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Publications by Masashi Kanemoto
Japanese Patients With Fabry Disease Predominantly Showing Cardiac and Neurological Manifestation With Novel Missense Mutation: R220P
Journal of Cardiology
Cardiovascular Medicine
Cardiology
A Rare Case of Complete Stent Fracture, Coronary Arterial Transection, and Pseudoaneurysm Formation Induced by Repeated Stenting
Case Reports in Cardiology
Cardiovascular Medicine
Cardiology
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Novel Α-Galactosidase a Mutation (K391E) in a Young Woman With Severe Cardiac and Renal Manifestations of Fabry Disease
International Heart Journal
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TRPM4 Mutation in Patients With Ventricular Noncompaction and Cardiac Conduction Disease
Circulation. Genomic and precision medicine
Genetics
Cardiovascular Medicine
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AB050. Later Onset Fabry Disease, Cardiac Damage Progress in Silence-Experience With a Highly Prevalent Mutation
Annals of Translational Medicine
Medicine
Cognitive Impairment and Fabry Disease: A Case Report With Mutation S126G
Neuropsychological Trends
Molecular Neuroscience
Physiological Psychology
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X-Linked Adrenal Hypoplasia Congenita With a Novel DAX1 Missense Mutation
Endocrine Abstracts
Epidemiological and Clinical Profile of Patients With Fabry Disease
Revista de Enfermagem UFPE on line
A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia
Reproductive Sciences
Gynecology
Obstetrics
Clinical Presentation in Female Patients With Fabry Disease
Journal of Medical Genetics
Genetics
Two Novel Missense Mutations in the Myostatin Gene Identified in Japanese Patients With Duchenne Muscular Dystrophy
BMC Medical Genetics
Genetics