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D R Johns

Showing results (11-20 of 76) with videos related to

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American Journal of Human Genetics|April 1, 1992
Mitochondrial ND-I mutation in Leber hereditary optic neuropathyD R Johns
The New England Journal of Medicine|November 22, 1990
Improved molecular-genetic diagnosis of Leber's hereditary optic neuropathyD R Johns
Genomics|October 1, 1989
Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNAD R Johns, O Hurko
The New England Journal of Medicine|August 10, 1989
Dystrophin and Duchenne's muscular dystrophyO Hurko, D R Johns
Neurologic Clinics|February 1, 1991
Neuro-ophthalmologic manifestations of mitochondrial DNA disorders: chronic progressive external ophthalmoplegia, Kearns-Sayre syndrome, and Leber's hereditary optic neuropathyG Kosmorsky, D R Johns
Lancet (London, England)|April 13, 1991
Mitochondrial leucine tRNA mutation in neurological diseasesD R Johns, O Hurko
Seminars in Neurology|March 1, 1996
Clinical spectrum of mitochondrial diseasesR Fadic, D R Johns
Biochemical and Biophysical Research Communications|February 14, 1991
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathyD R Johns, J Berman
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 1, 1994
Cuban epidemic optic neuropathy. Mitochondrial DNA analysisD R Johns, A A Sadun
Biochemical and Biophysical Research Communications|October 29, 1993
Cytochrome c oxidase mutations in Leber hereditary optic neuropathyD R Johns, M J Neufeld
Pageof 8

Showing results (11-20 of 76) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|April 1, 1992
Mitochondrial ND-I mutation in Leber hereditary optic neuropathyD R Johns
The New England Journal of Medicine|November 22, 1990
Improved molecular-genetic diagnosis of Leber's hereditary optic neuropathyD R Johns
Genomics|October 1, 1989
Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNAD R Johns, O Hurko
The New England Journal of Medicine|August 10, 1989
Dystrophin and Duchenne's muscular dystrophyO Hurko, D R Johns
Neurologic Clinics|February 1, 1991
Neuro-ophthalmologic manifestations of mitochondrial DNA disorders: chronic progressive external ophthalmoplegia, Kearns-Sayre syndrome, and Leber's hereditary optic neuropathyG Kosmorsky, D R Johns
Lancet (London, England)|April 13, 1991
Mitochondrial leucine tRNA mutation in neurological diseasesD R Johns, O Hurko
Seminars in Neurology|March 1, 1996
Clinical spectrum of mitochondrial diseasesR Fadic, D R Johns
Biochemical and Biophysical Research Communications|February 14, 1991
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathyD R Johns, J Berman
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 1, 1994
Cuban epidemic optic neuropathy. Mitochondrial DNA analysisD R Johns, A A Sadun
Biochemical and Biophysical Research Communications|October 29, 1993
Cytochrome c oxidase mutations in Leber hereditary optic neuropathyD R Johns, M J Neufeld
Pageof 8