BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 15315789)

  • 1. Juvenile hemochromatosis HJV-related revealed by cardiogenic shock.
    Filali M; Le Jeunne C; Durand E; Grinda JM; Roetto A; Daraio F; Bruneval P; Jeunemaitre X; Gimenez-Roqueplo AP
    Blood Cells Mol Dis; 2004; 33(2):120-4. PubMed ID: 15315789
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A juvenile hemochromatosis patient homozygous for a novel deletion of cDNA nucleotide 81 of hemojuvelin.
    Lee P; Promrat K; Mallette C; Flynn M; Beutler E
    Acta Haematol; 2006; 115(1-2):123-7. PubMed ID: 16424663
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. HJV gene mutations in European patients with juvenile hemochromatosis.
    Gehrke SG; Pietrangelo A; Kascák M; Braner A; Eisold M; Kulaksiz H; Herrmann T; Hebling U; Bents K; Gugler R; Stremmel W
    Clin Genet; 2005 May; 67(5):425-8. PubMed ID: 15811010
    [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. Prevalence of the G320V mutation of the HJV gene, associated with juvenile hemochromatosis, in Greece.
    Pissia M; Polonifi K; Politou M; Lilakos K; Sakellaropoulos N; Papanikolaou G
    Haematologica; 2004 Jun; 89(6):742-3. PubMed ID: 15194541
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. [Mutation analysis of the pathogenic gene in a Chinese family with hereditary hemochromatosis].
    Yuanfeng L; Hongxing Z; Haitao Z; Xiaobo P; Lili B; Fuchu H; Zewu Q; Gangqiao Z
    Yi Chuan; 2014 Nov; 36(11):1152-8. PubMed ID: 25567873
    [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. Variable expressivity of HJV related hemochromatosis: "Juvenile" hemochromatosis?
    Hamdi-Rozé H; Ben Ali Z; Ropert M; Detivaud L; Aggoune S; Simon D; Pelletier G; Deugnier Y; David V; Bardou-Jacquet E
    Blood Cells Mol Dis; 2019 Feb; 74():30-33. PubMed ID: 30389309
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Homozygosity for a novel nonsense mutation (G66X) of the HJV gene causes severe juvenile hemochromatosis with fatal cardiomyopathy.
    Jánosi A; Andrikovics H; Vas K; Bors A; Hubay M; Sápi Z; Tordai A
    Blood; 2005 Jan; 105(1):432. PubMed ID: 15611318
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. [Juvenile haemochromatosis caused by a homozygous Gly320Val mutation in the haemojuvelin gene].
    Berg LB; Milman NT; Friis-Hansen L; Jensen PD; Fründ T
    Ugeskr Laeger; 2013 Apr; 175(16):1113-4. PubMed ID: 23651750
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Q312X mutation in the hemojuvelin gene is associated with cardiomyopathy due to juvenile haemochromatosis.
    Nagayoshi Y; Nakayama M; Suzuki S; Hokamaki J; Shimomura H; Tsujita K; Fukuda M; Yamashita T; Nakamura Y; Sugiyama S; Ogawa H
    Eur J Heart Fail; 2008 Oct; 10(10):1001-6. PubMed ID: 18725184
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.