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Review Article

Primary myopathies and the heart

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Pages 9-24 | Received 18 Jul 2007, Published online: 12 Jul 2009

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Claudia Stöllberger & Josef Finsterer. (2019) Understanding left ventricular hypertrabeculation/noncompaction: pathomorphologic findings and prognostic impact of neuromuscular comorbidities. Expert Review of Cardiovascular Therapy 17:2, pages 95-109.
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Articles from other publishers (57)

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Evan M. Harvey, Murad Almasri & Hugo R. Martinez. 2021. Cardiomyopathy - Disease of the Heart Muscle. Cardiomyopathy - Disease of the Heart Muscle.
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Hugo R. Martinez, Gary S. Beasley, John Jefferies & Jeffrey A. Towbin. 2020. Pediatric and Congenital Cardiology, Cardiac Surgery and Intensive Care. Pediatric and Congenital Cardiology, Cardiac Surgery and Intensive Care 1 41 .
Claudia Stöllberger, Matthias Hasun, Maria Winkler-Dworak & Josef Finsterer. (2020) Usefulness of Neuromuscular Co-morbidity, Left Bundle Branch Block, and Atrial Fibrillation to Predict the Long-Term Prognosis of Left Ventricular Hypertrabeculation/Noncompaction. The American Journal of Cardiology 128, pages 168-173.
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Jeffrey A. Towbin, Kaitlin Ryan & Jason Goldberg. 2019. Noncompaction Cardiomyopathy. Noncompaction Cardiomyopathy 95 126 .
Martin J. Goddard. (2018) The spectrum of inheritable cardiac disease in sudden cardiac death: investigation and pathology. Diagnostic Histopathology 24:9, pages 346-356.
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C. Stöllberger, C. Wegner & J. Finsterer. (2018) Left ventricular hypertrabeculation/noncompaction, cardiac phenotype, and neuromuscular disordersLinksventrikuläre Hypertrabekulierung/Noncompaction, kardialer Phänotyp und neuromuskuläre Erkrankungen. Herz.
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Karen Koitka, Arun Dahiya, Ada Lo, Gregory M. Scalia, John J. Atherton & Sandhir B. Prasad. (2017) Myofibrillar Cardiomyopathy due to a Novel Desmin Gene Mutation: Complementary Role of Echocardiography, Cardiac Magnetic Resonance, and Genetic Testing in Delineating Diagnosis. CASE 1:1, pages 28-33.
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J.A. Towbin. 2017. Cardioskeletal Myopathies in Children and Young Adults. Cardioskeletal Myopathies in Children and Young Adults 153 171 .
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ROBERTA MANUGUERRA, SERGIO CALLEGARI & DOMENICO CORRADI. (2016) Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence. Journal of Cardiovascular Electrophysiology 27:2, pages 242-252.
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Claudia Stöllberger, Gerhard Blazek, Martin Gessner, Katharina Bichler, Christian Wegner & Josef Finsterer. (2015) Neuromuscular comorbidity, heart failure, and atrial fibrillation as prognostic factors in left ventricular hypertrabeculation/noncompactionNeuromuskuläre Komorbidität, Herzinsuffizienz und Vorhofflimmern bestimmen die Prognose bei linksventrikulärer Hypertrabekulierung/Noncompaction. Herz 40:6, pages 906-911.
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Josef Finsterer, Romana Höftberger, Boris Rolinski, Claudia Stöllberger, Adelheid Wöhrer & Walter Benedikt Winkler. (2014) Presumed mitochondrial disease manifesting with recurrent syncopes. Journal of Cardiovascular Medicine 15:2, pages 167-169.
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Kim L. McBride & Vidu Garg. (2010) Impact of Mendelian inheritance in cardiovascular disease. Annals of the New York Academy of Sciences 1214:1, pages 122-137.
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Maria Marques, Isabel Barbin, Ana Taniguti, Daniela Oggian, R. Ferretti & H. Santo Neto. (2010) Myocardial fibrosis is unaltered by long-term administration of L-arginine in dystrophin deficient mdx mice: A histomorphometric analysis . Acta Biologica Hungarica 61:2, pages 168-174.
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S. Lutz, B. Stiegler, W. Kress, M. von der Hagen & U. Schara. (2009) Kongenitale StrukturmyopathienCongenital myopathies. medizinische genetik 21:3, pages 316-321.
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J. T. KisselE. L. DimbergA. M. Emslie-SmithD. SelcenB. M. Keegan. (2009) A 49-year-old man with contractures, weakness, and cardiac arrhythmia. Neurology 72:23, pages 2036-2043.
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M. C. Sharma, D. Jain, C. Sarkar & H. H. Goebel. (2009) Congenital myopathies - a comprehensive update of recent advancements. Acta Neurologica Scandinavica 119:5, pages 281-292.
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