PubMed (OMIM) for id: 51422

Year	Number of Results
1959	1
1967	1
1969	1
1978	2
1982	1
1984	1
1985	1
1987	1
1988	1
1992	1
1993	1
1995	1
1997	2
1999	2
2000	4
2001	5
2002	1
2003	2
2004	2
2005	3
2006	2
2007	1
2008	2
2009	1
2024	0

1

Severe hypertrophic cardiomyopathy in an infant with a novel PRKAG2 gene mutation: potential differences between infantile and adult onset presentation.

Kelly BP, Russell MW, Hennessy JR, Ensing GJ. Kelly BP, et al. Pediatr Cardiol. 2009 Nov;30(8):1176-9. doi: 10.1007/s00246-009-9521-3. Pediatr Cardiol. 2009. PMID: 19787389

2

AMP-activated protein kinase: structure and regulation.

Sanz P. Sanz P. Curr Protein Pept Sci. 2008 Oct;9(5):478-92. doi: 10.2174/138920308785915254. Curr Protein Pept Sci. 2008. PMID: 18855699 Free article. Review.

3

Shared genetic causes of cardiac hypertrophy in children and adults.

Morita H, Rehm HL, Menesses A, McDonough B, Roberts AE, Kucherlapati R, Towbin JA, Seidman JG, Seidman CE. Morita H, et al. N Engl J Med. 2008 May 1;358(18):1899-908. doi: 10.1056/NEJMoa075463. Epub 2008 Apr 9. N Engl J Med. 2008. PMID: 18403758 Free PMC article.

4

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. Akman HO, et al. Pediatr Res. 2007 Oct;62(4):499-504. doi: 10.1203/PDR.0b013e3181462b86. Pediatr Res. 2007. PMID: 17667862

5

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. Bayrak F, et al. Eur J Heart Fail. 2006 Nov;8(7):712-5. doi: 10.1016/j.ejheart.2006.03.006. Epub 2006 May 22. Eur J Heart Fail. 2006. PMID: 16716659 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. Laforêt P, et al. Neuromuscul Disord. 2006 Mar;16(3):178-82. doi: 10.1016/j.nmd.2005.12.004. Epub 2006 Feb 17. Neuromuscul Disord. 2006. PMID: 16487706

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. Burwinkel B, et al. Am J Hum Genet. 2005 Jun;76(6):1034-49. doi: 10.1086/430840. Epub 2005 May 2. Am J Hum Genet. 2005. PMID: 15877279 Free PMC article.

8

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. Arad M, et al. N Engl J Med. 2005 Jan 27;352(4):362-72. doi: 10.1056/NEJMoa033349. N Engl J Med. 2005. PMID: 15673802 Free article.

9

Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome.

Sidhu JS, Rajawat YS, Rami TG, Gollob MH, Wang Z, Yuan R, Marian AJ, DeMayo FJ, Weilbacher D, Taffet GE, Davies JK, Carling D, Khoury DS, Roberts R. Sidhu JS, et al. Circulation. 2005 Jan 4;111(1):21-9. doi: 10.1161/01.CIR.0000151291.32974.D5. Epub 2004 Dec 20. Circulation. 2005. PMID: 15611370 Free PMC article.

10

Radiofrequency ablation in children with asymptomatic Wolff-Parkinson-White syndrome.

Pappone C, Manguso F, Santinelli R, Vicedomini G, Sala S, Paglino G, Mazzone P, Lang CC, Gulletta S, Augello G, Santinelli O, Santinelli V. Pappone C, et al. N Engl J Med. 2004 Sep 16;351(12):1197-205. doi: 10.1056/NEJMoa040625. N Engl J Med. 2004. PMID: 15371577 Free article. Clinical Trial.

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