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 *

121 related articles for article (PubMed ID: 25441019)

  • 1. [Usefulness of a diagnostic algorithm hyperferritinemia: A case report of a Spanish family with hereditary hemochromatosis and mutation in SLC40A1 gene].
    Vargas JA; Muñoz A; Samper B; Bornstein B
    Med Clin (Barc); 2015 Jul; 145(1):42-3. PubMed ID: 25441019
    [No Abstract]   [Full Text] [Related]  

  • 2. Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV.
    Speletas M; Kioumi A; Loules G; Hytiroglou P; Tsitouridis J; Christakis J; Germenis AE
    Blood Cells Mol Dis; 2008; 40(3):353-9. PubMed ID: 17997113
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Type 4B hereditary hemochromatosis due to heterozygous p.D157A mutation in SLC40A1 complicated with hypopituitarism.
    Honma Y; Karasuyama T; Kumamoto K; Shimajiri S; Toki Y; Tatsumi Y; Sumida K; Koikawa K; Morino K; Oe S; Miyagawa K; Yamasaki M; Shibata M; Abe S; Ikuta K; Hayashi H; Harada M
    Med Mol Morphol; 2021 Mar; 54(1):60-67. PubMed ID: 32607777
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron.
    Koyama C; Wakusawa S; Hayashi H; Ueno T; Suzuki R; Yano M; Saito H; Okazaki T
    Intern Med; 2005 Sep; 44(9):990-3. PubMed ID: 16258219
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel gain of function mutation in the SLC40A1 gene associated with hereditary haemochromatosis type 4.
    Chen SR; Yang LQ; Chong YT; Jie YS; Wu YK; Yang J; Lin GL; Li XH
    Intern Med J; 2015 Jun; 45(6):672-6. PubMed ID: 26059880
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pediatric Ferroportin Disease.
    Galicia-Poblet G; Cid-París E; López-Andrés N; Losada-Pajares A; Jurado-López JC; Moreno-Carralero MI; Morán-Jiménez MJ
    J Pediatr Gastroenterol Nutr; 2016 Dec; 63(6):e205-e207. PubMed ID: 25742196
    [No Abstract]   [Full Text] [Related]  

  • 7. Identification of mutations in SLC40A1 that affect ferroportin function and phenotype of human ferroportin iron overload.
    Mayr R; Griffiths WJ; Hermann M; McFarlane I; Halsall DJ; Finkenstedt A; Douds A; Davies SE; Janecke AR; Vogel W; Cox TM; Zoller H
    Gastroenterology; 2011 Jun; 140(7):2056-63, 2063.e1. PubMed ID: 21396368
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Type 4B hereditary hemochromatosis associated with a novel mutation in the SLC40A1 gene: A case report and a review of the literature.
    Zhang W; Lv T; Huang J; Ou X
    Medicine (Baltimore); 2017 Sep; 96(38):e8064. PubMed ID: 28930842
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel missense mutation c.470 A>C (p.D157A) in the SLC40A1 gene as a cause of ferroportin disease in a family with hyperferritinaemia.
    Saja K; Bignell P; Robson K; Provan D
    Br J Haematol; 2010 Jun; 149(6):914-6. PubMed ID: 20230395
    [No Abstract]   [Full Text] [Related]  

  • 10. G80S-linked ferroportin disease: the first clinical description in a Greek family.
    Mougiou A; Pietrangelo A; Caleffi A; Kourakli A; Karakantza M; Zoumbos N
    Blood Cells Mol Dis; 2008; 41(1):138-9. PubMed ID: 18420432
    [No Abstract]   [Full Text] [Related]  

  • 11. A Novel Phenotype of a Hereditary Hemochromatosis Type 4 with Ferroportin-1 Mutation, Presenting with Juvenile Cataracts.
    Yamakawa N; Oe K; Yukawa N; Murakami K; Nakashima R; Imura Y; Yoshifuji H; Ohmura K; Miura Y; Tomosugi N; Kawabata H; Takaori-Kondo A; Mimori T
    Intern Med; 2016; 55(18):2697-701. PubMed ID: 27629970
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ferroportin disease: A novel SLC40A1 mutation.
    Ravasi G; Pelucchi S; Russo A; Mariani R; Piperno A
    Dig Liver Dis; 2020 Jun; 52(6):688-690. PubMed ID: 32360131
    [No Abstract]   [Full Text] [Related]  

  • 13. Identification of hereditary hemochromatosis pedigrees and a novel SLC40A1 mutation in Chinese population.
    An P; Jiang L; Guan Y; Wang H; Wang J; Tian Y; Yang W; Shi Y; Xue J; Min J; Wang F
    Blood Cells Mol Dis; 2017 Mar; 63():34-36. PubMed ID: 28110135
    [No Abstract]   [Full Text] [Related]  

  • 14. Characterization of three novel pathogenic SLC40A1 mutations and genotype/phenotype correlations in 7 Italian families with type 4 hereditary hemochromatosis.
    Majore S; Bonaccorsi di Patti MC; Valiante M; Polticelli F; Cortese A; Di Bartolomeo S; De Bernardo C; De Muro M; Faienza F; Radio FC; Grammatico P; Musci G
    Biochim Biophys Acta Mol Basis Dis; 2018 Feb; 1864(2):464-470. PubMed ID: 29154924
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of HFE mutations and non-HFE gene mutations (TFR2 and SLC40A1) in patients with phenotypic hemochromatosis from the Basque Country.
    Castiella A; Zapata E; De Juan MD; Zubiaurre L; Iribarren A; Otazua P; Fernandez J; Aragón L; Zuriarrain O; Gorostidi A
    Int J Lab Hematol; 2016 Feb; 38(1):e5-7. PubMed ID: 26547814
    [No Abstract]   [Full Text] [Related]  

  • 16. Clinical presentation and molecular pathophysiology of autosomal dominant hemochromatosis caused by a novel ferroportin mutation.
    Griffiths WJ; Mayr R; McFarlane I; Hermann M; Halsall DJ; Zoller H; Cox TM
    Hepatology; 2010 Mar; 51(3):788-95. PubMed ID: 19937651
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel ferroportin mutation in a Canadian family with autosomal dominant hemochromatosis.
    Morris TJ; Litvinova MM; Ralston D; Mattman A; Holmes D; Lockitch G
    Blood Cells Mol Dis; 2005; 35(3):309-14. PubMed ID: 16111902
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin.
    Lee PL; Gelbart T; West C; Halloran C; Felitti V; Beutler E
    Blood Cells Mol Dis; 2001; 27(5):783-802. PubMed ID: 11783942
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.
    Njajou OT; Vaessen N; Joosse M; Berghuis B; van Dongen JW; Breuning MH; Snijders PJ; Rutten WP; Sandkuijl LA; Oostra BA; van Duijn CM; Heutink P
    Nat Genet; 2001 Jul; 28(3):213-4. PubMed ID: 11431687
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Hereditary hemochromatosis].
    Tokarev IuN; Settarova DA
    Klin Med (Mosk); 1988 Mar; 66(3):136-42. PubMed ID: 3292825
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.