Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
European Journal of Immunology|March 5, 2003
CD4 T cell activation by myelin oligodendrocyte glycoprotein is suppressed by adult but not cord blood CD25+ T cellsKajsa Wing, Susanne Lindgren, Gittan Kollberg, et al.
European Journal of Human Genetics : EJHG|October 14, 2018
Mitochondrial complex IV deficiency caused by a novel frameshift variant in MT-CO2 associated with myopathy and perturbed acylcarnitine profileSara Roos, Kalliopi Sofou, Carola Hedberg-Oldfors, et al.
Neuromuscular Disorders : NMD|January 14, 2009
A novel homozygous RRM2B missense mutation in association with severe mtDNA depletionGittan Kollberg, Niklas Darin, Karin Benan, et al.
The New England Journal of Medicine|October 12, 2007
Cardiomyopathy and exercise intolerance in muscle glycogen storage disease 0Gittan Kollberg, Már Tulinius, Thomas Gilljam, et al.
European Journal of Human Genetics : EJHG|February 11, 2005
Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutationsGittan Kollberg, Monica Jansson, Asa Pérez-Bercoff, et al.
European Journal of Human Genetics : EJHG|July 12, 2012
A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathySara Roos, Niklas Darin, Gittan Kollberg, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 13, 2012
Phenotypic and genotypic variability in Alpers syndromeKalliopi Sofou, Ali-Reza Moslemi, Gittan Kollberg, et al.
Brain Pathology (Zurich, Switzerland)|November 22, 2021
Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients with mitochondrial myopathy associated with the homoplasmic m.14674T>C variantSara Roos, Carola Hedberg-Oldfors, Kittichate Visuttijai, et al.
Journal of Neuropathology and Experimental Neurology|August 10, 2006
POLG1 mutations associated with progressive encephalopathy in childhoodGittan Kollberg, Ali-Reza Moslemi, Niklas Darin, et al.
The EMBO Journal|January 19, 2012
Nonsense mutations in the COX1 subunit impair the stability of respiratory chain complexes rather than their assemblyHue-Tran Hornig-Do, Takashi Tatsuta, Angela Buckermann, et al.
Pageof 3