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E Holme

Showing results (51-60 of 111) with videos related to

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Annals of Neurology|March 23, 2001
The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalitiesN Darin, A Oldfors, A R Moslemi, et al.
Human Genetics|March 1, 1996
Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gneM Houshmand, N G Larsson, A Oldfors, et al.
Neuropediatrics|October 12, 2005
Two new mutations in the MTATP6 gene associated with Leigh syndromeA-R Moslemi, N Darin, M Tulinius, et al.
Immunogenetics|January 1, 1988
Quantitation of human C4A and C4B, in serum and plasma by enzyme-linked immunoadsorbent assayE Holme, S J Cross, J Veitch, et al.
Acta Neuropathologica|January 1, 1990
Neuropathology in Kearns-Sayre syndromeA Oldfors, I M Fyhr, E Holme, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Treatment of two children with hereditary tyrosinaemia type I and long-standing renal disease with a 4-hydroxyphenylpyruvate dioxygenase inhibitor (NTBC)E Pronicka, E Rowinska, Z Bentkowski, 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.
Clinical and Experimental Immunology|January 1, 1986
Decreased C3b receptors (CR1) on erythrocytes from patients with systemic lupus erythematosusE Holme, A Fyfe, A Zoma, 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.
Pageof 12

Showing results (51-60 of 111) with videos related to

Sort By:
Pageof 12
Annals of Neurology|March 23, 2001
The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalitiesN Darin, A Oldfors, A R Moslemi, et al.
Human Genetics|March 1, 1996
Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gneM Houshmand, N G Larsson, A Oldfors, et al.
Neuropediatrics|October 12, 2005
Two new mutations in the MTATP6 gene associated with Leigh syndromeA-R Moslemi, N Darin, M Tulinius, et al.
Immunogenetics|January 1, 1988
Quantitation of human C4A and C4B, in serum and plasma by enzyme-linked immunoadsorbent assayE Holme, S J Cross, J Veitch, et al.
Acta Neuropathologica|January 1, 1990
Neuropathology in Kearns-Sayre syndromeA Oldfors, I M Fyhr, E Holme, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Treatment of two children with hereditary tyrosinaemia type I and long-standing renal disease with a 4-hydroxyphenylpyruvate dioxygenase inhibitor (NTBC)E Pronicka, E Rowinska, Z Bentkowski, 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.
Clinical and Experimental Immunology|January 1, 1986
Decreased C3b receptors (CR1) on erythrocytes from patients with systemic lupus erythematosusE Holme, A Fyfe, A Zoma, 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.
Pageof 12