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pro vyhledávání: '"F. R. Heller"'
An improved method for detection of low density lipoprotein receptor defects in human T lymphocytes.
Autor:
F R Verhoeye, O Descamps, B Husson, J C Hondekijn, M F Ronveaux-Dupal, J F Lontie, F R Heller
Publikováno v:
Journal of Lipid Research, Vol 37, Iss 6, Pp 1377-1384 (1996)
Familial hypercholesterolemia (FH) results from an inherited functional defect of the low density lipoprotein (LDL) receptor and is complicated by premature atherosclerosis. FH diagnosis is obtained by sophisticated techniques or is suggested by clin
Externí odkaz:
https://doaj.org/article/7ba5190b7dfb481b8562665a0e8cf015
Publikováno v:
European Journal of Clinical Investigation. 33:1-9
Background In the present study we assessed whether the presence of genetic mutations typical of familial hypercholesterolaemia (FH) was associated with greater atherosclerosis in the coronary vessels in patients with severe hypercholesterolaemia and
Impact of genetic defects on atherosclerosis in patients suspected of familial hypercholesterolaemia
Publikováno v:
European Journal of Clinical Investigation. 31:958-965
Background Among patients with severe hypercholesterolaemia and a family history of early cardiovascular disease, we assessed whether patients with mutations of low-density lipoprotein (LDL) receptor and apolipoprotein B genes related to familial hyp
Publikováno v:
Hepatology. 29:427-433
Out of a prospective series of 142 consecutive episodes of hypoxic (ischemic) hepatitis (HH), we identified 17 episodes associated with an acute exacerbation of chronic respiratory failure (CRF) without left cardiac failure. In the aim to evaluate th
Autor:
G. Kloppel, R. Abs, F. R. Heller, E. Reyniers, Michel Meurisse, K. De Boulle, P. J. Willems, Albert Beckers, Achille Stevenaert
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 79:1498-1502
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant inherited disorder characterized by nodular proliferation of the parathyroid glands and tumors of the anterior pituitary gland, the endocrine pancreas, and the neuroendocrine cell sy
Publikováno v:
Acta Clinica Belgica. 48:209-212
We report a case of association between genetic haemochromatosis and mixed gonadal dysgenesis. To our knowledge, this case is the first reported in the literature. We discuss the mechanisms of hypogonadism observed in this patient.
Publikováno v:
European Heart Journal. 13:569-573
A family with ‘syndrome myxoma’ is reported. In this very rare condition, myxoma can be associated with cutaneous lesions, extracardiac tumours and endocrine over-activity.
Autor:
F R Heller
Publikováno v:
Acta Clinica Belgica. 54:299-301
Studies in which hypolipidemic therapy were used for preventing cardiovascular diseases are analyzed on the basis of the number of patients to treat to avoid a clinical event, one of the most accepted evidence-based medicine criteria. The benefit of
Autor:
F R, Heller
Publikováno v:
Acta clinica Belgica. 63(2)
Publikováno v:
Medicine. 82(6)
The centrilobular liver cell necrosis observed in hypoxic hepatitis is generally attributed to failure of hepatic blood perfusion. Accordingly, this injury of the liver is commonly recognized under the terms "shock liver" or "ischemic hepatitis." Dur