Leroux A - Search Results

1

Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum.

Ewenczyk C, Leroux A, Roubergue A, Laugel V, Afenjar A, Saudubray JM, Beauvais P, Billette de Villemeur T, Vidailhet M, Roze E. Ewenczyk C, et al. Among authors: leroux a. Brain. 2008 Mar;131(Pt 3):760-1. doi: 10.1093/brain/awm337. Epub 2008 Jan 17. Brain. 2008. PMID: 18202104 Review.

2

[Clinical and biological forms of cytochrome b5 reductase deficiency].

Kaplan JC, Leroux A, Beauvais P. Kaplan JC, et al. Among authors: leroux a. C R Seances Soc Biol Fil. 1979;173(2):368-79. C R Seances Soc Biol Fil. 1979. PMID: 159760 French.

3

[Congenital recessive methemoglobinemia: a unique disease and variations (proceedings)].

Leroux A, Beauvais P, Kaplan JC. Leroux A, et al. Nouv Rev Fr Hematol Blood Cells. 1977;18(1):217. Nouv Rev Fr Hematol Blood Cells. 1977. PMID: 896445 French. No abstract available.

4

[Hereditary methemoglobinemia with mental retardation and neurologic disorders. Clinical and biochemical study of a case].

Beauvais P, Leroux A, Kaplan JC. Beauvais P, et al. Among authors: leroux a. Nouv Presse Med. 1976 Dec 4;5(41):2793-5. Nouv Presse Med. 1976. PMID: 995609 French. No abstract available.

5

Prenatal diagnosis of recessive congenital methaemoglobinaemia type II: novel mutation in the NADH-cytochrome b5 reductase gene leading to stop codon read-through.

Leroux A, Leturcq F, Deburgrave N, Szajnert MF. Leroux A, et al. Eur J Haematol. 2005 May;74(5):389-95. doi: 10.1111/j.1600-0609.2004.00388.x. Eur J Haematol. 2005. PMID: 15813912

6

Four new mutations in the NADH-cytochrome b5 reductase gene from patients with recessive congenital methemoglobinemia type II.

Vieira LM, Kaplan JC, Kahn A, Leroux A. Vieira LM, et al. Among authors: leroux a. Blood. 1995 Apr 15;85(8):2254-62. Blood. 1995. PMID: 7718898 Free article.

7

Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases.

Junien C, Leroux A, Lostanlen D, Reghis A, Boue J, Nicolas H, Boue A, Kaplan JC. Junien C, et al. Among authors: leroux a. Prenat Diagn. 1981 Jan;1(1):17-24. doi: 10.1002/pd.1970010106. Prenat Diagn. 1981. PMID: 7346809

8

Soluble NADH-cytochrome b5 reductase from rabbit liver cytosol: partial purification and characterization.

Lostanlen D, Vieira de Barros A, Leroux A, Kaplan JC. Lostanlen D, et al. Among authors: leroux a. Biochim Biophys Acta. 1978 Sep 11;526(1):42-51. doi: 10.1016/0005-2744(78)90288-7. Biochim Biophys Acta. 1978. PMID: 28780

9

Congenital methemoglobin-reductase (cytochrome b5 reductase) deficiency associated with mental retardation in a Spanish girl.

Vives-Corrons JL, Pujades A, Vela E, Corretger JM, Leroux A, Kaplan JC. Vives-Corrons JL, et al. Among authors: leroux a. Acta Haematol. 1978;59(6):348-53. doi: 10.1159/000207786. Acta Haematol. 1978. PMID: 97893

10

Soluble and microsomal forms of NADH-cytochrome beta 5 reductase from human placenta. Similarity with NADH-methemoglobin reductase from human erythrocytes.

Leroux A, Torlinski L, Kaplan JC. Leroux A, et al. Biochim Biophys Acta. 1977 Mar 15;481(1):50-62. doi: 10.1016/0005-2744(77)90136-x. Biochim Biophys Acta. 1977. PMID: 402944

In congenital methemoglobinemia associated with mental retardation a generalized deficiency of NADH-cytochrome beta 5 reductase (NADH : ferricytochrome beta 5 oxidoreductase, EC 1.6.2.2) has been found in soluble extracts of red blood cells, as well as in deoxycholate-trea …

In congenital methemoglobinemia associated with mental retardation a generalized deficiency of NADH-cytochrome beta 5 reductase (NADH …

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