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Brain & Development|May 1, 1991
EEG findings in children and adolescents with mitochondrial encephalomyopathies: a study of 25 casesM H Tulinius, I HagnePediatric Neurology|July 1, 1996
Early-onset myopathy with tubular aggregatesM H Tulinius, A Lundberg, A OldforsBiochimica Et Biophysica Acta|May 24, 1995
Inheritance and expression of mitochondrial DNA point mutationsE Holme, M H Tulinius, N G Larsson, et al.Muscle & Nerve. Supplement|January 1, 1995
Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomasN G Larsson, M H Tulinius, E Holme, et al.Pediatric Neurology|May 1, 1989
Mitochondrial myopathy and cardiomyopathy in siblingsM H Tulinius, B O Eriksson, O Hjalmarson, et al.The Journal of Pediatrics|August 1, 1991
Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigationsM H Tulinius, E Holme, B Kristiansson, et al.The Journal of Pediatrics|August 1, 1991
Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromesM H Tulinius, E Holme, B Kristiansson, et al.Biochimica Et Biophysica Acta|April 12, 1994
Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathyM Houshmand, N G Larsson, E Holme, et al.American Journal of Human Genetics|February 1, 1992
Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her childN G Larsson, H G Eiken, H Boman, et al.American Journal of Human Genetics|December 1, 1992
Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndromeN G Larsson, M H Tulinius, E Holme, et al.Pageof 2