223 related articles for article (PubMed ID: 29334594)
1. Thoracic aortic aneurysm in patients with loss of function Filamin A mutations: Clinical characterization, genetics, and recommendations.
Chen MH; Choudhury S; Hirata M; Khalsa S; Chang B; Walsh CA
Am J Med Genet A; 2018 Feb; 176(2):337-350. PubMed ID: 29334594
[TBL] [Abstract][Full Text] [Related]
2. 47 patients with FLNA associated periventricular nodular heterotopia.
Lange M; Kasper B; Bohring A; Rutsch F; Kluger G; Hoffjan S; Spranger S; Behnecke A; Ferbert A; Hahn A; Oehl-Jaschkowitz B; Graul-Neumann L; Diepold K; Schreyer I; Bernhard MK; Mueller F; Siebers-Renelt U; Beleza-Meireles A; Uyanik G; Janssens S; Boltshauser E; Winkler J; Schuierer G; Hehr U
Orphanet J Rare Dis; 2015 Oct; 10():134. PubMed ID: 26471271
[TBL] [Abstract][Full Text] [Related]
3. Sinus of Valsalva Aneurysm in Females.
Wang Y; Wu B; Li J; Shu X
Int Heart J; 2022 Nov; 63(6):1201-1204. PubMed ID: 36372407
[TBL] [Abstract][Full Text] [Related]
4. A novel truncating mutation in FLNA causes periventricular nodular heterotopia, Ehlers-Danlos-like collagenopathy and macrothrombocytopenia.
Ieda D; Hori I; Nakamura Y; Ohshita H; Negishi Y; Shinohara T; Hattori A; Kato T; Inukai S; Kitamura K; Kawai T; Ohara O; Kunishima S; Saitoh S
Brain Dev; 2018 Jun; 40(6):489-492. PubMed ID: 29449050
[TBL] [Abstract][Full Text] [Related]
5. Asymmetrical aortic root aneurism in patient with Filamin A mutation.
Martin-Suarez S; Gliozzi G; Pagano V; Leone O; Foà A; Ruggiero A; Snaidero S; Cerchierini E; Pacini D
J Card Surg; 2022 Oct; 37(10):3408-3412. PubMed ID: 35819109
[TBL] [Abstract][Full Text] [Related]
6. Cardiovascular, Brain, and Lung Involvement in a Newborn With a Novel FLNA Mutation: A Case Report and Literature Review.
Meliota G; Vairo U; Ficarella R; Milella L; Faienza MF; D'Amato G
Adv Neonatal Care; 2022 Apr; 22(2):125-131. PubMed ID: 33852449
[TBL] [Abstract][Full Text] [Related]
7. Insights on the Pathogenesis of Aneurysm through the Study of Hereditary Aortopathies.
Creamer TJ; Bramel EE; MacFarlane EG
Genes (Basel); 2021 Jan; 12(2):. PubMed ID: 33514025
[TBL] [Abstract][Full Text] [Related]
8. Phenotypic manifestations in
Loft Nagel J; Jønch AE; Nguyen NTTN; Bygum A
BMJ Case Rep; 2022 Apr; 15(4):. PubMed ID: 35414575
[TBL] [Abstract][Full Text] [Related]
9. Microdeletion in Xq28 with a polymorphic inversion in a patient with FLNA-associated progressive lung disease.
Yoshii K; Matsumoto H; Hirasawa K; Sakauchi M; Hara H; Ito S; Osawa M; Fukami M; Horikawa R; Nagata S
Respir Investig; 2019 Jul; 57(4):395-398. PubMed ID: 30987847
[TBL] [Abstract][Full Text] [Related]
10. A review of filamin A mutations and associated interstitial lung disease.
Sasaki E; Byrne AT; Phelan E; Cox DW; Reardon W
Eur J Pediatr; 2019 Feb; 178(2):121-129. PubMed ID: 30547349
[TBL] [
