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American Journal of Medical Genetics. Part A|October 23, 2023
Novel compound heterozygous ATP1A2 variants in a patient with fetal akinesia/hypokinesia sequenceShogo Furukawa, Mitsuhiro Kato, Toshihiro Nomura, et al.
Human Genome Variation|February 19, 2022
Two novel heterozygous variants in ATP1A3 cause movement disordersShogo Furukawa, Sachiko Miyamoto, Shinobu Fukumura, et al.
Clinical Imaging|June 18, 2018
Semiquantitative analysis using standardized uptake value in 123I-FP-CIT SPECT/CTAkira Toriihara, Hiromitsu Daisaki, Akihiro Yamaguchi, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|April 17, 2025
Emergence of Japanese encephalitis in a previously non-reported area: Three consecutive annual cases from a tertiary center in Narita, Chiba, JapanKoki Yoshizawa, Emiri Muranaka, Ryota Hase, et al.
Brain & Development|September 26, 2025
Muscle and thyroid manifestations in TANGO2 deficiency disorder: a case study of novel biallelic variantsRyo Sugiyama, Yuko Shimizu-Motohashi, Yuka Sakata, et al.
Internal Medicine (Tokyo, Japan)|March 12, 2015
Primary cerebral lymphomatoid granulomatosis progressing to methotrexate-associated lymphoproliferative disease under immunosuppressive therapyHiroaki Tanaka, Shogo Furukawa, Yusuke Takeda, et al.
Frontiers in Aging Neuroscience|March 19, 2020
The Relationship Between the Striatal Dopaminergic Neuronal and Cognitive Function With AgingHongliang Li, Shigeki Hirano, Shogo Furukawa, et al.
Journal of Human Genetics|January 6, 2026
Identification of 5' untranslated region variants in genes involved in neurodevelopmental disordersTaiju Hayashi, Sachiko Miyamoto, Yusaku Endo, et al.
Internal Medicine (Tokyo, Japan)|September 21, 2021
Behçet's Disease with Bilateral Renal Infarction Due to MucormycosisKumiko Shimoyama, Tomoyuki Niwa, Shogo Furukawa, et al.
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