| 1 |
35360035 | Atrial Lesions in a Pedigree With PRKAG2 Cardiomyopathy: Involvement of Disrupted AMP-Activated Protein Kinase Signaling. | 2022 |
2 |
| 2 |
33509202 | Novel PRKAG2 variant presenting as liver cirrhosis: report of a family with 2 cases and review of literature. | 2021 Jan 28 |
2 |
| 3 |
29298659 | Cardiac manifestations of PRKAG2 mutation. | 2018 Jan 3 |
2 |
| 4 |
29452156 | Establishment of a PRKAG2 cardiac syndrome disease model and mechanism study using human induced pluripotent stem cells. | 2018 Apr |
1 |
| 5 |
29480501 | Human γ2-AMPK Mutations. | 2018 |
1 |
| 6 |
29593177 | Molecular Pathogenesis of Familial Wolff-Parkinson-White Syndrome. | 2018 |
2 |
| 7 |
27142047 | Severe Cardiomyopathy as the Isolated Presenting Feature in an Adult with Late-Onset Pompe Disease: A Case Report. | 2017 |
1 |
| 8 |
28258649 | Cardiac manifestations of inherited metabolic disease in children. | 2017 May |
1 |
| 9 |
28550180 | A novel, de novo mutation in the PRKAG2 gene: infantile-onset phenotype and the signaling pathway involved. | 2017 Aug 1 |
1 |
| 10 |
27496753 | Glycogen Storage Disease Because of a PRKAG2 Mutation Causing Severe Biventricular Hypertrophy and High-Grade Atrio-Ventricular Block. | 2016 Aug |
1 |
| 11 |
28009297 | Integrative Analysis of PRKAG2 Cardiomyopathy iPS and Microtissue Models Identifies AMPK as a Regulator of Metabolism, Survival, and Fibrosis. | 2016 Dec 20 |
2 |
| 12 |
26496977 | Cardiovascular magnetic resonance findings in patients with PRKAG2 gene mutations. | 2015 Oct 24 |
1 |
| 13 |
24503893 | Mutation in the γ2-subunit of AMP-activated protein kinase stimulates cardiomyocyte proliferation and hypertrophy independent of glycogen storage. | 2014 Mar 14 |
1 |
| 14 |
23778007 | Identification and functional analysis of a novel PRKAG2 mutation responsible for Chinese PRKAG2 cardiac syndrome reveal an important role of non-CBS domains in regulating the AMPK pathway. | 2013 Oct |
1 |
| 15 |
19787389 | Severe hypertrophic cardiomyopathy in an infant with a novel PRKAG2 gene mutation: potential differences between infantile and adult onset presentation. | 2009 Nov |
1 |
| 16 |
19920047 | In vivo assessment of myocardial glucose uptake by positron emission tomography in adults with the PRKAG2 cardiac syndrome. | 2009 Nov |
1 |
| 17 |
20031621 | Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogen. | 2009 Oct |
1 |
| 18 |
17667862 | Fatal infantile cardiac glycogenosis with phosphorylase kinase deficiency and a mutation in the gamma2-subunit of AMP-activated protein kinase. | 2007 Oct |
1 |
| 19 |
17990392 | [AMP-activated protein kinase: how a mistake in energy gauge causes glycogen storage]. | 2007 Oct |
1 |
| 20 |
16487706 | A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis. | 2006 Mar |
1 |
| 21 |
15673802 | Glycogen storage diseases presenting as hypertrophic cardiomyopathy. | 2005 Jan 27 |
2 |
| 22 |
16275868 | Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy. | 2005 Nov 15 |
1 |
| 23 |
16619977 | [Cardiomyopathies due to defective energy metabolism: morphological and functional features]. | 2005 Dec |
1 |
| 24 |
12546691 | Glycogen storage disease as a unifying mechanism of disease in the PRKAG2 cardiac syndrome. | 2003 Feb |
1 |
| 25 |
11827995 | Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy. | 2002 Feb |
1 |