173 related articles for article (PubMed ID: 37280519)
21. The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis.
Shen H; Gao Z; Ye Q
Genet Test Mol Biomarkers; 2024 Jan; 28(1):33-38. PubMed ID: 38294355
[No Abstract] [Full Text] [Related]
22. Identification of variants in 94 Chinese patients with hereditary spherocytosis by next-generation sequencing.
Wang WJ; Xie JD; Yao H; Ding ZX; Jiang AR; Ma L; Shen HJ; Chen SN
Clin Genet; 2023 Jan; 103(1):67-78. PubMed ID: 36203343
[TBL] [Abstract][Full Text] [Related]
23. A previously unrecognized Ankyrin-1 mutation associated with Hereditary Spherocytosis in an Italian family.
Lazzareschi I; Curatola A; Pedicelli C; Castiglia D; Buonsenso D; Gatto A; Attinà G; Valentini P
Eur J Haematol; 2019 Nov; 103(5):523-526. PubMed ID: 31400153
[TBL] [Abstract][Full Text] [Related]
24. A clinical and experimental study of adult hereditary spherocytosis in the Chinese population.
Xue J; He Q; Xie XJ; Su AL; Cao SB
Kaohsiung J Med Sci; 2020 Jul; 36(7):552-560. PubMed ID: 32133777
[TBL] [Abstract][Full Text] [Related]
25. [Clinical manifestations of erythrocyte membrane protein coding gene mutations in hereditary spherocytosis].
Sun XJ; Li HY; Li DP; Liu YZ; Zhang JY; Yin YK; Su MH; Pan H; Li QL; Hu B; Liu H; Shi J
Zhonghua Xue Ye Xue Za Zhi; 2018 Nov; 39(11):912-916. PubMed ID: 30486587
[No Abstract] [Full Text] [Related]
26. 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]
27. The Spectrum of
Chonat S; Risinger M; Sakthivel H; Niss O; Rothman JA; Hsieh L; Chou ST; Kwiatkowski JL; Khandros E; Gorman MF; Wells DT; Maghathe T; Dagaonkar N; Seu KG; Zhang K; Zhang W; Kalfa TA
Front Physiol; 2019; 10():815. PubMed ID: 31333484
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. The Complexity of Genotype-Phenotype Correlations in Hereditary Spherocytosis: A Cohort of 95 Patients: Genotype-Phenotype Correlation in Hereditary Spherocytosis.
van Vuren A; van der Zwaag B; Huisjes R; Lak N; Bierings M; Gerritsen E; van Beers E; Bartels M; van Wijk R
Hemasphere; 2019 Aug; 3(4):e276. PubMed ID: 31723846
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.
Hughes MR; Anderson N; Maltby S; Wong J; Berberovic Z; Birkenmeier CS; Haddon DJ; Garcha K; Flenniken A; Osborne LR; Adamson SL; Rossant J; Peters LL; Minden MD; Paulson RF; Wang C; Barber DL; McNagny KM; Stanford WL
Exp Hematol; 2011 Mar; 39(3):305-20, 320.e1-2. PubMed ID: 21193012
[TBL] [Abstract][Full Text] [Related]
32. A Novel
Jang W; Kim SK; Nahm CH; Choi JW; Kim JJ; Moon Y
Ann Clin Lab Sci; 2021 Jan; 51(1):136-139. PubMed ID: 33653793
[TBL] [Abstract][Full Text] [Related]
33. Molecular Genetic Mechanisms of Hereditary Spherocytosis: Current Perspectives.
He BJ; Liao L; Deng ZF; Tao YF; Xu YC; Lin FQ
Acta Haematol; 2018; 139(1):60-66. PubMed ID: 29402830
[TBL] [Abstract][Full Text] [Related]
34. The updated beta-spectrin mutations in patients with hereditary spherocytosis by targeted next-generation sequencing.
Fan J; Yao L; Lu D; Yao Y; Sun Y; Tian Y; Mou L; Chen L; Zhao L; Qiao S; Hu S; Zhu Y
J Hum Genet; 2021 Dec; 66(12):1153-1158. PubMed ID: 34140613
[TBL] [Abstract][Full Text] [Related]
35. Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis.
Guan H; Liang X; Zhang R; Wang H; Liu W; Zhang R; Yang J; Liu S
Hematology; 2018 Jul; 23(6):357-361. PubMed ID: 29099659
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Clinical Exome Sequencing Reveals Novel Mutations in
Chiguer A; Lyahyai J; El Kadiri Y; Cherkaoui Jaouad I; Doubaj Y; Sefiani A
Hemoglobin; 2024 Jun; ():1-4. PubMed ID: 38831725
[TBL] [Abstract][Full Text] [Related]
38. Identification of a novel
Wang X; Yi B; Mu K; Shen N; Zhu Y; Hu Q; Lu Y
Oncotarget; 2017 Nov; 8(57):96791-96797. PubMed ID: 29228571
[TBL] [Abstract][Full Text] [Related]
39. Hereditary spherocytosis caused by copy number variation in SPTB gene identified through targeted next-generation sequencing.
Jang W; Kim J; Chae H; Kim M; Koh KN; Park CJ; Kim Y
Int J Hematol; 2019 Aug; 110(2):250-254. PubMed ID: 30903564
[TBL] [Abstract][Full Text] [Related]
40. Concomitant Hereditary Spherocytosis and Pyruvate Kinase Deficiency in a Spanish Family with Chronic Hemolytic Anemia: Contribution of Laser Ektacytometry to Clinical Diagnosis.
Vives Corrons JL; Krishnevskaya E; Montllor L; Leguizamon V; Garcia Bernal M
Cells; 2022 Mar; 11(7):. PubMed ID: 35406697
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
