Nelson I - Search Results

1

[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy].

Marsac C, Degoul F, Bonne G, Romero N, Nelson I, Fardeau M, François D, Ponsot G, Harpey JP, Eymard B, et al. Marsac C, et al. Among authors: nelson i. Rev Neurol (Paris). 1991;147(6-7):462-6. Rev Neurol (Paris). 1991. PMID: 1962051 French.

2

Kearns-Sayre syndrome with sideroblastic anemia: molecular investigations.

Nelson I, Bonne G, Degoul F, Marsac C, Ponsot G, Lestienne P. Nelson I, et al. Neuropediatrics. 1992 Aug;23(4):199-205. doi: 10.1055/s-2008-1071341. Neuropediatrics. 1992. PMID: 1407387

3

Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.

Degoul F, Nelson I, Lestienne P, Francois D, Romero N, Duboc D, Eymard B, Fardeau M, Ponsot G, Paturneau-Jouas M, et al. Degoul F, et al. Among authors: nelson i. J Neurol Sci. 1991 Feb;101(2):168-77. doi: 10.1016/0022-510x(91)90042-6. J Neurol Sci. 1991. PMID: 1851820

4

Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies.

Degoul F, Nelson I, Amselem S, Romero N, Obermaier-Kusser B, Ponsot G, Marsac C, Lestienne P. Degoul F, et al. Among authors: nelson i. Nucleic Acids Res. 1991 Feb 11;19(3):493-6. doi: 10.1093/nar/19.3.493. Nucleic Acids Res. 1991. PMID: 2011523 Free PMC article.

5

[Nucleotide mapping and a kinetic model of a heteroplasmic deletion of 4,666 base pairs from mitochondrial DNA in the Kearns-Sayre syndrome].

Nelson I, d'Auriol L, Galibert F, Ponsot G, Lestienne P. Nelson I, et al. C R Acad Sci III. 1989;309(10):403-7. C R Acad Sci III. 1989. PMID: 2514965 French.

6

Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscle.

Romero NB, Lestienne P, Marsac C, Paturneau-Jouas M, Nelson I, François D, Eymard B, Fardeau M. Romero NB, et al. Among authors: nelson i. J Neurol Sci. 1989 Nov;93(2-3):297-309. doi: 10.1016/0022-510x(89)90199-8. J Neurol Sci. 1989. PMID: 2556504

7

Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.

Nelson I, Degoul F, Obermaier-Kusser B, Romero N, Borrone C, Marsac C, Vayssiere JL, Gerbitz K, Fardeau M, Ponsot G, Lestienne P. Nelson I, et al. Nucleic Acids Res. 1989 Oct 25;17(20):8117-24. doi: 10.1093/nar/17.20.8117. Nucleic Acids Res. 1989. PMID: 2813058 Free PMC article.

8

Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic mice.

Nelson I, Gerasimov S, Marsac C, Lestienne P, Boursot P. Nelson I, et al. Mamm Genome. 1993 Nov;4(11):680-3. doi: 10.1007/BF00360907. Mamm Genome. 1993. PMID: 8281018 No abstract available.

9

Higher maternal than paternal inheritance of diabetes in GK rats.

Gauguier D, Nelson I, Bernard C, Parent V, Marsac C, Cohen D, Froguel P. Gauguier D, et al. Among authors: nelson i. Diabetes. 1994 Feb;43(2):220-4. doi: 10.2337/diab.43.2.220. Diabetes. 1994. PMID: 8288046

10

Distinctive serum miRNA profile in mouse models of striated muscular pathologies.

Vignier N, Amor F, Fogel P, Duvallet A, Poupiot J, Charrier S, Arock M, Montus M, Nelson I, Richard I, Carrier L, Servais L, Voit T, Bonne G, Israeli D. Vignier N, et al. Among authors: nelson i. PLoS One. 2013;8(2):e55281. doi: 10.1371/journal.pone.0055281. Epub 2013 Feb 13. PLoS One. 2013. PMID: 23418438 Free PMC article.

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