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Z Argov

Showing results (91-100 of 112) with videos related to

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Journal of Applied Physiology (Bethesda, Md. : 1985)|February 1, 1992
Substrate regulation of mitochondrial oxidative phosphorylation in hypercapnic rabbit muscleS Nioka, Z Argov, G P Dobson, et al.
Annals of Neurology|December 16, 1998
Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme geneA Lossos, Z Meiner, V Barash, et al.
Neurology|August 19, 2007
Treatment of human myasthenia gravis with oral antisense suppression of acetylcholinesteraseZ Argov, D McKee, S Agus, 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.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|November 1, 1994
Transient neurological events during dipyridamole stress test: an arterial steal phenomenon?D Schechter, M Bocher, Y Berlatzky, et al.
Neurology|February 1, 1995
Hereditary leukoencephalopathy and palmoplantar keratoderma: a new disorder with increased skin collagen contentA Lossos, H Cooperman, D Soffer, et al.
Neurology|May 5, 1998
Effects of aerobic training in patients with mitochondrial myopathiesT Taivassalo, N De Stefano, Z Argov, et al.
Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.
Muscle & Nerve|October 27, 1997
Biochemical and genetic studies in a family with mitochondrial myopathyT D Heiman-Patterson, Z Argov, J M Chavin, 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.
Pageof 12

Showing results (91-100 of 112) with videos related to

Sort By:
Pageof 12
Journal of Applied Physiology (Bethesda, Md. : 1985)|February 1, 1992
Substrate regulation of mitochondrial oxidative phosphorylation in hypercapnic rabbit muscleS Nioka, Z Argov, G P Dobson, et al.
Annals of Neurology|December 16, 1998
Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme geneA Lossos, Z Meiner, V Barash, et al.
Neurology|August 19, 2007
Treatment of human myasthenia gravis with oral antisense suppression of acetylcholinesteraseZ Argov, D McKee, S Agus, 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.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|November 1, 1994
Transient neurological events during dipyridamole stress test: an arterial steal phenomenon?D Schechter, M Bocher, Y Berlatzky, et al.
Neurology|February 1, 1995
Hereditary leukoencephalopathy and palmoplantar keratoderma: a new disorder with increased skin collagen contentA Lossos, H Cooperman, D Soffer, et al.
Neurology|May 5, 1998
Effects of aerobic training in patients with mitochondrial myopathiesT Taivassalo, N De Stefano, Z Argov, et al.
Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.
Muscle & Nerve|October 27, 1997
Biochemical and genetic studies in a family with mitochondrial myopathyT D Heiman-Patterson, Z Argov, J M Chavin, 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.
Pageof 12