-
1
-
-
78649960584
-
Neuromuscular disorders in left ventricular hypertrabeculation/ noncompaction
-
J. Finsterer, C. Stöllberger, and G. Fazio Neuromuscular disorders in left ventricular hypertrabeculation/noncompaction Curr Pharm Des 16 2010 2895 2904
-
(2010)
Curr Pharm des
, vol.16
, pp. 2895-2904
-
-
Finsterer, J.1
Stöllberger, C.2
Fazio, G.3
-
2
-
-
34250377470
-
Inclusion body myositis: Current pathogenetic concepts and diagnostic and therapeutic approaches
-
M. Needham, and F.L. Mastaglia Inclusion body myositis: current pathogenetic concepts and diagnostic and therapeutic approaches Lancet Neurol 6 2007 620 631
-
(2007)
Lancet Neurol
, vol.6
, pp. 620-631
-
-
Needham, M.1
Mastaglia, F.L.2
-
3
-
-
84866329572
-
Pathogenesis and therapy of inclusion body myositis
-
S.A. Greenberg Pathogenesis and therapy of inclusion body myositis Curr Opin Neurol 25 2012 630 639
-
(2012)
Curr Opin Neurol
, vol.25
, pp. 630-639
-
-
Greenberg, S.A.1
-
4
-
-
0028787389
-
Inclusion body myositis and myopathies
-
R.C. Griggs, V. Askanas, and S. DiMauro Inclusion body myositis and myopathies Ann Neurol 38 1995 705 713
-
(1995)
Ann Neurol
, vol.38
, pp. 705-713
-
-
Griggs, R.C.1
Askanas, V.2
Dimauro, S.3
-
6
-
-
0019481203
-
Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation
-
I. Nonaka, N. Sunohara, S. Ishiura, and E. Satoyoshi Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation J Neurol Sci 51 1981 141 155
-
(1981)
J Neurol Sci
, vol.51
, pp. 141-155
-
-
Nonaka, I.1
Sunohara, N.2
Ishiura, S.3
Satoyoshi, E.4
-
7
-
-
27144483812
-
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene
-
D. Haubenberger, R.E. Bittner, and S. Rauch-Shorny Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene Neurology 65 2005 1304 1305
-
(2005)
Neurology
, vol.65
, pp. 1304-1305
-
-
Haubenberger, D.1
Bittner, R.E.2
Rauch-Shorny, S.3
-
9
-
-
17044449684
-
Left ventricular hypertrabeculation/noncompaction
-
C. Stöllberger, and J. Finsterer Left ventricular hypertrabeculation/noncompaction J Am Soc Echocardiogr 17 2004 91 100
-
(2004)
J Am Soc Echocardiogr
, vol.17
, pp. 91-100
-
-
Stöllberger, C.1
Finsterer, J.2
-
10
-
-
34249277737
-
Cardiologic and neurologic findings in left ventricular hypertrabeculation/noncompaction relating to echocardiographic indication
-
C. Stöllberger, M. Winkler-Dworak, G. Blazek, and J. Finsterer Cardiologic and neurologic findings in left ventricular hypertrabeculation/ noncompaction relating to echocardiographic indication Int J Cardiol 119 2007 28 32
-
(2007)
Int J Cardiol
, vol.119
, pp. 28-32
-
-
Stöllberger, C.1
Winkler-Dworak, M.2
Blazek, G.3
Finsterer, J.4
-
11
-
-
79960188921
-
Left ventricular hypertrabeculation/noncompaction in hereditary inclusion body myopathy
-
J. Finsterer, C. Stöllberger, and R. Höftberger Left ventricular hypertrabeculation/noncompaction in hereditary inclusion body myopathy Int J Cardiol 150 2011 e67 e69
-
(2011)
Int J Cardiol
, vol.150
-
-
Finsterer, J.1
Stöllberger, C.2
Höftberger, R.3
-
12
-
-
84861839657
-
Stroke and stroke-like episodes in muscle disease
-
J. Finsterer Stroke and stroke-like episodes in muscle disease Open Neurol J 6 2012 26 36
-
(2012)
Open Neurol J
, vol.6
, pp. 26-36
-
-
Finsterer, J.1
-
13
-
-
21744448369
-
Noncompaction in myotonic dystrophy type 1 on cardiac MRI
-
J. Finsterer, C. Stölberger, and W. Kopsa Noncompaction in myotonic dystrophy type 1 on cardiac MRI Cardiology 103 2005 167 168
-
(2005)
Cardiology
, vol.103
, pp. 167-168
-
-
Finsterer, J.1
Stölberger, C.2
Kopsa, W.3
-
14
-
-
42649101980
-
Left ventricular non-compaction in a patient with myotonic dystrophy type 2
-
K. Wahbi, C. Meune, and G. Bassez Left ventricular non-compaction in a patient with myotonic dystrophy type 2 Neuromuscul Disord 18 2008 331 333
-
(2008)
Neuromuscul Disord
, vol.18
, pp. 331-333
-
-
Wahbi, K.1
Meune, C.2
Bassez, G.3
-
15
-
-
23644452964
-
Left ventricular hypertrabeculation/noncompaction as a cardiac manifestation of Duchenne muscular dystrophy under non-invasive positive-pressure ventilation
-
J. Finsterer, E. Gelpi, and C. Stöllberger Left ventricular hypertrabeculation/noncompaction as a cardiac manifestation of Duchenne muscular dystrophy under non-invasive positive-pressure ventilation Acta Cardiol 60 2005 445 448
-
(2005)
Acta Cardiol
, vol.60
, pp. 445-448
-
-
Finsterer, J.1
Gelpi, E.2
Stöllberger, C.3
-
17
-
-
0344873698
-
Mutations in cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction
-
M. Vatta, B. Mohapatra, and S. Jimenez Mutations in cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction J Am Coll Cardiol 42 2003 2014 2027
-
(2003)
J Am Coll Cardiol
, vol.42
, pp. 2014-2027
-
-
Vatta, M.1
Mohapatra, B.2
Jimenez, S.3
-
18
-
-
3042519038
-
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations
-
M. Hermida-Prieto, L. Monserrat, and A. Castro-Beiras Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations Am J Cardiol 94 2004 50 54
-
(2004)
Am J Cardiol
, vol.94
, pp. 50-54
-
-
Hermida-Prieto, M.1
Monserrat, L.2
Castro-Beiras, A.3
-
19
-
-
2542486394
-
Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK binding protein-12
-
A.B. Kenton, X. Sanchez, and K.J. Coveler Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK binding protein-12 Mol Genet Metab 82 2004 162 166
-
(2004)
Mol Genet Metab
, vol.82
, pp. 162-166
-
-
Kenton, A.B.1
Sanchez, X.2
Coveler, K.J.3
-
20
-
-
78751575267
-
Oculopharyngodistal myopathy - A possible association with cardiomyopathy
-
W. Thevathasan, W. Squier, D.H. Maciver, D.A. Hilton, E. Fathers, and D. Hilton-Jones Oculopharyngodistal myopathy - a possible association with cardiomyopathy Neuromuscul Disord 21 2011 121 125
-
(2011)
Neuromuscul Disord
, vol.21
, pp. 121-125
-
-
Thevathasan, W.1
Squier, W.2
Maciver, D.H.3
Hilton, D.A.4
Fathers, E.5
Hilton-Jones, D.6
-
21
-
-
84868638909
-
Left ventricular noncompaction cardiomyopathy and aortopathy in a patient with recessive dystrophic epidermolysis bullosa
-
T.D. Ryan, S.M. Ware, A.W. Lucky, J.A. Towbin, J.L. Jefferies, and R.B. Hinton Left ventricular noncompaction cardiomyopathy and aortopathy in a patient with recessive dystrophic epidermolysis bullosa Circ Heart Fail 5 2012 e81 e82
-
(2012)
Circ Heart Fail
, vol.5
-
-
Ryan, T.D.1
Ware, S.M.2
Lucky, A.W.3
Towbin, J.A.4
Jefferies, J.L.5
Hinton, R.B.6
-
22
-
-
0344844423
-
Clinical characterization of left ventricular noncompaction in children: A relatively common form of cardiomyopathy
-
R.H. Pignatelli, C.J. McMahon, and W.J. Dreyer Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy Circulation 108 2003 2672 2678
-
(2003)
Circulation
, vol.108
, pp. 2672-2678
-
-
Pignatelli, R.H.1
McMahon, C.J.2
Dreyer, W.J.3
-
23
-
-
84865958738
-
Thrombolysis of ischemic stroke from noncompaction in metabolic myopathy
-
J. Finsterer, C. Stöllberger, and G. Sodeck Thrombolysis of ischemic stroke from noncompaction in metabolic myopathy Neurologist 18 2012 296 297
-
(2012)
Neurologist
, vol.18
, pp. 296-297
-
-
Finsterer, J.1
Stöllberger, C.2
Sodeck, G.3
-
24
-
-
4043152735
-
Myoadenylate-deaminase gene mutation associated with left ventricular hypertrabeculation/non-compaction
-
J. Finsterer, B. Schoser, and C. Stöllberger Myoadenylate-deaminase gene mutation associated with left ventricular hypertrabeculation/non-compaction Acta Cardiol 59 2004 453 456
-
(2004)
Acta Cardiol
, vol.59
, pp. 453-456
-
-
Finsterer, J.1
Schoser, B.2
Stöllberger, C.3
-
25
-
-
84867655657
-
Noncompaction myocardium in association with type Ib glycogen storage disease
-
B. Goeppert, M. Lindner, and M.N. Vogel Noncompaction myocardium in association with type Ib glycogen storage disease Pathol Res Pract 208 2012 620 622
-
(2012)
Pathol Res Pract
, vol.208
, pp. 620-622
-
-
Goeppert, B.1
Lindner, M.2
Vogel, M.N.3
-
26
-
-
84864515189
-
Malonyl coenzyme A decarboxylase deficiency: Early dietary restriction and time course of cardiomyopathy
-
C.E. Prada, J.L. Jefferies, and M.A. Grenier Malonyl coenzyme A decarboxylase deficiency: early dietary restriction and time course of cardiomyopathy Pediatrics 130 2012 e456 e460
-
(2012)
Pediatrics
, vol.130
-
-
Prada, C.E.1
Jefferies, J.L.2
Grenier, M.A.3
-
27
-
-
81955164203
-
Coffin-Lowry syndrome and left ventricular noncompaction cardiomyopathy with a restrictive pattern
-
H.R. Martinez, M.C. Niu, V.R. Sutton, R. Pignatelli, M. Vatta, and J.L. Jefferies Coffin-Lowry syndrome and left ventricular noncompaction cardiomyopathy with a restrictive pattern Am J Med Genet A 155A 2011 3030 3034
-
(2011)
Am J Med Genet A
, vol.155 A
, pp. 3030-3034
-
-
Martinez, H.R.1
Niu, M.C.2
Sutton, V.R.3
Pignatelli, R.4
Vatta, M.5
Jefferies, J.L.6
-
28
-
-
33645473866
-
Left ventricular hypertrabeculation/noncompaction with PMP22 duplication-based Charcot-Marie-Tooth disease type 1A
-
G. Corrado, N. Checcarelli, M. Santarone, C. Stollberger, and J. Finsterer Left ventricular hypertrabeculation/noncompaction with PMP22 duplication-based Charcot-Marie-Tooth disease type 1A Cardiology 105 2006 142 145
-
(2006)
Cardiology
, vol.105
, pp. 142-145
-
-
Corrado, G.1
Checcarelli, N.2
Santarone, M.3
Stollberger, C.4
Finsterer, J.5
-
29
-
-
84862009401
-
Poliomyelitis and left ventricular hypertrabeculation (noncompaction)
-
J. Finsterer, and C. Stöllberger Poliomyelitis and left ventricular hypertrabeculation (noncompaction) Int J Cardiol 158 2012 e15 e16
-
(2012)
Int J Cardiol
, vol.158
-
-
Finsterer, J.1
Stöllberger, C.2
-
30
-
-
79955032183
-
Left ventricular noncompaction in Sotos syndrome
-
H.R. Martinez, J.W. Belmont, W.J. Craigen, M.D. Taylor, and J.L. Jefferies Left ventricular noncompaction in Sotos syndrome Am J Med Genet A 155A 2011 1115 1118
-
(2011)
Am J Med Genet A
, vol.155 A
, pp. 1115-1118
-
-
Martinez, H.R.1
Belmont, J.W.2
Craigen, W.J.3
Taylor, M.D.4
Jefferies, J.L.5
-
31
-
-
70350622068
-
High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuria
-
L.E. Profitlich, B. Kirmse, M.P. Wasserstein, G.A. Diaz, and S. Srivastava High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuria Mol Genet Metab 98 2009 344 348
-
(2009)
Mol Genet Metab
, vol.98
, pp. 344-348
-
-
Profitlich, L.E.1
Kirmse, B.2
Wasserstein, M.P.3
Diaz, G.A.4
Srivastava, S.5
|