Showing results (1-10 of 118) with videos related to

Sort By:
Pageof 12
Pediatrics International : Official Journal of the Japan Pediatric Society|April 16, 2014
Branchio-oto-renal syndrome: comprehensive review based on nationwide surveillance in JapanNaoya Morisada, Kandai Nozu, Kazumoto Iijima
The Pediatric Infectious Disease Journal|October 6, 2020
Infant Pyogenic Liver Abscess Complicated With Autoimmune Neutropenia: Two CasesShogo Otake, Rin Tamashiro, Naoya Morisada, et al.
Case Reports in Genetics|February 23, 2023
4q25 Microdeletion with Axenfeld-Rieger Syndrome and Developmental DelayYukino Kawanami, Tomoko Horinouchi, Naoya Morisada, et al.
Pediatric Nephrology (Berlin, Germany)|February 22, 2012
Alport-like glomerular basement membrane changes with renal-coloboma syndromeHiromi Ohtsubo, Naoya Morisada, Hiroshi Kaito, et al.
The Tohoku Journal of Experimental Medicine|September 20, 2019
Rapidly Progressive Nephronophthisis in a 2-Year-Old Boy with a Homozygous SDCCAG8 MutationYoshitaka Watanabe, Shuichiro Fujinaga, Koji Sakuraya, et al.
The Journal of Obstetrics and Gynaecology Research|March 12, 2023
Genetic autopsy and genetic counseling for a case of fatal oligohydramnios due to de novo 17q12 deletion syndromeKana Hiromoto, Naoya Morisada, Shinya Tairaku, et al.
American Journal of Medical Genetics. Part A|April 30, 2019
Male CDPX2 patient with EBP mosaicism and asymmetrically lateralized skin lesions with strict midline demarcationTomoko Horinouchi, Naoya Morisada, Hiroyasu Uemura, et al.
Clinical Case Reports|April 6, 2026
An Infant With Hyper IgE Syndrome Mimicking Acute LeukemiaYuichiro Matsui, Suguru Uemura, Kenji Kishimoto, et al.
Pageof 12