Rötig A - Search Results

1

Cerebral blood flow and acute episodes of Leigh syndrome in neurometabolic disorders.

Loiselet K, Ruzzenente B, Roux CJ, Barcia G, Pennisi A, Desguerre I, Rötig A, Munnich A, Boddaert N; Paediatric Radiology and Metabolics Group. Loiselet K, et al. Among authors: rotig a. Dev Med Child Neurol. 2021 Jun;63(6):705-711. doi: 10.1111/dmcn.14814. Epub 2021 Jan 28. Dev Med Child Neurol. 2021. PMID: 33511646 Free article.

2

Isolation and characterization of mitochondria from human B lymphoblastoid cell lines.

Bourgeron T, Chretien D, Rötig A, Munnich A, Rustin P. Bourgeron T, et al. Among authors: rotig a. Biochem Biophys Res Commun. 1992 Jul 15;186(1):16-23. doi: 10.1016/s0006-291x(05)80769-7. Biochem Biophys Res Commun. 1992. PMID: 1321601

3

[Metabolic, enzymological and molecular assessment of mitochondrial cytopathies].

Munnich A, Rotig A. Munnich A, et al. Among authors: rotig a. Pediatrie. 1991;46(6-7):509-14. Pediatrie. 1991. PMID: 1664083 French.

4

Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome.

Rötig A, Cormier V, Koll F, Mize CE, Saudubray JM, Veerman A, Pearson HA, Munnich A. Rötig A, et al. Genomics. 1991 Jun;10(2):502-4. doi: 10.1016/0888-7543(91)90342-c. Genomics. 1991. PMID: 1712754

5

Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy.

Cormier V, Rotig A, Tardieu M, Colonna M, Saudubray JM, Munnich A. Cormier V, et al. Among authors: rotig a. Am J Hum Genet. 1991 Apr;48(4):643-8. Am J Hum Genet. 1991. PMID: 2014791 Free PMC article.

6

Widespread multi-tissue deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome.

Cormier V, Rötig A, Quartino AR, Forni GL, Cerone R, Maier M, Saudubray JM, Munnich A. Cormier V, et al. Among authors: rotig a. J Pediatr. 1990 Oct;117(4):599-602. doi: 10.1016/s0022-3476(05)80698-5. J Pediatr. 1990. PMID: 2213388 No abstract available.

7

The measurement of the rotenone-sensitive NADH cytochrome c reductase activity in mitochondria isolated from minute amount of human skeletal muscle.

Chretien D, Bourgeron T, Rötig A, Munnich A, Rustin P. Chretien D, et al. Among authors: rotig a. Biochem Biophys Res Commun. 1990 Nov 30;173(1):26-33. doi: 10.1016/s0006-291x(05)81016-2. Biochem Biophys Res Commun. 1990. PMID: 2256918

8

[Respiratory chain diseases in infancy. Clinical presentation and diagnosis].

García Silva MT, Bonnefont JP, Rotig A, Romero N, Vassault A, Colonna M, Coude M, Rabier D, Munnich A, Fardeau M, et al. García Silva MT, et al. Among authors: rotig a. An Esp Pediatr. 1989 Nov;31(5):421-30. An Esp Pediatr. 1989. PMID: 2559637 Review. Spanish.

9

Phenotypic expression of mitochondrial genotypes in cultured skin fibroblasts and in Epstein-Barr virus-transformed lymphocytes in Pearson syndrome.

Rötig A, Bourgeron T, Rustin P, Munnich A. Rötig A, et al. Muscle Nerve Suppl. 1995;3:S159-64. doi: 10.1002/mus.880181431. Muscle Nerve Suppl. 1995. PMID: 7541513

10

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.

Bourgeron T, Rustin P, Chretien D, Birch-Machin M, Bourgeois M, Viegas-Péquignot E, Munnich A, Rötig A. Bourgeron T, et al. Among authors: rotig a. Nat Genet. 1995 Oct;11(2):144-9. doi: 10.1038/ng1095-144. Nat Genet. 1995. PMID: 7550341

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

307 results

Search Page

Filters