188 related articles for article (PubMed ID: 36463227)
41. Utility of mean sphered cell volume and mean reticulocyte volume for the diagnosis of hereditary spherocytosis.
Arora RD; Dass J; Maydeo S; Arya V; Kotwal J; Bhargava M
Hematology; 2018 Aug; 23(7):413-416. PubMed ID: 29338606
[TBL] [Abstract][Full Text] [Related]
42. Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature.
Xie L; Xing Z; Li C; Liu SX; Wen FQ
BMC Med Genomics; 2021 Mar; 14(1):77. PubMed ID: 33706756
[TBL] [Abstract][Full Text] [Related]
43. Flow cytometric osmotic fragility test and eosin-5'-maleimide dye-binding tests are better than conventional osmotic fragility tests for the diagnosis of hereditary spherocytosis.
Arora RD; Dass J; Maydeo S; Arya V; Radhakrishnan N; Sachdeva A; Kotwal J; Bhargava M
Int J Lab Hematol; 2018 Jun; 40(3):335-342. PubMed ID: 29573337
[TBL] [Abstract][Full Text] [Related]
44. Next generation sequencing reveals co-existence of hereditary spherocytosis and Dubin-Johnson syndrome in a Chinese gril: A case report.
Li Y; Li Y; Yang Y; Yang WR; Li JP; Peng GX; Song L; Fan HH; Ye L; Xiong YZ; Wu ZJ; Zhou K; Zhao X; Jing LP; Zhang FK; Zhang L
World J Clin Cases; 2019 Oct; 7(20):3303-3309. PubMed ID: 31667183
[TBL] [Abstract][Full Text] [Related]
45. 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]
46. Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1.
Allegrini B; NGuyen LD; Mignotet M; Etchebest C; Fenneteau O; Platon J; Lambilliotte A; Guizouarn H; Da Costa L
Blood Cells Mol Dis; 2023 Nov; 103():102780. PubMed ID: 37516005
[TBL] [Abstract][Full Text] [Related]
47. 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]
48. Literature review on genotype-phenotype correlation in patients with hereditary spherocytosis.
Yang L; Shu H; Zhou M; Gong Y
Clin Genet; 2022 Dec; 102(6):474-482. PubMed ID: 36071563
[TBL] [Abstract][Full Text] [Related]
49. A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.
Jenkins PB; Abou-Alfa GK; Dhermy D; Bursaux E; Féo C; Scarpa AL; Lux SE; Garbarz M; Forget BG; Gallagher PG
J Clin Invest; 1996 Jan; 97(2):373-80. PubMed ID: 8567957
[TBL] [Abstract][Full Text] [Related]
50. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population.
Yawata Y; Kanzaki A; Yawata A; Doerfler W; Ozcan R; Eber SW
Int J Hematol; 2000 Feb; 71(2):118-35. PubMed ID: 10745622
[TBL] [Abstract][Full Text] [Related]
51. Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of
Tian Y; Wang Y; Yang J; Gao P; Xu H; Wu Y; Li M; Chen H; Lu D; Yan H
Front Genet; 2023; 14():1221853. PubMed ID: 37795245
[TBL] [Abstract][Full Text] [Related]
52. 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]
53. Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
Trabelsi N; Bouguerra G; Haddad F; Ouederni M; Darragi I; Boudrigua I; Chaouachi D; Barmat M; Fouzai C; Bejaoui M; Menif S; Kraiem I; Abbes S
Cell Physiol Biochem; 2021 Mar; 55(1):117-129. PubMed ID: 33667330
[TBL] [Abstract][Full Text] [Related]
54. Atypical hereditary spherocytosis phenotype associated with pseudohypokalaemia and a new variant in the band 3 protein.
Ramasamy I
BMJ Case Rep; 2020 Dec; 13(12):. PubMed ID: 33298499
[TBL] [Abstract][Full Text] [Related]
55. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
Tshilolo L; Kagambega F; Sztern B; Vertongen F; Gulbis B
Rev Med Brux; 1998 Oct; 19(5 Pt 1):417-23. PubMed ID: 9844481
[TBL] [Abstract][Full Text] [Related]
56. 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]
57. Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family.
Leung KF; Au WY; Chan AY; Chan LC; Waye JS; Chui DH; Ma SK
Clin Lab Haematol; 2001 Feb; 23(1):53-5. PubMed ID: 11422231
[TBL] [Abstract][Full Text] [Related]
58. Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report.
Du Z; Luo G; Wang K; Bing Z; Pan S
BMC Pediatr; 2021 Jun; 21(1):291. PubMed ID: 34182956
[TBL] [Abstract][Full Text] [Related]
59. [Clinical and genotypic analysis of hereditary spherocytosis combined with cholestasis among pediatric patients].
Jiang T; Tang L; Zhang H; Li SJ; Ouyang WX
Zhonghua Gan Zang Bing Za Zhi; 2023 Sep; 31(9):943-946. PubMed ID: 37872089
[No Abstract] [Full Text] [Related]
60. Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.
Han JH; Kim S; Jang H; Kim SW; Lee MG; Koh H; Lee JH
PLoS One; 2015; 10(6):e0131251. PubMed ID: 26107955
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
