Nana Sakakibara
11PUBLICATIONS
42CO-AUTHORS
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Publications (11)
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|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 13, 2024
Clinical, Pathological, and Genetic Characteristics of Patients with Digenic Alport Syndrome.Yuta Inoki, Tomoko Horinouchi, Tomohiko Yamamura
|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
|Apr 14, 2022
Clear Evidence of LAMA5 Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome.Yukimasa Taniguchi, China Nagano, Kiyotoshi Sekiguchi
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Frequent Collaborators
8 joint publications
Kandai Nozu
8 joint publications
Tomoko Horinouchi
7 joint publications
China Nagano
6 joint publications
Tomohiko Yamamura
5 joint publications
Kazumoto Iijima
3 joint publications
Hiroaki Nagase
2 joint publications
Koichi Nakanishi
2 joint publications
Takeshi Ninchoji
1 joint publications
Yutaka Takaoka
1 joint publications
Hideaki Kitakado
