Paroxysmal nocturnal hemoglobinuria: the path to diagnosis

The aim of study was to describe the case of diagnosis of orphan disease — paroxysmal nocturnal hemoglobinuria in clinical practice of the therapist on an outpatient basis.Materials and methods. The patient Sh., 47 years, due to the gradual increase in the volume of the abdomen, the appearance of sw...

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發表在:	Klinicist
Main Authors:	E. F. Makhnyr, N. O. Inasaridze
格式:	Article
語言:	俄语
出版:	ABV-press 2019-04-01
主題:	paroxysmal nocturnal hemoglobinuria marchiafava—michele disease strubing—marchiafava disease harley disease rare (orphan) disease eculizumab immunophenotyping of peripheral blood phosphatidylinositol glycan class a hemolytic-uremic syndrome thrombotic microangiopathy
在線閱讀:	https://klinitsist.abvpress.ru/Klin/article/view/372