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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 27667161)

  • 1. Next-generation sequencing of hereditary hemochromatosis-related genes: Novel likely pathogenic variants found in the Portuguese population.
    Faria R; Silva B; Silva C; Loureiro P; Queiroz A; Fraga S; Esteves J; Mendes D; Fleming R; Vieira L; Gonçalves J; Faustino P
    Blood Cells Mol Dis; 2016 Oct; 61():10-5. PubMed ID: 27667161
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes.
    Radio FC; Majore S; Aurizi C; Sorge F; Biolcati G; Bernabini S; Giotti I; Torricelli F; Giannarelli D; De Bernardo C; Grammatico P
    Blood Cells Mol Dis; 2015 Jun; 55(1):71-5. PubMed ID: 25976471
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.
    Wallace DF; Subramaniam VN
    Genet Med; 2016 Jun; 18(6):618-26. PubMed ID: 26633544
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 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. 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]  

  • 10. TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy.
    Radio FC; Majore S; Binni F; Valiante M; Ricerca BM; De Bernardo C; Morrone A; Grammatico P
    Blood Cells Mol Dis; 2014; 52(2-3):83-7. PubMed ID: 24055163
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. MRI-Based Iron Phenotyping and Patient Selection for Next-Generation Sequencing of Non-Homeostatic Iron Regulator Hemochromatosis Genes.
    Viveiros A; Schaefer B; Panzer M; Henninger B; Plaikner M; Kremser C; Franke A; Franzenburg S; Hoeppner MP; Stauder R; Janecke A; Tilg H; Zoller H
    Hepatology; 2021 Nov; 74(5):2424-2435. PubMed ID: 34048062
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of Genes for Hereditary Hemochromatosis.
    Gerhard GS; Paynton BV; DiStefano JK
    Methods Mol Biol; 2018; 1706():353-365. PubMed ID: 29423808
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants.
    Barton JC; Lafreniere SA; Leiendecker-Foster C; Li H; Acton RT; Press RD; Eckfeldt JH
    Am J Hematol; 2009 Nov; 84(11):710-4. PubMed ID: 19787796
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of Novel Mutations by Targeted NGS Panel in Patients with Hyperferritinemia.
    Ravasi G; Pelucchi S; Bertola F; Capelletti MM; Mariani R; Piperno A
    Genes (Basel); 2021 Nov; 12(11):. PubMed ID: 34828384
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P; Esculié-Coste C; Bismuth M; Giansily-Blaizot M; Larrey D; Schved JF
    Blood Cells Mol Dis; 2001; 27(1):290-3. PubMed ID: 11358390
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Non-HFE hemochromatosis.
    Pietrangelo A
    Semin Liver Dis; 2005 Nov; 25(4):450-60. PubMed ID: 16315138
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New Mutations in
    Hernández G; Ferrer-Cortès X; Venturi V; Musri M; Pilquil MF; Torres PMM; Rodríguez IH; Mínguez MÀR; Kelleher NJ; Pelucchi S; Piperno A; Alberca EP; Ricós GG; Giró EC; Pérez-Montero S; Tornador C; Villà-Freixa J; Sánchez M
    Genes (Basel); 2021 Dec; 12(12):. PubMed ID: 34946929
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.