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E Holme

Showing results (31-40 of 111) with videos related to

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Neuromuscular Disorders : NMD|July 23, 1998
Threshold expression of the tRNA(Lys) A8344G mutation in single muscle fibresA R Moslemi, M Tulinius, E Holme, et al.
Clinical and Experimental Immunology|April 1, 1985
Prevention of immune precipitation by purified components of the alternative pathwayJ K Naama, E Holme, E Hamilton, et al.
Neurology|July 17, 1999
Autosomal dominant progressive external ophthalmoplegia: distribution of multiple mitochondrial DNA deletionsA R Moslemi, A Melberg, E Holme, et al.
Brain : a Journal of Neurology|April 1, 1993
Mitochondrial DNA deletions in inclusion body myositisA Oldfors, N G Larsson, C Lindberg, et al.
Annals of Neurology|November 1, 1996
Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegiaA R Moslemi, A Melberg, E Holme, et al.
Neurology|January 27, 1998
Rhabdomyolysis in autosomal dominant progressive external ophthalmoplegiaA Melberg, E Holme, A Oldfors, et al.
Acta Neuropathologica|January 1, 1995
Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibresA Oldfors, E Holme, M Tulinius, et al.
Acta Neuropathologica|January 1, 1989
Cytochrome c oxidase deficiency in infancyA Oldfors, H Sommerland, E Holme, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Inheritance and expression of mitochondrial DNA point mutationsE Holme, M H Tulinius, N G Larsson, et al.
Journal of the American Academy of Dermatology|September 1, 1996
IgA class anticardiolipin antibodies in cutaneous leukocytoclastic vasculitisA D Burden, D M Tillman, P Foley, et al.
Pageof 12

Showing results (31-40 of 111) with videos related to

Sort By:
Pageof 12
Neuromuscular Disorders : NMD|July 23, 1998
Threshold expression of the tRNA(Lys) A8344G mutation in single muscle fibresA R Moslemi, M Tulinius, E Holme, et al.
Clinical and Experimental Immunology|April 1, 1985
Prevention of immune precipitation by purified components of the alternative pathwayJ K Naama, E Holme, E Hamilton, et al.
Neurology|July 17, 1999
Autosomal dominant progressive external ophthalmoplegia: distribution of multiple mitochondrial DNA deletionsA R Moslemi, A Melberg, E Holme, et al.
Brain : a Journal of Neurology|April 1, 1993
Mitochondrial DNA deletions in inclusion body myositisA Oldfors, N G Larsson, C Lindberg, et al.
Annals of Neurology|November 1, 1996
Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegiaA R Moslemi, A Melberg, E Holme, et al.
Neurology|January 27, 1998
Rhabdomyolysis in autosomal dominant progressive external ophthalmoplegiaA Melberg, E Holme, A Oldfors, et al.
Acta Neuropathologica|January 1, 1995
Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibresA Oldfors, E Holme, M Tulinius, et al.
Acta Neuropathologica|January 1, 1989
Cytochrome c oxidase deficiency in infancyA Oldfors, H Sommerland, E Holme, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Inheritance and expression of mitochondrial DNA point mutationsE Holme, M H Tulinius, N G Larsson, et al.
Journal of the American Academy of Dermatology|September 1, 1996
IgA class anticardiolipin antibodies in cutaneous leukocytoclastic vasculitisA D Burden, D M Tillman, P Foley, et al.
Pageof 12