Nelson I - Search Results

1

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

2

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

3

[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.

4

Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR.

Obermaier-Kusser B, Müller-Höcker J, Nelson I, Lestienne P, Enter C, Riedele T, Gerbitz KD. Obermaier-Kusser B, et al. Among authors: nelson i. Biochem Biophys Res Commun. 1990 Jun 29;169(3):1007-15. doi: 10.1016/0006-291x(90)91994-4. Biochem Biophys Res Commun. 1990. PMID: 1973036

5

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.

6

Mitochondrial DNA in postmortem brain from patients with Parkinson's disease.

Lestienne P, Nelson I, Riederer P, Reichmann H, Jellinger K. Lestienne P, et al. Among authors: nelson i. J Neurochem. 1991 May;56(5):1819. doi: 10.1111/j.1471-4159.1991.tb02087.x. J Neurochem. 1991. PMID: 2013767 No abstract available.

7

Mutation detection in Leber's hereditary optic neuropathy by PCR with allele-specific priming.

Nørby S, Lestienne P, Nelson I, Rosenberg T. Nørby S, et al. Among authors: nelson i. Biochem Biophys Res Commun. 1991 Mar 15;175(2):631-6. doi: 10.1016/0006-291x(91)91612-g. Biochem Biophys Res Commun. 1991. PMID: 2018507

8

[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.

9

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

10

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.

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