Pissard S - Search Results

1

Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region.

Ghedira ES, Lecerf L, Faubert E, Costes B, Moradkhani K, Bachir D, Galactéros F, Pissard S. Ghedira ES, et al. Among authors: pissard s. Haematologica. 2013 Feb;98(2):305-8. doi: 10.3324/haematol.2012.061994. Epub 2012 Jul 16. Haematologica. 2013. PMID: 22801970 Free PMC article.

2

A potential regulatory region for the expression of fetal hemoglobin in sickle cell disease.

Pissard S, Beuzard Y. Pissard S, et al. Blood. 1994 Jul 1;84(1):331-8. Blood. 1994. PMID: 7517214 Free article.

3

Severe hemolytic anemia in a Vietnamese family, associated with novel mutations in the gene encoding for pyruvate kinase.

Costa C, Albuisson J, Le TH, Max-Audit I, Dinh KT, Tosi M, Goossens M, Pissard S. Costa C, et al. Among authors: pissard s. Haematologica. 2005 Jan;90(1):25-30. Haematologica. 2005. PMID: 15642665

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: pissard s. Hemoglobin. 2005;29(3):229-33. doi: 10.1081/hem-200066335. Hemoglobin. 2005. PMID: 16114188

5

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. 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.

6

Pyruvate kinase (PK) deficiency in newborns: the pitfalls of diagnosis.

Pissard S, de Montalembert M, Bachir D, Max-Audit I, Goossens M, Wajcman H, Bader-Meunier B. Pissard S, et al. J Pediatr. 2007 Apr;150(4):443-5. doi: 10.1016/j.jpeds.2007.01.039. J Pediatr. 2007. PMID: 17382129

7

Evaluation of the free α-hemoglobin pool in red blood cells: a new test providing a scale of β-thalassemia severity.

Vasseur C, Pissard S, Domingues-Hamdi E, Marden MC, Galactéros F, Baudin-Creuza V. Vasseur C, et al. Among authors: pissard s. Am J Hematol. 2011 Feb;86(2):199-202. doi: 10.1002/ajh.21918. Am J Hematol. 2011. PMID: 21264907 Free article.

8

A second observation of the rare frameshift mutation in the β-globin gene: codon 46 (+A) (Hbb:c.138_139insA).

Ghedira ES, Dupin-Deguine D, Duffilot D, Lemetayer N, Faubert E, Pissard S. Ghedira ES, et al. Among authors: pissard s. Hemoglobin. 2011;35(2):157-61. doi: 10.3109/03630269.2011.557460. Hemoglobin. 2011. PMID: 21417574

9

Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease.

Badens C, Joly P, Agouti I, Thuret I, Gonnet K, Fattoum S, Francina A, Simeoni MC, Loundou A, Pissard S. Badens C, et al. Among authors: pissard s. Haematologica. 2011 Nov;96(11):1712-4. doi: 10.3324/haematol.2011.046748. Epub 2011 Jul 26. Haematologica. 2011. PMID: 21791466 Free PMC article. Clinical Trial.

10

Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: description of seven new G6PD mutants.

Moradkhani K, Mekki C, Bahuau M, Te VL, Holder M, Pissard S, Préhu C, Rose C, Wajcman H, Galactéros F. Moradkhani K, et al. Among authors: pissard s. Am J Hematol. 2012 Feb;87(2):208-10. doi: 10.1002/ajh.22218. Epub 2011 Dec 3. Am J Hematol. 2012. PMID: 22139979 Free article.

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