196 related articles for article (PubMed ID: 31126250)
21. [The characteristic of hereditary spherocytosis related gene mutation in 37 Chinese hereditary spherocytisis patients].
Peng GX; Yang WR; Zhao X; Jin LP; Zhang L; Zhou K; Li Y; Ye L; Li Y; Li JP; Fan HH; Song L; Yang Y; Xiong YZ; Wu ZJ; Wang HJ; Zhang FK
Zhonghua Xue Ye Xue Za Zhi; 2018 Nov; 39(11):898-903. PubMed ID: 30486584
[No Abstract] [Full Text] [Related]
22. Genotype-phenotype correlation in children with hereditary spherocytosis.
Tole S; Dhir P; Pugi J; Drury LJ; Butchart S; Fantauzzi M; Langer JC; Baker JM; Blanchette VS; Kirby-Allen M; Carcao MD
Br J Haematol; 2020 Nov; 191(3):486-496. PubMed ID: 32436265
[TBL] [Abstract][Full Text] [Related]
23. A novel variant of SLC4A1 for hereditary spherocytosis in a Chinese family: a case report and systematic review.
Li J; Wang X; Zheng N; Wang X; Liu Y; Xue L
BMC Med Genomics; 2022 Dec; 15(1):250. PubMed ID: 36463227
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. [Analysis of the characteristics of SPTB gene variants among 16 children with Hereditary spherocytosis].
Ge Y; Li J; Han Y; Xie H; Shangguan S; Jiang Q; Chen X; Liu R
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Mar; 40(3):269-275. PubMed ID: 36854399
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. [Clinical characteristics and genetic analysis of hereditary spherocytosis caused by mutations of ANK1 and SPTB genes].
Gong J; He XL; Zou RY; Chen KK; You YL; Zou H; Tian X; Zhu CG
Zhongguo Dang Dai Er Ke Za Zhi; 2019 Apr; 21(4):370-374. PubMed ID: 31014431
[TBL] [Abstract][Full Text] [Related]
28. Spectrum of Ankyrin Mutations in Hereditary Spherocytosis: A Case Report and Review of the Literature.
Luo Y; Li Z; Huang L; Tian J; Xiong M; Yang Z
Acta Haematol; 2018; 140(2):77-86. PubMed ID: 30227413
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.
Hao L; Li S; Ma D; Chen S; Zhang B; Xiao D; Zhang J; Jiang N; Jiang S; Ma J
J Cell Mol Med; 2019 Jun; 23(6):4454-4463. PubMed ID: 31016877
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature.
Wang D; Song L; Shen L; Zhang K; Lv Y; Gao M; Ma J; Wan Y; Gai Z; Liu Y
Front Pharmacol; 2021; 12():644352. PubMed ID: 34335240
[No Abstract] [Full Text] [Related]
33. 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]
34. 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]
35. Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.
Choi HS; Choi Q; Kim JA; Im KO; Park SN; Park Y; Shin HY; Kang HJ; Kook H; Kim SY; Kim SJ; Kim I; Kim JY; Kim H; Park KD; Park KB; Park M; Park SK; Park ES; Park JA; Park JE; Park JK; Baek HJ; Seo JH; Shim YJ; Ahn HS; Yoo KH; Yoon HS; Won YW; Lee KS; Lee KC; Lee MJ; Lee SA; Lee JA; Lee JM; Lee JH; Lee JW; Lim YT; Jung HJ; Chueh HW; Choi EJ; Jung HL; Kim JH; Lee DS;
Orphanet J Rare Dis; 2019 May; 14(1):114. PubMed ID: 31122244
[TBL] [Abstract][Full Text] [Related]
36. [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]
37. Identification of a novel ANK1 mutation in hereditary spherocytosis co-existing with BWS.
Zhang Q; Zhang C; Wang Y; Hao S; Shi J; Feng X; Zheng L; Wang X; Xue C; Zhou B; Liu F; Zhao F; Li X; Deng L; Hou J; Meng Z
Mol Genet Genomic Med; 2022 Apr; 10(4):e1903. PubMed ID: 35218326
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. SPTB related spherocytosis in a three-generation family presenting with kidney failure in adulthood due to co-occurrence of UMOD disease causing variant.
Meglic A; Debeljak M; Kovac J; Trampus Bakija A; Rajic V; Kojc N; Trebusak Podkrajsek K
Nefrologia (Engl Ed); 2020; 40(4):421-428. PubMed ID: 32113667
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
