PubMed (OMIM) for id: 12162

Year	Number of Results
1959	1
1967	1
1969	1
1978	2
1982	1
1987	1
1992	1
1995	1
1997	2
1999	1
2000	4
2001	5
2002	1
2003	1
2004	2
2005	2
2024	0

1

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.

2

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.

3

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.

4

Hereditary occurrence of the pre-excitation (Wolff-Parkinson-White) syndrome with re-entry mechanism and concealed conduction.

HARNISCHFEGER WW. HARNISCHFEGER WW. Circulation. 1959 Jan;19(1):28-40. doi: 10.1161/01.cir.19.1.28. Circulation. 1959. PMID: 13619017 No abstract available.

5

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. Arad M, et al. Circulation. 2003 Jun 10;107(22):2850-6. doi: 10.1161/01.CIR.0000075270.13497.2B. Epub 2003 Jun 2. Circulation. 2003. PMID: 12782567

6

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. Arad M, et al. J Clin Invest. 2002 Feb;109(3):357-62. doi: 10.1172/JCI14571. J Clin Invest. 2002. PMID: 11827995 Free PMC article.

7

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. Gollob MH, et al. Circulation. 2001 Dec 18;104(25):3030-3. doi: 10.1161/hc5001.102111. Circulation. 2001. PMID: 11748095

8

A gene responsible for familial Wolff-Parkinson-White syndrome.

Anderson KP, Vidaillet HJ Jr, Josephson ME. Anderson KP, et al. N Engl J Med. 2001 Oct 4;345(14):1063-4. doi: 10.1056/NEJM200110043451412. N Engl J Med. 2001. PMID: 11586962 No abstract available.

9

An activating mutation in the gamma1 subunit of the AMP-activated protein kinase.

Hamilton SR, Stapleton D, O'Donnell JB Jr, Kung JT, Dalal SR, Kemp BE, Witters LA. Hamilton SR, et al. FEBS Lett. 2001 Jul 6;500(3):163-8. doi: 10.1016/s0014-5793(01)02602-3. FEBS Lett. 2001. PMID: 11445078 Free article.

10

Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.

Gollob MH, Green MS, Tang AS, Gollob T, Karibe A, Ali Hassan AS, Ahmad F, Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R. Gollob MH, et al. N Engl J Med. 2001 Jun 14;344(24):1823-31. doi: 10.1056/NEJM200106143442403. N Engl J Med. 2001. PMID: 11407343 Free article.

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