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M Sadeh

Showing results (101-110 of 119) with videos related to

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Journal of Neural Transmission (Vienna, Austria : 1996)|July 13, 2006
Skin biopsy for assessment of autonomic denervation in Parkinson's diseaseR Dabby, R Djaldetti, M Shahmurov, et al.
Neurology|October 3, 2007
Minocycline treatment in acute stroke: an open-label, evaluator-blinded studyY Lampl, M Boaz, R Gilad, et al.
Human Genetics|May 14, 1999
Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier motherS M Tanner, K H Orstavik, M Kristiansen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 24, 2007
A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletionE Leshinsky-Silver, M Michelson, S Cohen, et al.
Journal of Medical Genetics|May 1, 1997
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle diseaseS Iyengar, H Kalinsky, S Weiss, et al.
Journal of the Neurological Sciences|March 4, 1999
Subacute painful lumbosacral polyradiculoneuropathy in immunocompromised patientsI Steiner, O Cohen, R R Leker, et al.
Annals of Neurology|April 1, 1997
Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1Z Argov, E Tiram, I Eisenberg, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13I Eisenberg, H Hochner, M Shemesh, et al.
Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.
Neuromuscular Disorders : NMD|September 11, 2007
Dysferlinopathy in the Jews of the Caucasus: a frequent mutation in the dysferlin geneE Leshinsky-Silver, Z Argov, L Rozenboim, et al.
Pageof 12

Showing results (101-110 of 119) with videos related to

Sort By:
Pageof 12
Journal of Neural Transmission (Vienna, Austria : 1996)|July 13, 2006
Skin biopsy for assessment of autonomic denervation in Parkinson's diseaseR Dabby, R Djaldetti, M Shahmurov, et al.
Neurology|October 3, 2007
Minocycline treatment in acute stroke: an open-label, evaluator-blinded studyY Lampl, M Boaz, R Gilad, et al.
Human Genetics|May 14, 1999
Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier motherS M Tanner, K H Orstavik, M Kristiansen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 24, 2007
A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletionE Leshinsky-Silver, M Michelson, S Cohen, et al.
Journal of Medical Genetics|May 1, 1997
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle diseaseS Iyengar, H Kalinsky, S Weiss, et al.
Journal of the Neurological Sciences|March 4, 1999
Subacute painful lumbosacral polyradiculoneuropathy in immunocompromised patientsI Steiner, O Cohen, R R Leker, et al.
Annals of Neurology|April 1, 1997
Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1Z Argov, E Tiram, I Eisenberg, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13I Eisenberg, H Hochner, M Shemesh, et al.
Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.
Neuromuscular Disorders : NMD|September 11, 2007
Dysferlinopathy in the Jews of the Caucasus: a frequent mutation in the dysferlin geneE Leshinsky-Silver, Z Argov, L Rozenboim, et al.
Pageof 12