Clinical diagnostics of fibrillinopathies (type 1)

Abstract

Diagnostic criteria are presented for the syndromes related to mutations of fibrillin gene type 1 (such as Marfan syndrome, ectopia lentis, MASS phenotype, mitral valve prolapse syndrome, stiff skin syndrome, Shprintzen-Goldberg syndrome) and for the acromelic group of dysplasias (such as geleophysic dysplasia, Weill-Marchesani syndrome, and acromicria). Russ J Cardiol 2013; 2 (100): 89-93

Cocarnit as a Part of Complex Therapy in Patients with Coronary Artery Disease and Chronic Heart Failure: A Clinical Experience

“…Препарат Кокарнит содержит никотинамид 20 мг, кокарбоксилазу 50 мг, цианокобаламин 500 мкг, динатрия аденозинтрифосфат тригидрат (АТФ) 10 мг, что определяет его комплексное воздействие на ряд метаболических процессов в организме [19].…”