BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 31286966)

  • 1. Genotypic and phenotypic spectra of hemojuvelin mutations in primary hemochromatosis patients: a systematic review.
    Kong X; Xie L; Zhu H; Song L; Xing X; Yang W; Chen X
    Orphanet J Rare Dis; 2019 Jul; 14(1):171. PubMed ID: 31286966
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
    Santos PC; Cançado RD; Pereira AC; Schettert IT; Soares RA; Pagliusi RA; Hirata RD; Hirata MH; Teixeira AC; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
    Blood Cells Mol Dis; 2011 Apr; 46(4):302-7. PubMed ID: 21411349
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China.
    Wu L; Zhang W; Li Y; Zhou D; Zhang B; Xu A; Wu Z; Wu L; Li S; Wang X; Zhao X; Wang Q; Li M; Wang Y; You H; Huang J; Ou X; Jia J
    Orphanet J Rare Dis; 2021 Sep; 16(1):398. PubMed ID: 34583728
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease.
    Sandhu K; Flintoff K; Chatfield MD; Dixon JL; Ramm LE; Ramm GA; Powell LW; Subramaniam VN; Wallace DF
    Blood; 2018 Jul; 132(1):101-110. PubMed ID: 29743178
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population.
    Barton JC; Rivers CA; Niyongere S; Bohannon SB; Acton RT
    BMC Med Genet; 2004 Dec; 5():29. PubMed ID: 15610558
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism.
    Santiago de Sousa Azulay R; Magalhães M; Tavares MDG; Dualibe R; Barbosa L; Sá Gaspar S; Faria AM; Nascimento GC; Damianse SDSP; Rocha VCC; Gomes MB; Dos Santos Faria M
    Am J Case Rep; 2020 Apr; 21():e923108. PubMed ID: 32327622
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin.
    Lee PL; Beutler E; Rao SV; Barton JC
    Blood; 2004 Jun; 103(12):4669-71. PubMed ID: 14982867
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians.
    Dhillon BK; Chopra G; Jamwal M; Chandak GR; Duseja A; Malhotra P; Chawla YK; Garewal G; Das R
    Blood Cells Mol Dis; 2018 Nov; 73():14-21. PubMed ID: 30195625
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular diagnostic and pathogenesis of hereditary hemochromatosis.
    Santos PCJL; Krieger JE; Pereira AC
    Int J Mol Sci; 2012; 13(2):1497-1511. PubMed ID: 22408404
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Non-
    Lv T; Zhang W; Xu A; Li Y; Zhou D; Zhang B; Li X; Zhao X; Wang Y; Wang X; Duan W; Wang Q; Xu H; Zheng J; Zhao R; Zhu L; Dong Y; Lu L; Chen Y; Long J; Zheng S; Wang W; You H; Jia J; Ou X; Huang J
    J Med Genet; 2018 Oct; 55(10):650-660. PubMed ID: 30166352
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patient.
    Daraio F; Ryan E; Gleeson F; Roetto A; Crowe J; Camaschella C
    Blood Cells Mol Dis; 2005; 35(2):174-6. PubMed ID: 15967692
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Juvenile Hemochromatosis: A Case Report and Review of the Literature.
    Takami A; Tatsumi Y; Sakai K; Toki Y; Ikuta K; Oohigashi Y; Takagi J; Kato K; Takami K
    Pharmaceuticals (Basel); 2020 Aug; 13(8):. PubMed ID: 32824233
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interaction of hemojuvelin with neogenin results in iron accumulation in human embryonic kidney 293 cells.
    Zhang AS; West AP; Wyman AE; Bjorkman PJ; Enns CA
    J Biol Chem; 2005 Oct; 280(40):33885-94. PubMed ID: 16103117
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Juvenile hemochromatosis associated with heterozygosity for novel hemojuvelin mutations and with unknown cofactors.
    Pelusi S; Rametta R; Della Corte C; Congia R; Dongiovanni P; Pulixi EA; Fargion S; Fracanzani AL; Nobili V; Valenti L
    Ann Hepatol; 2014; 13(5):568-71. PubMed ID: 25152992
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
    Brissot P; Moirand R; Jouanolle AM; Guyader D; Le Gall JY; Deugnier Y; David V
    J Hepatol; 1999 Apr; 30(4):588-93. PubMed ID: 10207799
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The mechanisms of systemic iron homeostasis and etiology, diagnosis, and treatment of hereditary hemochromatosis.
    Kawabata H
    Int J Hematol; 2018 Jan; 107(1):31-43. PubMed ID: 29134618
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes.
    Pietrangelo A; Caleffi A; Henrion J; Ferrara F; Corradini E; Kulaksiz H; Stremmel W; Andreone P; Garuti C
    Gastroenterology; 2005 Feb; 128(2):470-9. PubMed ID: 15685557
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
    Martinelli AL; Filho R; Cruz S; Franco R; Tavella M; Secaf M; Ramalho L; Zucoloto S; Rodrigues S; Zago M
    Genet Mol Res; 2005 Mar; 4(1):31-8. PubMed ID: 15841433
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis.
    Press RD; Flora K; Gross C; Rabkin JM; Corless CL
    Am J Clin Pathol; 1998 May; 109(5):577-84. PubMed ID: 9576576
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.