Cochaux P - Search Results

1

Transplanted sickle-cell disease patients with autologous bone marrow recovery after graft failure develop increased levels of fetal haemoglobin which corrects disease severity.

Ferster A, Corazza F, Vertongen F, Bujan W, Devalck C, Fondu P, Cochaux P, Lambermont M, Khaladji Z, Sariban E. Ferster A, et al. Among authors: cochaux p. Br J Haematol. 1995 Aug;90(4):804-8. doi: 10.1111/j.1365-2141.1995.tb05199.x. Br J Haematol. 1995. PMID: 7545424

2

Neonatal haemoglobinopathy screening: review of a 10-year programme in Brussels.

Gulbis B, Ferster A, Cotton F, Lebouchard MP, Cochaux P, Vertongen F. Gulbis B, et al. Among authors: cochaux p. J Med Screen. 2006;13(2):76-8. doi: 10.1258/096914106777589650. J Med Screen. 2006. PMID: 16792829

3

[Sickle cell disease: exotic disease or a Belgian public health problem?].

Gulbis B, Ferster A, Kentos A, N'Gay Munungi D, Cotton F, Rongé E, Dresse MF, Bradstreet C, Cochaux P, Vertongen F. Gulbis B, et al. Among authors: cochaux p. Rev Med Brux. 2005 Sep;26(4):S309-13. Rev Med Brux. 2005. PMID: 16240879 Free article. Review. French.

4

[Prevention of hemoglobinopathies in Brussels: a necessity?].

Gulbis B, Cotton F, Hansen V, Ferster A, Toppet M, Cochaux P, Parma J, Vassart G, Fondu P, Vertongen F. Gulbis B, et al. Among authors: cochaux p. Rev Med Brux. 2001 Jun;22(3):133-40. Rev Med Brux. 2001. PMID: 11488080 Review. French.

5

Hb Ube-2 [alpha68(E17)Asn-Asp] and Hb Hafnia [beta116(G18)His-->Gln] observed during neonatal screening in Brussels.

Cotton F, Hansen V, Lin C, Parma J, Cochaux P, Damis E, Vertongen F, Gulbis B. Cotton F, et al. Among authors: cochaux p. Hemoglobin. 2000 Feb;24(1):65-9. doi: 10.3109/03630260009002276. Hemoglobin. 2000. PMID: 10722118 No abstract available.

6

Rapid and easy prenatal diagnosis of sickle cell anemia using double-dye LNA probe technology.

Housni HE, Vandesompele J, Vannuffel P, Gulbis B, Parma J, Cochaux P. Housni HE, et al. Among authors: cochaux p. Br J Haematol. 2007 Feb;136(3):509-10. doi: 10.1111/j.1365-2141.2006.06447.x. Br J Haematol. 2007. PMID: 17233849 Free article. No abstract available.

7

[Molecular and diagnostic genetics].

Cochaux P, Velu T, Abramowicz M, Vassart G. Cochaux P, et al. Rev Med Brux. 1990 Jun;11(6):188-94. Rev Med Brux. 1990. PMID: 2196651 French.

8

Prevalence of the major mutation of the CF gene in Belgian patients.

Cochaux P, Van Geffel R, Baran D, Vassart G. Cochaux P, et al. Adv Exp Med Biol. 1991;290:353-4. doi: 10.1007/978-1-4684-5934-0_34. Adv Exp Med Biol. 1991. PMID: 1950745 No abstract available.

9

[Applications of molecular genetics to clinical genetics].

Vassart G, Cochaux P. Vassart G, et al. Among authors: cochaux p. Nephrologie. 1988;9(6):249-51. Nephrologie. 1988. PMID: 3070428 Review. French. No abstract available.

10

Prevalence of the delta F508 deletion of the cystic fibrosis gene in Belgian patients.

Cochaux P, van Geffel R, Baran D, Poncin J, Vassart G. Cochaux P, et al. Hum Genet. 1990 Sep;85(4):400. doi: 10.1007/BF02428275. Hum Genet. 1990. PMID: 2210745

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