Results 241 to 250 of about 15,219 (276)

Two-dimensional Strain Echocardiography in the Evaluation of Ventricular Function in Patients with Newly Diagnosed Hereditary Hemochromatosis

, 2019
Martín Aladio, Florencia Yamasato, Ariel K. Saad, Juan Sordá, Oscar Grosso, Esteban González Ballerga, Jorge Daruich, Sara Berensztein   +7 more
openalex   +1 more source

Expression of hemochromatosis in homozygous subjects. Implications for early diagnosis and prevention [PDF]

, 1990
Axelsen, E, Board, P G, Halliday, J W, Powell, L W, Summers, K M, Webb, S   +5 more
core  

2039 T2* CMR in hereditary hemochromatosis

Journal of Cardiovascular Magnetic Resonance, 2008
O'Hanlon Rory, Bucciarelli-Ducci Chiara, Anderson Lisa, Westwood Mark, Kirk Paul, Grasso Agata, Pennell Dudley   +6 more
doaj   +1 more source

Eicosanoids and Oxylipin Signature in Hereditary Hemochromatosis Patients Are Similar to Dysmetabolic Iron Overload Syndrome Patients but Are Impacted by Dietary Iron Absorption.

Ann Nutr Metab
Lobbes H, Dalle C, Pereira B, Ruivard M, Mazur A, Gladine C.   +5 more
europepmc   +1 more source

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Hereditary hemochromatosis

Seminars in Hematology, 2002
Hereditary hemochromatosis (hh, type 1 hemochromatosis) is an autosomal recessive trait characterized by hyperabsorption of dietary iron. The disease trait occurs in approximately five per thousand Caucasians of northern European descent. The causative gene, designated HFE, was isolated and characterized in 1996; most individuals with hh are homozygous
Richard S, Ajioka, James P, Kushner
openaire   +2 more sources

Hereditary hemochromatosis of tongue

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 2011
Hereditary hemochromatosis (HH) refers to several inherited disorders of iron metabolism leading to tissue iron overload. Classical HH is associated with mutations in HFE (C282Y homozygotes or C282Y/H63D compound heterozygotes) and is almost exclusively found in populations of northern European descent.
Sanjay Rastogi, Neha Verma, Hessa Al Wayli   +2 more
openaire   +3 more sources

Hereditary Hemochromatosis in Spain

Genetic Testing, 2000
The C282Y mutation of the HFE gene has been reported as the main cause of hereditary hemochromatosis (HH). Another missense mutation (H63D) has also been detected at an increased frequency in a compound heterozygote state with the C282Y mutation in HH patients.
Ysamar Barrio, Enrique Quintero, Rafael Oliva, Mayka Sanchez, Joan Rodés, Miquel Bruguera, Roberto Mazzara   +6 more
openaire   +3 more sources

Hereditary Hemochromatosis

2007
Iron is a major component of the Earth’s crust, but its own chemistry greatly limits utilization and also sets the basis for its toxicity. Hereditary hemochromatosis (HH) is the most common cause of iron overload in humans. For much of the twentieth century, HH was regarded as a monogenic disorder characterized by excess tissue deposits of iron ...
CORRADINI, Elena, FERRARA, Francesca, PIETRANGELO, Antonello   +2 more
openaire   +2 more sources