186 related articles for article (PubMed ID: 33210974)
1. 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]
2. 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]
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. [Genetic Analysis and Prenatal Diagnosis of a Family with Hereditary Spherocytosis Caused by a Novel Compound Heterozygous Mutation of SPTB Gene].
Qin YM; Liao L; Deng XL; Huang J; Wei HY; Lin FQ
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2022 Apr; 30(2):552-558. PubMed ID: 35395996
[TBL] [Abstract][Full Text] [Related]
5. Effects of
Herrera-Tirado IM; Espinoza-Mata LL; Rizo-delaTorre LDC; Becerra-Solano LE; Ibarra-Cortés B; Perea-Díaz FJ
Genet Test Mol Biomarkers; 2022 May; 26(5):270-276. PubMed ID: 35638908
[No Abstract] [Full Text] [Related]
6. Whole exome sequencing identified a novel mutation (p.Ala1884Pro) of β-spectrin in a Chinese family with hereditary spherocytosis.
Fan LL; Liu JS; Huang H; Du R; Xiang R
J Gene Med; 2019 Feb; 21(2-3):e3073. PubMed ID: 30690801
[TBL] [Abstract][Full Text] [Related]
7. Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
Park J; Jeong DC; Yoo J; Jang W; Chae H; Kim J; Kwon A; Choi H; Lee JW; Chung NG; Kim M; Kim Y
Clin Genet; 2016 Jul; 90(1):69-78. PubMed ID: 26830532
[TBL] [Abstract][Full Text] [Related]
8. Targeted next-generation sequencing identified novel mutations associated with hereditary anemias in Brazil.
Svidnicki MCCM; Zanetta GK; Congrains-Castillo A; Costa FF; Saad STO
Ann Hematol; 2020 May; 99(5):955-962. PubMed ID: 32266426
[TBL] [Abstract][Full Text] [Related]
9. A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin.
Li S; Guo P; Mi L; Chai X; Xi K; Liu T; Lu L; Li J
Ann Hematol; 2022 Apr; 101(4):731-738. PubMed ID: 35099593
[TBL] [Abstract][Full Text] [Related]
10. Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian study.
Aggarwal A; Jamwal M; Sharma P; Sachdeva MUS; Bansal D; Malhotra P; Das R
Br J Haematol; 2020 Mar; 188(5):784-795. PubMed ID: 31602632
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. A novel essential splice site variant in SPTB in a large hereditary spherocytosis family.
Nieminen TT; Liyanarachchi S; Comiskey DF; Wang Y; Li W; Hendrickson IV; Brock P; de la Chapelle A; He H
Mol Genet Genomic Med; 2021 May; 9(5):e1641. PubMed ID: 33943044
[TBL] [Abstract][Full Text] [Related]
13. Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency.
Miraglia del Giudice E; Lombardi C; Francese M; Nobili B; Conte ML; Amendola G; Cutillo S; Iolascon A; Perrotta S
Br J Haematol; 1998 May; 101(2):251-4. PubMed ID: 9609518
[TBL] [Abstract][Full Text] [Related]
14. Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis.
Xie F; Lei L; Cai B; Gan L; Gao Y; Liu X; Zhou L; Jiang J
Mol Genet Genomic Med; 2021 Apr; 9(4):e1577. PubMed ID: 33620149
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion.
Ly Thi Thanh H; Le Thi Thanh H; Hoang Luong L; Huy Tran T; Liu SC; Truong HN; Ta TV; Bui TH; Tran VK
Taiwan J Obstet Gynecol; 2018 Jun; 57(3):435-441. PubMed ID: 29880180
[TBL] [Abstract][Full Text] [Related]
16. Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype.
Miraglia del Giudice E; Perrotta S; Nobili B; Pinto L; Cutillo L; Iolascon A
Br J Haematol; 1993 Nov; 85(3):553-7. PubMed ID: 8136278
[TBL] [Abstract][Full Text] [Related]
17. Targeted next-generation sequencing identified a novel
Sun Q; Xie Y; Wu P; Li S; Hua Y; Lu X; Zhao W
Hematology; 2019 Dec; 24(1):583-587. PubMed ID: 31390973
[No Abstract] [Full Text] [Related]
18. 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]
19. A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review.
Shih YH; Huang YC; Lin CY; Lin HY; Kuo SF; Lin JS; Shen MC
Medicine (Baltimore); 2023 Jan; 102(4):e32708. PubMed ID: 36705355
[TBL] [Abstract][Full Text] [Related]
20. Clinical and molecular evaluation of non-dominant hereditary spherocytosis.
Miraglia del Giudice E; Nobili B; Francese M; D'Urso L; Iolascon A; Eber S; Perrotta S
Br J Haematol; 2001 Jan; 112(1):42-7. PubMed ID: 11167781
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
