Search Results - "Mozdon, M A"

Clinical profile and therapeutic aspects of mycosis fungoides: a retrospective analysis of 210 cases in Russia by Gorenkova, L. G., Zvonkov, E. E., Mangasarova, Ya. K., Chabaeva, Yu. A., Kulikov, S. M., Kovrigina, A. M., Kuzmina, L. A., Sidorova, Yu. V., Mozdon, M. A.

“…Background. Mycosis fungoides (MF) is classified as an orphan disease. Due to the rarity of pathology, and until recently the absence of an expert group and a…”
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Iron deficiency anemia in a patient with hereditary hemorrhagic telangiectasia. Case report by Mozdon, M A, Ponomarev, R V, Tsvetaeva, N V, Shabrin, A V, Ermachenkova, E I, Larichev, S E, Lukina, E A

“…Rendu-Osler-Weber disease or hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease. It is characterized by vascular dysplasia with…”
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