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Journal Abstract Search

100 related items for PubMed ID: 21070929

  • 1. Singleton-merten syndrome and impaired cardiac function.
    Valverde I, Rosenthal E, Tzifa A, Desai P, Bell A, Pushparajah K, Qureshi S, Beerbaum P, Simpson J.
    J Am Coll Cardiol; 2010 Nov 16; 56(21):1760. PubMed ID: 21070929
    [No Abstract] [Full Text] [Related]

  • 2. Transcatheter Aortic Valve Replacement for Severe Aortic Regurgitation in Singleton-Merten Syndrome.
    Cannata S, Freitas D, Lucchese G, Frigiola A, Hancock J, Head C, Young C, Prendergast B, Redwood S.
    JACC Cardiovasc Interv; 2018 Nov 12; 11(21):e173-e174. PubMed ID: 30343025
    [No Abstract] [Full Text] [Related]

  • 3. Long term clinical outcome of dental implants placed in a patient with Singleton-Merten syndrome.
    Rodriguez R, Hartmann N, Figgener L, Kleinheinz J, Weingart D.
    J Prosthodont Res; 2015 Jul 12; 59(3):199-204. PubMed ID: 26043888
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  • 4. Progressive supra-aortic stenosis in a young adult with the findings of Singleton Merten Syndrome.
    Ozyuksel A, Ersoy C, Canturk E, Akcevin A.
    BMJ Case Rep; 2014 Sep 05; 2014():. PubMed ID: 25193816
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  • 7. Singleton-Merten syndrome: A rare cause of femoral head necrosis.
    Assaf E, Bdeir M, Mohs E, Dally FJ, Gravius S, Weis CA, Darwich A.
    Am J Med Genet A; 2021 Oct 05; 185(10):3170-3175. PubMed ID: 34189824
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  • 9. [Singleton-Merten syndrome].
    Sakazume S.
    Ryoikibetsu Shokogun Shirizu; 2001 Oct 05; (34 Pt 2):640-1. PubMed ID: 11528940
    [No Abstract] [Full Text] [Related]

  • 10. Further evidence for specific IFIH1 mutation as a cause of Singleton-Merten syndrome with phenotypic heterogeneity.
    Pettersson M, Bergendal B, Norderyd J, Nilsson D, Anderlid BM, Nordgren A, Lindstrand A.
    Am J Med Genet A; 2017 May 05; 173(5):1396-1399. PubMed ID: 28319323
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  • 11. MDA5-Associated Neuroinflammation and the Singleton-Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum.
    Buers I, Rice GI, Crow YJ, Rutsch F.
    J Interferon Cytokine Res; 2017 May 05; 37(5):214-219. PubMed ID: 28475458
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  • 14. Hereditary Disorders of Cardiovascular Calcification.
    Rutsch F, Buers I, Nitschke Y.
    Arterioscler Thromb Vasc Biol; 2021 Jan 05; 41(1):35-47. PubMed ID: 33176451
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  • 15. Thrombus in the distal aortic arch after apicoaortic conduit for severe aortic stenosis.
    Kotani S, Hattori K, Kato Y, Shibata T.
    Interact Cardiovasc Thorac Surg; 2010 Mar 05; 10(3):486-8. PubMed ID: 20007638
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  • 16. Singleton-Merten Syndrome-like Skeletal Abnormalities in Mice with Constitutively Activated MDA5.
    Soda N, Sakai N, Kato H, Takami M, Fujita T.
    J Immunol; 2019 Sep 01; 203(5):1356-1368. PubMed ID: 31366715
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  • 17. A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome.
    Rutsch F, MacDougall M, Lu C, Buers I, Mamaeva O, Nitschke Y, Rice GI, Erlandsen H, Kehl HG, Thiele H, Nürnberg P, Höhne W, Crow YJ, Feigenbaum A, Hennekam RC.
    Am J Hum Genet; 2015 Feb 05; 96(2):275-82. PubMed ID: 25620204
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  • 18. Musculoskeletal Disease in MDA5-Related Type I Interferonopathy: A Mendelian Mimic of Jaccoud's Arthropathy.
    de Carvalho LM, Ngoumou G, Park JW, Ehmke N, Deigendesch N, Kitabayashi N, Melki I, Souza FFL, Tzschach A, Nogueira-Barbosa MH, Ferriani V, Louzada-Junior P, Marques W, Lourenço CM, Horn D, Kallinich T, Stenzel W, Hur S, Rice GI, Crow YJ.
    Arthritis Rheumatol; 2017 Oct 05; 69(10):2081-2091. PubMed ID: 28605144
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  • 20. Singleton-Merten syndrome: an autosomal dominant disorder with variable expression.
    Feigenbaum A, Müller C, Yale C, Kleinheinz J, Jezewski P, Kehl HG, MacDougall M, Rutsch F, Hennekam RC.
    Am J Med Genet A; 2013 Feb 05; 161A(2):360-70. PubMed ID: 23322711
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