메뉴 건너뛰기




Volumn 84, Issue 11, 2006, Pages 687-696

Hemoglobinopathies in Tunisia. An updated review of the epidemiological and molecular data;Les hemoglobinopathies en Tunisie. Revue actualisée des données épidémiologiques et moléculaires

Author keywords

Epidemiology; Hemoglobinopathies; Mutations; Tunisia

Indexed keywords

EDETIC ACID; HEMOGLOBIN; IRON;

EID: 33846139589     PISSN: 00414131     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (43)

References (39)
  • 2
    • 33846135774 scopus 로고    scopus 로고
    • Institut National de statistique: Tunisie
    • Institut National de statistique: Annuaire de la statistique de la Tunisie (2001).
    • (2001) Annuaire de la statistique de la
  • 3
    • 0024624615 scopus 로고
    • Consanguinity in the population of Northern Tunisia
    • Riou S., El Younsi C., Chaaabouni H.: Consanguinity in the population of Northern Tunisia. Tunisie Medicale, 1989, 67: 167-172.
    • (1989) Tunisie Medicale , vol.67 , pp. 167-172
    • Riou, S.1    El Younsi, C.2    Chaaabouni, H.3
  • 5
    • 0003336829 scopus 로고    scopus 로고
    • The Hemoglobinopathies Techniques of Identification
    • New York: Marcel Dekker, Inc
    • Huisman THJ.; Jonxis JHP: The Hemoglobinopathies Techniques of Identification. In; Clinical and Biochemical Analysis. Vol.6 New York: Marcel Dekker, Inc.
    • Clinical and Biochemical Analysis , vol.6
    • Huisman, T.H.J.1    Jonxis, J.H.P.2
  • 7
    • 4544319099 scopus 로고    scopus 로고
    • Molecular Basis of -thalassemia in the population of Tunisia
    • Fattoum S., Messaoud T., Bibi A: Molecular Basis of -thalassemia in the population of Tunisia. Hemoglobin, 2004, 28: 177-187.
    • (2004) Hemoglobin , vol.28 , pp. 177-187
    • Fattoum, S.1    Messaoud, T.2    Bibi, A.3
  • 8
    • 0027449674 scopus 로고
    • Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven mediterranean β-thalassemia mutations by covalent reverse dot-blot analysis: Application diagnosis in Sicily
    • Maggio A., Giambona A., Cai SP., Wall J., Kan YW., Chehab FF: Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven mediterranean β-thalassemia mutations by covalent reverse dot-blot analysis: Application diagnosis in Sicily. Blood, 1993, 81: 239-242.
    • (1993) Blood , vol.81 , pp. 239-242
    • Maggio, A.1    Giambona, A.2    Cai, S.P.3    Wall, J.4    Kan, Y.W.5    Chehab, F.F.6
  • 9
    • 0024376665 scopus 로고
    • Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes
    • Sutton M., Bouhassira EE., and Nagel RL.: Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes. Am. J. Hematol., 1989, 32: 66.
    • (1989) Am. J. Hematol , vol.32 , pp. 66
    • Sutton, M.1    Bouhassira, E.E.2    Nagel, R.L.3
  • 10
    • 4544289190 scopus 로고    scopus 로고
    • Comprehensive scanning method for rapid detection of β-globin gene mutations and polymorphisms
    • Ghanem N., Girodon E., Vidaud M., Martin J., Fanen P., Plassa F., Goossens MA.: Comprehensive scanning method for rapid detection of β-globin gene mutations and polymorphisms. Hum Mutat., 2000, 1: 277-341.
    • (2000) Hum Mutat , vol.1 , pp. 277-341
    • Ghanem, N.1    Girodon, E.2    Vidaud, M.3    Martin, J.4    Fanen, P.5    Plassa, F.6    Goossens, M.A.7
  • 11
    • 0033983971 scopus 로고    scopus 로고
    • Cutting GR.: Single -tube multiplex-PCR screen for common deletional determinants of α-thalassemia
    • Chong SS., Boehm CD., Higgs DR., Cutting GR.: Single -tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood 2000, 95: 360-362.
    • (2000) Blood , vol.95 , pp. 360-362
    • Chong, S.S.1    Boehm, C.D.2    Higgs, D.R.3
  • 12
    • 0028263783 scopus 로고
    • Detection of common deletional α-thalassemia - 2 determinants by PCR
    • Baysal E, and Huisman THJ.: Detection of common deletional α-thalassemia - 2 determinants by PCR. Am. J. Hematol., 1994, 46: 208-213.
    • (1994) Am. J. Hematol , vol.46 , pp. 208-213
    • Baysal, E.1    Huisman, T.H.J.2
  • 13
    • 0032870749 scopus 로고    scopus 로고
    • A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism: Strategy for rapid screening of the polyadenylation signal mutation αTsaudi (AATAAA → AATAAG) in the α2-globin gene
    • Jassim N., Al Arrayed S., Gerard N., Al Muharraq H., Al Ajmi A., Ramasawmy R., and Krishnamoorthy R.: A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism: strategy for rapid screening of the polyadenylation signal mutation αTsaudi (AATAAA → AATAAG) in the α2-globin gene. Hemoglobin, 1999, 23: 213-220.
    • (1999) Hemoglobin , vol.23 , pp. 213-220
    • Jassim, N.1    Al Arrayed, S.2    Gerard, N.3    Al Muharraq, H.4    Al Ajmi, A.5    Ramasawmy, R.6    Krishnamoorthy, R.7
  • 15
    • 0026691572 scopus 로고
    • PCR-based strategy to detect the common severe determinant of α-Thalassemia
    • Bowden DK., Vickers MA., Higgs DR. A PCR-based strategy to detect the common severe determinant of α-Thalassemia. Br J Haematol., 1992; 84: 104-108.
    • (1992) Br J Haematol , vol.84 , pp. 104-108
    • Bowden, D.K.1    Vickers, M.A.2    Higgs DR., A.3
  • 19
    • 0026734802 scopus 로고
    • Hb Bab saadoun or α2β2 18 (CD 7) Leu →Pro, a mildy unstable variant found in an Arabian from Tunisia
    • Molchanova TR, Wilson JB., Gu LH., Guemira F., Fattoum S., and Huisman THJ. Hb Bab saadoun or α2β2 18 (CD 7) Leu →Pro, a mildy unstable variant found in an Arabian from Tunisia. Hemoglobin 1992; 16: 267-273.
    • (1992) Hemoglobin , vol.16 , pp. 267-273
    • Molchanova, T.R.1    Wilson, J.B.2    Gu, L.H.3    Guemira, F.4    Fattoum, S.5    Huisman, T.H.J.6
  • 20
    • 33748927102 scopus 로고    scopus 로고
    • Detection of two rare β-thalassemia alleles found in the Tunisian population: Codon 47 (+A) and Codon 106/107 (+G)
    • Bibi A., Messaoud T., Beldjord C., and Fattoum S. Detection of two rare β-thalassemia alleles found in the Tunisian population: Codon 47 (+A) and Codon 106/107 (+G) Hemoglobin 2006; 30: 1-11.
    • (2006) Hemoglobin , vol.30 , pp. 1-11
    • Bibi, A.1    Messaoud, T.2    Beldjord, C.3    Fattoum, S.4
  • 22
  • 23
    • 0025753747 scopus 로고
    • Sikle cell anemia in the Tunisian population: Haplotype and HbF expression
    • Abbes S., Fattoum S., Vidaud M., Gossens M. and Rosa J. Sikle cell anemia in the Tunisian population: haplotype and HbF expression. Hemoglobin 1991; 15: 1-9.
    • (1991) Hemoglobin , vol.15 , pp. 1-9
    • Abbes, S.1    Fattoum, S.2    Vidaud, M.3    Gossens, M.4    Rosa, J.5
  • 24
    • 4544309391 scopus 로고    scopus 로고
    • Anovel α- thalassemia Nonsens Mutation in Codon 23 of the α 2-Globin Gene (GAG →TAG) in a Tunisian Family
    • Siala H., Fattoum S., Messaoud T., Ouali F., Gérard N., Krishnamoorthy R.: Anovel α- thalassemia Nonsens Mutation in Codon 23 of the α 2-Globin Gene (GAG →TAG) in a Tunisian Family. Hemoglobin, 2004; 28: 249-254.
    • (2004) Hemoglobin , vol.28 , pp. 249-254
    • Siala, H.1    Fattoum, S.2    Messaoud, T.3    Ouali, F.4    Gérard, N.5    Krishnamoorthy, R.6
  • 25
    • 28844434222 scopus 로고    scopus 로고
    • First description in Tunisia of a point mutation in the α1 globin gene (α1, codon 119, CCT→ TCT): Hb Groene Hart associated with -α3.7
    • Siala H., Ouali F., Messaoud T., Star R., Fattoum S. First description in Tunisia of a point mutation in the α1 globin gene (α1, codon 119, CCT→ TCT): Hb Groene Hart associated with -α3.7. Hemoglobin, 2005; 29: 263-268.
    • (2005) Hemoglobin , vol.29 , pp. 263-268
    • Siala, H.1    Ouali, F.2    Messaoud, T.3    Star, R.4    Fattoum, S.5
  • 27
    • 28544436549 scopus 로고    scopus 로고
    • Prevalence et typologie des anemies chez les enfants de moins de 5ans: Etude épidémiologique dans le Grand Tunis et Le Sud Ouest
    • El Ati J., Gaigi S., Béji C., Haddad S., Cherif S., Amina F., Fattoum S., Ben Abdeladhim A. Prevalence et typologie des anemies chez les enfants de moins de 5ans: Etude épidémiologique dans le Grand Tunis et Le Sud Ouest. La Tunisie Médicale 2005; 83: 511-518.
    • (2005) La Tunisie Médicale , vol.83 , pp. 511-518
    • El Ati, J.1    Gaigi, S.2    Béji, C.3    Haddad, S.4    Cherif, S.5    Amina, F.6    Fattoum, S.7    Ben Abdeladhim, A.8
  • 30
    • 77049164783 scopus 로고
    • Protection afforded by sickle-cell trait against subtertian malarial infection
    • Allison AC. Protection afforded by sickle-cell trait against subtertian malarial infection. Br Med J 1954; 1: 290-4.
    • (1954) Br Med J , vol.1 , pp. 290-294
    • Allison, A.C.1
  • 31
    • 4544255724 scopus 로고    scopus 로고
    • Contribution to the description of the β-thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity
    • Chouk I., B. Daoud B., Mellouli F., Bejaoui M., Gérard N., Dellagi K., Abbés S.: Contribution to the description of the β-thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity. Hemoglobin, 2004; 28: 189-195.
    • (2004) Hemoglobin , vol.28 , pp. 189-195
    • Chouk, I.B.1    Daoud, B.2    Mellouli, F.3    Bejaoui, M.4    Gérard, N.5    Dellagi, K.6    Abbés, S.7
  • 32
    • 4544332591 scopus 로고    scopus 로고
    • Compound Heterozygosity for two New Mutations in the β-globin gene [cd 9(+TA) and Polyadenylation Site (AATAAA → AAAAAA)] Leads to Thalassemia Intermedia in a Tunisian Patient
    • Jacquette A., Le Roux G., Lacombe CH., Goossens M., Pissard S.: Compound Heterozygosity for two New Mutations in the β-globin gene [cd 9(+TA) and Polyadenylation Site (AATAAA → AAAAAA)] Leads to Thalassemia Intermedia in a Tunisian Patient. Hemoglobin, 2004; 28: 243-248.
    • (2004) Hemoglobin , vol.28 , pp. 243-248
    • Jacquette, A.1    Le Roux, G.2    Lacombe, C.H.3    Goossens, M.4    Pissard, S.5
  • 33
    • 4544247915 scopus 로고    scopus 로고
    • Thalassemia in Tunisia: More Tasks Ahead
    • Wajeman H.; Krishnamoorthy R: Thalassemia in Tunisia: More Tasks Ahead. Hemoglobin, 2004; 28: 171-172.
    • (2004) Hemoglobin , vol.28 , pp. 171-172
    • Wajeman, H.1    Krishnamoorthy, R.2
  • 38
    • 0034855133 scopus 로고    scopus 로고
    • The thalassemia syndromes: Molecular characterization in the Spanish population
    • Villegas A., Ropero P., Gonzolez F.A., Anguita E., and Espinos D. The thalassemia syndromes: Molecular characterization in the Spanish population. Hemoglobin 2001; 25: 273-283.
    • (2001) Hemoglobin , vol.25 , pp. 273-283
    • Villegas, A.1    Ropero, P.2    Gonzolez, F.A.3    Anguita, E.4    Espinos, D.5
  • 39
    • 0031010067 scopus 로고    scopus 로고
    • β-thalassaemia in the immigrant and non -immigrant German populations
    • Vetter B., Schwarz C., Konne E. and Kulozik E. β-thalassaemia in the immigrant and non -immigrant German populations. Br J Haematol 1997; 97: 266-272.
    • (1997) Br J Haematol , vol.97 , pp. 266-272
    • Vetter, B.1    Schwarz, C.2    Konne, E.3    Kulozik, E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.