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pro vyhledávání: '"Alexan I. Yerevanian"'
Autor:
Alexan I, Yerevanian, Francy, Shu
Publikováno v:
Neurology. 96(7)
Autor:
Alexan I Yerevanian, Francy Shu
Publikováno v:
Neurology.
Hereditary transthyretin amyloidosis (hATTR) is an autosomal dominant, rapidly progressive, multisystem disease with substantial clinical heterogeneity, typically marked by lesions in the peripheral nervous system (median neuropathy, sensorimotor pol
Publikováno v:
BMJ Case Rep
A 56-year-old man with a remote history of bilateral recurrent facial palsies presented with a week of ophthalmoplegia with intact deep tendon reflexes and lack of ataxia, cerebrospinal fluid with albuminocytologic dissociation and elevated serum ant
Publikováno v:
Journal of Molecular and Cellular Cardiology. 50:803-812
While progress in conventional treatments is making steady and incremental gains to reduce mortality associated with heart failure, there remains a need to explore potentially new therapeutic approaches. Heart failure induced by different etiologies