Mitchell G - Search Results

1

Approach to the patient with a fatty acid oxidation disorder.

Saudubray JM, Mitchell G, Bonnefont JP, Schwartz G, Nuttin C, Munnich A, Brivet M, Vassault A, Demaugre F, Rabier D, et al. Saudubray JM, et al. Among authors: mitchell g. Prog Clin Biol Res. 1992;375:271-88. Prog Clin Biol Res. 1992. PMID: 1438373 Review. No abstract available.

2

Hepatic and muscular presentations of carnitine palmitoyl transferase deficiency: two distinct entities.

Demaugre F, Bonnefont JP, Mitchell G, Nguyen-Hoang N, Pelet A, Rimoldi M, Di Donato S, Saudubray JM. Demaugre F, et al. Among authors: mitchell g. Pediatr Res. 1988 Sep;24(3):308-11. doi: 10.1203/00006450-198809000-00006. Pediatr Res. 1988. PMID: 3211616

3

The effect of D-carnitine on palmitate oxidation in cultured fibroblasts.

Mitchell G, Saudubray JM, Pellet A, Demaugre F, Labarthe JC. Mitchell G, et al. Clin Chim Acta. 1984 Oct 29;143(1):23-7. doi: 10.1016/0009-8981(84)90033-0. Clin Chim Acta. 1984. PMID: 6499212 No abstract available.

4

Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids.

Duran M, Mitchell G, de Klerk JB, de Jager JP, Hofkamp M, Bruinvis L, Ketting D, Saudubray JM, Wadman SK. Duran M, et al. Among authors: mitchell g. J Pediatr. 1985 Sep;107(3):397-404. doi: 10.1016/s0022-3476(85)80514-x. J Pediatr. 1985. PMID: 4032135

5

[Heterogeneity of carnitine palmitoyltransferase deficiencies. Deficiency of CPT I in the hepatic form and CPT II in the muscular form].

Bonnefont JP, Ogier H, Mitchell G, Demaugre F, Pelet A, Saudubray JM, Frezal J. Bonnefont JP, et al. Among authors: mitchell g. Arch Fr Pediatr. 1985 Aug-Sep;42 Suppl 1:613-7. Arch Fr Pediatr. 1985. PMID: 4083994 French.

6

Infantile onset carnitine palmitoyltransferase 2 deficiency: Cortical polymicrogyria, schizencephaly, and gray matter heterotopias in an adolescent with normal development.

Shelihan I, Rossignol E, Décarie JC, Bonnefont JP, Brivet M, Brunel-Guitton C, Mitchell GA. Shelihan I, et al. JIMD Rep. 2021 Sep 29;63(1):3-10. doi: 10.1002/jmd2.12243. eCollection 2022 Jan. JIMD Rep. 2021. PMID: 35028265 Free PMC article.

7

Hudson memorial lecture. Neonatal management of organic acidurias. Clinical update.

Saudubray JM, Ogier H, Charpentier C, Depondt E, Coudé FX, Munnich A, Mitchell G, Rey F, Rey J, Frézal J. Saudubray JM, et al. Among authors: mitchell g. J Inherit Metab Dis. 1984;7 Suppl 1:2-9. doi: 10.1007/978-94-009-5612-4_2. J Inherit Metab Dis. 1984. PMID: 6434839

8

Antenatal diagnosis of glutaricaciduria type II.

Mitchell G, Saudubray JM, Benoit Y, Rocchiccioli F, Charpentier C, Ogier H, Boue J. Mitchell G, et al. Lancet. 1983 May 14;1(8333):1099. doi: 10.1016/s0140-6736(83)91929-3. Lancet. 1983. PMID: 6133123 No abstract available.

9

Deficient liver biotinidase activity in multiple carboxylase deficiency.

Gaudry M, Munnich A, Saudubray JM, Ogier H, Mitchell G, Marsac C, Causse M, Marquet A, Frezal J. Gaudry M, et al. Among authors: mitchell g. Lancet. 1983 Aug 13;2(8346):397. doi: 10.1016/s0140-6736(83)90363-x. Lancet. 1983. PMID: 6135889 No abstract available.

10

One gene, several messages. From multifunctional proteins to endogenous opiates.

Frézal J, Munnich A, Mitchell G. Frézal J, et al. Among authors: mitchell g. Hum Genet. 1983;64(4):311-4. doi: 10.1007/BF00292362. Hum Genet. 1983. PMID: 6311726 No abstract available.

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