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 *

158 related articles for article (PubMed ID: 23651750)

  • 1. [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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. [Genetic iron overloads and hepatic insulin-resistance iron overload syndrome: an update].
    Ruivard M
    Rev Med Interne; 2009 Jan; 30(1):35-42. PubMed ID: 18584923
    [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. 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]  

  • 8. [Diagnosis and treatment of primary hemochromatosis].
    Swinkels DW; Marx JJ
    Ned Tijdschr Geneeskd; 1999 Jul; 143(27):1404-8. PubMed ID: 10422553
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Diagnosis of 5 patients with possible primary hemochromatosis].
    Jacobs EM; de Vries RA; Elving LD; Stalenhoef AF; Swinkels DW
    Ned Tijdschr Geneeskd; 2003 Apr; 147(14):666-70. PubMed ID: 12712652
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Diagnosis and management of genetic haemochromatosis.
    Dooley JS
    Best Pract Res Clin Haematol; 2002 Jun; 15(2):277-93. PubMed ID: 12401308
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Causes of iron overload in blood donors - a clinical study.
    Laursen AH; Bjerrum OW; Friis-Hansen L; Hansen TO; Marott JL; Magnussen K
    Vox Sang; 2018 Feb; 113(2):110-119. PubMed ID: 29230833
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group.
    Corti P; Ferrari GM; Faraguna MC; Capitoli G; Longo F; Corradini E; Casini T; Boscarol G; Pinto VM; Ghilardi R; Russo G; Colombatti R; Mariani R; Piperno A
    Br J Haematol; 2024 Jan; 204(1):306-314. PubMed ID: 37990447
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Hemochromatosis--from an underdiagnosed curiosity to a common disease].
    Hagve TA; Asberg A; Ulvik R; Borch-Iohnsen B; Thorstensen K
    Tidsskr Nor Laegeforen; 2009 Apr; 129(9):863-6. PubMed ID: 19415085
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary haemochromatosis: detection and management.
    Vautier G; Murray M; Olynyk JK
    Med J Aust; 2001 Oct; 175(8):418-21. PubMed ID: 11700835
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Clinical evaluation of a hemochromatosis next-generation sequencing gene panel.
    Lanktree MB; Sadikovic B; Waye JS; Levstik A; Lanktree BB; Yudin J; Crowther MA; Pare G; Adams PC
    Eur J Haematol; 2017 Mar; 98(3):228-234. PubMed ID: 27753142
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical expression of haemochromatosis in Irish C282Y homozygotes identified through family screening.
    Gleeson F; Ryan E; Barrett S; Crowe J
    Eur J Gastroenterol Hepatol; 2004 Sep; 16(9):859-63. PubMed ID: 15316409
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.
    Wrede CE; Hutzler S; Bollheimer LC; Buettner R; Hellerbrand C; Schöelmerich J; Palitzsch KD
    Isr Med Assoc J; 2004 Jan; 6(1):30-3. PubMed ID: 14740507
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.