-
1
-
-
33644809319
-
Is Wolff-Parkinson-White syndrome a genetic disease?
-
Ehtisham J, Watkins H. Is Wolff-Parkinson-White syndrome a genetic disease? J Cardiovasc Electrophysiol 2005: 16: 1258-1262.
-
(2005)
J Cardiovasc Electrophysiol
, vol.16
, pp. 1258-1262
-
-
Ehtisham, J.1
Watkins, H.2
-
2
-
-
0037329297
-
Glycogen storage disease as a unifying mechanism of disease in the PRKAG2 cardiac syndrome
-
Gollob MH. Glycogen storage disease as a unifying mechanism of disease in the PRKAG2 cardiac syndrome. Biochem Soc Trans 2003: 31: 228-231.
-
(2003)
Biochem Soc Trans
, vol.31
, pp. 228-231
-
-
Gollob, M.H.1
-
3
-
-
0035859215
-
Identification of a gene responsible for familial Wolff-Parkinson-White syndrome
-
Gollob MH, Green MS, Tang AS et al. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. N Engl J Med 2001: 344: 1823-1831.
-
(2001)
N Engl J Med
, vol.344
, pp. 1823-1831
-
-
Gollob, M.H.1
Green, M.S.2
Tang, A.S.3
-
4
-
-
0035910109
-
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 et al. Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy. Circulation 2001: 104: 3030-3033.
-
(2001)
Circulation
, vol.104
, pp. 3030-3033
-
-
Gollob, M.H.1
Seger, J.J.2
Gollob, T.N.3
-
5
-
-
33750370906
-
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. Ventricular pre-excitation and cardiac hypertrophy mimicking hypertrophic cardiomyopathy in a Turkish family with a novel PRKAG2 mutation. Eur J Heart Fail 2006: 8: 712-715.
-
(2006)
Eur J Heart Fail
, vol.8
, pp. 712-715
-
-
Bayrak, F.1
Komurcu-Bayrak, E.2
Mutlu, B.3
Kahveci, G.4
Basaran, Y.5
Erginel-Unaltuna, N.6
-
6
-
-
19944434362
-
Glycogen storage diseases presenting as hypertrophic cardiomyopathy
-
Arad M, Maron BJ, Gorham JM et al. Glycogen storage diseases presenting as hypertrophic cardiomyopathy. N Engl J Med 2005: 352: 362-372.
-
(2005)
N Engl J Med
, vol.352
, pp. 362-372
-
-
Arad, M.1
Maron, B.J.2
Gorham, J.M.3
-
7
-
-
33644977251
-
A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis
-
Laforet P, Richard P, Said MA et al. A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis. Neuromuscul Disord 2006: 16: 178-182.
-
(2006)
Neuromuscul Disord
, vol.16
, pp. 178-182
-
-
Laforet, P.1
Richard, P.2
Said, M.A.3
-
8
-
-
20044391423
-
Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history
-
Murphy RT, Mogensen J, McGarry K et al. Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history. J Am Coll Cardiol 2005: 45: 922-930.
-
(2005)
J Am Coll Cardiol
, vol.45
, pp. 922-930
-
-
Murphy, R.T.1
Mogensen, J.2
McGarry, K.3
-
10
-
-
0035872209
-
Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis
-
Blair E, Redwood C, Ashrafian H et al. Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis. Hum Mol Genet 2001: 10: 1215-1220.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1215-1220
-
-
Blair, E.1
Redwood, C.2
Ashrafian, H.3
-
11
-
-
0036167225
-
Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy
-
Arad M, Benson DW, Perez-Atayde AR et al. Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy. J Clin Invest 2002: 109: 357-362.
-
(2002)
J Clin Invest
, vol.109
, pp. 357-362
-
-
Arad, M.1
Benson, D.W.2
Perez-Atayde, A.R.3
-
12
-
-
84907597512
-
Familial conduction system abnormalities associated with ventricular pre-excitation and cardiac hypertrophy-A Department of Investigation and Analysis
-
Xing Z. Familial conduction system abnormalities associated with ventricular pre-excitation and cardiac hypertrophy-A Department of Investigation and Analysis. Chin J Cardiol 2007: 35: 258-259.
-
(2007)
Chin J Cardiol
, vol.35
, pp. 258-259
-
-
Xing, Z.1
-
13
-
-
84856559876
-
AMPK gamma2 subunit gene PRKAG2 polymorphism associated with cognitive impairment as well as diabetes in old age
-
Kim E, Lee SH, Lee KS et al. AMPK gamma2 subunit gene PRKAG2 polymorphism associated with cognitive impairment as well as diabetes in old age. Psychoneuroendocrinology 2012: 37: 358-365.
-
(2012)
Psychoneuroendocrinology
, vol.37
, pp. 358-365
-
-
Kim, E.1
Lee, S.H.2
Lee, K.S.3
-
14
-
-
0034541333
-
Molecular cloning, genomic organization, and mapping of PRKAG2: a heart abundant gamma2 subunit of 5'-AMP-activated protein kinase, to human chromosome 7q36
-
Lang T, Yu L, Tu Q et al. Molecular cloning, genomic organization, and mapping of PRKAG2: a heart abundant gamma2 subunit of 5'-AMP-activated protein kinase, to human chromosome 7q36. Genomics 2000: 70: 258-263.
-
(2000)
Genomics
, vol.70
, pp. 258-263
-
-
Lang, T.1
Yu, L.2
Tu, Q.3
-
15
-
-
19944429566
-
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 et al. 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. Circulation 2005: 111: 21-29.
-
(2005)
Circulation
, vol.111
, pp. 21-29
-
-
Sidhu, J.S.1
Rajawat, Y.S.2
Rami, T.G.3
-
16
-
-
85047691317
-
CBS domains form energy-sensing modules whose binding of adenosine ligands is disrupted by disease mutations
-
Scott JW, Hawley SA, Green KA et al. CBS domains form energy-sensing modules whose binding of adenosine ligands is disrupted by disease mutations. J Clin Invest 2004: 113: 274-284.
-
(2004)
J Clin Invest
, vol.113
, pp. 274-284
-
-
Scott, J.W.1
Hawley, S.A.2
Green, K.A.3
-
17
-
-
0037782349
-
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy
-
Arad M, Moskowitz IP, Patel VV et al. Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy. Circulation 2003: 107: 2850-2856.
-
(2003)
Circulation
, vol.107
, pp. 2850-2856
-
-
Arad, M.1
Moskowitz, I.P.2
Patel, V.V.3
-
18
-
-
34447125085
-
A PRKAG2 mutation causes biphasic changes in myocardial AMPK activity and does not protect against ischemia
-
Banerjee SK, Ramani R, Saba S et al. A PRKAG2 mutation causes biphasic changes in myocardial AMPK activity and does not protect against ischemia. Biochem Biophys Res Commun 2007: 360: 381-387.
-
(2007)
Biochem Biophys Res Commun
, vol.360
, pp. 381-387
-
-
Banerjee, S.K.1
Ramani, R.2
Saba, S.3
-
19
-
-
0030881788
-
Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form
-
Verloes A, Massin M, Lombet J et al. Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form. Am J Med Genet 1997: 72: 135-142.
-
(1997)
Am J Med Genet
, vol.72
, pp. 135-142
-
-
Verloes, A.1
Massin, M.2
Lombet, J.3
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