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Literature DB >> 22587749

Severe dilated cardiomyopathy in a patient with myotonic dystrophy type 2 and homozygous repeat expansion in ZNF9.

Teresa M Lee¹, Mathew S Maurer, Izabela Karbassi, Corey Braastad, Sat D Batish, Wendy K Chung.

Abstract

Entities: Chemical Disease Gene Species

Mesh：

Substances：

Year: 2011 PMID： 22587749 PMCID： PMC3678523 DOI： 10.1111/j.1751-7133.2011.00265.x

Source DB: PubMed Journal: Congest Heart Fail ISSN： 1527-5299

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12 in total

Review 1. The myotonic dystrophies: diagnosis and management.

Authors: Chris Turner; David Hilton-Jones
Journal: J Neurol Neurosurg Psychiatry Date: 2010-02-22 Impact factor: 10.154

Review 2. Cardiac involvement in primary myopathies.

Authors: J Finsterer; C Stöllberger
Journal: Cardiology Date: 2000 Impact factor: 1.869

Review 3. Cardiac involvement in patients with muscular dystrophies: magnetic resonance imaging phenotype and genotypic considerations.

Authors: David Verhaert; Kathryn Richards; Jill A Rafael-Fortney; Subha V Raman
Journal: Circ Cardiovasc Imaging Date: 2011-01 Impact factor: 7.792

Review 4. Sudden cardiac death in myotonic dystrophy type 2.

Authors: B G H Schoser; K Ricker; C Schneider-Gold; C Hengstenberg; J Dürre; B Bültmann; W Kress; J W Day; L P W Ranum
Journal: Neurology Date: 2004-12-28 Impact factor: 9.910

5. Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2).

Authors: J W Day; R Roelofs; B Leroy; I Pech; K Benzow; L P Ranum
Journal: Neuromuscul Disord Date: 1999-01 Impact factor: 4.296

6. Usefulness of clinical and electrocardiographic data for predicting adverse cardiac events in patients with myotonic dystrophy.

Authors: Robert Breton; Jean Mathieu
Journal: Can J Cardiol Date: 2009-02 Impact factor: 5.223

Severe dilated cardiomyopathy in a patient with myotonic dystrophy type 2 and homozygous repeat expansion in ZNF9.

Review 1. The myotonic dystrophies: diagnosis and management.

Review 2. Cardiac involvement in primary myopathies.

Review 3. Cardiac involvement in patients with muscular dystrophies: magnetic resonance imaging phenotype and genotypic considerations.

Review 4. Sudden cardiac death in myotonic dystrophy type 2.

5. Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2).

6. Usefulness of clinical and electrocardiographic data for predicting adverse cardiac events in patients with myotonic dystrophy.

7. Cardiac and skeletal muscle involvement in myotonic dystrophy type 2 (DM2): a quantitative 31P-MRS and MRI study.

8. Homozygosity for CCTG mutation in myotonic dystrophy type 2.

9. Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: a case control study.

10. Left ventricular non-compaction in a patient with myotonic dystrophy type 2.

Review 1. Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects.

Review 2. Biomolecular diagnosis of myotonic dystrophy type 2: a challenging approach.

Review 3. Recent advances in myotonic dystrophy type 2.

Review 4. Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the Nerves.

5. Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism.

Review 6. Modeling of Myotonic Dystrophy Cardiac Phenotypes in Drosophila.

7. A rare case report of severe cardiomyopathy associated with myotonic dystrophy type 2.