315 related articles for article (PubMed ID: 6162733)
1. Haemoglobin O Arab, beta-thalassaemia and glucose-6-phosphate dehydrogenase deficiency in a Hungarian family.
Horányi M; Szelényi J; Rona G; Lang A; Lehmann H; Hollán SR
Folia Haematol Int Mag Klin Morphol Blutforsch; 1980; 107(4):654-60. PubMed ID: 6162733
[TBL] [Abstract][Full Text] [Related]
2. [Haemoglobinosis C/beta-thalassemia double heterozygosity in an Algerian patient with total suppression of haemoglobin A synthesis (author's transl)].
Boreux G; Farquet JJ; Pugin P; Miescher PA; Klein D
J Genet Hum; 1978 Mar; 26(1):1-15. PubMed ID: 670935
[TBL] [Abstract][Full Text] [Related]
3. Hemoglobin A2, E and F levels and the incidence of hemoglobin E, beta-thalassemia, and glucose-6-phosphate dehydrogenase deficiency in lymphoma.
Panich V; Na-Nakorn S; Piankijagum A
J Med Assoc Thai; 1974 Jan; 57(1):3-10. PubMed ID: 4814776
[No Abstract] [Full Text] [Related]
4. [Triple erythrocyte disorders: thalassemia, hemoglobinopathy L Glucose-6-phosphate dehydrogenase deficiency in a girl from Polesine. First study].
De Filippis A
Haematologica; 1969; 54(10):685-702. PubMed ID: 4994285
[No Abstract] [Full Text] [Related]
5. Anemia in patients with coinherited thalassemia and glucose-6-phosphate dehydrogenase deficiency.
Pornprasert S; Phanthong S
Hemoglobin; 2013; 37(6):536-43. PubMed ID: 23944358
[TBL] [Abstract][Full Text] [Related]
6. Effect of alpha thalassaemia, G-6-PD deficiency and Hb F on the nature of sickle cell anaemia in south-western Saudi Arabia.
el-Hazmi MA; al-Swailem AR; Bahakim HM; al-Faleh FZ; Warsy AS
Trop Geogr Med; 1990 Jul; 42(3):241-7. PubMed ID: 1705730
[TBL] [Abstract][Full Text] [Related]
7. Leg ulcer in a patient with beta-thalassemia and glucose-6-phosphate-dehydrogenase deficiency.
Lotti T; Benci M; Palleschi GM; Cantini F; Palchetti R; Albertacci A
Int J Dermatol; 1990; 29(6):426-7. PubMed ID: 2397966
[No Abstract] [Full Text] [Related]
8. Haemolytic anaemia.
Weatherall DJ
Practitioner; 1978 Aug; 221(1322):194-202. PubMed ID: 724613
[No Abstract] [Full Text] [Related]
9. Spectrum of haemolytic anaemias in Punjab, North India.
Dash S; Dash RJ
Trop Geogr Med; 1980 Dec; 32(4):312-6. PubMed ID: 7210170
[TBL] [Abstract][Full Text] [Related]
10. Hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency.
Olivares N; Medina C; Sánchez-Corona J; Rivas F; Rivera H; Hernández A; Delgado JL; Ibarra B; Cantú JM; Vaca G; Martínez C
Arch Invest Med (Mex); 1979; 10(4):177-86. PubMed ID: 539862
[TBL] [Abstract][Full Text] [Related]
11. Haemoglobin E-thalassaemia disease complicated by pregnancy.
Ong HC
Trop Geogr Med; 1974 Mar; 26(1):94-5. PubMed ID: 4830626
[No Abstract] [Full Text] [Related]
12. Sickle cell haemoglobin, thalassaemia and G-6-PD enzyme deficiency genes in Garasiya tribe inhabited malaria endemic areas of Sirohi District, Rajasthan (India).
Choubisa SL
J Commun Dis; 2009 Mar; 41(1):13-8. PubMed ID: 19886170
[TBL] [Abstract][Full Text] [Related]
13. Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: a molecular and hematological analysis.
Fucharoen S; Fucharoen G; Sanchaisuriya K; Surapot S
Blood Cells Mol Dis; 2005; 35(2):196-200. PubMed ID: 15982909
[TBL] [Abstract][Full Text] [Related]
14. [Haemolytic anaemia due to glucose-6-phosphatehydrogenase deficiency in a Slovak family (author's transl)].
Gocárová K; Strnová J; Sasinka M; Plenta I; Chmeliar J
Cas Lek Cesk; 1976 Aug; 115(33-34):1031-5. PubMed ID: 975174
[No Abstract] [Full Text] [Related]
15. Hereditary hemolytic anemia associated with glucose-6-phosphate dehydrogenase deficiency (Mediterranean type).
Benbassat J; Ben-Ishay D
Isr J Med Sci; 1969; 5(5):1053-9. PubMed ID: 5369703
[No Abstract] [Full Text] [Related]
16. Survey on haemoglobin variants, beta-thalassaemia, glucose-6-phosphate dehydrogenase deficiency and haptoglobin types in Turkish people living in Manavgat, Serik and Boztepe (Antalya).
Aksoy M; Dinçol G; Erdem S
Hum Hered; 1980; 30(1):3-6. PubMed ID: 7353885
[TBL] [Abstract][Full Text] [Related]
17. [Concurrence on two siblings of three haemoglobin abnormal genes: haemoglobin S, beta-thalassaemia and hereditary persistence of foetal haemoglobin (author's transl)].
Guerrero García R; Rosillo de León J; Landero de Ruíz N; Padilla C; Ruíz Reyes G
Sangre (Barc); 1978; 23(5):578-86. PubMed ID: 741340
[No Abstract] [Full Text] [Related]
18. Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace.
Aksoy M; Kutlar A; Kutlar F; Dinçol G; Erdem S; Baştesbihçi S
J Med Genet; 1985 Aug; 22(4):288-90. PubMed ID: 4045955
[TBL] [Abstract][Full Text] [Related]
19. Genetic Blood Disorders Survey in the Sultanate of Oman.
Al-Riyami A; Ebrahim GJ
J Trop Pediatr; 2003 Jul; 49 Suppl 1():i1-20. PubMed ID: 12934793
[TBL] [Abstract][Full Text] [Related]
20. Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype level.
Sanna G; Frau F; Melis MA; Galanello R; De Virgiliis S; Cao A
Br J Haematol; 1980 Apr; 44(4):555-61. PubMed ID: 7378315
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
