Odièvre M - Search Results

1

Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

Poll-The BT, Saudubray JM, Ogier HA, Odièvre M, Scotto JM, Monnens L, Govaerts LC, Roels F, Cornelis A, Schutgens RB, et al. Poll-The BT, et al. Among authors: odievre m. Eur J Pediatr. 1987 Sep;146(5):477-83. doi: 10.1007/BF00441598. Eur J Pediatr. 1987. PMID: 2445576

2

Familial hypermethioninemia partially responsive to dietary restriction.

Labrune P, Perignon JL, Rault M, Brunet C, Lutun H, Charpentier C, Saudubray JM, Odievre M. Labrune P, et al. Among authors: odievre m. J Pediatr. 1990 Aug;117(2 Pt 1):220-6. doi: 10.1016/s0022-3476(05)80533-5. J Pediatr. 1990. PMID: 2380820

3

Antenatal diagnosis of infantile Refsum's disease.

Poll-The BT, Poulos A, Sharp P, Boue J, Ogier H, Odièvre M, Saudubray JM. Poll-The BT, et al. Among authors: odievre m. Clin Genet. 1985 May;27(5):524-6. doi: 10.1111/j.1399-0004.1985.tb00246.x. Clin Genet. 1985. PMID: 2408795 No abstract available.

4

Absence of hepatic peroxisomes in a case of infantile Refsum's disease.

Ogier H, Roels F, Cornelis A, Poll The BT, Scotto JM, Odievre M, Sandubray JM. Ogier H, et al. Among authors: odievre m. Scand J Clin Lab Invest. 1985 Dec;45(8):767-8. doi: 10.3109/00365518509155292. Scand J Clin Lab Invest. 1985. PMID: 2417305 No abstract available.

5

Infantile phytanic acid storage disease, a possible variant of Refsum's disease: three cases, including ultrastructural studies of the liver.

Scotto JM, Hadchouel M, Odievre M, Laudat MH, Saudubray JM, Dulac O, Beucler I, Beaune P. Scotto JM, et al. Among authors: odievre m. J Inherit Metab Dis. 1982;5(2):83-90. doi: 10.1007/BF01799998. J Inherit Metab Dis. 1982. PMID: 6188882

6

Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency.

Bougnères PF, Saudubray JM, Marsac C, Bernard O, Odièvre M, Girard J. Bougnères PF, et al. Among authors: odievre m. J Pediatr. 1981 May;98(5):742-6. doi: 10.1016/s0022-3476(81)80834-7. J Pediatr. 1981. PMID: 7014807

7

Severe giant cell hepatitis with autoimmune hemolytic anemia in early childhood.

Bernard O, Hadchouel M, Scotto J, Odièvre M, Alagille D. Bernard O, et al. Among authors: odievre m. J Pediatr. 1981 Nov;99(5):704-11. doi: 10.1016/s0022-3476(81)80388-5. J Pediatr. 1981. PMID: 7299542

8

[Comparison of percutaneous needle biopsy and liver surgical biopsy for the diagnosis of neonatal cholestasis (author's transl)].

Eliot N, Hadchouel M, Gautier M, Scotto J, Odièvre M. Eliot N, et al. Among authors: odievre m. Gastroenterol Clin Biol. 1978 Dec;2(12):1025-9. Gastroenterol Clin Biol. 1978. PMID: 570530 French. No abstract available.

9

Decreased ketogenesis due to deficiency of hepatic carnitine acyl transferase.

Bougneres PF, Saudubray JM, Marsac C, Bernard O, Odievre M, Girard JR. Bougneres PF, et al. Among authors: odievre m. N Engl J Med. 1980 Jan 10;302(2):123-4. N Engl J Med. 1980. PMID: 7350426 No abstract available.

10

Effect of lactation in a mother with galactosemia.

Brivet M, Raymond JP, Konopka P, Odievre M, Lemonnier A. Brivet M, et al. Among authors: odievre m. J Pediatr. 1989 Aug;115(2):280-2. doi: 10.1016/s0022-3476(89)80084-8. J Pediatr. 1989. PMID: 2754558 No abstract available.

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