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Publications by Hiroaki Wakakuri

Novel Α-Galactosidase a Mutation (K391E) in a Young Woman With Severe Cardiac and Renal Manifestations of Fabry Disease

International Heart Journal

Cardiovascular Medicine

English

Related publications

Fabry Disease: Twenty Novel Α-Galactosidase a Mutations Causing the Classical Phenotype

Journal of Human Genetics

English

Fabry Disease: Twenty Novel Α-Galactosidase a Mutations and Genotype-Phenotype Correlations in Classical and Variant Phenotypes

Molecular Medicine

Molecular Medicine

Molecular Biology

English

Receptor-Mediated Endocytosis of Α-Galactosidase a in Human Podocytes in Fabry Disease

Multidisciplinary

English

Α-Galactosidase a Genotype N215S Induces a Specific Cardiac Variant of Fabry DiseaseCLINICAL PERSPECTIVE

Circulation: Cardiovascular Genetics

English

Adipocytes Participate in Storage in Α-Galactosidase Deficiency (Fabry Disease)

Journal of Inherited Metabolic Disease

English

Japanese Patients With Fabry Disease Predominantly Showing Cardiac and Neurological Manifestation With Novel Missense Mutation: R220P

Journal of Cardiology

Cardiovascular Medicine

English

Distribution of -Galactosidase a in Normal Human Kidney and Renal Accumulation and Distribution of Recombinant -Galactosidase a in Fabry Mice

Journal of the American Society of Nephrology : JASN

English

Cardiovascular Manifestations of Fabry Disease and the Novel Therapeutic Strategies

Journal of Nippon Medical School

English

Replacement of Α-Galactosidase a in Fabry Disease: Effect on Fibroblast Cultures Compared With Biopsied Tissues of Treated Patients

Virchows Archiv

Forensic Medicine

Molecular Biology

English