Treatment with low-dose tacrolimus inhibits bleeding complications in a patient with hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) can be found in patients suffering from a loss-of-function mutation of the gene encoding for the activin receptor-like kinase 1 (ALK-1), a bone morphogenetic protein (BMP) type 1 receptor. Interestingly, ALK-1 mutations also lead to hereditary hemorrhagic telang...

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Detalles Bibliográficos
Autores principales: Sommer, N, Droege, F, Gamen, KE, Geisthoff, U, Gall, H, Tello, K, Richter, MJ, Deubner, LM, Schmiedel, R, Hecker, M, Spiekerkoetter, E, Wirsching, K, Seeger, W, Ghofrani, HA, Pullamsetti, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432681/
https://www.ncbi.nlm.nih.gov/pubmed/30260738
http://dx.doi.org/10.1177/2045894018805406

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