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 *

176 related articles for article (PubMed ID: 30130274)

  • 1. Ferroportin Disease Caused by a Heterozygous Variant p.Cys326Phe in the SLC40A1 Gene and the Efficacy of Therapeutic Phlebotomy in Children.
    Shimura M; Nishimata S; Saito N; Tsutsumi N; Suzuki S; Morishima Y; Kashiwagi Y; Numabe H; Kawashima H
    J Pediatr Hematol Oncol; 2019 Jul; 41(5):e325-e328. PubMed ID: 30130274
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Long-term phlebotomy successfully alleviated hepatic iron accumulation in a ferroportin disease patient with a mutation in SLC40A1: a case report.
    Nishina S; Tomiyama Y; Ikuta K; Tatsumi Y; Toki Y; Kato A; Kato K; Yoshioka N; Sasaki K; Hara Y; Hino K
    BMC Gastroenterol; 2021 Mar; 21(1):111. PubMed ID: 33673803
    [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. 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]  

  • 5. SLC40A1 c.1402G-->a results in aberrant splicing, ferroportin truncation after glycine 330, and an autosomal dominant hemochromatosis phenotype.
    Lee PL; Gelbart T; West C; Barton JC
    Acta Haematol; 2007; 118(4):237-41. PubMed ID: 18160816
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case report of hereditary hemochromatosis caused by mutation of SLC40A1 gene.
    Yin X; Zhang Y; Gao H; Jin QL; Wen XY
    Medicine (Baltimore); 2019 Nov; 98(44):e17526. PubMed ID: 31689754
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.
    Del-Castillo-Rueda A; Moreno-Carralero MI; Cuadrado-Grande N; Alvarez-Sala-Walther LA; Enríquez-de-Salamanca R; Méndez M; Morán-Jiménez MJ
    Gene; 2012 Oct; 508(1):15-20. PubMed ID: 22890139
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Iron chelators reverse organ damage in type 4B hereditary hemochromatosis: Case reports.
    Wu LY; Song ZY; Li QH; Mou LJ; Yu YY; Shen SS; Song XX
    Medicine (Baltimore); 2021 Apr; 100(13):e25258. PubMed ID: 33787609
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Two novel mutations in the SLC40A1 and HFE genes implicated in iron overload in a Spanish man.
    Del-Castillo-Rueda A; Moreno-Carralero MI; Alvarez-Sala-Walther LA; Cuadrado-Grande N; Enríquez-de-Salamanca R; Méndez M; Morán-Jiménez MJ
    Eur J Haematol; 2011 Mar; 86(3):260-4. PubMed ID: 21175851
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnosis and management of hereditary hemochromatosis.
    Salgia RJ; Brown K
    Clin Liver Dis; 2015 Feb; 19(1):187-98. PubMed ID: 25454304
    [TBL] [Abstract][Full Text] [Related]  

  • 14. SLC40A1-related hemochromatosis associated with a p.Y333H mutation in mainland China: a pedigree report and literature review.
    Li Y; Duan F; Yang S
    BMC Med Genomics; 2024 Jun; 17(1):161. PubMed ID: 38886778
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Management of iron overload during pregnancy and childbirth in a patient with ferroportin disease].
    Ohara K; Tsuge N; Watanabe S; Eda H; Ogasawara F; Kondo T; Yoshida S; Kojima K
    Rinsho Ketsueki; 2023; 64(11):1410-1414. PubMed ID: 38072426
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Haemochromatosis.
    Brissot P; Pietrangelo A; Adams PC; de Graaff B; McLaren CE; Loréal O
    Nat Rev Dis Primers; 2018 Apr; 4():18016. PubMed ID: 29620054
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Monitoring of hepcidin levels in a patient with G80S-linked ferroportin disease undergoing iron depletion by phlebotomy.
    Wolff F; Bailly B; Gulbis B; Cotton F
    Clin Chim Acta; 2014 Mar; 430():20-1. PubMed ID: 24370385
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.