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Pediatric Nephrology (Berlin, Germany)|July 20, 2020
Comparison of clinical and genetic characteristics between Dent disease 1 and Dent disease 2Nana Sakakibara, China Nagano, Shinya Ishiko, et al.Epilepsy & Behavior : E&B|November 27, 2021
Multivariate analysis of the impact of weather and air pollution on emergency department visits for unprovoked seizure among children: A retrospective clinical observational studyHiroshi Yamaguchi, Kandai Nozu, Shinya Ishiko, et al.Kidney360|April 4, 2022
Heterozygous Urinary Abnormality-Causing Variants of <i>COL4A3</i> and <i>COL4A4</i> Affect Severity of Autosomal Recessive Alport SyndromeTomoko Horinouchi, Tomohiko Yamamura, China Nagano, et al.International Journal of Environmental Research and Public Health|November 13, 2021
Impact of the State of Emergency during the COVID-19 Pandemic in 2020 on Asthma Exacerbations among Children in Kobe City, JapanHiroshi Yamaguchi, Kandai Nozu, Shinya Ishiko, et al.Minerva Pediatrics|September 13, 2021
Current management for foreign body and toxic agent ingestion in a pediatric primary emergency centerTakeshi Ninchoji, Kandai Nozu, Atsushi Kondo, et al.Clinical and Experimental Nephrology|March 24, 2020
Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1Tomohiko Inoue, China Nagano, Masafumi Matsuo, et al.Biomarker Insights|November 3, 2025
Latent Intrarenal Renin-Angiotensin-Aldosterone System Activation Could Persist Until Early School-Aged in Children with a History of Low Birth WeightShingo Ishimori, Shinya Ishiko, Junya Fujimura, et al.American Journal of Medical Genetics. Part A|July 5, 2022
Detecting pathogenic deep intronic variants in Gitelman syndromeRini Rossanti, Tomoko Horinouchi, Nana Sakakibara, et al.Kidney International Reports|September 14, 2023
Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in <i>LAMB2</i>-Associated DiseaseRyota Suzuki, Nana Sakakibara, Yuta Ichikawa, et al.Journal of Human Genetics|February 10, 2022
Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese populationNana Sakakibara, Kandai Nozu, Tomohiko Yamamura, et al.Pageof 5