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M Sadeh

Showing results (21-30 of 119) with videos related to

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Harefuah|October 15, 1980
[The F wave: electrodiagnosis and clinical applications]I Sarova-Pinhas, M Sadeh
Cellular and Molecular Biology, Including Cyto-Enzymology|January 1, 1981
Histochemistry of human laryngeal musclesM Sadeh, J Kronenberg, E Gaton
Muscle & Nerve|June 1, 1997
Stimulated single-fiber electromyography in Lambert-Eaton myasthenic syndrome before and after 3,4-diaminopyridineM Sadeh, Y River, Z Argov
Annals of Neurology|September 1, 1988
Hexosaminidase A deficiency manifesting as spinal muscular atrophy of late onsetA Karni, R Navon, M Sadeh
Acta Neurologica Scandinavica|March 1, 1990
Familial myoedema, muscular hypertrophy and stiffnessM Sadeh, M Berg, U Sandbank
Early Human Development|June 15, 1999
Laminin alpha2 deficient congenital muscular dystrophy: prenatal diagnosisD Nass, I Goldberg, M Sadeh
Acta Neurologica Scandinavica|July 10, 2004
Transient global amnesia -- not always a benign processY Lampl, M Sadeh, M Lorberboym
Israel Journal of Medical Sciences|April 1, 1990
Creutzfeldt-Jakob disease associated with peripheral neuropathyM Sadeh, Y Chagnac, Y Goldhammer
Muscle & Nerve|February 1, 1993
Single fiber EMG in a congenital myasthenic syndrome associated with facial malformationsM Sadeh, I Blatt, Y Goldhammer
Journal of Neurology|January 1, 1982
Periodic ataxia: an unusual non-familial variation with paroxysmal EEG featuresJ Braham, T Siegal, M Sadeh
Pageof 12

Showing results (21-30 of 119) with videos related to

Sort By:
Pageof 12
Harefuah|October 15, 1980
[The F wave: electrodiagnosis and clinical applications]I Sarova-Pinhas, M Sadeh
Cellular and Molecular Biology, Including Cyto-Enzymology|January 1, 1981
Histochemistry of human laryngeal musclesM Sadeh, J Kronenberg, E Gaton
Muscle & Nerve|June 1, 1997
Stimulated single-fiber electromyography in Lambert-Eaton myasthenic syndrome before and after 3,4-diaminopyridineM Sadeh, Y River, Z Argov
Annals of Neurology|September 1, 1988
Hexosaminidase A deficiency manifesting as spinal muscular atrophy of late onsetA Karni, R Navon, M Sadeh
Acta Neurologica Scandinavica|March 1, 1990
Familial myoedema, muscular hypertrophy and stiffnessM Sadeh, M Berg, U Sandbank
Early Human Development|June 15, 1999
Laminin alpha2 deficient congenital muscular dystrophy: prenatal diagnosisD Nass, I Goldberg, M Sadeh
Acta Neurologica Scandinavica|July 10, 2004
Transient global amnesia -- not always a benign processY Lampl, M Sadeh, M Lorberboym
Israel Journal of Medical Sciences|April 1, 1990
Creutzfeldt-Jakob disease associated with peripheral neuropathyM Sadeh, Y Chagnac, Y Goldhammer
Muscle & Nerve|February 1, 1993
Single fiber EMG in a congenital myasthenic syndrome associated with facial malformationsM Sadeh, I Blatt, Y Goldhammer
Journal of Neurology|January 1, 1982
Periodic ataxia: an unusual non-familial variation with paroxysmal EEG featuresJ Braham, T Siegal, M Sadeh
Pageof 12