Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 2
2005 1
2007 2
2010 1
2012 1
2013 1
2015 2
2017 3
2019 3
2020 4
2021 4
2022 5
2023 0
Text availability
Article attribute
Article type
Publication date

Search Results

29 results
Results by year
Filters applied: . Clear all
Page 1
The Role of Propranolol as a Repurposed Drug in Rare Vascular Diseases.
Cuesta AM, Gallardo-Vara E, Casado-Vela J, Recio-Poveda L, Botella LM, Albiñana V. Cuesta AM, et al. Among authors: botella lm. Int J Mol Sci. 2022 Apr 11;23(8):4217. doi: 10.3390/ijms23084217. Int J Mol Sci. 2022. PMID: 35457036 Free PMC article. Review.
A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2.
Errasti Díaz S, Peñalva M, Recio-Poveda L, Vilches S, Casado-Vela J, Pérez Pérez J, Botella LM, Albiñana V, Cuesta AM. Errasti Díaz S, et al. Among authors: botella lm. J Clin Med. 2022 May 28;11(11):3053. doi: 10.3390/jcm11113053. J Clin Med. 2022. PMID: 35683441 Free PMC article.
European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)?
Dupuis-Girod S, Shovlin CL, Kjeldsen AD, Mager HJ, Sabba C, Droege F, Fargeton AE, Fialla AD, Gandolfi S, Hermann R, Lenato GM, Manfredi G, Post MC, Rennie C, Suppressa P, Sure U; ePag group; Buscarini E. Dupuis-Girod S, et al. Eur J Med Genet. 2022 Oct;65(10):104575. doi: 10.1016/j.ejmg.2022.104575. Epub 2022 Aug 5. Eur J Med Genet. 2022. PMID: 35940549 Free article.
29 results