Zobrazeno 1 - 10
of 51
pro vyhledávání: '"J F, De Plaen"'
Publikováno v:
Journal of Internal Medicine. 255:130-136
We report the history of a patient and his daughter, both affected with hypoplasia of the abdominal aorta and its branches, leading to early and dramatic complications. In the index patient, renal ischaemia as a result of severe hypoplasia of the abd
Publikováno v:
Journal of Internal Medicine. 246:113-116
Head and neck paraganglioma is a rare tumour, especially in its familial form. We report a case of a multifocal head and neck paraganglioma in a young man with a family history of cervical tumours. At the age of 24, exploration of a left cervical swe
Publikováno v:
Clinical Rheumatology. 15:174-180
Diffuse arterial involvement in giant cell arteritis (GCA) is well recognized. By contrast, GCA clinically isolated to large vessels without cephalic, rheumatologic or systemic symptoms represents a much rarer manifestation of the disease. We report
Autor:
A Amery, N. D. Pandita-Gunawardena, A. Hickey, G. Donnarel, L. Thijs, M. Escande, Xavier Girerd, D. G. Beevers, J. F. De Plaen, Françoise Forette, J.A. Staessen, T. Strasser, I. Perilliat, M. Ruilope, J Cox, P. W. De Leeuw, L. Terzoli, R. H. Fagard, D. Slovick, P. Bert, R. J. Webster, R. Varis, Denis Clement
Publikováno v:
Aging Clinical and Experimental Research. 3:373-382
Vascular dementia (VD) is the second most common cause of dementia in the elderly after Alzheimer’s disease (AD). Prevalence estimates from community surveys indicate that, on average, 5% of persons over 65 and 15 to 20% of people over 80 suffer fr
Publikováno v:
Journal of internal medicine. 241(1)
Publikováno v:
The American journal of the medical sciences. 312(3)
The combination of hypertension, hypokaliemia, and male pseudohermaphroditism or amenorrhea must prompt a search for a rare adrenal enzymatic defect, 17 alpha-hydroxylase/17,20-lyase deficiency. This is a report of the observation of a male patient i
Publikováno v:
Annales d'endocrinologie. 56(2)
The glucocorticoid suppressible hyperaldosteronism (GSH) is a rare form of systemic hypertension. We report a family--a father and his two children--with this disease. GSH represents a peculiar form of primary hyperaldosteronism, with usually an abse
Publikováno v:
Nephrologie. 14(3)
Renal infarction can be complicated by arterial hypertension, which is sometimes severe and may present as hypertensive encephalopathy and epilepsy. We report such a case in whom angiographic studies revealed a stenosis of the left renal artery and a
Publikováno v:
Bulletin de la Societe belge d'ophtalmologie. 250
Publikováno v:
Nephrologie. 14(2)