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E Wilichowski

Showing results (11-20 of 34) with videos related to

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Molecular and Cellular Probes|February 1, 1994
Deletion screening of mitochondrial DNA via multiprimer DNA amplificationB P Ernst, E Wilichowski, M Wagner, et al.
Neuropediatrics|December 22, 1999
Quantitative proton magnetic resonance spectroscopy of cerebral metabolic disturbances in patients with MELASE Wilichowski, P J Pouwels, J Frahm, et al.
Klinika Oczna|June 1, 1995
[Retinitis pigmentosa in Kearns-Sayre syndrome resulting from mutation of mitochondrial DNA "de novo"]A T Midro, R Zalewska, G Skrzypczak-Adamiak, et al.
Klinische Padiatrie|July 5, 2006
[Pitfalls in the diagnosis of congenital hyperinsulinism: a case report and review of the literature]J R Fernandez Alvarez, H Rabe, E Wilichowski, et al.
Human Genetics|January 1, 1987
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markersE Wilichowski, M Krawczak, E Seemanova, et al.
Neuropediatrics|December 1, 1994
Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosisF A Hanefeld, B P Ernst, E Wilichowski, et al.
Neuroradiology|March 23, 2004
Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathyK Brockmann, J Finsterbusch, U Schara, et al.
Annals of Neurology|June 18, 1998
Identical mitochondrial DNA in monozygotic twins with discordant adrenoleukodystrophy phenotypeE Wilichowski, A Ohlenbusch, G C Korenke, et al.
The Pediatric Infectious Disease Journal|April 1, 1996
Fatal Pseudallescheria boydii panencephalitis in a child after near-drowningE Wilichowski, H J Christen, H Schiffmann, et al.
Neuropediatrics|October 1, 1993
Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopyF Hanefeld, U Holzbach, B Kruse, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Molecular and Cellular Probes|February 1, 1994
Deletion screening of mitochondrial DNA via multiprimer DNA amplificationB P Ernst, E Wilichowski, M Wagner, et al.
Neuropediatrics|December 22, 1999
Quantitative proton magnetic resonance spectroscopy of cerebral metabolic disturbances in patients with MELASE Wilichowski, P J Pouwels, J Frahm, et al.
Klinika Oczna|June 1, 1995
[Retinitis pigmentosa in Kearns-Sayre syndrome resulting from mutation of mitochondrial DNA "de novo"]A T Midro, R Zalewska, G Skrzypczak-Adamiak, et al.
Klinische Padiatrie|July 5, 2006
[Pitfalls in the diagnosis of congenital hyperinsulinism: a case report and review of the literature]J R Fernandez Alvarez, H Rabe, E Wilichowski, et al.
Human Genetics|January 1, 1987
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markersE Wilichowski, M Krawczak, E Seemanova, et al.
Neuropediatrics|December 1, 1994
Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosisF A Hanefeld, B P Ernst, E Wilichowski, et al.
Neuroradiology|March 23, 2004
Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathyK Brockmann, J Finsterbusch, U Schara, et al.
Annals of Neurology|June 18, 1998
Identical mitochondrial DNA in monozygotic twins with discordant adrenoleukodystrophy phenotypeE Wilichowski, A Ohlenbusch, G C Korenke, et al.
The Pediatric Infectious Disease Journal|April 1, 1996
Fatal Pseudallescheria boydii panencephalitis in a child after near-drowningE Wilichowski, H J Christen, H Schiffmann, et al.
Neuropediatrics|October 1, 1993
Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopyF Hanefeld, U Holzbach, B Kruse, et al.
Pageof 4