Tulinius M - Search Results

1

Neuropathology in Kearns-Sayre syndrome.

Oldfors A, Fyhr IM, Holme E, Larsson NG, Tulinius M. Oldfors A, et al. Among authors: tulinius m. Acta Neuropathol. 1990;80(5):541-6. doi: 10.1007/BF00294616. Acta Neuropathol. 1990. PMID: 2251912

2

Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.

Oldfors A, Larsson NG, Holme E, Tulinius M, Kadenbach B, Droste M. Oldfors A, et al. Among authors: tulinius m. J Neurol Sci. 1992 Jul;110(1-2):169-77. doi: 10.1016/0022-510x(92)90025-g. J Neurol Sci. 1992. PMID: 1324295

3

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome.

Larsson NG, Holme E, Kristiansson B, Oldfors A, Tulinius M. Larsson NG, et al. Among authors: tulinius m. Pediatr Res. 1990 Aug;28(2):131-6. doi: 10.1203/00006450-199008000-00011. Pediatr Res. 1990. PMID: 2395603

4

Cytochrome c oxidase deficiency in infancy.

Oldfors A, Sommerland H, Holme E, Tulinius M, Kristiansson B. Oldfors A, et al. Among authors: tulinius m. Acta Neuropathol. 1989;77(3):267-75. doi: 10.1007/BF00687578. Acta Neuropathol. 1989. PMID: 2538042

5

Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosis.

Oldfors A, Tulinius M, Holme E, Kalimo H, Kristiansson B, Eriksson BO. Oldfors A, et al. Among authors: tulinius m. Acta Neuropathol. 1987;74(3):287-93. doi: 10.1007/BF00688194. Acta Neuropathol. 1987. PMID: 3673521

6

Tissue distribution and disease manifestations of the tRNA(Lys) A-->G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibres.

Oldfors A, Holme E, Tulinius M, Larsson NG. Oldfors A, et al. Among authors: tulinius m. Acta Neuropathol. 1995;90(3):328-33. doi: 10.1007/BF00296519. Acta Neuropathol. 1995. PMID: 8525809

7

Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria.

Holme E, Greter J, Jacobson CE, Larsson NG, Lindstedt S, Nilsson KO, Oldfors A, Tulinius M. Holme E, et al. Among authors: tulinius m. Pediatr Res. 1992 Dec;32(6):731-5. doi: 10.1203/00006450-199212000-00022. Pediatr Res. 1992. PMID: 1287564

8

Multiple symmetric lipomas with high levels of mtDNA with the tRNA(Lys) A-->G(8344) mutation as the only manifestation of disease in a carrier of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.

Holme E, Larsson NG, Oldfors A, Tulinius M, Sahlin P, Stenman G. Holme E, et al. Among authors: tulinius m. Am J Hum Genet. 1993 Mar;52(3):551-6. Am J Hum Genet. 1993. PMID: 8447321 Free PMC article.

9

Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gne.

Houshmand M, Larsson NG, Oldfors A, Tulinius M, Holme E. Houshmand M, et al. Among authors: tulinius m. Hum Genet. 1996 Mar;97(3):269-73. doi: 10.1007/BF02185750. Hum Genet. 1996. PMID: 8786060

10

Threshold expression of the tRNA(Lys) A8344G mutation in single muscle fibres.

Moslemi AR, Tulinius M, Holme E, Oldfors A. Moslemi AR, et al. Among authors: tulinius m. Neuromuscul Disord. 1998 Jun;8(5):345-9. doi: 10.1016/s0960-8966(98)00029-7. Neuromuscul Disord. 1998. PMID: 9673990

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