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Titlebook: Gallopamil; Pharmacological and Martin Kaltenbach,Rüdiger Hopf Conference proceedings 1984 Springer-Verlag Berlin Heidelberg 1984 Angina p

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https://doi.org/10.1007/978-1-4939-1320-6ane potential. They reach the receptor in the sodium channel from the cytoplasm side of the membrane and act in the charged form (. et al. 1980; . 1977 a, b; . 1973). There are many similarities between this block and the calcium channel block by D 600. For example, in recent years we have shown in
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Pauline K. Robinson,James E. Birrenels; these are mainly studies in vitro on basilar artery strips (for review of literature see Flaim 1982). In 1973 Vlahov and Enzenross reported that the constriction of feline pia vessels induced in vivo by reducing the pH was inhibited by local administration of gallopamil (D 600) in concentration
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Nicolle Sitte,Thomas von Zglinickif af-terload partially or totally compensates for the negative inotropic effect of these substances; thus some authors report that ventricular function is unchanged and others that it is improved. This trial was intended to investigate in a consecutive group of coronary patients the response of haem
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Biology of Aging and its Modulationpatients with coronary heart disease (. 1980; . et al. 1978). Because there are distinct differences in the pharmacokinetics and pharmacodynamics of the substances available it is necessary to establish precisely the recommended dosages and dosage intervals for each new preparation of this group. Th
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Biology of Aging and its Modulationon has been reported for diltiazem and nifedipine; this effect is less pronounced with verapamil. Rafflenbeul and Lichtlen have reported only recently (1982) a 29% increase in the calibre of some coronary stenoses after sublingual nifedipine. The same stenoses showed a 33% dilatation after sublingua
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Rafi T. Kevorkian,John E. Morley80; . 1977; . and . 1980; . et al. 1981 ; . et al. 1981). There are appreciable differences between the individual calcium antagonists as regards chemical structure and profile of action (. 1977). This trial was to establish whether oral administration of the calcium antagonist gallopa-mil (D 600),
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