128 related articles for article (PubMed ID: 38504512)
1. Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A review.
Thaker P; Mahajan N; Mukherjee MB; Colah RB
Int J Lab Hematol; 2024 Jun; 46(3):434-450. PubMed ID: 38504512
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis of a novel hemoglobinopathy of compound heterozygosity of hemoglobin S/hemoglobin Q India.
Parab S; Sakhare S; Sengupta C; Velumani A
Clin Chim Acta; 2015 Mar; 442():33-5. PubMed ID: 25576799
[TBL] [Abstract][Full Text] [Related]
3. A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK.
Khalil MSM; Timbs AT; Henderson SJ; Schuh A; El-Khawanky MM; Old JM
Hemoglobin; 2020 May; 44(3):195-200. PubMed ID: 32597250
[TBL] [Abstract][Full Text] [Related]
4. Prevalence and molecular characterization of structural hemoglobin variants in the Dongguan region of Guangdong province, southern China.
Lou JW; Wang T; Liu YH; He Y; Zhong BM; Liu JX; Zhao Y; Ye WL; Li DZ
Hemoglobin; 2014; 38(4):282-6. PubMed ID: 24985555
[TBL] [Abstract][Full Text] [Related]
5. Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband.
Sidhwa K; Daruwalla MR; Pawar R; Nadkarni A; Hariharan P; Mehta P; Gupta AD
Indian J Pathol Microbiol; 2019; 62(2):323-325. PubMed ID: 30971568
[TBL] [Abstract][Full Text] [Related]
6. Rare hemoglobin variants in Tunisian population.
Zorai A; Moumni I; Mosbahi I; Douzi K; Chaouachi D; Guemira F; Abbes S
Int J Lab Hematol; 2015 Apr; 37(2):148-54. PubMed ID: 24905386
[TBL] [Abstract][Full Text] [Related]
7. Phenotypic expression of HbO Indonesia in two Indian families and its interaction with sickle hemoglobin.
Gupta AD; Nadkarni A; Mehta P; Goriwale M; Ramani M; Chaudhary P; Mehrotra V; Colah R
Indian J Pathol Microbiol; 2017; 60(1):79-83. PubMed ID: 28195097
[TBL] [Abstract][Full Text] [Related]
8. A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC.
Edison ES; Sathya M; Rajkumar SV; Nair SC; Srivastava A; Shaji RV
Int J Lab Hematol; 2012 Oct; 34(5):556-8. PubMed ID: 22471768
[TBL] [Abstract][Full Text] [Related]
9. Diagnosis of a rare double heterozygous Hb D Punjab/Hb Q India hemoglobinopathy using Sebia capillary zone electrophoresis.
Parab S; Sakhare S; Sengupta C; Velumani A
Indian J Pathol Microbiol; 2014; 57(4):626-8. PubMed ID: 25308024
[TBL] [Abstract][Full Text] [Related]
10. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM
Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
[TBL] [Abstract][Full Text] [Related]
11. Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, India.
Meher S; Dehury S; Mohanty PK; Patel S; Pattanayak C; Bhattacharya S; Das K; Sarkar B
Hemoglobin; 2016 Aug; 40(4):270-2. PubMed ID: 27254408
[TBL] [Abstract][Full Text] [Related]
12. Hemoglobin profile and molecular characteristics of the complex interaction of hemoglobin Doi-Saket [α9(A7) asn > lys, HBA2:c.30C > a], a novel α2α1 hybrid globin variant, with hemoglobin E [β26(B8) Glu > lys, HBB:c.79G > A] and deletional α
Panyasai S; Khongthai K; Satthakarn S
Ann Med; 2023; 55(2):2264174. PubMed ID: 37796611
[TBL] [Abstract][Full Text] [Related]
13. Hb TAYBE: clinical and morphological findings IN 43 patients.
Koren A; Levin C; Zalman L; Palmor H; Filon D; Chubar E; Resnitzky P; Bennett M
Eur J Haematol; 2016 Aug; 97(2):137-44. PubMed ID: 26519868
[TBL] [Abstract][Full Text] [Related]
14. Five Rare β Globin Chain Hemoglobin Variants in India.
Colah RB; Nadkarni A; Gorakshakar A; Sawant P; Gorivale M; Mehta P; Sawant M; Ghosh K
Indian J Hematol Blood Transfus; 2016 Jun; 32(Suppl 1):282-6. PubMed ID: 27408413
[TBL] [Abstract][Full Text] [Related]
15. Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population.
Farashi S; Garous NF; Vakili S; Ashki M; Imanian H; Azarkeivan A; Najmabadi H
Hemoglobin; 2016; 40(1):53-5. PubMed ID: 26574177
[TBL] [Abstract][Full Text] [Related]
16. Capillary Electrophoresis Resolves Inconclusive HPLC Analysis for Hemoglobin Variants: a Study of Two Cases.
Li Y; Tian M; Qin T; Wan L
Clin Lab; 2018 Jul; 64(7):1305-1309. PubMed ID: 30146834
[TBL] [Abstract][Full Text] [Related]
17. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
Viprakasit V; Ekwattanakit S; Chalaow N; Riolueang S; Wijit S; Tanyut P; Chat-Uthai N; Tachavanich K
Acta Haematol; 2014; 131(2):88-94. PubMed ID: 24081251
[TBL] [Abstract][Full Text] [Related]
18. Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or
Khalil MSM; Timbs AT; Henderson SJ; Schuh A; Old JM
Hemoglobin; 2020 Sep; 44(5):364-367. PubMed ID: 32924661
[TBL] [Abstract][Full Text] [Related]
19. Potential pitfalls in the diagnosis of Hb Handsworth in areas with high prevalence of HbS.
Al Zadjali S; Al-Riyami AZ; Gravell D; Al Haddabi H; Al Rawahi M; Al Falahi K; Daar S
Int J Lab Hematol; 2014 Aug; 36(4):488-92. PubMed ID: 24165563
[TBL] [Abstract][Full Text] [Related]
20. Mutational spectrum of delta-globin gene in the Portuguese population.
Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
