Similar articles for PMID: 20954559

Year	Number of Results
1992	1
1993	1
1994	1
1995	2
1997	2
1998	2
1999	1
2000	1
2001	1
2002	1
2003	4
2004	7
2005	3
2006	5
2007	3
2008	5
2009	14
2010	11
2011	8
2012	6
2013	6
2014	4
2015	3
2016	4
2017	7
2018	2
2019	4
2020	3
2021	2
2024	0

1

A rare case of alpha-thalassaemia intermedia in a Malay patient double heterozygous for alpha(+)-thalassaemia and a mutation in alpha1 globin gene CD59 (GGC --> GAC).

George E, Jama T, Azian AS, Rahimah A, Zubaidah Z. George E, et al. Med J Malaysia. 2009 Dec;64(4):321-2. Med J Malaysia. 2009. PMID: 20954559 Free article.

2

alpha-thalassaemia masked by beta gene defects and a new polyadenylation site mutation on the alpha2-globin gene.

Harteveld CL, Oosterhuis WP, Schoenmakers CH, Ananta H, Kos S, Bakker Verweij M, van Delft P, Arkesteijn SG, Phylipsen M, Giordano PC. Harteveld CL, et al. Eur J Haematol. 2010 Apr;84(4):354-8. doi: 10.1111/j.1600-0609.2009.01380.x. Epub 2009 Nov 12. Eur J Haematol. 2010. PMID: 19912309

3

Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.

Azma RZ, Othman A, Azman N, Alauddin H, Ithnin A, Yusof N, Razak NF, Sardi NH, Hussin NH. Azma RZ, et al. Malays J Pathol. 2012 Jun;34(1):57-62. Malays J Pathol. 2012. PMID: 22870600 Free article.

4

Two new alpha1-globin gene point mutations: Hb Nedlands (HBA1:c.86C>T) [alpha28(B9)Ala-->Val] and Hb Queens Park (HBA1:c.98T>A) [alpha32(B13)Met-->Lys].

Phylipsen M, Prior JF, Lim E, Lingam N, Finlayson J, Arkesteijn SG, Harteveld CL, Giordano PC. Phylipsen M, et al. Hemoglobin. 2010 Jan;34(2):123-6. doi: 10.3109/03630261003679854. Hemoglobin. 2010. PMID: 20353346

5

Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand.

Chunpanich S, Ayukarn K, Sanchaisuriya K, Fucharoen G, Fucharoen S. Chunpanich S, et al. Clin Lab Haematol. 2004 Oct;26(5):355-8. doi: 10.1111/j.1365-2257.2004.00627.x. Clin Lab Haematol. 2004. PMID: 15485467

6

Observation of a rare hemoglobin variant [Hb Lulu island, beta107(G9)Gly-->Asp, GGC-->GAC] co-inherited with a beta+-thalassemia mutation [IVS-I-110 (G-->A)] or in the heterozygous state in a Greek-Albanian family.

Papassotiriou I, Stamoulakatou A, Wajcman H, Kister J, Dimisianos G, Lazaropoulou C, Kanavaki I, Vavourakis E, Kattamis A, Kanavakis E, Traeger-Synodinos J. Papassotiriou I, et al. Hemoglobin. 2006;30(4):409-18. doi: 10.1080/03630260600867842. Hemoglobin. 2006. PMID: 16987796

7

Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG).

Eng B, Walker L, Waye JS. Eng B, et al. Hemoglobin. 2009;33(1):72-4. doi: 10.1080/03630260802625980. Hemoglobin. 2009. PMID: 19205977

8

[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.

9

[Genetic screening for alpha-thalassemia deletional determinants by GapPCR method].

Katol J, Takao M, Ideguchi H, Sawada H, Kawashima H, Ono J. Katol J, et al. Rinsho Byori. 2006 Nov;54(11):1095-100. Rinsho Byori. 2006. PMID: 17240829 Japanese.

10

A new alpha(0)-thalassemia deletion found in a Dutch family (--(AW)).

Phylipsen M, Vogelaar IP, Schaap RA, Arkesteijn SG, Boxma GL, van Helden WC, Wildschut IC, de Bruin-Roest AC, Giordano PC, Harteveld CL. Phylipsen M, et al. Blood Cells Mol Dis. 2010 Aug 15;45(2):133-5. doi: 10.1016/j.bcmd.2010.05.004. Epub 2010 Jun 1. Blood Cells Mol Dis. 2010. PMID: 20682466

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