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PedAM

Pediatric Disease Annotations & Medicines




Disease cardiomyopathy
Phenotype C0028326|noonan syndrome
Sentences 6
PubMedID- PMC3944423 A lethal course of hypertrophic cardiomyopathy in noonan syndrome due to a novel germline mutation in the kras gene: case study.
PubMedID- 22980313 Background: studies of cardiomyopathy in children with noonan syndrome (ns) have been primarily small case series or cross-sectional studies with small or no comparison groups.
PubMedID- 20450268 Arrhythmogenic cardiomyopathy in a patient with noonan syndrome.
PubMedID- 23239527 Severe hypertrophic cardiomyopathy in noonan syndrome-consider sequencing genes encoding sarcomeric proteins.
PubMedID- 21269411 Survival implications: hypertrophic cardiomyopathy in noonan syndrome.
PubMedID- 24382853 A lethal course of hypertrophic cardiomyopathy in noonan syndrome due to a novel germline mutation in the kras gene: case study.

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