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F Jerusalem

Showing results (71-80 of 85) with videos related to

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Der Nervenarzt|June 1, 1990
[Ophthalmoplegia-plus: clinical variability, biochemical defects of the mitochondria respiratory chain and deletions of the mitochondria genome]S Zierz, O von Wersebe, K D Gerbitz, et al.
Journal of the Neurological Sciences|November 1, 1974
Morphometric analysis of skeletal muscle capillary ultrastructure in inflammatory myopathiesF Jerusalem, M Rakusa, A G Engel, et al.
Deutsche Medizinische Wochenschrift (1946)|April 4, 1980
[Carnitine deficiency myopathy (author's transl)]F Jerusalem, A G Engel, C Sengupta, et al.
Archives of Neurology|April 1, 1978
The syndrome of 'continuous muscle fiber activity.'J Lütschg, F Jerusalem, H P Ludin, et al.
Annals of Neurology|May 1, 1988
Motor neuron syndrome and monoclonal IgM with antibody activity against gangliosides GM1 and GD1bE Nardelli, A J Steck, T Barkas, et al.
Journal of Neurology|January 1, 1980
Myotonic dystrophy--early detection and genetic counsellingT Schubert, F Jerusalem, A C Martenet, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Neuropathy and monoclonal IgM M-protein with antibody activity against gangliosidesE Nardelli, A J Steck, M Schluep, et al.
Acta Neuropathologica|January 1, 1982
Evidence for a chronic axonal atrophy in oculopharyngeal "muscular dystrophy"A Probst, W Tackmann, H R Stoeckli, et al.
Muscle & Nerve|August 1, 1988
Immunofluorescent evidence for presence of interleukin-1 in normal and diseased human skeletal muscleW Schubert, L Kontozis, G Sticker, et al.
Journal of Neurology|February 1, 1994
Abnormal dystrophin expression in patients with limb girdle syndromesS Beyenburg, S Zierz, K Arahata, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Der Nervenarzt|June 1, 1990
[Ophthalmoplegia-plus: clinical variability, biochemical defects of the mitochondria respiratory chain and deletions of the mitochondria genome]S Zierz, O von Wersebe, K D Gerbitz, et al.
Journal of the Neurological Sciences|November 1, 1974
Morphometric analysis of skeletal muscle capillary ultrastructure in inflammatory myopathiesF Jerusalem, M Rakusa, A G Engel, et al.
Deutsche Medizinische Wochenschrift (1946)|April 4, 1980
[Carnitine deficiency myopathy (author's transl)]F Jerusalem, A G Engel, C Sengupta, et al.
Archives of Neurology|April 1, 1978
The syndrome of 'continuous muscle fiber activity.'J Lütschg, F Jerusalem, H P Ludin, et al.
Annals of Neurology|May 1, 1988
Motor neuron syndrome and monoclonal IgM with antibody activity against gangliosides GM1 and GD1bE Nardelli, A J Steck, T Barkas, et al.
Journal of Neurology|January 1, 1980
Myotonic dystrophy--early detection and genetic counsellingT Schubert, F Jerusalem, A C Martenet, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Neuropathy and monoclonal IgM M-protein with antibody activity against gangliosidesE Nardelli, A J Steck, M Schluep, et al.
Acta Neuropathologica|January 1, 1982
Evidence for a chronic axonal atrophy in oculopharyngeal "muscular dystrophy"A Probst, W Tackmann, H R Stoeckli, et al.
Muscle & Nerve|August 1, 1988
Immunofluorescent evidence for presence of interleukin-1 in normal and diseased human skeletal muscleW Schubert, L Kontozis, G Sticker, et al.
Journal of Neurology|February 1, 1994
Abnormal dystrophin expression in patients with limb girdle syndromesS Beyenburg, S Zierz, K Arahata, et al.
Pageof 9