Clinical case of recurrent aHUS after allogeneic cadaveric kidney transplantation
Introduction. Atypical hemolytic uremic syndrome (aHUS) is a systemic orphan disease that reproduces as an uncontrolled activation of the alternative pathway of the complement system and is expressed as systemic thrombotic microangiopathy (TMA). The classical triad of aHUS symptoms are hemolytic ane...
Tallennettuna:
| Päätekijät: | , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Russo |
| Julkaistu: |
Federal Research Center of Transplantology and Artificial Organs named after V.I.Shumakov
2024-01-01
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| Sarja: | Вестник трансплантологии и искусственных органов |
| Aiheet: | |
| Linkit: | https://journal.transpl.ru/vtio/article/view/1641 |
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