April 20, 2018 (v1)
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Uploaded on: December 4, 2022
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March 18, 2021 (v1)Publication
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March 18, 2021 (v1)Publication
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July 14, 2023 (v1)Publication
Background: Hereditary hemorrhagic telangiectasia (HHT) is a rare vascular disease with autosomal dominant inheritance. Disease-causing variants in endoglin (ENG) and activin A receptor type II-like 1 (ACVRL1) genes are detected in more than 90% of cases submitted to molecular diagnosis. Methods: We used data from the RiHHTa (Computerized...
Uploaded on: October 11, 2023 -
August 20, 2021 (v1)Publication
Background: Patients infected with the human immunodeficiency virus (HIV) have an increased risk of cardiovascular disease due to increased inflammation and persistent immune activation. CD163 is a macrophage scavenger receptor that is involved in monocyte-macrophage activation in HIV-infected patients. CD163 interacts with TWEAK, a member of...
Uploaded on: December 4, 2022 -
November 17, 2022 (v1)Publication
To analyze the frequency and clinical phenotype of neurosarcoidosis (NS) in one of the largest nationwide cohorts of patients with sarcoidosis reported from southern Europe. NS was evaluated according to the Diagnostic Criteria for Central Nervous System and Peripheral Nervous System Sarcoidosis recently proposed by Stern et al. Pathologic...
Uploaded on: December 4, 2022