Zobrazeno 1 - 10
of 12
pro vyhledávání: '"József Höhn"'
Publikováno v:
Magyar Onkológia. 54:125-128
Metastatic liver disease is a challenging and life-threatening situation oft en with dismal prognosis. Nearly half of the patients with colorectal cancer develop liver metastasis during the course of their diseases. Hepatic resection is the treatment
Autor:
Blanka Veréb, Alíz Nikolényi, László Tiszlavicz, Katalin Hideghéthy, Gellért Baradnay, Eszter Mán, József Höhn, Anikó Maráz, György Lázár, István Németh, László Varga, Zsolt Simonka
Publikováno v:
Magyar Onkológia. 54:129-135
2/nap 5-FU es 20 mg/m 2 /nap leucovorin kemoterapia, az utobbi időben kiegeszitve celzott an a makroszkopos tumorra biztonsagi zonaval 3x1,8 Gy előrehozott boost besugarzassal. Restaging vizsgalatokat kovetően atlagosan 8 hett el az onkologiai kez
Publikováno v:
Cardiovascular Drugs and Therapy. 17:115-121
Levosimendan, a new type of inodilator drugs, is known to activate membrane adenosine 3′,5′-triphosphate-sensitive potassium (KATP) channels in some vascular smooth muscles and causes vasorelaxation. The involvement of potassium channels in the m
Autor:
Ádám Balogh, Éva Makula, József Höhn, Gábor Kocsis Savanya, Mihály Boros, Erzsébet László Kókai, András Petri
Publikováno v:
Langenbeck's Archives of Surgery. 387:229-233
Background and aims. In a search for the optimal management of nonparasitic liver cysts, a study was made of the effectiveness of different methods. Patients and methods. Between 1 January 1982 and 15 December 2001 we treated 132 patients with nonpar
Publikováno v:
Langenbeck's Archives of Surgery. 387:27-31
Background and aims: Our aim is to give an audit of our experience over the past two decades in the form of a retrospective study. Patients/methods: In two equal periods between 01.01.1982 and 31.03.2001, 56 patients (37 males and 19 females) with py
Publikováno v:
Journal of Pharmacy and Pharmacology. 52:213-217
In the present study the vasorelaxing capacity of cromakalim, an ATP-sensitive potassium-channel (KATP channel) activator, and that of levosimendan, a new positive inotropic and vasodilating drug with calcium sensitizing and potassium-channel-activat
Autor:
Ádám Balogh, András Varró, János Pataricza, József Höhn, Gábor Tóth, Julius Gy. Papp, András Petri
Publikováno v:
Pharmacology and Toxicology. 94:271-273
The involvement of potassium channels in the venodilating capacity of the inodilator levosimendan in human saphenous vein preparations was investigated. Levosimendan caused relaxation with 50% effective concentration (EC50) of 0.32 +/- 0.04 microM in
Publikováno v:
Journal of Pharmacy and Pharmacology. 47:921-925
A comparative study was performed on the sensitivity of in-vitro vasorelaxation by nitroglycerin and cromakalim to block glibenclamide, a blocker of ATP-sensitive potassium channels, and iberiotoxin, a selective inhibitor of large-conductance calcium
Publikováno v:
Hepato-gastroenterology. 55(82-83)
The aim of this study is to give an audit of the experiences in the Institute of Experimental Surgery, at the University of Szeged, over the past 2 decades in the form of a retrospective study.Between January 1982 and December 2001, 132 patients with
Publikováno v:
Cardiovascular drugs and therapy. 17(2)
Levosimendan, a new type of inodilator drugs, is known to activate membrane adenosine 3',5'-triphosphate-sensitive potassium (KATP) channels in some vascular smooth muscles and causes vasorelaxation. The involvement of potassium channels in the mecha