نتایج جستجو برای: hemochromatosis

تعداد نتایج: 2753  

Journal: :Gastroenterology 1980

Journal: :Journal of General Internal Medicine 1989

Journal: :Arthritis & Rheumatism 1964

Journal: :Clinical chemistry 2003
Séverine Fruchon Mounia Bensaid Nicolas Borot Marie-Paule Roth Hélène Coppin

2011
Yadollah Zahedpasha

A case of neonatal hemochromatosis is reported in a premature 35-week infant who presented at birth with coffee ground vomiting and gradual appearance of grayish icter and colorless stool. Neonatal hemochromatosis was confirmed by elevated ferritin levels and extrahepatic siderosis detected in liver biopsy.

Journal: :Canadian Journal of Gastroenterology 1990

2017
Maciej Szemraj Katarzyna Oszajca Janusz Szemraj Piotr Jurowski

BACKGROUND Congenital hemochromatosis is a disorder caused by mutations of genes involved in iron metabolism, leading to increased levels of iron concentration in tissues and serum. High concentrations of iron can lead to the development of AMD. The aim of this study was to analyze circulating miRNAs in the serum of congenital hemochromatosis patients with AMD and their correlation with the exp...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
S P Hussain K Raja P A Amstad M Sawyer L J Trudel G N Wogan L J Hofseth P G Shields T R Billiar C Trautwein T Hohler P R Galle D H Phillips R Markin A J Marrogi C C Harris

Hemochromatosis and Wilson disease (WD), characterized by the excess hepatic deposition of iron and copper, respectively, produce oxidative stress and increase the risk of liver cancer. Because the frequency of p53 mutated alleles in nontumorous human tissue may be a biomarker of oxyradical damage and identify individuals at increased cancer risk, we have determined the frequency of p53 mutated...

Journal: :Blood 2005
Pierre-Alexandre Krayenbuehl Thomas Walczyk Ronny Schoenberg Friedhelm von Blanckenburg Georg Schulthess

It has recently been shown that the iron isotopic composition of blood differs between individuals and sexes, which is supposed to reflect individual differences in iron metabolism. We hypothesized that patients suffering from hereditary hemochromatosis would demonstrate alterations in the iron isotopic composition of blood due to persistent up-regulation of intestinal iron absorption. Blood fr...

2005
LEON M. PTASZEK ERIK T. PRICE MARY Y. HU PHILLIP C. YANG

The hallmark of hemochromatosis is the deposition of iron in multiple tissue types, most notably the skin, liver, pancreas, thyroid, and heart. Definitive diagnosis of iron deposition generally requires invasive methods, such as direct tissue biopsy. We describe a 40 year-old woman with end-stage liver disease secondary to hereditary hemochromatosis and alcohol abuse, who was referred to the ca...

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