Rinaldo P - Search Results

1

Clinical and biochemical features of fatty acid oxidation disorders.

Rinaldo P, Raymond K, al-Odaib A, Bennett MJ. Rinaldo P, et al. Curr Opin Pediatr. 1998 Dec;10(6):615-21. doi: 10.1097/00008480-199810060-00014. Curr Opin Pediatr. 1998. PMID: 9848022 Review.

2

Fatty acid oxidation disorders.

Rinaldo P, Matern D, Bennett MJ. Rinaldo P, et al. Annu Rev Physiol. 2002;64:477-502. doi: 10.1146/annurev.physiol.64.082201.154705. Annu Rev Physiol. 2002. PMID: 11826276 Review.

3

Sudden and unexpected neonatal death: a protocol for the postmortem diagnosis of fatty acid oxidation disorders.

Rinaldo P, Yoon HR, Yu C, Raymond K, Tiozzo C, Giordano G. Rinaldo P, et al. Semin Perinatol. 1999 Apr;23(2):204-10. doi: 10.1016/s0146-0005(99)80052-4. Semin Perinatol. 1999. PMID: 10331471 Review.

4

Inborn errors of mitochondrial fatty acid oxidation.

Bennett MJ, Rinaldo P, Strauss AW. Bennett MJ, et al. Among authors: rinaldo p. Crit Rev Clin Lab Sci. 2000 Feb;37(1):1-44. doi: 10.1080/10408360091174169. Crit Rev Clin Lab Sci. 2000. PMID: 10737439 Review.

5

Two-tier approach to the newborn screening of methylenetetrahydrofolate reductase deficiency and other remethylation disorders with tandem mass spectrometry.

Tortorelli S, Turgeon CT, Lim JS, Baumgart S, Day-Salvatore DL, Abdenur J, Bernstein JA, Lorey F, Lichter-Konecki U, Oglesbee D, Raymond K, Matern D, Schimmenti L, Rinaldo P, Gavrilov DK. Tortorelli S, et al. Among authors: rinaldo p. J Pediatr. 2010 Aug;157(2):271-5. doi: 10.1016/j.jpeds.2010.02.027. Epub 2010 Apr 14. J Pediatr. 2010. PMID: 20394947

6

Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing.

Smith EH, Thomas C, McHugh D, Gavrilov D, Raymond K, Rinaldo P, Tortorelli S, Matern D, Highsmith WE, Oglesbee D. Smith EH, et al. Among authors: rinaldo p. Mol Genet Metab. 2010 Jul;100(3):241-50. doi: 10.1016/j.ymgme.2010.04.001. Epub 2010 Apr 8. Mol Genet Metab. 2010. PMID: 20434380

7

Intact alpha-subunit is required for membrane-binding of human mitochondrial trifunctional beta-oxidation protein, but is not necessary for conferring 3-ketoacyl-CoA thiolase activity to the beta-subunit.

Weinberger MJ, Rinaldo P, Strauss AW, Bennett MJ. Weinberger MJ, et al. Among authors: rinaldo p. Biochem Biophys Res Commun. 1995 Apr 6;209(1):47-52. doi: 10.1006/bbrc.1995.1468. Biochem Biophys Res Commun. 1995. PMID: 7726862 Free article.

8

Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency.

Bhala A, Willi SM, Rinaldo P, Bennett MJ, Schmidt-Sommerfeld E, Hale DE. Bhala A, et al. Among authors: rinaldo p. J Pediatr. 1995 Jun;126(6):910-5. doi: 10.1016/s0022-3476(95)70207-5. J Pediatr. 1995. PMID: 7776094

9

Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: a new defect of fatty acid oxidation.

Bennett MJ, Weinberger MJ, Kobori JA, Rinaldo P, Burlina AB. Bennett MJ, et al. Among authors: rinaldo p. Pediatr Res. 1996 Jan;39(1):185-8. doi: 10.1203/00006450-199601000-00031. Pediatr Res. 1996. PMID: 8825408

10

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women.

Ibdah JA, Bennett MJ, Rinaldo P, Zhao Y, Gibson B, Sims HF, Strauss AW. Ibdah JA, et al. Among authors: rinaldo p. N Engl J Med. 1999 Jun 3;340(22):1723-31. doi: 10.1056/NEJM199906033402204. N Engl J Med. 1999. PMID: 10352164 Free article.

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