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

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2001 1
2005 1
2007 1
2009 2
2010 2
2011 3
2012 4
2013 9
2014 6
2015 6
2016 6
2017 10
2018 6
2019 7
2020 14
2021 17
2022 10
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Similar articles for PMID: 34857515

91 results

Results by year

Filters applied: . Clear all
Page 1
ACTA2-Related Dysgyria: An Under-Recognized Malformation of Cortical Development.
Subramanian S, Biswas A, Alves CAPF, Sudhakar SV, Shekdar KV, Krishnan P, Shroff M, Taranath A, Arrigoni F, Aldinger KA, Leventer RJ, Dobyns WB, Mankad K. Subramanian S, et al. AJNR Am J Neuroradiol. 2022 Jan;43(1):146-150. doi: 10.3174/ajnr.A7364. Epub 2021 Dec 2. AJNR Am J Neuroradiol. 2022. PMID: 34857515 Free PMC article.
Expanding the Distinctive Neuroimaging Phenotype of ACTA2 Mutations.
D'Arco F, Alves CA, Raybaud C, Chong WKK, Ishak GE, Ramji S, Grima M, Barkovich AJ, Ganesan V. D'Arco F, et al. AJNR Am J Neuroradiol. 2018 Nov;39(11):2126-2131. doi: 10.3174/ajnr.A5823. Epub 2018 Sep 27. AJNR Am J Neuroradiol. 2018. PMID: 30262641 Free PMC article.
European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants.
van de Laar IMBH, Arbustini E, Loeys B, Björck E, Murphy L, Groenink M, Kempers M, Timmermans J, Roos-Hesselink J, Benke K, Pepe G, Mulder B, Szabolcs Z, Teixidó-Turà G, Robert L, Emmanuel Y, Evangelista A, Pini A, von Kodolitsch Y, Jondeau G, De Backer J. van de Laar IMBH, et al. Orphanet J Rare Dis. 2019 Nov 21;14(1):264. doi: 10.1186/s13023-019-1186-2. Orphanet J Rare Dis. 2019. PMID: 31752940 Free PMC article.
Brain Abnormalities in Patients with Germline Variants in H3F3: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors.
Alves CAPF, Sherbini O, D'Arco F, Steel D, Kurian MA, Radio FC, Ferrero GB, Carli D, Tartaglia M, Balci TB, Powell-Hamilton NN, Schrier Vergano SA, Reutter H, Hoefele J, Günthner R, Roeder ER, Littlejohn RO, Lessel D, Lüttgen S, Kentros C, Anyane-Yeboa K, Catarino CB, Mercimek-Andrews S, Denecke J, Lyons MJ, Klopstock T, Bhoj EJ, Bryant L, Vanderver A. Alves CAPF, et al. AJNR Am J Neuroradiol. 2022 Jul;43(7):1048-1053. doi: 10.3174/ajnr.A7555. Epub 2022 Jun 30. AJNR Am J Neuroradiol. 2022. PMID: 35772801 Free PMC article.
91 results