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Judge, Daniel
One or more keywords matched the following items that are connected to
Judge, Daniel
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Pedigree
Academic Article
Exercise has a disproportionate role in the pathogenesis of arrhythmogenic right ventricular dysplasia/cardiomyopathy in patients without desmosomal mutations.
Academic Article
Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype?
Academic Article
Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome.
Academic Article
Genetic evaluation of familial cardiomyopathy.
Academic Article
Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article
Characterization of microsatellite markers flanking FBN1: utility in the diagnostic evaluation for Marfan syndrome.
Academic Article
Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2.
Academic Article
Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype.
Academic Article
Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article
Giant Ring Mitochondria in a Patient With Heart Failure and Cerebral White Matter Disease Resulting From an MT-TL1 Mitochondrial Gene Mutation.
Academic Article
The Role of Genetics in Peripartum Cardiomyopathy.
Academic Article
Role of Genetic Testing in Inherited Cardiovascular Disease: A Review.
Academic Article
Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia.
Academic Article
Use of genetics in the clinical evaluation of cardiomyopathy.
Academic Article
Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article
Risk stratification in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.
Academic Article
Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC).
Academic Article
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo.
Academic Article
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features.
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Pedigree