These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
176 related articles for article (PubMed ID: 28814167)
1. Cardio-cephalic neural crest syndrome: A novel hypothesis of vascular neurocristopathy. Komiyama M Interv Neuroradiol; 2017 Dec; 23(6):572-576. PubMed ID: 28814167 [TBL] [Abstract][Full Text] [Related]
2. Moyamoya angiopathy in PHACE syndrome not associated with RNF213 variants. Hadisurya J; Guey S; Grangeon L; Wieczorek D; Corpechot M; Schwitalla JC; Kraemer M Childs Nerv Syst; 2019 Jul; 35(7):1231-1237. PubMed ID: 31037424 [TBL] [Abstract][Full Text] [Related]
3. Cephalic/cardiac neural crest cell and moyamoya disease. Ota T; Komiyama M Neuroradiol J; 2021 Dec; 34(6):529-533. PubMed ID: 34078151 [TBL] [Abstract][Full Text] [Related]
4. Moyamoya syndrome and PHACE syndrome: clinical and radiographic characterization of the intracranial arteriopathy and response to surgical revascularization. Jernigan S; Storey A; Hammer C; Riordan C; Orbach DB; Scott RM; Smith E J Neurosurg Pediatr; 2019 Apr; 23(4):493-497. PubMed ID: 30717056 [TBL] [Abstract][Full Text] [Related]
5. Moyamoya Vasculopathy in PHACE Syndrome: Six New Cases and Review of the Literature. Tortora D; Severino M; Accogli A; Martinetti C; Vercellino N; Capra V; Rossi A; Pavanello M World Neurosurg; 2017 Dec; 108():291-302. PubMed ID: 28887276 [TBL] [Abstract][Full Text] [Related]
6. Tuberomammillary Fusion and Moya-Moya Vasculopathy Associated with PHACE Syndrome. Freitas LF; Miranda EC; Amaro AP; Narvaez EO; Duarte ML Neuropediatrics; 2024 Jun; 55(3):213-214. PubMed ID: 37716357 [No Abstract] [Full Text] [Related]
7. 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]
8. Utilisation of advanced MRI techniques to understand neurovascular complications of PHACE syndrome: a case of arterial stenosis and dissection. Eisenmenger LB; Rivera-Rivera LA; Johnson KM; Drolet BA BMJ Case Rep; 2020 Sep; 13(9):. PubMed ID: 32928832 [TBL] [Abstract][Full Text] [Related]
9. PHACE syndrome in a preterm infant. Steggerda SJ; Tan RNGB; de Laat PCJ Neurology; 2020 Oct; 95(16):751-752. PubMed ID: 32913025 [No Abstract] [Full Text] [Related]
10. RNF213 variants in a child with PHACE syndrome and moyamoya vasculopathy. Schilter KF; Steiner JE; Demos W; Maheshwari M; Prokop JW; Worthey E; Drolet BA; Siegel DH Am J Med Genet A; 2017 Sep; 173(9):2557-2561. PubMed ID: 28686325 [TBL] [Abstract][Full Text] [Related]
15. PHACE syndrome: clinical manifestations, diagnostic criteria, and management. Rotter A; Samorano LP; Rivitti-Machado MC; Oliveira ZNP; Gontijo B An Bras Dermatol; 2018 Jun; 93(3):405-411. PubMed ID: 29924216 [TBL] [Abstract][Full Text] [Related]
16. Moyamoya disease is a vascular form of neurocristopathy: disease of the embryologic cephalic neural crest. Komiyama M Childs Nerv Syst; 2017 Apr; 33(4):567-568. PubMed ID: 28299436 [No Abstract] [Full Text] [Related]