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Items: 1 to 20 of 82

1.

β-Thalassemia trait association with autoimmune diseases: β-globin locus proximity to the immunity genes or role of hemorphins?

Altinoz MA, Gedikoglu G, Deniz G.

Immunopharmacol Immunotoxicol. 2012 Apr;34(2):181-90. doi: 10.3109/08923973.2011.599391. Epub 2011 Jul 28. Review.

PMID:
21793795
2.

Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approach.

Basak AN, Tuzmen S.

Methods Mol Biol. 2011;700:291-307. doi: 10.1007/978-1-61737-954-3_19.

PMID:
21204041
3.

Hemoglobins, Hemorphins, and 11p15.5 Chromosomal Region in Cancer Biology and İmmunity with Special Emphasis for Brain Tumors.

Altinoz MA, Elmaci I, Ince B, Ozpinar A, Sav AM.

J Neurol Surg A Cent Eur Neurosurg. 2016 May;77(3):247-57. doi: 10.1055/s-0035-1566120. Epub 2016 Mar 2. Review.

PMID:
26935297
4.

The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island.

Giambona A, Vinciguerra M, Cannata M, Cassarà F, Fiorentino G, Leto F, Gioco PL, Renda D, Passarello C, Maggio A.

Blood Cells Mol Dis. 2011 Apr 15;46(4):282-7. doi: 10.1016/j.bcmd.2011.01.006. Epub 2011 Feb 24.

PMID:
21353607
5.

Hypochromic microcytic anemia with a variant hemoglobin.

Bain BJ.

Am J Hematol. 2009 Jan;84(1):59. doi: 10.1002/ajh.21300. No abstract available.

6.
7.

Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand.

Nuntakarn L, Fucharoen S, Fucharoen G, Sanchaisuriya K, Jetsrisuparb A, Wiangnon S.

Blood Cells Mol Dis. 2009 Jan-Feb;42(1):32-5. doi: 10.1016/j.bcmd.2008.09.002. Epub 2008 Oct 23.

PMID:
18951049
8.
9.
10.

Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.

Colah R, Gorakshakar A, Nadkarni A, Phanasgaonkar S, Surve R, Sawant P, Mohanty D, Ghosh K.

Blood Cells Mol Dis. 2009 May-Jun;42(3):241-6. doi: 10.1016/j.bcmd.2008.12.006. Epub 2009 Feb 28.

PMID:
19254853
11.

Genetic modifiers of beta-thalassemia.

Thein SL.

Haematologica. 2005 May;90(5):649-60. Review.

12.

Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels.

Vrettou C, Kanavakis E, Traeger-Synodinos J, Metaxotou-Mavrommati A, Basiakos I, Maragoudaki E, Stamoulakatou A, Papassotiriou I, Kattamis C.

Hemoglobin. 2000 Aug;24(3):203-20.

PMID:
10975440
13.

Molecular basis of thalassemia intermedia in Iran.

Akbari MT, Izadi P, Izadyar M, Kyriacou K, Kleanthous M.

Hemoglobin. 2008;32(5):462-70. doi: 10.1080/03630260802341851.

PMID:
18932071
14.

Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene.

Traeger-Synodinos J, Papassotiriou I, Vrettou C, Skarmoutsou C, Stamoulakatou A, Kanavakis E.

Haematologica. 2001 Apr;86(4):363-7.

15.

Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.

Nadkarni A, Gorakshakar A, Surve R, Sawant P, Phanasgaonkar S, Nair S, Ghosh K, Colah RB.

Hemoglobin. 2009;33(1):59-65. doi: 10.1080/03630260802626012.

PMID:
19205975
16.

beta+-Thalassemia trait: hematologic and hemoglobin synthesis studies.

Pootrakul S, Assawamunkong S, Na-Nakorn S.

Hemoglobin. 1976-1977;1(1):75-83.

PMID:
1052172
17.

Hemoglobin Hakkari: an autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin gene.

Kanathezhath B, Hazard FK, Guo H, Kidd J, Azimi M, Kuypers FA, Vichinsky EP, Lal A.

Pediatr Blood Cancer. 2010 Feb;54(2):332-5. doi: 10.1002/pbc.22167.

PMID:
19852066
18.

Quantities of alpha Q chain variants in heterozygotes with and without a concomitant beta-thalassemia trait.

Qin WB, Baysal E, Wong KF, Molchanova TP, Pobedimskaya DD, Sharma S, Wilson JB, Huisman TH.

Am J Hematol. 1994 Jan;45(1):91-3.

PMID:
8250015
19.

The importance of β globin deletion analysis in the evaluation of patients with β thalassemia.

Mikula M, Buller-Burckle A, Gallivan M, Sun W, Franklin CR, Strom CM.

Int J Lab Hematol. 2011 Jun;33(3):310-7. doi: 10.1111/j.1751-553X.2010.01287.x. Epub 2011 Jan 11.

PMID:
21219590
20.

Xmn I polymorphism associated with concomitant activation of Gγ and Aγ globin gene transcription on a β0-thalassemia chromosome.

Haj Khelil A, Morinière M, Laradi S, Khelif A, Perrin P, Ben Chibani J, Baklouti F.

Blood Cells Mol Dis. 2011 Feb 15;46(2):133-8. doi: 10.1016/j.bcmd.2010.11.002. Epub 2010 Dec 8.

PMID:
21144779

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