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Nihon Rinsho Men'Eki Gakkai Kaishi = Japanese Journal of Clinical Immunology|May 3, 2007
[MVK gene abnormality and new approach to treatment of hyper IgD syndrome and periodic fever syndrome]Takuya NarutoBlood|December 17, 2011
Functional heterogeneity of human effector CD8+ T cellsHiroshi Takata, Takuya Naruto, Masafumi TakiguchiJournal of Clinical Medicine|April 3, 2021
The Benefits and Respective Side-Effects of PE Therapy for Intractable Kawasaki DiseaseMasaaki Mori, Susumu Yamazaki, Takuya NarutoHuman Genome Variation|April 16, 2016
A novel PTCH1 mutation in a patient with Gorlin syndromeNana Okamoto, Takuya Naruto, Tomohiro Kohmoto, et al.Human Genome Variation|April 13, 2018
Primary microcephaly caused by novel compound heterozygous mutations in ASPMNobuhiko Okamoto, Tomohiro Kohmoto, Takuya Naruto, et al.American Journal of Medical Genetics. Part A|November 14, 2025
A Novel Intronic Variant in FRMPD4 Disrupts Splicing: Case Report of an X-Linked Neurodevelopmental DisorderTomoko Satake, Yasuhiro Kawai, Koki Nagai, et al.Human Genome Variation|May 22, 2020
Tatton-Brown-Rahman syndrome with a novel DNMT3A mutation presented severe intellectual disability and autism spectrum disorderTakayuki Yokoi, Yumi Enomoto, Takuya Naruto, et al.World Journal of Clinical Cases|December 26, 2022
Kawasaki disease without changes in inflammatory biomarkers: A case reportKosei Yamashita, Takeru Kanazawa, Yoshifusa Abe, et al.Human Genome Variation|August 1, 2018
Nonsyndromic intellectual disability with novel heterozygous SCN2A mutation and epilepsyTakayuki Yokoi, Yumi Enomoto, Yoshinori Tsurusaki, et al.American Journal of Medical Genetics. Part A|August 30, 2023
A Japanese patient with Teebi hypertelorism syndrome and a novel CDH11 EC1 domain variantYukiko Kuroda, Yoko Saito, Yumi Enomoto, et al.Pageof 11