Metaxotou-Mavromati A - Search Results

1

The interaction of alpha zero thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H.

Kanavakis E, Traeger-Synodinos J, Papasotiriou I, Vrettou C, Metaxotou-Mavromati A, Stamoulakatou A, Lagona E, Kattamis C. Kanavakis E, et al. Among authors: metaxotou mavromati a. Br J Haematol. 1996 Feb;92(2):332-5. doi: 10.1046/j.1365-2141.1996.d01-1487.x. Br J Haematol. 1996. PMID: 8602995

2

The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalence.

Traeger-Synodinos J, Tzetis M, Kanavakis E, Metaxotou-Mavromati A, Kattamis C. Traeger-Synodinos J, et al. Among authors: metaxotou mavromati a. Br J Haematol. 1991 Oct;79(2):302-5. doi: 10.1111/j.1365-2141.1991.tb04537.x. Br J Haematol. 1991. PMID: 1720325

3

Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia.

Metaxotou-Mavromati A, Kattamis C, Matathia L, Tzetis M, Kanavakis E. Metaxotou-Mavromati A, et al. J Med Genet. 1988 Mar;25(3):195-9. doi: 10.1136/jmg.25.3.195. J Med Genet. 1988. PMID: 3351907 Free PMC article.

4

The triplicated alpha gene locus and beta thalassaemia.

Kanavakis E, Metaxotou-Mavromati A, Kattamis C, Wainscoat JS, Wood WG. Kanavakis E, et al. Br J Haematol. 1983 Jun;54(2):201-7. doi: 10.1111/j.1365-2141.1983.tb02088.x. Br J Haematol. 1983. PMID: 6189508

5

Globin gene mapping in normal Hb A2 types of beta-thalassaemia.

Kanavakis E, Metaxotou-Mavromati A, Kattamis C, Aksoy M, Weatherall DJ, Wood WG. Kanavakis E, et al. Br J Haematol. 1982 May;51(1):59-64. doi: 10.1111/j.1365-2141.1982.tb07289.x. Br J Haematol. 1982. PMID: 7073990

6

Molecular characterization of homozygous (high HbA2) beta-thalassemia intermedia in Greece.

Kanavakis E, Traeger-Synodinos J, Tzetis M, Metaxotou-Mavromati A, Ladis V, Kattamis C. Kanavakis E, et al. Among authors: metaxotou mavromati a. Pediatr Hematol Oncol. 1995 Jan-Feb;12(1):37-45. doi: 10.3109/08880019509029526. Pediatr Hematol Oncol. 1995. PMID: 7703040

7

The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies.

Traeger-Synodinos J, Kanavakis E, Vrettou C, Maragoudaki E, Michael T, Metaxotou-Mavromati A, Kattamis C. Traeger-Synodinos J, et al. Among authors: metaxotou mavromati a. Br J Haematol. 1996 Dec;95(3):467-71. doi: 10.1046/j.1365-2141.1996.d01-1939.x. Br J Haematol. 1996. PMID: 8943886

8

An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant.

Traeger-Synodinos J, Metaxotou-Mavromati A, Kanavakis E, Vrettou C, Papassotiriou I, Michael T, Kattamis C. Traeger-Synodinos J, et al. Among authors: metaxotou mavromati a. Hemoglobin. 1998 May;22(3):209-15. doi: 10.3109/03630269809113135. Hemoglobin. 1998. PMID: 9629496

9

The heterogeneity of normal Hb A2-beta thalassaemia in Greece.

Kattamis C, Metaxotou-Mavromati A, Wood WG, Nash JR, Weatherall DJ. Kattamis C, et al. Br J Haematol. 1979 May;42(1):109-23. doi: 10.1111/j.1365-2141.1979.tb03703.x. Br J Haematol. 1979. PMID: 465353

10

Clinical and hematologic phenotype of homozygous beta+ (high A2)-thalassemia with low Hb F.

Kattamis CA, Metaxotou-Mavromati A, Mitsioni A, Kanavakis E. Kattamis CA, et al. Birth Defects Orig Artic Ser. 1987;23(5A):303-7. Birth Defects Orig Artic Ser. 1987. PMID: 2446674 No abstract available.

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