Pages that link to "Q72848599"
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The following pages link to The cardiomyopathy of progressive muscular dystrophy (Q72848599):
Displaying 50 items.
- High incidence of electrocardiogram abnormalities in young patients with duchenne muscular dystrophy (Q24316932) (← links)
- A highly stable and nonintegrated human artificial chromosome (HAC) containing the 2.4 Mb entire human dystrophin gene (Q24631410) (← links)
- Echocardiographic evaluation of fibrous replacement in the myocardium of patients with Duchenne muscular dystrophy (Q30536911) (← links)
- Cardiac involvement in Beagle-based canine X-linked muscular dystrophy in Japan (CXMDJ): electrocardiographic, echocardiographic, and morphologic studies (Q33265240) (← links)
- Myocardial inflammation in Duchenne Muscular Dystrophy as a precipitating factor for heart failure: a prospective study (Q33584263) (← links)
- Dystrophin analysis in idiopathic dilated cardiomyopathy (Q33596006) (← links)
- Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex (Q33732306) (← links)
- Assessment of left ventricular regional function in affected and carrier dogs with duchenne muscular dystrophy using speckle tracking echocardiography (Q33910571) (← links)
- Latent physiological factors of complex human diseases revealed by independent component analysis of clinarrays (Q34259513) (← links)
- Mutation rate in Duchenne type of muscular dystrophy (Q34634019) (← links)
- The nosology of the spinal muscular atrophies (Q34634645) (← links)
- Abnormalities of the electrocardiogram in hereditary myopathies (Q34635213) (← links)
- Cardiomyopathy and neuromyopathic disorders: clinical aspects. (Q35143398) (← links)
- Cardiomyopathy and neuromyopathic disorders: pathological aspects (Q35143414) (← links)
- Cardiac involvement in the Kugelberg-Welander syndrome (Q35263869) (← links)
- Development of Duchenne-type cardiomyopathy. Morphologic studies in a canine model. (Q35817154) (← links)
- X-Linked Dilated Cardiomyopathy: A Cardiospecific Phenotype of Dystrophinopathy (Q35818371) (← links)
- Age-matched comparison reveals early electrocardiography and echocardiography changes in dystrophin-deficient dogs (Q35819142) (← links)
- Effect of adopting a new histological grading system of acute rejection after heart transplantation. (Q35843162) (← links)
- Association of Congenital Heart Disease with Syndromes or Other Defects (Q35879938) (← links)
- GRMD cardiac and skeletal muscle metabolism gene profiles are distinct (Q36340997) (← links)
- Q wave T wave vector discordance in hypertrophic cardiomyopathy: septal hypertrophy and strain pattern (Q36766759) (← links)
- Translating golden retriever muscular dystrophy microarray findings to novel biomarkers for cardiac/skeletal muscle function in Duchenne muscular dystrophy (Q36813841) (← links)
- X-linked recessive (Duchenne) muscular dystrophy (DMD) and purine metabolism: Effects of oral allopurinol and adenylate (Q39179958) (← links)
- Complete genetic correction of ips cells from Duchenne muscular dystrophy (Q39641162) (← links)
- Clinical pathologic conference. Duchenne's muscular dystrophy (Q39833353) (← links)
- Left ventricular T2 distribution in Duchenne muscular dystrophy (Q39835697) (← links)
- An evaluation of some carrier detection techniques in Duchenne muscular dystrophy (Q39904919) (← links)
- Cardiac problems in patients with neurologic disease. (Q40446998) (← links)
- Neurogenic skeletal myopathy in patients with primary cardiomyopathy (Q40990508) (← links)
- Echocardiographic assessment of left ventricular function in Duchenne's muscular dystrophy (Q41331538) (← links)
- Cardiorespiratory changes in progressive muscular dystrophy (Q41361266) (← links)
- ECG abnormalities in myopathies, coronary heart disease and controls (Q41635733) (← links)
- Sequential changes of orthogonal electrocardiograms in progressive muscular dystrophy of the Duchenne type (Q41660061) (← links)
- The heart in Leber's optic atrophy (Q41846698) (← links)
- Succinylcholine-induced cardiac arrest in unsuspected Duchenne muscular dystrophy (Q42256600) (← links)
- Subclinical cardiomyopathy in Becker muscular dystrophy (Q42577975) (← links)
- Limb girdle type muscular dystrophy associated with a Wolff-Parkinson-White syndrome (Q42587830) (← links)
- Presence of mechanical dyssynchrony in duchenne muscular dystrophy (Q42615657) (← links)
- Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy (Q44163813) (← links)
- Acute pulmonary edema as the inaugural symptom of Becker's muscular dystrophy in a 19-year-old patient (Q44187392) (← links)
- Myocardiopathy in Duchenne progressive muscular dystrophy (Q44436285) (← links)
- Duchenne's cardiomyopathy in a canine model: electrocardiographic and echocardiographic studies (Q44688951) (← links)
- The pathology of the heart in progressive muscular dystrophy: epimyocardial fibrosis (Q44764309) (← links)
- Cardiac arrest during induction of anesthesia in Duchenne muscular dystrophy (Q44962851) (← links)
- Cardiac transplantation in Becker muscular dystrophy (Q45091890) (← links)
- CT features of myocardial fat and correlation with clinical background in patients without cardiac disease (Q45342082) (← links)
- Steroid therapy and cardiac function in Duchenne muscular dystrophy. (Q46577754) (← links)
- Spinal deformity in progressive neuromuscular disease. Natural history and management. (Q46636459) (← links)
- A 900 bp genomic region from the mouse dystrophin promoter directs lacZ reporter expression only to the right heart of transgenic mice (Q48048927) (← links)