126 related articles for article (PubMed ID: 27979672)
1. [Neonatal expression of beta-thalassemia trait associated with hereditary spherocytosis in two monozygotic twins].
Ben Hamouda H; Mahjoub B; Soua H; Laradi S; Miled A; Sfar MT
Arch Pediatr; 2017 Feb; 24(2):126-130. PubMed ID: 27979672
[TBL] [Abstract][Full Text] [Related]
2. Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene.
Chen M; Ye YP; Liao L; Deng XL; Qiu YL; Lin FQ
Hematology; 2020 Dec; 25(1):438-445. PubMed ID: 33210974
[No Abstract] [Full Text] [Related]
3. Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs‑negative hemolytic jaundice.
Wang X; Liu A; Lu Y; Hu Q
Mol Med Rep; 2019 Apr; 19(4):2801-2807. PubMed ID: 30816434
[TBL] [Abstract][Full Text] [Related]
4. A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the
Yang K; Ren Q; Wu Y; Zhou Y; Yin X
Hemoglobin; 2019 Mar; 43(2):140-144. PubMed ID: 31190573
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Red blood cell indexes in patients in patients with hereditary spherocytosis and beta-thalassemia combination.
Akar N; Gökçe H
Pediatr Hematol Oncol; 2002 Dec; 19(8):569-73. PubMed ID: 12487832
[TBL] [Abstract][Full Text] [Related]
7. Diagnostic difficulty of beta-thalassemia syndrome in a multi-transfused patient: contribution of myelogram and studying parents.
Trawinski É; Fenneteau O; Le Mouel L; Ithier G; Couque N
Ann Biol Clin (Paris); 2017 Oct; 75(5):562-568. PubMed ID: 28958966
[TBL] [Abstract][Full Text] [Related]
8. Hereditary spherocytosis in a newborn with carrier state parents--a family study.
Tsai YM; Wang SY; Lee PP
Zhonghua Yi Xue Za Zhi (Taipei); 1989 Aug; 44(2):129-34. PubMed ID: 2819575
[TBL] [Abstract][Full Text] [Related]
9. First report of a nonsense mutation at codon 15(TGG-->TAG) in exon 1 of the beta globin gene in a beta thalassemia trait in State of Orissa, India.
Nishank SS; Ranjit M; Chhotray GP
Hematology; 2008 Feb; 13(1):65-7. PubMed ID: 18534069
[TBL] [Abstract][Full Text] [Related]
10. A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis.
Zhu F; Liang M; Xu L; Peng Z; Cai D; Wei X; Lin L; Shang X
Gene; 2020 Feb; 726():144226. PubMed ID: 31669644
[TBL] [Abstract][Full Text] [Related]
11. Combination of a triple alpha-globin gene with beta-thalassemia in a gypsy family: importance of the genetic testing in the diagnosis and search for a donor for bone marrow transplantation for one of their children.
Yus Cebrian F; Recasens Flores Mdel V; Izquierdo Álvarez S; Parra Salinas I; Rodriguez-Vigil Iturrate C
BMC Res Notes; 2016 Apr; 9():220. PubMed ID: 27080228
[TBL] [Abstract][Full Text] [Related]
12. Tokyo-1 Mutation: Hereditary Spherocytosis in a Hispanic Newborn Presenting as Early Onset Severe Hyperbilirubinemia.
Tan AW; Leung P; Patil UP
Fetal Pediatr Pathol; 2018 Aug; 37(4):296-300. PubMed ID: 30207817
[TBL] [Abstract][Full Text] [Related]
13. Precise diagnosis of a hereditary spherocytosis patient with complicated hematological phenotype.
Liang G; Lin Z; Zhang Y; Zhang Q; Zhu D; Liang X; Xie H; Wei X; Shang X
Mol Genet Genomics; 2024 May; 299(1):57. PubMed ID: 38787432
[TBL] [Abstract][Full Text] [Related]
14. Novel α-spectrin mutation in trans with α-spectrin causing severe neonatal jaundice from hereditary spherocytosis.
Nussenzveig RH; Christensen RD; Prchal JT; Yaish HM; Agarwal AM
Neonatology; 2014; 106(4):355-7. PubMed ID: 25277063
[TBL] [Abstract][Full Text] [Related]
15. Genetic diagnosis and pathogenic analysis of an atypical hereditary spherocytosis combined with UGT1A1 partial deficiency: A case report.
Yi Y; Dang X; Li Y; Zhao C; Tang H; Shi X
Mol Med Rep; 2018 Jan; 17(1):382-387. PubMed ID: 29115431
[TBL] [Abstract][Full Text] [Related]
16. Managing anemia in pediatric office practice: Part 1.
Segel GB; Hirsh MG; Feig SA
Pediatr Rev; 2002 Mar; 23(3):75-84. PubMed ID: 11875180
[No Abstract] [Full Text] [Related]
17. 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. PubMed ID: 11325640
[TBL] [Abstract][Full Text] [Related]
18. Molecular analysis of beta-thalassemia in South Vietnam.
Svasti S; Hieu TM; Munkongdee T; Winichagoon P; Van Be T; Van Binh T; Fucharoen S
Am J Hematol; 2002 Oct; 71(2):85-8. PubMed ID: 12353305
[TBL] [Abstract][Full Text] [Related]
19. Misdiagnosis of two cases of hereditary spherocytosis in a family and review of published reports.
Deng Z; Liao L; Yang W; Lin F
Clin Chim Acta; 2015 Feb; 441():6-9. PubMed ID: 25485852
[TBL] [Abstract][Full Text] [Related]
20. A Novel ANK1 Mutation in a Neonatal Hereditary Spherocytosis Case: Diagnostic Challenges and Familial Genetic Analysis.
Li J; Guo H; Zhu Z; Sun J
Acta Haematol; 2022; 145(6):575-581. PubMed ID: 35817016
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
