Tomohiko Yamamura

11PUBLICATIONS
41CO-AUTHORS
Medical infection agents (incl. prions)Infant and child healthGene and molecular therapyDevelopmental genetics (incl. sex determination)Neurology and neuromuscular diseases
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Publications (11)

|Jan 08, 2025
Exon Skipping Therapies for Rare Kidney Diseases.

Tomohiko Yamamura, Kandai Nozu

|Aug 13, 2024
Clinical, Pathological, and Genetic Characteristics of Patients with Digenic Alport Syndrome.

Yuta Inoki, Tomoko Horinouchi, Tomohiko Yamamura

|Sep 30, 2022
Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis.

China Nagano, Shigeo Hara, Norishige Yoshikawa

|May 18, 2022
Evaluation of Suspected Autosomal Alport Syndrome Synonymous Variants.

Rini Rossanti, Tomoko Horinouchi, Tomohiko Yamamura

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