208 related articles for article (PubMed ID: 31602632)
41. 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]
42. 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]
43. Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.
Gallagher PG; Forget BG
Blood Cells Mol Dis; 1998 Dec; 24(4):539-43. PubMed ID: 9887280
[No Abstract] [Full Text] [Related]
44. High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis.
Miraglia del Giudice E; Francese M; Nobili B; Morlé L; Cutillo S; Delaunay J; Perrotta S
J Pediatr; 1998 Jan; 132(1):117-20. PubMed ID: 9470011
[TBL] [Abstract][Full Text] [Related]
45. Genetic and Clinical Characteristics of Patients With Hereditary Spherocytosis in Hubei Province of China.
Wang X; Zhang A; Huang M; Chen L; Hu Q; Lu Y; Cheng L
Front Genet; 2020; 11():953. PubMed ID: 33014018
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. 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]
48. 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]
49. Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report.
Chai S; Jiao R; Sun X; Fu P; Zhao Q; Sang M
BMC Med Genet; 2020 Nov; 21(1):223. PubMed ID: 33187473
[TBL] [Abstract][Full Text] [Related]
50. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity].
Eber SW
Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935
[TBL] [Abstract][Full Text] [Related]
51. 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]
52. A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis?
Bogusławska DM; Heger E; Listowski M; Wasiński D; Kuliczkowski K; Machnicka B; Sikorski AF
Br J Haematol; 2014 Oct; 167(2):269-71. PubMed ID: 24903897
[No Abstract] [Full Text] [Related]
53. 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]
54. 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]
55. Ankyrin gene mutations in japanese patients with hereditary spherocytosis.
Nakanishi H; Kanzaki A; Yawata A; Yamada O; Yawata Y
Int J Hematol; 2001 Jan; 73(1):54-63. PubMed ID: 11372755
[TBL] [Abstract][Full Text] [Related]
56. A novel splicing mutation of ANK1 is associated with phenotypic heterogeneity of hereditary spherocytosis in a Chinese family.
Xu L; Wei X; Liang G; Zhu D; Zhang Y; Zhang Y; Shang X
Biochim Biophys Acta Mol Basis Dis; 2023 Jan; 1869(1):166595. PubMed ID: 36336297
[TBL] [Abstract][Full Text] [Related]
57. Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes.
Shen H; Huang H; Luo K; Yi Y; Shi X
BMC Med Genet; 2019 May; 20(1):90. PubMed ID: 31126250
[TBL] [Abstract][Full Text] [Related]
58. Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis.
Savvides P; Shalev O; John KM; Lux SE
Blood; 1993 Nov; 82(10):2953-60. PubMed ID: 8219186
[TBL] [Abstract][Full Text] [Related]
59. 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]
60. 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]
