These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
286 related articles for article (PubMed ID: 30816434)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to alpha-spectrin deficiency. Yaish HM; Christensen RD; Agarwal A J Perinatol; 2013 May; 33(5):404-6. PubMed ID: 23624969 [TBL] [Abstract][Full Text] [Related]
8. An Wang X; Mao L; Shen N; Peng J; Zhu Y; Hu Q; Lu Y Oncotarget; 2017 Dec; 8(68):113282-113286. PubMed ID: 29348906 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. [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]
13. A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome. Nato Y; Kageyama Y; Suzuki K; Shimojima Yamamoto K; Kanno H; Miyashita H Intern Med; 2023 Jan; 62(1):107-111. PubMed ID: 35650129 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosis. Bai L; Zheng L; Li B; Huang H; Shi X; Yi Y Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2023 Apr; 48(4):565-574. PubMed ID: 37385619 [TBL] [Abstract][Full Text] [Related]
16. Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing. Qin L; Nie Y; Zhang H; Chen L; Zhang D; Lin Y; Ru K J Hum Genet; 2020 Apr; 65(4):427-434. PubMed ID: 31980736 [TBL] [Abstract][Full Text] [Related]
17. A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis. Zhu F; Liang M; Xu L; Peng Z; Cai D; Wei X; Lin L; Shang X Gene; 2020 Feb; 726():144226. PubMed ID: 31669644 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Clinical utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience. Agarwal AM; McMurty V; Clayton AL; Bolia A; Reading NS; Mani C; Patel JL; Rets A Eur J Haematol; 2023 Jun; 110(6):688-695. PubMed ID: 36825813 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]