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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

310 related items for PubMed ID: 31054269

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Liver transplantation normalizes serum hepcidin level and cures iron metabolism alterations in HFE hemochromatosis.
    Bardou-Jacquet E, Philip J, Lorho R, Ropert M, Latournerie M, Houssel-Debry P, Guyader D, Loréal O, Boudjema K, Brissot P.
    Hepatology; 2014 Mar; 59(3):839-47. PubMed ID: 23775519
    [Abstract] [Full Text] [Related]

  • 26. Synopsis of the Dutch multidisciplinary guideline for the diagnosis and treatment of hereditary haemochromatosis.
    Swinkels DW, Jorna AT, Raymakers RA.
    Neth J Med; 2007 Dec; 65(11):452-5. PubMed ID: 18079569
    [Abstract] [Full Text] [Related]

  • 27. Hemochromatosis: pathophysiology, evaluation, and management of hepatic iron overload with a focus on MRI.
    Golfeyz S, Lewis S, Weisberg IS.
    Expert Rev Gastroenterol Hepatol; 2018 Aug; 12(8):767-778. PubMed ID: 29966105
    [Abstract] [Full Text] [Related]

  • 28. Pulmonary Haemosiderosis Secondary to Hereditary Haemochromatosis; a Case Report.
    Jehangir W, Karabachev AD, Umyarova ER.
    J Cancer Allied Spec; 2020 Aug; 6(1):e281. PubMed ID: 37197141
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Iron overload and HFE gene mutations in Polish patients with liver cirrhosis.
    Sikorska K, Romanowski T, Stalke P, Iżycka-Świeszewska E, Bielawski KP.
    Hepatobiliary Pancreat Dis Int; 2011 Jun; 10(3):270-5. PubMed ID: 21669570
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Hereditary Hemochromatosis: Rapid Evidence Review.
    Kane SF, Roberts C, Paulus R.
    Am Fam Physician; 2021 Sep 01; 104(3):263-270. PubMed ID: 34523883
    [Abstract] [Full Text] [Related]

  • 36. Diagnostic difficulties of primary hemochromatosis in a patient with posthemorrhagic anemia.
    Podzolkov VI, Pokrovskaya AE, Vargina TS, Oganesyan KA.
    Ter Arkh; 2019 May 16; 91(4):118-121. PubMed ID: 31094485
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Hereditary hemochromatosis: laboratory evaluation.
    Moyer TP, Highsmith WE, Smyrk TC, Gross JB.
    Clin Chim Acta; 2011 Aug 17; 412(17-18):1485-92. PubMed ID: 21510925
    [Abstract] [Full Text] [Related]

  • 39. [Iron overload disease: recent findings].
    Licata A, Brucato V, Di Marco V, Barbaria F, Craxì A.
    Ann Ital Med Int; 2004 Aug 17; 19(3):145-54. PubMed ID: 15529941
    [Abstract] [Full Text] [Related]

  • 40. Juvenile haemochromatosis.
    Griffiths WJH, Besser M, Bowden DJ, Kelly DA.
    Lancet Child Adolesc Health; 2021 Jul 17; 5(7):524-530. PubMed ID: 33861982
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 16.