Similar articles for PMID: 34857515

Year	Number of Results
2000	1
2001	1
2002	1
2005	2
2007	1
2009	2
2010	2
2011	5
2012	5
2013	10
2014	7
2015	6
2016	7
2017	11
2018	13
2019	10
2020	13
2021	16
2022	3

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

2

Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features.

Blumkin L, Leibovitz Z, Krajden-Haratz K, Arad A, Yosovich K, Gindes L, Zerem A, Ben-Sira L, Lev D, Nissenkorn A, Kidron D, Dobyns WB, Malinger G, Bahi-Buisson N, Leventer RJ, Lerman-Sagie T. Blumkin L, et al. Eur J Paediatr Neurol. 2020 May;26:46-60. doi: 10.1016/j.ejpn.2020.03.001. Epub 2020 Mar 4. Eur J Paediatr Neurol. 2020. PMID: 32169460

3

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.

4

A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations.

Munot P, Saunders DE, Milewicz DM, Regalado ES, Ostergaard JR, Braun KP, Kerr T, Lichtenbelt KD, Philip S, Rittey C, Jacques TS, Cox TC, Ganesan V. Munot P, et al. Brain. 2012 Aug;135(Pt 8):2506-14. doi: 10.1093/brain/aws172. Epub 2012 Jul 24. Brain. 2012. PMID: 22831780 Free PMC article.

5

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.

6

Cerebral arteriopathy in ACTA2 mutations: a spectrum of disease highlighted by a case of variable penetrance in two siblings.

Tschoe C, Kim TE, Fargen KM, Wolfe SQ. Tschoe C, et al. J Neurosurg Pediatr. 2021 Jan 29;27(4):446-451. doi: 10.3171/2020.8.PEDS20391. J Neurosurg Pediatr. 2021. PMID: 33513575

7

Cerebral arteriopathy associated with heterozygous Arg179Cys mutation in the ACTA2 gene: Report in 2 newborn siblings.

de Grazia J, Delgado I, Sanchez-Montanez A, Boronat S, Del Campo M, Vazquez E. de Grazia J, et al. Brain Dev. 2017 Jan;39(1):62-66. doi: 10.1016/j.braindev.2016.08.003. Epub 2016 Aug 25. Brain Dev. 2017. PMID: 27567161

8

Cerebrovascular Disease Progression in Patients With ACTA2 Arg179 Pathogenic Variants.

Lauer A, Speroni SL, Patel JB, Regalado E, Choi M, Smith E, Kalpathy-Kramer J, Caruso P, Milewicz DM, Musolino PL. Lauer A, et al. Neurology. 2021 Jan 26;96(4):e538-e552. doi: 10.1212/WNL.0000000000011210. Epub 2020 Nov 16. Neurology. 2021. PMID: 33199432 Free PMC article.

9

The natural history of a family with aortic dissection associated with a novel ACTA2 variant.

Delsart P, Vanlerberghe C, Juthier F, Sobocinski J, Domanski O, Longere B, Hanna N, Arnaud P, Marsili L. Delsart P, et al. Ann Vasc Surg. 2021 Nov;77:348.e7-348.e11. doi: 10.1016/j.avsg.2021.05.034. Epub 2021 Aug 23. Ann Vasc Surg. 2021. PMID: 34437965

10

ACTA2 Cerebral Arteriopathy: Not Just a Puff of Smoke.

Cuoco JA, Busch CM, Klein BJ, Benko MJ, Stein R, Nicholson AD, Marvin EA. Cuoco JA, et al. Cerebrovasc Dis. 2018;46(3-4):161-171. doi: 10.1159/000493863. Epub 2018 Oct 9. Cerebrovasc Dis. 2018. PMID: 30300893 Free article. Review.

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