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Brain & Development|September 20, 2011
Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromesAi Hoshino, Makiko Saitoh, Akira Oka, et al.
Japanese Journal of Infectious Diseases|December 28, 2017
Human Parainfluenza Virus Type 3 Infections in Patients with Hematopoietic Stem Cell Transplants: the Mode of Nosocomial Infections and PrognosisSatsuki Kakiuchi, Masanori Tsuji, Hidekazu Nishimura, et al.
Journal of Cell Science|June 3, 2020
A cellular model of albumin endocytosis uncovers a link between membrane and nuclear proteinsSeiya Urae, Yutaka Harita, Tomohiro Udagawa, et al.
Pediatric Nephrology (Berlin, Germany)|May 19, 2022
Urine alpha 1-microglobulin-to-creatinine ratio and beta 2-microglobulin-to-creatinine ratio for detecting CAKUT with kidney dysfunction in childrenRiku Hamada, Kaori Kikunaga, Tetsuji Kaneko, et al.
Brain & Development|September 23, 2008
A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRITerumi Murakami, Yukiko K Hayashi, Megumu Ogawa, et al.
Clinical Ophthalmology (Auckland, N.Z.)|August 12, 2009
A single nucleotide polymorphism analysis of the LAMA1 gene in Japanese patients with high myopiaSayaka Sasaki, Masao Ota, Akira Meguro, et al.
Annals of the Rheumatic Diseases|August 18, 2009
Genetics of Behçet disease inside and outside the MHCAkira Meguro, Hidetoshi Inoko, Masao Ota, et al.
Virology Journal|August 5, 2020
Association of human cytomegalovirus (HCMV) neutralizing antibodies with antibodies to the HCMV glycoprotein complexesMiho Shibamura, Tomoki Yoshikawa, Souichi Yamada, et al.
Pediatric Neurology|December 4, 2003
New GAA mutations in Japanese patients with GSDII (Pompe disease)Judy R Pipo, Jian-Hua Feng, Toshiyuki Yamamoto, et al.
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