Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 2
173
Views
13
CrossRef citations to date
0
Altmetric
Original Article

Hemoglobin Variants in Cyprus

, , , , , & show all
Pages 81-94 | Received 01 May 2008, Accepted 09 Dec 2008, Published online: 07 Jul 2009

REFERENCES

  • Kyrri A, Felekis X, Kalogerou E, Christopoulos G, Makariou C, Loizidou D, et al. Hb Limassol [β8(A5)Lys→Asn]: A new hemoglobin variant. Hemoglobin. 2001; 25(4)421–424
  • Fessas C, Karaklis A, Loukopoulos D, Stamatoyannopoulos G, Fessas P. Haemoglobin Nicosia. An α-chain variant and its combination with β-thalassaemia. Br J Haematol. 1965; 11(3)323–330
  • Pauling L, Itano HA, Singer SJ, Ibert CW. Sickle cell anemia, a molecular disease. Science. 1949; 109(2835)443–458
  • Baglioni C. Abnormal human haemoglobins. VII. Chemical studies on Haemoglobin D. Biochim Biophys Acta. 1962; 59(2)437–449
  • Gerald PS, Diamond LK. A new hereditary hemoglobinopathy (the Lepore trait) and its interaction with thalassemia trait. Blood. 1958; 13(9)835–844
  • Strahler JR, Rosenbloom BB, Hanash SM. A silent, neutral substitution detected by reverse-phase high-performance liquid chromatography: Hemoglobin Beirut. Science. 1983; 221(4613)860–862
  • Fessas P, Loukopoulos D, Loutradi-Anagnostou A, Komis G. ‘Silent’ β-thalassaemia caused by a ‘silent’ β-chain mutant: The pathogenesis of a syndrome of thalassaemia intermedia. Br J Haematol. 1982; 51(4)577–583
  • Christodoulou I, Papanastasiou P, Karababa PH, Mouroutsou A, Boussiou M, Sinopoulou K, et al. Molecular study of β-globin variants in the Greek population. 8th International Conference on Thalassaemias and The Haemoglobinopathies. Athens 2001
  • Boi-Doku FS, Lehmann H, Beale D. Haemoglobin G-Accra. Nature. 1964; 203(4943)363–365
  • Wajcman H, Belkhodja O, Labie D. Hb Setif: G1 (94) Asp-Tyr. A new chain hemoglobin variant with substitution of the residue involved in hydrogen bond between unlike subunits. FEBS Lett. 1972; 27(2)298–300
  • Griffiths KD, Lang A, Lehmann H, Mann JR, Plowman D, Raine DN. Haemoglobin Handsworth α18(A16)Gly→Arg. FEBS Lett. 1977; 75(1)93–95
  • Wajcman H, Blouquit Y, Gombaud-Saintonge G, Riou J, Galacteros F. Hb Fontainebleau [α21(B2)Ala→Pro], a new silent mutant hemoglobin. Hemoglobin. 1989; 13(5)421–428
  • Samperi P, Mancuso GR, Dibenedetto SP, Di Cataldo A, Ragusa R, Schiliro G. High performance liquid chromatography (HPLC): A simple method to quantify Hb C, O-Arab, Agenogi and F. Clin Lab Haematol. 1991; 13(2)169–175
  • Weatherall D, Clegg JB. The Thalassaemia Syndromes3rd. Blackwell Scientific Publications, Oxford 1981
  • Itano HA, Pauling L. A rapid diagnostic test for sickle cell anemia. Blood. 1949; 4(1)66–68
  • Carrell RW, Kay R. A simple method for the detection of unstable haemoglobins. Br J Haematol. 1972; 23(5)615–619
  • Betke K, Marti HR, Schlicht I. Estimation of small percentages of foetal haemoglobin. Nature. 1959; 184(4702)1877–1878
  • Fenn JB, Mann M, Meng CK, Wong SF, Whitehouse CM. Electrospray ionization for mass spectrometry of large biomolecules. Science. 1989; 246(4926)64–71
  • Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988; 16(3)1215
  • Kyriacou K, Kyrri A, Kalogirou E, Vasiliades PH, Angastinitis M, Loannou PA, et al. Hb Bart's levels in cord blood and α-thalassemia mutations in Cyprus. Hemoglobin. 2000; 24(3)171–180
  • Baysal E, Indrak K, Bozkurt G, Berkalp A, Aritkan E, old JM, et al. The β-thalassaemia mutations in the population of Cyprus. Br J Haematol. 1992; 81(4)607–609
  • Plato CC, Rucknagel DL, Geshowitz H. Studies on the distribution of glucose-6-phosphate dehydrogenase deficiency, thalassemia, and other genetic traits in the coastal and mountain villages of Cyprus. Am J Hum Genet. 1964; 16(3)267–283
  • Boussiou M, Loukopoulos D, Christakis J, Fessas PH. The origin of the sickle cell mutation in Greece: Evidence from âs globin gene cluster polymorphisms. Hemoglobin. 1991; 15(6)459–467
  • Kyrris CP. History of Cyprus. Lambousa Publications; 1996, NicosiaCyprus
  • Efremov GD. Hemoglobins Lepore and anti-Lepore. Hemoglobin. 1978; 2(3)197–233
  • Baglioni C, Ventruto V. Human abnormal hemoglobins. 11. A chemical study of Hemoglobin Lepore from a homozygote individual. Eur J Biochem. 1968; 5(1)29–32
  • Fessas P, Stamatoyannopoulos G, Karaklis A. Hemoglobin ‘pylos’: Study of a hemoglobinopathy resembling thalassemia in the heterozygous, homozygous and double heterozygous state. Blood. 1962; 19(1)1–22
  • Baglioni C. Abnormal human hemoglobins. X. A study of Hemoglobin Lepore Boston. Biochim Biophys Acta. 1965; 97(1)37–46
  • Labie D, Schroeder WA, Huisman THJ. The amino acid sequence of the δβ chains of Hemoglobin Lepore Augusta = Lepore Washington. Biochim Biophys Acta. 1966; 127(2)428–437
  • Quattrin N, Ventruto V. Hemoglobin Lepore: Its significance for thalassemia and clinical manifestations. Ann NY Acad Sci. 1974; 232: 65–75
  • Bircan I, Sisli S, Guven A, Cali S, Yegin O, Ertug H, et al. Hemoglobinopathies in the district of Antalya, Turkey. Pediatr Hematol Oncol. 1993; 10(3)289–291
  • Chami B, Blouquit Y, Bardakdjian-Michau J, Riou J, Wajcman H, Rosa J, et al. Hemoglobin variants in North Africa. Hemoglobin. 1994; 18(1)39–51
  • Bird GW, Lehmann H. Haemoglobin D in India. BMJ. 1956; 1(4965)514
  • Hynes M, Lehmann H. Haemoglobin D in a Persian girl: Presumably the first case of Haemoglobin-D-thalassaemia. BMJ. 1956; 2(4998)923–924
  • Gouttas A, Tsevrenis H, Papaspyrou A, Pougouras P, Fertakis A, Vorias N. [Hemoglobinosis D in Greece.]. Sangre (Barc). 1960; 31: 303–306
  • Stewart JN, MacIver JG. Sickle cell-Haemoglobin-D disease in a mulatto girl. Lancet. 1956; 270(6906)23–25
  • Stout C, Holland CK, Bird RM. Hemoglobin D in an Oklahoma family. Arch Int Med. 1964; 114(2)296–300

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.