159 related articles for article (PubMed ID: 24293535)
1. Cerebral arteriopathy associated with Arg179His ACTA2 mutation.
Amans MR; Stout C; Fox C; Narvid J; Hetts SW; Cooke DL; Higashida RT; Dowd CF; McSwain H; Halbach VV
BMJ Case Rep; 2013 Nov; 2013():. PubMed ID: 24293535
[TBL] [Abstract][Full Text] [Related]
2. Cerebral arteriopathy associated with Arg179His ACTA2 mutation.
Amans MR; Stout C; Fox C; Narvid J; Hetts SW; Cooke DL; Higashida RT; Dowd CF; McSwain H; Halbach VV
J Neurointerv Surg; 2014 Nov; 6(9):e46. PubMed ID: 24353327
[TBL] [Abstract][Full Text] [Related]
3. ACTA2 Cerebral Arteriopathy: Not Just a Puff of Smoke.
Cuoco JA; Busch CM; Klein BJ; Benko MJ; Stein R; Nicholson AD; Marvin EA
Cerebrovasc Dis; 2018; 46(3-4):161-171. PubMed ID: 30300893
[TBL] [Abstract][Full Text] [Related]
4. Triple bypass for multisystem smooth muscle dysfunction syndrome due to Arg179His ACTA2 mutation.
Morita S; Yamaguchi K; Akagawa H; Ishikawa T; Funatsu T; Eguchi S; Ishikawa T; Niwa A; Nonaka T; Kawamata T
J Stroke Cerebrovasc Dis; 2022 Sep; 31(9):106402. PubMed ID: 35248443
[TBL] [Abstract][Full Text] [Related]
5. Neonatal stroke and progressive leukoencephalopathy in a child with an ACTA2 mutation.
Moosa AN; Traboulsi EI; Reid J; Prieto L; Moran R; Friedman NR
J Child Neurol; 2013 Apr; 28(4):531-4. PubMed ID: 22752479
[TBL] [Abstract][Full Text] [Related]
6. Indirect and direct revascularization of ACTA2 cerebral arteriopathy: feasibility of the superficial temporal artery to anterior cerebral artery bypass with posterior auricular artery interposition graft: case report.
Rutledge WC; Choudhri O; Walcott BP; Benet A; Fox CK; Gupta N; Lawton MT
J Neurosurg Pediatr; 2016 Sep; 18(3):339-43. PubMed ID: 27176728
[TBL] [Abstract][Full Text] [Related]
7. Iris anomalies and the incidence of
Taubenslag KJ; Scanga HL; Huey J; Lee J; Medsinge A; Sylvester CL; Cheng KP; Nischal KK
Br J Ophthalmol; 2019 Apr; 103(4):499-503. PubMed ID: 29875232
[TBL] [Abstract][Full Text] [Related]
8. 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
Brain; 2012 Aug; 135(Pt 8):2506-14. PubMed ID: 22831780
[TBL] [Abstract][Full Text] [Related]
9. High-resolution iris and retinal imaging in multisystemic smooth muscle dysfunction syndrome due to a novel Asn117Lys substitution in ACTA2: a case report.
Mc Glacken-Byrne AB; Prentice D; Roshandel D; Brown MR; Tuch P; Yau KS; Sivadorai P; Davis MR; Laing NG; Chen FK
BMC Ophthalmol; 2020 Feb; 20(1):68. PubMed ID: 32093627
[TBL] [Abstract][Full Text] [Related]
10. "Twig-like" cerebral vessels are not pathognomonic for ACTA A2 mutations: A case report.
Nagarajan K; Swamiappan E; Anbazhagan S; Dalal A; Adithan S; Krings T
Interv Neuroradiol; 2018 Aug; 24(4):463-468. PubMed ID: 29591721
[TBL] [Abstract][Full Text] [Related]
11. Nonsurgical treatment of cerebral ischemia associated with ACTA2 cerebral arteriopathy: a case report and literature review.
Muroi A; Shiono J; Ihara S; Morisaki H; Nakai Y
Childs Nerv Syst; 2022 Jun; 38(6):1209-1212. PubMed ID: 34546411
[TBL] [Abstract][Full Text] [Related]
12. 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
Brain Dev; 2017 Jan; 39(1):62-66. PubMed ID: 27567161
[TBL] [Abstract][Full Text] [Related]
13. Refractory cerebral infarction in a child with an ACTA2 mutation.
Kanamori K; Sakaguchi Y; Tsuda K; Ihara S; Miyama S
Brain Dev; 2021 Apr; 43(4):585-589. PubMed ID: 33342581
[TBL] [Abstract][Full Text] [Related]
14. 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
J Neurosurg Pediatr; 2021 Jan; 27(4):446-451. PubMed ID: 33513575
[TBL] [Abstract][Full Text] [Related]
15. Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome.
Logeswaran T; Friedburg C; Hofmann K; Akintuerk H; Biskup S; Graef M; Rad A; Weber A; Neubauer BA; Schranz D; Bouvagnet P; Lorenz B; Hahn A
Am J Med Genet A; 2017 Apr; 173(4):959-965. PubMed ID: 28328125
[TBL] [Abstract][Full Text] [Related]
16. Cerebral arteriopathy and ischemic stroke in a pediatric MYH11 patient.
Raghuram A; Sanchez S; Lu Y; Hickerson M; Mayorga MBS; Romero JM; Matsumoto S; Musolino PL; Samaniego EA
J Stroke Cerebrovasc Dis; 2023 Mar; 32(3):106938. PubMed ID: 36621119
[TBL] [Abstract][Full Text] [Related]
17. ACTA2 leukovasculopathy: A rare pediatric white matter disorder.
Sabo TM; Stokes MA; Karbhari N; Veltkamp DL; Pfeifer CM
Radiol Case Rep; 2020 Aug; 15(8):1285-1288. PubMed ID: 32595813
[TBL] [Abstract][Full Text] [Related]
18. Fibromuscular dysplasia as a cause of stroke in a 9-year-old girl.
Yiş U; Men S; Cakmakçi H; Demircioğlu F; Kurul SH; Oren H; Dirik E
Turk J Pediatr; 2011; 53(5):567-70. PubMed ID: 22272461
[TBL] [Abstract][Full Text] [Related]
19. Intracranial Vessel Wall MRI in Cryptogenic Stroke and Intracranial Vasculitis.
Destrebecq V; Sadeghi N; Lubicz B; Jodaitis L; Ligot N; Naeije G
J Stroke Cerebrovasc Dis; 2020 May; 29(5):104684. PubMed ID: 32151477
[TBL] [Abstract][Full Text] [Related]
20. [Posterior cerebral artery involvement in Moyamoya disease].
Harman M; Etlik O; Unal O; Sakarya ME
Tani Girisim Radyol; 2004 Mar; 10(1):23-5. PubMed ID: 15054698
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
