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.
225 related articles for article (PubMed ID: 31286966)
21. Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis. Wang Y; Du Y; Liu G; Guo S; Hou B; Jiang X; Han B; Chang Y; Nie G Int J Hematol; 2017 Apr; 105(4):521-525. PubMed ID: 27896572 [TBL] [Abstract][Full Text] [Related]
22. The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype. Le Gac G; Scotet V; Ka C; Gourlaouen I; Bryckaert L; Jacolot S; Mura C; Férec C Hum Mol Genet; 2004 Sep; 13(17):1913-8. PubMed ID: 15254010 [TBL] [Abstract][Full Text] [Related]
23. [Molecular genetic diagnostics and screening of hereditary hemochromatosis]. Zlocha J; Kovács L; Pozgayová S; Kupcová V; Durínová S Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764 [TBL] [Abstract][Full Text] [Related]
24. Hepatic iron metabolism gene expression profiles in HFE associated hereditary hemochromatosis. Gleeson F; Ryan E; Barrett S; Russell J; Crowe J Blood Cells Mol Dis; 2007; 38(1):37-44. PubMed ID: 17098454 [TBL] [Abstract][Full Text] [Related]
25. Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload. Badar S; Busti F; Ferrarini A; Xumerle L; Bozzini P; Capelli P; Pozzi-Mucelli R; Campostrini N; De Matteis G; Marin Vargas S; Giorgetti A; Delledonne M; Olivieri O; Girelli D Am J Hematol; 2016 Jun; 91(4):420-5. PubMed ID: 26799139 [TBL] [Abstract][Full Text] [Related]
26. Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes. Mendes AI; Ferro A; Martins R; Picanço I; Gomes S; Cerqueira R; Correia M; Nunes AR; Esteves J; Fleming R; Faustino P Ann Hematol; 2009 Mar; 88(3):229-34. PubMed ID: 18762941 [TBL] [Abstract][Full Text] [Related]
27. Juvenile hemochromatosis and hepatocellular carcinoma in a patient with a novel mutation in the HJV gene. Ramzan K; Imtiaz F; Al-Ashgar HI; AlSayed M; Sulaiman RA Eur J Med Genet; 2017 Jun; 60(6):308-311. PubMed ID: 28363629 [TBL] [Abstract][Full Text] [Related]
28. Two middle-age-onset hemochromatosis patients with heterozygous mutations in the hemojuvelin gene in a Chinese family. Li S; Xue J; Chen B; Wang Q; Shi M; Xie X; Zhang L Int J Hematol; 2014 Apr; 99(4):487-92. PubMed ID: 24584909 [TBL] [Abstract][Full Text] [Related]
29. Hemojuvelin (HJV) mutations in persons of European, African-American and Asian ancestry with adult onset haemochromatosis. Lee PL; Barton JC; Brandhagen D; Beutler E Br J Haematol; 2004 Oct; 127(2):224-9. PubMed ID: 15461631 [TBL] [Abstract][Full Text] [Related]
30. Molecular pathogenesis of hereditary hemochromatosis. Liu J; Pu C; Lang L; Qiao L; Abdullahi MA; Jiang C Histol Histopathol; 2016 Aug; 31(8):833-40. PubMed ID: 27031690 [TBL] [Abstract][Full Text] [Related]
31. Hemochromatosis: genetics helps to define a multifactorial disease. Burke W; Press N; McDonnell SM Clin Genet; 1998 Jul; 54(1):1-9. PubMed ID: 9727731 [TBL] [Abstract][Full Text] [Related]
32. Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis. Zhang W; Li Y; Xu A; Ouyang Q; Wu L; Zhou D; Wu L; Zhang B; Zhao X; Wang Y; Wang X; Duan W; Wang Q; You H; Huang J; Ou X; Jia J; Orphanet J Rare Dis; 2022 Jun; 17(1):216. PubMed ID: 35668470 [TBL] [Abstract][Full Text] [Related]
34. Early age-of-onset iron overload and homozygosity for the novel hemojuvelin mutation HJV R54X (exon 3; c.160A-->T) in an African American male of West Indies descent. Murugan RC; Lee PL; Kalavar MR; Barton JC Clin Genet; 2008 Jul; 74(1):88-92. PubMed ID: 18492090 [TBL] [Abstract][Full Text] [Related]
35. Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report. Militaru MS; Popp RA; Trifa AP J Gastrointestin Liver Dis; 2010 Jun; 19(2):191-3. PubMed ID: 20593054 [TBL] [Abstract][Full Text] [Related]
36. Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload. de Lima Santos PC; Pereira AC; Cançado RD; Schettert IT; Hirata RD; Hirata MH; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM Genet Test Mol Biomarkers; 2010 Dec; 14(6):803-6. PubMed ID: 21039223 [TBL] [Abstract][Full Text] [Related]
37. Juvenile hemochromatosis caused by a novel combination of hemojuvelin G320V/R176C mutations in a 5-year old girl. Aguilar-Martinez P; Lok CY; Cunat S; Cadet E; Robson K; Rochette J Haematologica; 2007 Mar; 92(3):421-2. PubMed ID: 17339196 [TBL] [Abstract][Full Text] [Related]
38. Identification of a novel mutation (C321X) in HJV. Huang FW; Rubio-Aliaga I; Kushner JP; Andrews NC; Fleming MD Blood; 2004 Oct; 104(7):2176-7. PubMed ID: 15138164 [TBL] [Abstract][Full Text] [Related]
39. Novel compound heterozygous mutations in the Xie LD; Kong XM; Shen JX; Wang TL; Ma J; Zhang YF; Chen XP World J Clin Cases; 2024 Jul; 12(19):3961-3970. PubMed ID: 38994316 [TBL] [Abstract][Full Text] [Related]