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E Wilichowski

Showing results (1-10 of 34) with videos related to

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Mycoses|November 1, 1995
Cerebral Pseudallescheria mycosis after near-drowningR Rüchel, E Wilichowski
The Laryngoscope|February 27, 2001
Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathiesP Zwirner, E Wilichowski
Neuropediatrics|October 8, 1998
Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutationsA Ohlenbusch, E Wilichowski, F Hanefeld
Muscle & Nerve|August 24, 1999
Supplementation with creatine monohydrate in children with mitochondrial encephalomyopathiesA Borchert, E Wilichowski, F Hanefeld
Neuropediatrics|February 24, 1999
Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genesE Wilichowski, A Ohlenbusch, F Hanefeld
Neuropediatrics|February 24, 1999
Characterization of the mitochondrial genome in childhood multiple sclerosis. III. Multiple sclerosis without optic neuritis and the non-LHON-associated genesA Ohlenbusch, E Wilichowski, F Hanefeld
Lancet (London, England)|June 22, 1996
Benign adipic aciduriaD H Hunneman, E Wilichowski, F Hanefeld
European Journal of Pediatrics|May 1, 1988
DNA analysis of ornithine transcarbamylase deficiencyU Wendel, E Wilichowski, J Schmidtke, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Rett syndrome--search for genetic markersF Hanefeld, U Hanefeld, E Wilichowski, et al.
Nucleic Acids Research|June 15, 1997
S1 nuclease hybrid analysis of mitochondrial DNA amplified by long-distance PCR: rapid screening for small-scale rearrangementsK Lundin, E Wilichowski, B P Ernst, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Mycoses|November 1, 1995
Cerebral Pseudallescheria mycosis after near-drowningR Rüchel, E Wilichowski
The Laryngoscope|February 27, 2001
Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathiesP Zwirner, E Wilichowski
Neuropediatrics|October 8, 1998
Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutationsA Ohlenbusch, E Wilichowski, F Hanefeld
Muscle & Nerve|August 24, 1999
Supplementation with creatine monohydrate in children with mitochondrial encephalomyopathiesA Borchert, E Wilichowski, F Hanefeld
Neuropediatrics|February 24, 1999
Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genesE Wilichowski, A Ohlenbusch, F Hanefeld
Neuropediatrics|February 24, 1999
Characterization of the mitochondrial genome in childhood multiple sclerosis. III. Multiple sclerosis without optic neuritis and the non-LHON-associated genesA Ohlenbusch, E Wilichowski, F Hanefeld
Lancet (London, England)|June 22, 1996
Benign adipic aciduriaD H Hunneman, E Wilichowski, F Hanefeld
European Journal of Pediatrics|May 1, 1988
DNA analysis of ornithine transcarbamylase deficiencyU Wendel, E Wilichowski, J Schmidtke, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Rett syndrome--search for genetic markersF Hanefeld, U Hanefeld, E Wilichowski, et al.
Nucleic Acids Research|June 15, 1997
S1 nuclease hybrid analysis of mitochondrial DNA amplified by long-distance PCR: rapid screening for small-scale rearrangementsK Lundin, E Wilichowski, B P Ernst, et al.
Pageof 4