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A pathological study of idiopathic haemochromatosis and its relationship to siderosis in liver cirrhosis. 1973

R Sinniah

UI MeSH Term Description Entries
D008103 Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. Cirrhosis, Liver,Fibrosis, Liver,Hepatic Cirrhosis,Liver Fibrosis,Cirrhosis, Hepatic
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D010182 Pancreatic Diseases Pathological processes of the PANCREAS. Disease, Pancreatic,Diseases, Pancreatic,Pancreatic Disease
D005260 Female Females
D006432 Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) Diabetes, Bronze,Bronze Diabetes,Bronzed Cirrhosis,Familial Hemochromatosis,Genetic Hemochromatosis,Haemochromatosis,Hemochromatoses,Iron Storage Disorder,Pigmentary Cirrhosis,Primary Hemochromatosis,Troisier-Hanot-Chauffard Syndrome,Von Recklenhausen-Applebaum Disease,Bronzed Cirrhoses,Cirrhoses, Bronzed,Cirrhoses, Pigmentary,Cirrhosis, Bronzed,Cirrhosis, Pigmentary,Disease, Von Recklenhausen-Applebaum,Diseases, Von Recklenhausen-Applebaum,Disorder, Iron Storage,Disorders, Iron Storage,Familial Hemochromatoses,Genetic Hemochromatoses,Haemochromatoses,Hemochromatose,Hemochromatoses, Familial,Hemochromatoses, Genetic,Hemochromatosis, Familial,Hemochromatosis, Genetic,Iron Storage Disorders,Pigmentary Cirrhoses,Recklenhausen-Applebaum Disease, Von,Recklenhausen-Applebaum Diseases, Von,Storage Disorder, Iron,Storage Disorders, Iron,Syndrome, Troisier-Hanot-Chauffard,Syndromes, Troisier-Hanot-Chauffard,Troisier Hanot Chauffard Syndrome,Troisier-Hanot-Chauffard Syndromes,Von Recklenhausen Applebaum Disease,Von Recklenhausen-Applebaum Diseases
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D012806 Siderosis A form of pneumoconiosis resulting from inhalation of iron in the mining dust or welding fumes. Sideroses

Related Publications

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Cirrhosis with secondary siderosis or primary haemochromatosis.
December 1967, Proceedings of the Royal Society of Medicine,
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Carbohydrate intolerance in idiopathic haemochromatosis and cirrhosis of the liver.
October 1973, The Quarterly journal of medicine,
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Pituitary function in idiopathic haemochromatosis and cirrhosis of the liver.
August 1972, Lancet (London, England),
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[Liver cirrhosis with siderosis].
February 1970, Revista clinica espanola,
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HAEMOCHROMATOSIS and transfusional siderosis.
November 1957, Lancet (London, England),
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Haemochromatosis African nutritional siderosis and experimental siderosis in animals.
July 1957, Lancet (London, England),
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[Relationship between hepatocellular carcinoma, liver cirrhosis and hepatitis B: a pathological study].
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[Liver cirrhosis with siderosis. II].
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The relationship of transfusional haemosiderosis to idiopathic haemochromatosis.
June 1953, South African journal of clinical science. Suid-Afrikaanse tydskrif vir kliniese wetenskap,
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Patterns of pathological iron storage. I. The nature and significance of transfusional siderosis and its relationship to idiopathic hemochromatosis and allied conditions.
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