Zobrazeno 1 - 9
of 9
pro vyhledávání: '"C Th B M, van Deursen"'
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 161
Hepatopulmonary syndrome is a severe complication of liver disease, with greatly increased mortality. The syndrome is characterized by increased blood-flow, intrapulmonary vasodilatation and angiogenesis, leading to effects including the formation of
Publikováno v:
BMJ, 342, 218-223. British Medical Journal
Summary points Hereditary haemochromatosis is an autosomal recessive genetic disease in which increased intestinal absorption of iron causes accumulation in tissues, primarily the liver, sometimes leading to organ damage. Liver deposits may result in
Publikováno v:
Journal of Neurology. 257:1465-1472
Involvement of peripheral nerves and skeletal muscles has been reported in the course of hereditary haemochromatosis (HH) but a systematic study is lacking. However, patients with HH report symptoms suggesting a possible polyneuropathy or myopathy. I
Autor:
E M G, Jacobs, A L M, Verbeek, H G, Kreeftenberg, C Th B M, van Deursen, J J M, Marx, A F H, Stalenhoef, D W, Swinkels, R A, de Vries
Publikováno v:
The Netherlands journal of medicine. 65(11)
HFE-related hereditary haemochromatosis (HH) is an iron overload disease attributed to the highly prevalent homozygosity for the C282Y mutation in the HFE gene. The pathophysiology of this error in iron metabolism is not completely elucidated yet, al
Autor:
E M G, Jacobs, J C M, Hendriks, J J M, Marx, C Th B M, van Deursen, H G, Kreeftenberg, R A, de Vries, A F H, Stalenhoef, A L M, Verbeek, D W, Swinkels
Publikováno v:
The Netherlands journal of medicine. 65(11)
Family screening has been suggested as a sophisticated model for the early detection of HFE-related hereditary haemochromatosis (HH). However, until now, controlled studies on the morbidity and mortality in families with HH are lacking.Data on iron p
Autor:
G J M, Mostard, C Th B M, van Deursen
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 146(5)
In a 53-year-old woman with abdominal pain, nausea and vomitus lasting for a month and leading to weight loss, abdominal CT showed abdominal spigelian hernia.
Publikováno v:
Acta obstetricia et gynecologica Scandinavica. 60(4)
Uterine inversion is a rare condition that occurs in various degrees. Predisposing and etiologic factors are discussed, as are therapy and prophylaxis. These points are illustrated by 4 own cases and by 172 cases collected from literature.
Publikováno v:
Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie. 27(6)
Summary: Results are presented from the determination of tissue iron and ferritin in 15 pathological livers (6with steatosis, 8 with fibrosis/cirrhosis and l with haemochromatosis). The histological assessment accordingto the Rowe System, after Perls