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N Telerman-Toppet

Showing results (51-60 of 56) with videos related to

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1991
Rhinocerebral mucormycosis in haemodialysis patients treated with desferrioxamine: possible role of recent surgery as an additional risk factorR Wens, J Devriendt, F Collart, et al.
Journal of Neurology|January 1, 1979
Charcot-Marie-Tooth disease associated with retinal pigment dystrophy and protanopia. Neurological, ophthalmological and genetic study of a familyP Khoubesserian, N van Regemorter, O Ohrn-Degueldre, et al.
Neurology|November 1, 1976
Changes in motor innervation and histochemical pattern of muscle fibers in some congenital myopathiesC Coërs, N Telerman-Toppet, J M Gérard, et al.
Journal of Neurology|October 7, 1977
Familial focal loss of cross striationsG K van Wijngaarden, J Bethlem, K P Dingemans, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblastsN Telerman-Toppet, D Biarent, J M Bouton, et al.
Neurology|January 1, 1992
Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNAH J Tritschler, F Andreetta, C T Moraes, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1991
Rhinocerebral mucormycosis in haemodialysis patients treated with desferrioxamine: possible role of recent surgery as an additional risk factorR Wens, J Devriendt, F Collart, et al.
Journal of Neurology|January 1, 1979
Charcot-Marie-Tooth disease associated with retinal pigment dystrophy and protanopia. Neurological, ophthalmological and genetic study of a familyP Khoubesserian, N van Regemorter, O Ohrn-Degueldre, et al.
Neurology|November 1, 1976
Changes in motor innervation and histochemical pattern of muscle fibers in some congenital myopathiesC Coërs, N Telerman-Toppet, J M Gérard, et al.
Journal of Neurology|October 7, 1977
Familial focal loss of cross striationsG K van Wijngaarden, J Bethlem, K P Dingemans, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblastsN Telerman-Toppet, D Biarent, J M Bouton, et al.
Neurology|January 1, 1992
Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNAH J Tritschler, F Andreetta, C T Moraes, et al.
Pageof 6