Nada MA - Search Results

1

Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene.

Andresen BS, Bross P, Vianey-Saban C, Divry P, Zabot MT, Roe CR, Nada MA, Byskov A, Kruse TA, Neve S, Kristiansen K, Knudsen I, Corydon MJ, Gregersen N. Andresen BS, et al. Among authors: nada ma. Hum Mol Genet. 1996 Apr;5(4):461-72. doi: 10.1093/hmg/5.4.461. Hum Mol Genet. 1996. PMID: 8845838

2

The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiency.

Andresen BS, Vianey-Saban C, Bross P, Divry P, Roe CR, Nada MA, Knudsen I, Gregersen N. Andresen BS, et al. Among authors: nada ma. J Inherit Metab Dis. 1996;19(2):169-72. doi: 10.1007/BF01799421. J Inherit Metab Dis. 1996. PMID: 8739957 No abstract available.

3

Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathy.

Brown-Harrison MC, Nada MA, Sprecher H, Vianey-Saban C, Farquhar J Jr, Gilladoga AC, Roe CR. Brown-Harrison MC, et al. Among authors: nada ma. Biochem Mol Med. 1996 Jun;58(1):59-65. doi: 10.1006/bmme.1996.0033. Biochem Mol Med. 1996. PMID: 8809347

4

Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients.

Vianey-Saban C, Divry P, Brivet M, Nada M, Zabot MT, Mathieu M, Roe C. Vianey-Saban C, et al. Clin Chim Acta. 1998 Jan 12;269(1):43-62. doi: 10.1016/s0009-8981(97)00185-x. Clin Chim Acta. 1998. PMID: 9498103

5

Investigation of beta-oxidation intermediates in normal and MCAD-deficient human fibroblasts using tandem mass spectrometry.

Nada MA, Chace DH, Sprecher H, Roe CR. Nada MA, et al. Biochem Mol Med. 1995 Feb;54(1):59-66. doi: 10.1006/bmme.1995.1009. Biochem Mol Med. 1995. PMID: 7551818

6

Improved detection of the G1528C mutation in LCHAD deficiency.

Ding JH, Yang BZ, Nada MA, Roe CR. Ding JH, et al. Among authors: nada ma. Biochem Mol Med. 1996 Jun;58(1):46-51. doi: 10.1006/bmme.1996.0031. Biochem Mol Med. 1996. PMID: 8809345

7

Evidence for intermediate channeling in mitochondrial beta-oxidation.

Nada MA, Rhead WJ, Sprecher H, Schulz H, Roe CR. Nada MA, et al. J Biol Chem. 1995 Jan 13;270(2):530-5. doi: 10.1074/jbc.270.2.530. J Biol Chem. 1995. PMID: 7822275 Free article.

8

Prenatal diagnosis of mitochondrial fatty acid oxidation defects.

Nada MA, Vianey-Saban C, Roe CR, Ding JH, Mathieu M, Wappner RS, Bialer MG, McGlynn JA, Mandon G. Nada MA, et al. Prenat Diagn. 1996 Feb;16(2):117-24. doi: 10.1002/(SICI)1097-0223(199602)16:2<117::AID-PD820>3.0.CO;2-Z. Prenat Diagn. 1996. PMID: 8650121

9

Inherited defects of fatty acid oxidation.

Roe CR, Nada MA. Roe CR, et al. Among authors: nada ma. World Rev Nutr Diet. 1994;75:22-5. doi: 10.1159/000423546. World Rev Nutr Diet. 1994. PMID: 7871828 Review. No abstract available.

10

Radioactive assay of 2,4-dienoyl-coenzyme A reductase.

Nada MA, Roe CR, Schulz H. Nada MA, et al. Anal Biochem. 1992 Feb 14;201(1):62-7. doi: 10.1016/0003-2697(92)90174-6. Anal Biochem. 1992. PMID: 1621963

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

63 results

Search Page

Filters