Belhani M - Search Results

1

Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problem.

Boudrahem-Addour N, Zidani N, Carion N, Labie D, Belhani M, Beldjord C. Boudrahem-Addour N, et al. Among authors: belhani m. Hemoglobin. 2009;33(1):24-36. doi: 10.1080/03630260802626061. Hemoglobin. 2009. PMID: 19205970

2

Oxidative status and plasma lipid profile in β-thalassemia patients.

Boudrahem-Addour N, Izem-Meziane M, Bouguerra K, Nadjem N, Zidani N, Belhani M, Djerdjouri B. Boudrahem-Addour N, et al. Among authors: belhani m. Hemoglobin. 2015;39(1):36-41. doi: 10.3109/03630269.2014.979997. Epub 2014 Nov 14. Hemoglobin. 2015. PMID: 25395219

3

[Clinical and biological aspects of beta-thalassemia. Apropos of 176 cases].

Belhani M, Dahmane M, Richard F, Trabuchet G, Benabadji M, Colonna P, Labie D. Belhani M, et al. Sem Hop. 1977 Apr 23;53(16):891-7. Sem Hop. 1977. PMID: 197608 French.

4

Indirect evaluation of a gene frequency: calculation of beta-thalassemia frequency in Algeria based on associated hemoglobin variants frequency.

Bachir D, Belhani M, Godet J, Nigon V, Colonna P. Bachir D, et al. Among authors: belhani m. Hum Hered. 1984;34(3):187-91. doi: 10.1159/000153460. Hum Hered. 1984. PMID: 6590459

5

[1st cases of alpha-thalassemia in Algeria: 12 cases of hemoglobinosis H].

Trabuchet G, Belhani M, Richard F, Hamladji RM, Benabadji M, Colonna P. Trabuchet G, et al. Among authors: belhani m. Sem Hop. 1977 Apr 23;53(16):885-9. Sem Hop. 1977. PMID: 197607 French.

6

Hemoglobin H disease from Algeria: genetic and molecular characterization.

Tabone P, Henni T, Belhani M, Colonna P, Verdier G, Godet J. Tabone P, et al. Among authors: belhani m. Acta Haematol. 1981;65(1):26-31. doi: 10.1159/000207145. Acta Haematol. 1981. PMID: 6791434

7

beta-O-thalassemia from Algeria: genetic and molecular characterization.

Godet J, Verdier G, Nigon V, Belhani M, Richard F, Colonna P, Mitchell J, Williamson R, Tolstoshev P. Godet J, et al. Among authors: belhani m. Blood. 1977 Sep;50(3):463-70. Blood. 1977. PMID: 884323 Free article.

8

Heterogeneity in beta 0 thalassemia from Algeria: genetic, clinical and molecular studies.

Belhani M, Morlé F, Colonna P, Godet J. Belhani M, et al. Hum Genet. 1980;54(2):251-7. doi: 10.1007/BF00278980. Hum Genet. 1980. PMID: 6156118

9

Alpha globin gene triplication in severe heterozygous beta thalassemia.

Henni T, Belhani M, Morle F, Bachir D, Tabone P, Colonna P, Godet J. Henni T, et al. Among authors: belhani m. Acta Haematol. 1985;74(4):236-9. doi: 10.1159/000206230. Acta Haematol. 1985. PMID: 3012927

10

[G-6PD deficiency in newborns in Algiers (author's transl)].

Richard F, Belhani M, Colonna P. Richard F, et al. Among authors: belhani m. Nouv Rev Fr Hematol. 1974 Jul-Aug;14(4):453-9. Nouv Rev Fr Hematol. 1974. PMID: 4280555 French. No abstract available.

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