Feillet F - Search Results

1

High prevalence of hyperhomocysteinemia related to folate deficiency and the 677C-->T mutation of the gene encoding methylenetetrahydrofolate reductase in coastal West Africa.

Amouzou EK, Chabi NW, Adjalla CE, Rodriguez-Guéant RM, Feillet F, Villaume C, Sanni A, Guéant JL. Amouzou EK, et al. Among authors: feillet f. Am J Clin Nutr. 2004 Apr;79(4):619-24. doi: 10.1093/ajcn/79.4.619. Am J Clin Nutr. 2004. PMID: 15051606 Free article.

2

Vitamin B12 status in marasmic children.

Feillet F, Guéant JL, Lambert D, Djalali M, Nicolas JP, Vidailhet M. Feillet F, et al. J Pediatr Gastroenterol Nutr. 1990 Aug;11(2):283-4. doi: 10.1097/00005176-199008000-00024. J Pediatr Gastroenterol Nutr. 1990. PMID: 2118566 No abstract available.

3

Concentrations of riboflavin and related organic acids in children with protein-energy malnutrition.

Capo-Chichi CD, Feillet F, Guéant JL, Amouzou K, Zonon N, Sanni A, Lefebvre E, Assimadi K, Vidailhet M. Capo-Chichi CD, et al. Among authors: feillet f. Am J Clin Nutr. 2000 Apr;71(4):978-86. doi: 10.1093/ajcn/71.4.978. Am J Clin Nutr. 2000. PMID: 10731506

4

Analysis of riboflavin and riboflavin cofactor levels in plasma by high-performance liquid chromatography.

Capo-chichi CD, Guéant JL, Feillet F, Namour F, Vidailhet M. Capo-chichi CD, et al. Among authors: feillet f. J Chromatogr B Biomed Sci Appl. 2000 Feb 28;739(1):219-24. doi: 10.1016/s0378-4347(99)00469-7. J Chromatogr B Biomed Sci Appl. 2000. PMID: 10744329

5

Evidence of cataplerosis in a patient with neonatal classical galactosemia presenting as citrin deficiency.

Feillet F, Merten M, Battaglia-Hsu SF, Rabier D, Kobayashi K, Straczek J, Brivet M, Favre E, Guéant JL. Feillet F, et al. J Hepatol. 2008 Mar;48(3):517-22. doi: 10.1016/j.jhep.2007.11.016. Epub 2007 Dec 31. J Hepatol. 2008. PMID: 18207281

6

Evaluation of neonatal BH4 loading test in neonates screened for hyperphenylalaninemia.

Feillet F, Chery C, Namour F, Kimmoun A, Favre E, Lorentz E, Battaglia-Hsu SF, Guéant JL. Feillet F, et al. Early Hum Dev. 2008 Sep;84(9):561-7. doi: 10.1016/j.earlhumdev.2008.01.003. Epub 2008 Mar 5. Early Hum Dev. 2008. PMID: 18321666

7

Acute decompensation of isovaleric acidemia induced by Graves' disease.

Kimmoun A, Abboud G, Strazeck J, Merten M, Guéant JL, Feillet F. Kimmoun A, et al. Among authors: feillet f. Intensive Care Med. 2008 Dec;34(12):2315-6. doi: 10.1007/s00134-008-1192-7. Epub 2008 Jul 8. Intensive Care Med. 2008. PMID: 18607566 No abstract available.

8

Life-threatening methylenetetrahydrofolate reductase (MTHFR) deficiency with extremely early onset: characterization of two novel mutations in compound heterozygous patients.

Forges T, Chery C, Audonnet S, Feillet F, Gueant JL. Forges T, et al. Among authors: feillet f. Mol Genet Metab. 2010 Jun;100(2):143-8. doi: 10.1016/j.ymgme.2010.03.002. Epub 2010 Mar 6. Mol Genet Metab. 2010. PMID: 20356773

9

Ovarian tissue cryopreservation and subsequent spontaneous pregnancies in a patient with classic galactosemia.

Forges T, Monnier P, Leheup B, Cheillan D, Brivet M, Barbarino A, Guéant JL, Feillet F. Forges T, et al. Among authors: feillet f. Fertil Steril. 2011 Jan;95(1):290.e1-3. doi: 10.1016/j.fertnstert.2010.06.014. Fertil Steril. 2011. PMID: 20663501 Free article.

10

Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome with compound AMN mutations in intron 3 and exon 7.

Namour F, Dobrovoljski G, Chery C, Audonnet S, Feillet F, Sperl W, Gueant JL. Namour F, et al. Among authors: feillet f. Haematologica. 2011 Nov;96(11):1715-9. doi: 10.3324/haematol.2011.043984. Epub 2011 Jul 12. Haematologica. 2011. PMID: 21750092 Free PMC article. Clinical Trial.

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