Results 101 to 110 of about 3,374,032 (169)

An unfortunate case of acquired hemochromatosis: a case report review of the clinical presentation, diagnosis, management, and prognosis

, 2016
Anam Tariq,1 Kevin Westra,2 Arben Santo3 1Department of Internal Medicine, Pinnacle Health Internal Medicine, 2Department of Gastroenterology, Harrisburg Gastroenterology, Harrisburg, PA, 3Department of Pathology, Virginia College of Osteopathic Medicine-
Santo A, Tariq A, Westra K
core  

Hereditary hemochromatosis: recent advances in molecular genetics and clinical management

Haematologica, 1997
BACKGROUND AND OBJECTIVE: Hereditary hemochromatosis (HC) is an inborn error of iron metabolism leading to increased intestinal iron absorption and progressive iron overload.
C Camaschella, A Piperno
doaj  

Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload

Haematologica, 2000
BACKGROUND AND OBJECTIVES: Hereditary hemochromatosis (HHC) is a common, recessively inherited, genetic disorder associated with an abnormality of the HFE gene.
E Vercesi, P Cerani, V Rolandi, A Rovati, G Bergamaschi   +4 more
doaj  

A rare large homozygous deletion of the HFE gene in a patient with hemochromatosis: a case report. [PDF]

Hematol Transfus Cell Ther
Gasimli R, Solmaz S, Subasioglu A.
europepmc   +1 more source

Cuproptosis in iron overload hepatocytes. [PDF]

Cell Death Dis
Sailer J, Gottal J, Kaub L, Jauch AT, Engler J, Eberhagen C, von Toerne C, Hansen-Palmus L, Wachinger V, Akdogan B, Engelhardt S, Knolle P, DiSpirito AA, Protzer U, Vujić Spasić M, Zischka H.   +15 more
europepmc   +1 more source

Serum IgA and IgM levels in hemochromatosis probands with HFE p.C282Y homozygosity. [PDF]

PLoS One
Barton JC, Barton JC, Bertoli LF, Acton RT.   +3 more
europepmc   +1 more source

Paroxysmal atrial fibrillation and hemochromatosis: A narrative review

Paroxysmal atrial fibrillation (PAF) and hemochromatosis have a complex relationship. This review explores its mechanisms, prevalence, correlations, and clinical manifestations.
Fakhor, Hajar, Rathi, Sushma, Ram, Nanik, Kumari, Komal, Attia, Nada M, Sidhu, Harmandeep K, Muzaffar, Momil, Wajid, Muhammad H, Majumder, Koushik, Ahmed, Gulzar   +9 more
core   +1 more source

One Clinical Picture, Two Clinical Entities: A Case Report and Literature Review of Neurofibromatosis and Hemochromatosis. [PDF]

Children (Basel)
Melit LE, Borka Balas R, Tripon F, Prisca RA, Toth T, Stangaciu A, Najjar K.   +6 more
europepmc   +1 more source

Homozygous TFR2 (c.2093_2096del) Mutation in an Asymptomatic Patient With Type 3 Hereditary Hemochromatosis, First Report From Saudi Arabia. [PDF]

Clin Case Rep
Raslan OM, Alamoudi DS.
europepmc   +1 more source

A Rare Case of Possible Iron Overload and B12 Deficiency in Autoimmune Polyglandular Syndrome Type 3B. [PDF]

Cureus
Kyan K, Kumar R, Craig D.
europepmc   +1 more source