Titlebook: O-(β-Hydroxyethyl)-rutoside; neue Ergebnisse in E Wolfgang Voelter (Leiter der Abteilung für Physika Conference proceedings 1983 Springer-V

戏服

,Variköse, eine geringfügige Gesundheitsstörung?,ar follow-up study..Preliminary results confirm that the subdivision of 3 groups (no varicosis, varicose disorder, varicose disease) performed on a statistical basis is of practical relevance. The disease group shows a high incidence of complaints, phlebitis and chronic venous insufficency, together

座右铭

,Sozioepidemiologische Studie über die Venenleiden bei einer erwachsenen Wohnbevölkerung in der Bunds, photographed. The persons examined correspond in age and professional distribution to the population of the Federal Republic..Almost three-fourths of all the women and one-half of all the men complained of problems with their feet, joints, and legs. Only 14% reported no changes in their venous sy

厌恶

,Epidemiologisch definiertes Problem: „venöses Beinleiden“- Stellenwert in der Allgemeinpraxis, investigated quantitatively and qualitatively..Data were gathered from a total of 3052 patients who consulted a general practitioner by chance. The classification of the morphological substrate and of the secondary change in chronic venous insufficiency of the venous disorder of the leg was made on

Cytokines

,Ein Überblick über neuere Versuche mit Paroven bei der Behandlung der chronisch-venösen Insuffizienus insufficiency. All three trials are shown to have provided very similar results with regard to rate and amount of improvement. Lessons learnt from these studies are included in the design of a new 1,100 patient multicentre study in the UK which will be reported on at the end of 1982.

ELATE

反应

Essential

Instrumental

,Die Wirkung von O-(β-Hydroxyethyl)-rutosiden auf die Symptomatik bei Patienten mit chronisch-venöseysmographic findings, calf circumference and subjective symptoms in patients with chronic venous insufficiency. 149 patients were recruited and 143 remained for analysis (71 HR und 72 placebo). HR was administered as an initial intravenous injection of 1,000 mg followed by oral treatment (500 mg × 3

Antagonism

青少年