212 related articles for article (PubMed ID: 31069991)
1. Molecular diagnostic update in hereditary hemolytic anemia and neonatal hyperbilirubinemia.
Rets A; Clayton AL; Christensen RD; Agarwal AM
Int J Lab Hematol; 2019 May; 41 Suppl 1():95-101. PubMed ID: 31069991
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Characterization of hereditary red blood cell membranopathies using combined targeted next-generation sequencing and osmotic gradient ektacytometry.
Vives-Corrons JL; Krishnevskaya E; Rodriguez IH; Ancochea A
Int J Hematol; 2021 Feb; 113(2):163-174. PubMed ID: 33074480
[TBL] [Abstract][Full Text] [Related]
4. Causes of hemolysis in neonates with extreme hyperbilirubinemia.
Christensen RD; Nussenzveig RH; Yaish HM; Henry E; Eggert LD; Agarwal AM
J Perinatol; 2014 Aug; 34(8):616-9. PubMed ID: 24762414
[TBL] [Abstract][Full Text] [Related]
5. Developmental, Genetic, Dietary, and Xenobiotic Influences on Neonatal Hyperbilirubinemia.
Yueh MF; Chen S; Nguyen N; Tukey RH
Mol Pharmacol; 2017 May; 91(5):545-553. PubMed ID: 28283555
[TBL] [Abstract][Full Text] [Related]
6. Molecular diagnosis of hereditary hemolytic anemias: Recent updates.
Agarwal AM; Rets AV
Int J Lab Hematol; 2023 Jun; 45 Suppl 2():79-86. PubMed ID: 37290893
[TBL] [Abstract][Full Text] [Related]
7. Epidemiological Study of Hereditary Hemolytic Anemia in the Korean Pediatric Population during 1997-2016: a Nationwide Retrospective Cohort Study.
Shim YJ; Jung HL; Shin HY; Kang HJ; Choi JY; Hah JO; Lee JM; Lim YT; Yang EJ; Baek HJ; Choi HS; Yoo KH; Park JE; Kim S; Kim JY; Park ES; Im HJ; Chueh HW; Kim SK; Lee JH; Yoo ES; Park HJ; Lee JA; Park M; Kang HS; Park JK; Lee NH; Park SK; Lee YH; Lee SW; Choi EJ; Kong SG;
J Korean Med Sci; 2020 Aug; 35(33):e279. PubMed ID: 32830468
[TBL] [Abstract][Full Text] [Related]
8. UGT1A1 gene and neonatal hyperbilirubinemia: a preliminary study from Bengkulu, Indonesia.
Amandito R; Putradista R; Jikesya C; Utaminingsih D; Rusin J; Rohsiswatmo R; Malik A
BMC Res Notes; 2018 Mar; 11(1):172. PubMed ID: 29534743
[TBL] [Abstract][Full Text] [Related]
9. Diagnostic yield of targeted next-generation sequencing for pediatric hereditary hemolytic anemia.
Choi YJ; Kim H; Ahn WK; Lee ST; Han JW; Choi JR; Lyu CJ; Hahn S; Shin S
BMC Med Genomics; 2023 Sep; 16(1):215. PubMed ID: 37697358
[TBL] [Abstract][Full Text] [Related]
10. Screening for G71R mutation of the UDP-glucuronosyltransferase 1 (UGT1A1) gene in neonates with pathologic and prolonged hyperbilirubinemia in Turkey.
Kilic I; Koseler A; Cakaloz I; Atalay E
Int J Clin Pharmacol Ther; 2010 Aug; 48(8):504-8. PubMed ID: 20650040
[TBL] [Abstract][Full Text] [Related]
11. [Roles of UGT 1A1 gene mutation in the development of neonatal hyperbilirubinemia in Guangxi].
Gao ZY; Zhong DN; Liu Y; Liu YN; Wei LM
Zhonghua Er Ke Za Zhi; 2010 Sep; 48(9):646-9. PubMed ID: 21092520
[TBL] [Abstract][Full Text] [Related]
12. Congenital Hemolytic Anemia.
Haley K
Med Clin North Am; 2017 Mar; 101(2):361-374. PubMed ID: 28189176
[TBL] [Abstract][Full Text] [Related]
13. Correlation between UGT1A1 polymorphism and neonatal hyperbilirubinemia of neonates in Wuhan.
Liu W; Chang LW; Xie M; Li WB; Rong ZH; Wu L; Chen L
J Huazhong Univ Sci Technolog Med Sci; 2017 Oct; 37(5):740-743. PubMed ID: 29058288
[TBL] [Abstract][Full Text] [Related]
14. [Hereditary hemolytic anemia in newborns: clinical significance of genetic diagnosis].
Ohga S; Ishimura M; Eguchi K; Hasegawa I; Ogura H; Utsugisawa T; Kanno H
Rinsho Ketsueki; 2020; 61(5):484-490. PubMed ID: 32507813
[TBL] [Abstract][Full Text] [Related]
15. Clinical and Genetic Etiologies of Neonatal Unconjugated Hyperbilirubinemia in the China Neonatal Genomes Project.
Mei H; Dong X; Wu B; Wang H; Lu Y; Hu L; Wang J; Cao Y; Zhang R; Cheng G; Wang L; Li Z; Yang L; Zhou W
J Pediatr; 2022 Apr; 243():53-60.e9. PubMed ID: 34953813
[TBL] [Abstract][Full Text] [Related]
16. Red Blood Cell Membrane-Related Gene Variants and Clinical Risk Factors in Chinese Neonates with Hyperbilirubinemia.
Lin F; Xu JX; Wu YH; Chen ZK; Chen MT; Ma YB; Li JD; Yang LY
Neonatology; 2023; 120(3):371-380. PubMed ID: 37040722
[TBL] [Abstract][Full Text] [Related]
17. Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding.
Sato H; Uchida T; Toyota K; Kanno M; Hashimoto T; Watanabe M; Nakamura T; Tamiya G; Aoki K; Hayasaka K
J Hum Genet; 2013 Jan; 58(1):7-10. PubMed ID: 23014115
[TBL] [Abstract][Full Text] [Related]
18. Clinical utility of next-generation sequencing in the diagnosis of hereditary haemolytic anaemias.
Agarwal AM; Nussenzveig RH; Reading NS; Patel JL; Sangle N; Salama ME; Prchal JT; Perkins SL; Yaish HM; Christensen RD
Br J Haematol; 2016 Sep; 174(5):806-14. PubMed ID: 27292444
[TBL] [Abstract][Full Text] [Related]
19. Hemolytic Disorders Causing Severe Neonatal Hyperbilirubinemia.
Christensen RD; Yaish HM
Clin Perinatol; 2015 Sep; 42(3):515-27. PubMed ID: 26250914
[TBL] [Abstract][Full Text] [Related]
20. Neonatal hemolytic jaundice: morphologic features of erythrocytes that will help you diagnose the underlying condition.
Christensen RD; Yaish HM; Lemons RS
Neonatology; 2014; 105(4):243-9. PubMed ID: 24526179
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]