Nana Sakakibara

13PUBLICATIONS
46CO-AUTHORS
HaematologyGene expression (incl. microarray and other genome-wide approaches)Nutrigenomics and personalised nutritionWomen's studies (incl. girls' studies)Neurology and neuromuscular diseases
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Publications (13)

|Oct 02, 2026
Heterozygous COL4A3/COL4A4 variants: diagnostic trends and clinical kidney outcomes.

|Sep 23, 2026
Symptom Burden and Clinical Clues in Gitelman Syndrome and Pseudo-Gitelman Syndrome.

|Mar 31, 2025
Tubular proteinuria due to hereditary endocytic receptor disorder of the proximal tubule: Dent disease and chronic benign proteinuria.

Nana Sakakibara, Kandai Nozu

|Aug 12, 2024
Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndrome.

Ryota Suzuki, Nana Sakakibara, Sae Murakami

|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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Frequent Collaborators

10 joint publications

Kandai Nozu

10 joint publications

Tomoko Horinouchi

9 joint publications

China Nagano

7 joint publications

Tomohiko Yamamura