-Eaton myasthenic syndrome IgG depletes presynaptic membrane active zone particles by antigenic modulationA Nagel, A G Engel, B Lang, et al.
Annals of Neurology|May 1, 1991
Eosinophilia myalgia syndrome: I. Immunocytochemical evidence for a T-cell-mediated immune effector responseA M Emslie-Smith, A G Engel, J Duffy, et al.
Journal of Medical Genetics|August 3, 2005
Spectrum of splicing errors caused by CHRNE mutations affecting introns and intron/exon boundariesK Ohno, A Tsujino, X-M Shen, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Frameshifting and splice-site mutations in the acetylcholine receptor epsilon subunit gene in three Turkish kinships with congenital myasthenic syndromesK Ohno, B Anlar, E Ozdirim, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1983
Passive transfer of Lambert-Eaton myasthenic syndrome with IgG from man to mouse depletes the presynaptic membrane active zonesH Fukunaga, A G Engel, B Lang, et al.
Pageof 25