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Results: 1 to 20 of 93

1.

Ventricular pre-excitation and cardiac hypertrophy mimicking hypertrophic cardiomyopathy in a Turkish family with a novel PRKAG2 mutation.

Bayrak F, Komurcu-Bayrak E, Mutlu B, Kahveci G, Basaran Y, Erginel-Unaltuna N.

Eur J Heart Fail. 2006 Nov;8(7):712-5. Epub 2006 May 22.

PMID:
16716659
[PubMed - indexed for MEDLINE]
2.

Glycogen storage diseases presenting as hypertrophic cardiomyopathy.

Arad M, Maron BJ, Gorham JM, Johnson WH Jr, Saul JP, Perez-Atayde AR, Spirito P, Wright GB, Kanter RJ, Seidman CE, Seidman JG.

N Engl J Med. 2005 Jan 27;352(4):362-72.

PMID:
15673802
[PubMed - indexed for MEDLINE]
Free Article
3.

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy.

Arad M, Benson DW, Perez-Atayde AR, McKenna WJ, Sparks EA, Kanter RJ, McGarry K, Seidman JG, Seidman CE.

J Clin Invest. 2002 Feb;109(3):357-62.

PMID:
11827995
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy.

Gollob MH, Green MS, Tang AS, Roberts R.

Curr Opin Cardiol. 2002 May;17(3):229-34. Review.

PMID:
12015471
[PubMed - indexed for MEDLINE]
5.

Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy.

Gollob MH, Seger JJ, Gollob TN, Tapscott T, Gonzales O, Bachinski L, Roberts R.

Circulation. 2001 Dec 18;104(25):3030-3.

PMID:
11748095
[PubMed - indexed for MEDLINE]
Free Article
6.

A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis.

Laforêt P, Richard P, Said MA, Romero NB, Lacene E, Leroy JP, Baussan C, Hogrel JY, Lavergne T, Wahbi K, Hainque B, Duboc D.

Neuromuscul Disord. 2006 Mar;16(3):178-82. Epub 2006 Feb 17.

PMID:
16487706
[PubMed - indexed for MEDLINE]
7.

Fatal congenital heart glycogenosis caused by a recurrent activating R531Q mutation in the gamma 2-subunit of AMP-activated protein kinase (PRKAG2), not by phosphorylase kinase deficiency.

Burwinkel B, Scott JW, Bührer C, van Landeghem FK, Cox GF, Wilson CJ, Grahame Hardie D, Kilimann MW.

Am J Hum Genet. 2005 Jun;76(6):1034-49. Epub 2005 May 2.

PMID:
15877279
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Molecular genetic analysis of PRKAG2 in sporadic Wolff-Parkinson-White syndrome.

Vaughan CJ, Hom Y, Okin DA, McDermott DA, Lerman BB, Basson CT.

J Cardiovasc Electrophysiol. 2003 Mar;14(3):263-8.

PMID:
12716108
[PubMed - indexed for MEDLINE]
9.

A familial form of conduction defect related to a mutation in the PRKAG2 gene.

Charron P, Genest M, Richard P, Komajda M, Pochmalicki G.

Europace. 2007 Aug;9(8):597-600. Epub 2007 May 4.

PMID:
17483151
[PubMed - indexed for MEDLINE]
Free Article
10.

Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome.

Patel VV, Arad M, Moskowitz IP, Maguire CT, Branco D, Seidman JG, Seidman CE, Berul CI.

J Am Coll Cardiol. 2003 Sep 3;42(5):942-51.

PMID:
12957447
[PubMed - indexed for MEDLINE]
Free Article
11.

Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history.

Murphy RT, Mogensen J, McGarry K, Bahl A, Evans A, Osman E, Syrris P, Gorman G, Farrell M, Holton JL, Hanna MG, Hughes S, Elliott PM, Macrae CA, McKenna WJ.

J Am Coll Cardiol. 2005 Mar 15;45(6):922-30.

PMID:
15766830
[PubMed - indexed for MEDLINE]
Free Article
12.

[A familial form of conduction defects associated with a PRKAG2 gene mutation].

Pochmalicki G, Genest M, Richard P, Komajda M, Charron P.

Arch Mal Coeur Vaiss. 2007 Sep;100(9):760-5. French.

PMID:
18033003
[PubMed - indexed for MEDLINE]
13.

Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.

Arad M, Moskowitz IP, Patel VV, Ahmad F, Perez-Atayde AR, Sawyer DB, Walter M, Li GH, Burgon PG, Maguire CT, Stapleton D, Schmitt JP, Guo XX, Pizard A, Kupershmidt S, Roden DM, Berul CI, Seidman CE, Seidman JG.

Circulation. 2003 Jun 10;107(22):2850-6. Epub 2003 Jun 2.

PMID:
12782567
[PubMed - indexed for MEDLINE]
Free Article
14.

A contemporary approach to hypertrophic cardiomyopathy.

Ho CY, Seidman CE.

Circulation. 2006 Jun 20;113(24):e858-62. Review. No abstract available.

PMID:
16785342
[PubMed - indexed for MEDLINE]
Free Article
15.

Mutation in the γ2-subunit of AMP-activated protein kinase stimulates cardiomyocyte proliferation and hypertrophy independent of glycogen storage.

Kim M, Hunter RW, Garcia-Menendez L, Gong G, Yang YY, Kolwicz SC Jr, Xu J, Sakamoto K, Wang W, Tian R.

Circ Res. 2014 Mar 14;114(6):966-75. doi: 10.1161/CIRCRESAHA.114.302364. Epub 2014 Feb 6.

PMID:
24503893
[PubMed - indexed for MEDLINE]
16.

[Same genotype and different phenotypes in a family with PRKAG2 gene mutation].

Hong K, Oliva A, Cheng XS, Brugada P, Brugada J, Sternick EB, Brugada R.

Zhonghua Xin Xue Guan Bing Za Zhi. 2007 Jun;35(6):552-4. Chinese.

PMID:
17711718
[PubMed - indexed for MEDLINE]
17.

[Inherited metabolic cardiomyopathies].

Germain DP, Linhart A, Desnos M, Hagège AA.

Presse Med. 2007 Mar;36 Spec No 1:1S48-54. Review. French.

PMID:
17546768
[PubMed - indexed for MEDLINE]
18.

Fatal infantile cardiac glycogenosis with phosphorylase kinase deficiency and a mutation in the gamma2-subunit of AMP-activated protein kinase.

Akman HO, Sampayo JN, Ross FA, Scott JW, Wilson G, Benson L, Bruno C, Shanske S, Hardie DG, Dimauro S.

Pediatr Res. 2007 Oct;62(4):499-504.

PMID:
17667862
[PubMed - indexed for MEDLINE]
19.

Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy.

Ahmad F, Arad M, Musi N, He H, Wolf C, Branco D, Perez-Atayde AR, Stapleton D, Bali D, Xing Y, Tian R, Goodyear LJ, Berul CI, Ingwall JS, Seidman CE, Seidman JG.

Circulation. 2005 Nov 15;112(20):3140-8. Epub 2005 Nov 7.

PMID:
16275868
[PubMed - indexed for MEDLINE]
Free Article
20.

Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis.

Oliveira SM, Ehtisham J, Redwood CS, Ostman-Smith I, Blair EM, Watkins H.

J Mol Cell Cardiol. 2003 Oct;35(10):1251-5.

PMID:
14519435
[PubMed - indexed for MEDLINE]

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