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Kidney International Reports|May 2, 2022
Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney DiseaseEri Okada, Naoya Morisada, Tomoko Horinouchi, et al.Kidney International Reports|May 14, 2023
Corrigendum to "Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease"Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866Eri Okada, Naoya Morisada, Tomoko Horinouchi, et al.Journal of Human Genetics|March 4, 2018
Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndromeAi Unzaki, Naoya Morisada, Kandai Nozu, et al.Clinical and Experimental Nephrology|May 28, 2019
Clinical characteristics of HNF1B-related disorders in a Japanese populationChina Nagano, Naoya Morisada, Kandai Nozu, et al.Journal of the American Society of Nephrology : JASN|July 1, 2018
Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport SyndromeTomoko Horinouchi, Kandai Nozu, Tomohiko Yamamura, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 29, 2021
Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndromeNana Sakakibara, Takeshi Ijuin, Tomoko Horinouchi, et al.Nature Communications|June 4, 2020
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5Tomohiko Yamamura, Tomoko Horinouchi, Tomomi Adachi, et al.Neurology|January 17, 2014
Genotype-phenotype correlations in alternating hemiplegia of childhoodMasayuki Sasaki, Atsushi Ishii, Yoshiaki Saito, et al.Pageof 12