133 related articles for article (PubMed ID: 35189650)
1. Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn.
Kalai M; Moumni I; Ouragini H; Chaouechi D; Boudriga I; Menif S
Am J Perinatol; 2024 Apr; 41(5):594-597. PubMed ID: 35189650
[TBL] [Abstract][Full Text] [Related]
2. [Association of Hbo Arab/beta-thalassemia discovered fortuitously in 2 brothers].
Mongalgi MA; Debbabi A; Guemira F; Fattoum S
Ann Pediatr (Paris); 1992 Apr; 39(4):268-70. PubMed ID: 1616242
[TBL] [Abstract][Full Text] [Related]
3. Anemia in patients with coinherited thalassemia and glucose-6-phosphate dehydrogenase deficiency.
Pornprasert S; Phanthong S
Hemoglobin; 2013; 37(6):536-43. PubMed ID: 23944358
[TBL] [Abstract][Full Text] [Related]
4. New Born Screening of Hemoglobinopathies in a Center Tunisian Population.
Chaouch L; Moumni I; Ben Abdallah J; Bouchahda R; Methlouthi J; Mahdhaoui N; Matamri W; Braham N; Bouguila F; Mejri L; Charefeddine B; Chaieb A; Khairi H; Menif S
J Pediatr Hematol Oncol; 2024 Jul; 46(5):e296-e299. PubMed ID: 38748601
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Molecular characterization of a discrete hemoglobinopathy upon investigation for a lung hydatic cyst in an old Tunisian patient.
Moumni I; Yalaoui S; Ghrairi N; Hamzaoui A; Zoraï A; Abbes S
Ann Biol Clin (Paris); 2011; 69(3):353-6. PubMed ID: 21659055
[TBL] [Abstract][Full Text] [Related]
7. εγ-Thalassemia, a New Hemoglobinopathy Category.
Oliveira JL; Thompson CH; Saravanaperumal SA; Koganti T; Jenkinson G; Hein MS; Kohorst MA; Hasadsri L; Nguyen PL; Matern D; Kipp BR; Klee EW; Wieben ED; Hoyer JD; Rangan A
Clin Chem; 2023 Jul; 69(7):711-717. PubMed ID: 37086467
[TBL] [Abstract][Full Text] [Related]
8. Distribution of thalassemias and associated hemoglobinopathies identified by prenatal diagnosis in Taiwan.
Peng CT; Liu SC; Peng YC; Lin TH; Wang SJ; Le CY; Shih MC; Tien N; Lu JJ; Lin CY
Blood Cells Mol Dis; 2013 Oct; 51(3):138-41. PubMed ID: 23689197
[TBL] [Abstract][Full Text] [Related]
9. [Beta-thalassemia and Hb D in patients with anemia].
Troĭtskaia OV; Antonova LA; Lozhechnik IG; Toshchan OV
Klin Lab Diagn; 1998 Mar; (3):16-23. PubMed ID: 9575728
[TBL] [Abstract][Full Text] [Related]
10. The coinheritance of beta- and alpha- thalassemia: a review of one patient and her family.
Mast KJ; Hammond S; Qualman SJ; Kahwash SB
Lab Hematol; 2009; 15(3):30-3. PubMed ID: 19758967
[TBL] [Abstract][Full Text] [Related]
11. The phenomena of balanced effect between α-globin gene and of β-globin gene.
Zhong L; Gan X; Xu L; Liang C; Xie Y; Lin W; Chen P; Liu M
BMC Med Genet; 2018 Aug; 19(1):145. PubMed ID: 30119651
[TBL] [Abstract][Full Text] [Related]
12. Hb S (
Azarkeivan A; Cohan N; Niazkar HR; Azizi A; Rad F
Hemoglobin; 2020 Mar; 44(2):109-112. PubMed ID: 32370567
[TBL] [Abstract][Full Text] [Related]
13. Hb Leiden-beta (0) thalassemia in a Chinese with severe hemolytic anemia.
Lie-Injo LE; Ganesan J; Randhawa ZI; Peterson D; Kane JP
Am J Hematol; 1977; 2(4):335-42. PubMed ID: 602924
[TBL] [Abstract][Full Text] [Related]
14. Carrier screening for thalassemia and hemoglobinopathies in Canada.
Langlois S; Ford JC; Chitayat D; ;
J Obstet Gynaecol Can; 2008 Oct; 30(10):950-959. PubMed ID: 19038079
[TBL] [Abstract][Full Text] [Related]
15. Interpretation of fetal hemoglobin only on newborn screening for hemoglobinopathy.
Heeney MM; Delgrosso K; Robinson R; Johnson CA; Daeschner CW; Campbell TA; Surrey S; Ware RE
J Pediatr Hematol Oncol; 2002; 24(6):499-502. PubMed ID: 12218602
[TBL] [Abstract][Full Text] [Related]
16. Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
Jha AN; Mishra H; Verma HK; Pandey I; Lakkakula BVKS
Hemoglobin; 2018 Mar; 42(2):84-90. PubMed ID: 30200838
[TBL] [Abstract][Full Text] [Related]
17. Hb A
Orts JA; Zúñiga Á; Bello Y; Fabregat AB; Vicente AI
Hemoglobin; 2016 Sep; 40(5):335-340. PubMed ID: 27535164
[TBL] [Abstract][Full Text] [Related]
18. Complex Interaction of Hb Q-Thailand with α
He S; Qin Q; Lin L; Chen Q; Yi S; Wei H; Du J; Zheng C; Qiu X; Chen B
Hemoglobin; 2017 Jan; 41(1):68-72. PubMed ID: 28475397
[TBL] [Abstract][Full Text] [Related]
19. An Unusual Compound Heterozygosity for Hb O-Arab (
van Gammeren AJ; Pelkmans L; Endschot CCWV; Roelofsen-de Beer RJAC; Harteveld CL
Hemoglobin; 2020 Jan; 44(1):61-63. PubMed ID: 31973650
[TBL] [Abstract][Full Text] [Related]
20. Coinheritance of HbD-Punjab/β+-thalassemia (IVSI+5 G-C) in patient with Gilbert's syndrome.
Petrenko AA; Pivnik AV; Kim PP; Demidova EY; Surin VL; Abdullaev AO; Sudarikov AB; Petrova NA; Maryina SA
Ter Arkh; 2018 Aug; 90(7):105-109. PubMed ID: 30701931
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
