Results 81 to 90 of about 3,374,032 (169)
Clinical and Experimental Obstetrics & Gynecology, 2020 Introduction: Iron deficiency anemia (IDA) is the most common form of anemia. Women who are pregnant or lactating and young children are the most affected.
A. Daniilidis +5 more
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Терапевтический архив, 2011 Aim. To estimate incidence of carriage of genetic polymorphisms coding hemostasis protein synthesis in patients with venous thromboembolic complications (VTEC) and healthy subjects in Moscow population; to detect VTEC genetic prognostic factors among the
Natal'ya Mikhaylovna Vorob'eva +11 more
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, 2000 The association of cirrhosis with diabetes mellitus and bronze skin pigmentation was first recognized more than a century ago, when the term hemochromatosis (HC) was given to the condition. Hereditary hemochromatosis, also previously described as genetic
Powell, Lawrie W. +4 more
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Protein-RNA interactions: a structural analysis [PDF]
, 2001 A detailed computational analysis of 32 protein-RNA complexes is presented. A number of physical and chemical properties of the intermolecular interfaces are calculated and compared with those observed in protein-double-stranded DNA and protein-single ...
Daley, DT +9 more
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Diabetes in HFE Hemochromatosis [PDF]
, 2017 Diabetes in whites of European descent with hemochromatosis was first attributed to pancreatic siderosis. Later observations revealed that the pathogenesis of diabetes in HFE hemochromatosis is multifactorial and its clinical manifestations are ...
Ronald T. Acton, James C. Barton
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Scientific Reports, 2018 Iron is a crucial micronutrient for both mammals and their associated pathogens, and extensive literature has shown that Mycobacterium tuberculosis (Mtb) bacilli inhibited from acquiring iron from the host are severely attenuated.
Rodrigo Abreu +4 more
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Biological Research, 2006 Hereditary hemochromatosis (HH) is the most common inherited disorder in people of Northern European descent. Over 83% of the cases of HH result from a single mutation of a Cys to Tyr in the HH protein, HFE.
CAROLINE A ENNS
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ER Stress and Iron Homeostasis: A New Frontier for the UPR
Biochemistry Research International, 2011 The C282Y mutation of HFE accounts for the majority of cases of the iron overload disease Hereditary Hemochromatosis (HH). The conformational changes introduced by this mutation impair the HFE association with β2-microglobulin
Susana J. Oliveira +2 more
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, 2023 Hemokromatoza je bolest obilježena pretjeranim nakupljanjem željeza u parenhimskim organima s posljedičnim oštećenjem tih organa. Primarna (hereditarna) hemokromatoza je najčešća metabolička genetska bolest u Europi.
Jankov, Katja
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Hemochromatosis: an endocrine liver disease.
, 2007 This review acknowledges the recent and dramatic advancement in the field of hemochromatosis and highlights the surprising analogies with a prototypic endocrine disease, diabetes. The term hemochromatosis should refer to a unique clinicopathologic subset
PIETRANGELO, Antonello
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