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CMR demonstration of multiple morphological phenotypes in Anderson-Fabry diseaseDOI 10.1186/1532-429x-17-s1-q68
A new phenotype of Fabry disease with intermediate severity between the classical form and the cardiac variant.Semantic proximity
A predominant cardiac phenotype of Anderson-Fabry disease in presence of a MYBPC3 gene mutation and a LAMA4 gene mutation.Semantic proximity
Many Faces of Fabry's Cardiomyopathy.Semantic proximity
The heart in Fabry's diseaseSemantic proximity
Cardiac manifestations of Fabry's disease: a story of mother and son.Semantic proximity
Guidelines to diagnosis and monitoring of Fabry disease and review of treatment experiences.Semantic proximity
Anderson-Fabry disease.Semantic proximity
The Changing Landscape of Fabry Disease.Semantic proximity
Hypertrophic cardiomyopathy and Anderson-Fabry disease: unravelling septal hypertrophy with T1-mapping CMR.Semantic proximity
Different Phenotypes of Anderson-Fabry Disease Identified with Cardiac Magnetic Resonance Imaging in a Family with the Same Late-Onset Mutation.Semantic proximity
Classical and non‐classical phenotypes of Erdheim–Chester disease: Correlating clinical, radiographic and genotypic findingsSemantic proximity
The Value of Advanced Cardiac Magnetic Resonance Imaging Technologies in Detecting the Characteristics of Cardiac Involvement in Anderson-Fabry DiseaseSemantic proximity
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