Tulinius M - Search Results

1

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.

Horvath R, Kemp JP, Tuppen HA, Hudson G, Oldfors A, Marie SK, Moslemi AR, Servidei S, Holme E, Shanske S, Kollberg G, Jayakar P, Pyle A, Marks HM, Holinski-Feder E, Scavina M, Walter MC, Coku J, Günther-Scholz A, Smith PM, McFarland R, Chrzanowska-Lightowlers ZM, Lightowlers RN, Hirano M, Lochmüller H, Taylor RW, Chinnery PF, Tulinius M, DiMauro S. Horvath R, et al. Among authors: tulinius m. Brain. 2009 Nov;132(Pt 11):3165-74. doi: 10.1093/brain/awp221. Epub 2009 Aug 31. Brain. 2009. PMID: 19720722 Free PMC article.

2

Behavioural strengths and difficulties in relation to intellectual functions and age in Swedish boys with Duchenne muscular dystrophy.

Gillenstrand J, Ekström AB, Kroksmark AK, Tulinius M, Broberg M. Gillenstrand J, et al. Among authors: tulinius m. Child Neuropsychol. 2023 Aug;29(6):959-972. doi: 10.1080/09297049.2022.2144814. Epub 2022 Nov 28. Child Neuropsychol. 2023. PMID: 36444135

3

Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.

Larsson NG, Tulinius MH, Holme E, Oldfors A, Andersen O, Wahlström J, Aasly J. Larsson NG, et al. Among authors: tulinius mh. Am J Hum Genet. 1992 Dec;51(6):1201-12. Am J Hum Genet. 1992. PMID: 1463006 Free PMC article.

4

Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations.

Tulinius MH, Holme E, Kristiansson B, Larsson NG, Oldfors A. Tulinius MH, et al. J Pediatr. 1991 Aug;119(2):242-50. doi: 10.1016/s0022-3476(05)80734-6. J Pediatr. 1991. PMID: 1861209

5

Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes.

Tulinius MH, Holme E, Kristiansson B, Larsson NG, Oldfors A. Tulinius MH, et al. J Pediatr. 1991 Aug;119(2):251-9. doi: 10.1016/s0022-3476(05)80735-8. J Pediatr. 1991. PMID: 1861210

6

Mitochondrial myopathy and cardiomyopathy in siblings.

Tulinius MH, Eriksson BO, Hjalmarson O, Holme E, Oldfors A. Tulinius MH, et al. Pediatr Neurol. 1989 May-Jun;5(3):182-8. doi: 10.1016/0887-8994(89)90069-6. Pediatr Neurol. 1989. PMID: 2742628

7

Inheritance and expression of mitochondrial DNA point mutations.

Holme E, Tulinius MH, Larsson NG, Oldfors A. Holme E, et al. Among authors: tulinius mh. Biochim Biophys Acta. 1995 May 24;1271(1):249-52. doi: 10.1016/0925-4439(95)00035-3. Biochim Biophys Acta. 1995. PMID: 7599216 Free article.

8

Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas.

Larsson NG, Tulinius MH, Holme E, Oldfors A. Larsson NG, et al. Among authors: tulinius mh. Muscle Nerve Suppl. 1995;3:S102-6. doi: 10.1002/mus.880181421. Muscle Nerve Suppl. 1995. PMID: 7603509 Review.

9

De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring.

Tulinius MH, Houshmand M, Larsson NG, Holme E, Oldfors A, Holmberg E, Wahlström J. Tulinius MH, et al. Hum Genet. 1995 Sep;96(3):290-4. doi: 10.1007/BF00210409. Hum Genet. 1995. PMID: 7649544

10

Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy.

Houshmand M, Larsson NG, Holme E, Oldfors A, Tulinius MH, Andersen O. Houshmand M, et al. Among authors: tulinius mh. Biochim Biophys Acta. 1994 Apr 12;1226(1):49-55. doi: 10.1016/0925-4439(94)90058-2. Biochim Biophys Acta. 1994. PMID: 8155739

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