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L Nijtmans

Showing results (1-10 of 7) with videos related to

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Italian Journal of Neurological Sciences|August 11, 2000
Nuclear gene defects in mitochondrial disordersM Zeviani, P Corona, L Nijtmans, et al.
Human Molecular Genetics|November 11, 1999
Characterization of SURF-1 expression and Surf-1p function in normal and disease conditionsV Tiranti, C Galimberti, L Nijtmans, et al.
Anticancer Research|November 1, 1992
Cytostatic activity of cisplatin in the presence of WR2721 and its thiol metabolite WR1065 in OVCAR-3 human ovarian cancer cells as compared to V79 fibroblastsM Treskes, L Nijtmans, A M Fichtinger-Schepman, et al.
Journal of Muscle Research and Cell Motility|February 1, 1995
New method for the accurate characterization of single human skeletal muscle fibres demonstrates a relation between mATPase and MyHC expression in pure and hybrid fibre typesJ A Sant'ana Pereira, A Wessels, L Nijtmans, et al.
American Journal of Medical Genetics. Part A|December 17, 2011
Infant with MCA and severe cutis laxa due to a de novo duplication 11p of paternal originT Gardeitchik, N de Leeuw, L Nijtmans, et al.
Human Molecular Genetics|November 7, 2000
A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndromeV Tiranti, P Corona, M Greco, et al.
Brain : a Journal of Neurology|December 3, 1999
Riboflavin therapy. Biochemical heterogeneity in two adult lipid storage myopathiesL Vergani, M Barile, C Angelini, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Italian Journal of Neurological Sciences|August 11, 2000
Nuclear gene defects in mitochondrial disordersM Zeviani, P Corona, L Nijtmans, et al.
Human Molecular Genetics|November 11, 1999
Characterization of SURF-1 expression and Surf-1p function in normal and disease conditionsV Tiranti, C Galimberti, L Nijtmans, et al.
Anticancer Research|November 1, 1992
Cytostatic activity of cisplatin in the presence of WR2721 and its thiol metabolite WR1065 in OVCAR-3 human ovarian cancer cells as compared to V79 fibroblastsM Treskes, L Nijtmans, A M Fichtinger-Schepman, et al.
Journal of Muscle Research and Cell Motility|February 1, 1995
New method for the accurate characterization of single human skeletal muscle fibres demonstrates a relation between mATPase and MyHC expression in pure and hybrid fibre typesJ A Sant'ana Pereira, A Wessels, L Nijtmans, et al.
American Journal of Medical Genetics. Part A|December 17, 2011
Infant with MCA and severe cutis laxa due to a de novo duplication 11p of paternal originT Gardeitchik, N de Leeuw, L Nijtmans, et al.
Human Molecular Genetics|November 7, 2000
A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndromeV Tiranti, P Corona, M Greco, et al.
Brain : a Journal of Neurology|December 3, 1999
Riboflavin therapy. Biochemical heterogeneity in two adult lipid storage myopathiesL Vergani, M Barile, C Angelini, et al.
Pageof 1