Bardakdjian-Michau J - Search Results

1

Decreased morbidity in homozygous sickle cell disease detected at birth.

Bardakdjian-Michau J, Guilloud-Batailie M, Maier-Redelsperger M, Elion J, Girot R, Feingold J, Galactéros F, de Montalembert M. Bardakdjian-Michau J, et al. Hemoglobin. 2002 Aug;26(3):211-7. doi: 10.1081/hem-120015024. Hemoglobin. 2002. PMID: 12403485

2

Two new hemoglobin variants with increased oxygen affinity: Hb Nantes [beta34(B16)Val-->Leu] and Hb Vexin [beta116(G18)His-->Leu].

Wajcman H, Bardakdjian-Michau J, Riou J, Préhu C, Kister J, Baudin-Creuza V, Promé D, Richelme-David S, Harousseau JL, Galactéros F. Wajcman H, et al. Among authors: bardakdjian michau j. Hemoglobin. 2003 Aug;27(3):191-9. doi: 10.1081/hem-120023384. Hemoglobin. 2003. PMID: 12908805 No abstract available.

3

Hemoglobin variants in North Africa.

Chami B, Blouquit Y, Bardakdjian-Michau J, Riou J, Wajcman H, Rosa J, Galactéros F. Chami B, et al. Hemoglobin. 1994 Jan;18(1):39-51. doi: 10.3109/03630269409014144. Hemoglobin. 1994. PMID: 8195007

4

Neonatal screening for sickle cell disease in France.

Bardakdjian-Michau J, Bahuau M, Hurtrel D, Godart C, Riou J, Mathis M, Goossens M, Badens C, Ducrocq R, Elion J, Perini JM. Bardakdjian-Michau J, et al. J Clin Pathol. 2009 Jan;62(1):31-3. doi: 10.1136/jcp.2008.058867. J Clin Pathol. 2009. PMID: 19103855

5

Hb Reims [alpha 2(23)(B4)Glu----Gly beta 2]: a new alpha chain variant with slightly decreased stability.

Bardakdjian-Michau J, Rosa J, Galactéros F, Lancelot M, Marquart FX. Bardakdjian-Michau J, et al. Hemoglobin. 1989;13(7-8):733-5. doi: 10.3109/03630268908998846. Hemoglobin. 1989. PMID: 2634669 No abstract available.

6

Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell disease.

Ducrocq R, Bévier A, Leneveu A, Maier-Redelsperger M, Bardakdjian-Michau J, Badens C, Elion J. Ducrocq R, et al. J Med Screen. 1998;5(1):27-30. doi: 10.1136/jms.5.1.27. J Med Screen. 1998. PMID: 9575456

7

Abnormal hemoglobins: laboratory methods.

Wajcman H, Préhu C, Bardakdjian-Michau J, Promé D, Riou J, Godart C, Mathis M, Hurtrel D, Galactéros F. Wajcman H, et al. Among authors: bardakdjian michau j. Hemoglobin. 2001 May;25(2):169-81. doi: 10.1081/hem-100104026. Hemoglobin. 2001. PMID: 11480779 Review.

8

A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry).

Cohen-Solal M, Préhu C, Wajcman H, Poyart C, Bardakdjian-Michau J, Kister J, Promé D, Valentin C, Bachir D, Galactéros F. Cohen-Solal M, et al. Br J Haematol. 1998 Dec;103(4):950-6. doi: 10.1046/j.1365-2141.1998.01094.x. Br J Haematol. 1998. PMID: 9886305 Free article.

9

Hb N-Timone [alpha 2 beta 2(8)(A5)Lys----Glu]: a new fast-moving variant with normal stability and oxygen affinity.

Léna-Russo D, Orsini A, Vovan L, Bardakdjian-Michau J, Lacombe C, Blouquit Y, Craescu CT, Galactéros F. Léna-Russo D, et al. Hemoglobin. 1989;13(7-8):743-7. doi: 10.3109/03630268908998848. Hemoglobin. 1989. PMID: 2634671 No abstract available.

10

[Neonatal detection of sickle cell disease].

Bardakdjian-Michau J. Bardakdjian-Michau J. J Gynecol Obstet Biol Reprod (Paris). 2003 Feb;32(1 Suppl):1S61-4. J Gynecol Obstet Biol Reprod (Paris). 2003. PMID: 12592166 Free article. Review. French.

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