Galactéros F - Search Results

1

A study of 36 unrelated cases with pure erythrocytosis revealed three new mutations in the erythropoietin receptor gene.

Al-Sheikh M, Mazurier E, Gardie B, Casadevall N, Galactéros F, Goossens M, Wajcman H, Préhu C, Ugo V. Al-Sheikh M, et al. Among authors: galacteros f. Haematologica. 2008 Jul;93(7):1072-5. doi: 10.3324/haematol.12260. Epub 2008 May 19. Haematologica. 2008. PMID: 18492694 Free article.

2

An identical mutation carried by different genes: Hb Frankfurt [alpha50(CE8)His->Gln].

Préhu C, Francina A, Behnken LJ, Promé D, Galactéros F, Wajcman H. Préhu C, et al. Among authors: galacteros f. Haematologica. 2003 May;88(5):ECR19. Haematologica. 2003. PMID: 12745288 No abstract available.

3

Hemoglobins with high oxygen affinity leading to erythrocytosis. New variants and new concepts.

Wajcman H, Galactéros F. Wajcman H, et al. Among authors: galacteros f. Hemoglobin. 2005;29(2):91-106. Hemoglobin. 2005. PMID: 15921161 Review.

4

Two French Caucasian families with dominant thalassemia-like phenotypes due to hyper unstable hemoglobin variants: Hb Sainte Seve [codon 118 (-T)] and codon 127 [CAG-->TAG (Gln-->stop]).

Préhu C, Pissard S, Al-Sheikh M, Le Niger C, Bachir D, Galactéros F, Wajcman H. Préhu C, et al. Among authors: galacteros f. Hemoglobin. 2005;29(3):229-33. doi: 10.1081/hem-200066335. Hemoglobin. 2005. PMID: 16114188

5

[Glucose 6-phosphate dehydrogenase deficiency: a protection against malaria and a risk for hemolytic accidents].

Wajcman H, Galactéros F. Wajcman H, et al. Among authors: galacteros f. C R Biol. 2004 Aug;327(8):711-20. doi: 10.1016/j.crvi.2004.07.010. C R Biol. 2004. PMID: 15506519 Free article. Review. French.

6

Chronic hemolytic anemia due to novel alpha-globin chain variants: critical location of the mutation within the gene sequence for a dominant effect.

Préhu C, Moradkhani K, Riou J, Bahuau M, Launay P, Martin N, Wajcman H, Goossens M, Galactéros F. Préhu C, et al. Among authors: galacteros f. Haematologica. 2009 Nov;94(11):1624-5. doi: 10.3324/haematol.2009.012971. Epub 2009 Oct 8. Haematologica. 2009. PMID: 19815833 Free PMC article. No abstract available.

7

Abnormal hemoglobins with high oxygen affinity and erythrocytosis.

Wajcman H, Galactéros F. Wajcman H, et al. Among authors: galacteros f. Hematol Cell Ther. 1996 Aug;38(4):305-12. doi: 10.1007/s00282-996-0305-4. Hematol Cell Ther. 1996. PMID: 8891722 Review.

8

Hb Montfermeil [beta 130(H8) Tyr-->Cys]: suggests a key role for the interaction between helix A and H in oxygen affinity of the hemoglobin molecule.

Kister J, Baudin-Creuza V, Kiger L, Préhu C, Papassotiriou I, Riou J, Galactéros F, Wajcman H. Kister J, et al. Among authors: galacteros f. Blood Cells Mol Dis. 2005 Mar-Apr;34(2):166-73. doi: 10.1016/j.bcmd.2004.12.003. Blood Cells Mol Dis. 2005. PMID: 15727901

9

Pyruvate kinase deficiency in France: a 3-year study reveals 27 new mutations.

Pissard S, Max-Audit I, Skopinski L, Vasson A, Vivien P, Bimet C, Goossens M, Galacteros F, Wajcman H. Pissard S, et al. Among authors: galacteros f. Br J Haematol. 2006 Jun;133(6):683-9. doi: 10.1111/j.1365-2141.2006.06076.x. Br J Haematol. 2006. PMID: 16704447 Free article.

10

A rare G6PD variant (c.383T>G; p.128Leu>Arg) with a molecular pathophysiological mechanism similar to that of G6PD A- (68Val>Met, 126Asn>Asp).

Moradkhani K, Bahuau M, Préhu C, Martin N, Bimet C, Galactéros F, Wajcman H. Moradkhani K, et al. Among authors: galacteros f. Blood Cells Mol Dis. 2009 Nov-Dec;43(3):226-9. doi: 10.1016/j.bcmd.2009.05.007. Epub 2009 Jul 25. Blood Cells Mol Dis. 2009. PMID: 19632868

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