Indrak K - Search Results

1

alpha-thalassemia resulting from a negative chromosomal position effect.

Barbour VM, Tufarelli C, Sharpe JA, Smith ZE, Ayyub H, Heinlein CA, Sloane-Stanley J, Indrak K, Wood WG, Higgs DR. Barbour VM, et al. Among authors: indrak k. Blood. 2000 Aug 1;96(3):800-7. Blood. 2000. PMID: 10910890 Free article.

2

The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed.

Divoky V, Baysal E, Oner R, Cürük MA, Walker EL 3rd, Indrak K, Huisman TH. Divoky V, et al. Among authors: indrak k. Hum Genet. 1994 Jan;93(1):77-8. doi: 10.1007/BF00218918. Hum Genet. 1994. PMID: 8270260

3

A Czechoslovakian teenager with Hb E-beta zero-thalassemia [IVS-I-1 (G----A)] complicated by the presence of an alpha-globin gene triplication.

Indrak K, Fei YJ, Li HW, Baysal E, Brabec V, Fortova H, Cermak J, Huisman TH. Indrak K, et al. Ann Hematol. 1991 Jul;63(1):42-4. doi: 10.1007/BF01714960. Ann Hematol. 1991. PMID: 1878422

4

A new alpha-thalassemia-2 deletion resulting in microcytosis and hypochromia and in vitro chain imbalance in the heterozygote.

Indrak K, Gu YC, Novotny J, Huisman TH. Indrak K, et al. Am J Hematol. 1993 Jun;43(2):144-5. doi: 10.1002/ajh.2830430214. Am J Hematol. 1993. PMID: 8342542

5

Molecular characterization of beta-thalassemia in Czechoslovakia.

Indrak K, Brabec V, Indrakova J, Chrobak L, Sakalova A, Jarosova M, Cermak J, Fei YJ, Kutlar F, Gu YC, et al. Indrak K, et al. Hum Genet. 1992 Feb;88(4):399-404. doi: 10.1007/BF00215673. Hum Genet. 1992. PMID: 1740317

6

Glucose-6 phosphate dehydrogenase mutations and haplotypes in various ethnic groups.

Xu W, Westwood B, Bartsocas CS, Malcorra-Azpiazu JJ, Indrák K, Beutler E. Xu W, et al. Among authors: indrak k. Blood. 1995 Jan 1;85(1):257-63. Blood. 1995. PMID: 7803800 Free article.

7

Two new EPO receptor mutations: truncated EPO receptors are most frequently associated with primary familial and congenital polycythemias.

Kralovics R, Indrak K, Stopka T, Berman BW, Prchal JF, Prchal JT. Kralovics R, et al. Among authors: indrak k. Blood. 1997 Sep 1;90(5):2057-61. Blood. 1997. PMID: 9292543 Free article.

8

Hb Hradec Kralove (Hb HK) or alpha 2 beta 2 115(G17)Ala-->Asp, a severely unstable hemoglobin variant resulting in a dominant beta-thalassemia trait in a Czech family.

Divoky V, Svobodova M, Indrak K, Chrobak L, Molchanova TP, Huisman TH. Divoky V, et al. Among authors: indrak k. Hemoglobin. 1993 Aug;17(4):319-28. doi: 10.3109/03630269308997485. Hemoglobin. 1993. PMID: 7693620

9

Molecular characterization of beta-thalassemia in Hungary.

Ringelhann B, Szelenyi JG, Horanyi M, Svobodova M, Divoky V, Indrak K, Hollân S, Marosi A, Laub M, Huisman TH. Ringelhann B, et al. Among authors: indrak k. Hum Genet. 1993 Oct;92(4):385-7. doi: 10.1007/BF01247340. Hum Genet. 1993. PMID: 8225319

10

[Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].

Indrák K, Divoký V, Brabec V, Indráková J, Svobodová M, Huisman TH. Indrák K, et al. Vnitr Lek. 1993 Oct;39(10):969-78. Vnitr Lek. 1993. PMID: 7694425 Czech.

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