Showing results (2071-2080 of 4,518) with videos related to
Sort By:
Pageof 452
Journal of Internal Medicine|April 1, 1997
Familial amyloidosis in one Chinese family: clinical, immunological, and molecular genetic analysisC T Chou, C C Lee, D M Chang, et al.Journal of Internal Medicine|November 3, 1998
The lymphocytic alveolitis in sarcoidosis is associated with increased amounts of soluble and cell-bound adhesion molecules in bronchoalveolar lavage fluid and serumM Berlin, J Lundahl, C M Sköld, et al.Journal of Internal Medicine|August 1, 1993
Efficacy of subcutaneous sumatriptan in the acute treatment of early-morning migraine: a placebo-controlled trial. Early-Morning Migraine Sumatriptan Study GroupM G Bousser, H D'Allens, A RichardJournal of Internal Medicine|February 1, 1997
The treatment of oesophageal varices: a debate and a discussionH O Conn, D Lebrec, J TerblancheJournal of Internal Medicine|February 1, 1997
Pitfalls in the diagnosis of hypereosinophilic syndrome: a report of two casesA S De Vriese, J C Kips, D P Vogelaers, et al.Journal of Internal Medicine|September 1, 1996
Population-based erythrocyte sedimentation rates in 3910 subjectively healthy Norwegian adults. A statistical study based on men and women from the Oslo areaP Wetteland, M Røger, H E Solberg, et al.Journal of Internal Medicine|September 1, 1996
Rising erythrocyte sedimentation rate during several years before diagnosis can be a predictive factor in 70% of renal cell carcinoma patients. The benefit of knowing subject-based reference valuesO H Iversen, M Røger, H E Solberg, et al.Journal of Internal Medicine|September 1, 1996
Exploring the declining case fatality in acute stroke. Population-based observations in the northern Sweden MONICA ProjectB Stegmayr, K AsplundJournal of Internal Medicine|September 1, 1996
Glomerular lipid deposition and proteinuria in a patient with familial dysbetalipoproteinaemiaK R Balson, J F Niall, J D BestJournal of Internal Medicine|March 1, 1997
Abnormal ambulatory electrocardiographic findings in patients with the Marfan syndromeA Savolainen, M Kupari, L Toivonen, et al.Pageof 452