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Journal of Clinical Medicine|November 28, 2018
Efficacy and Safety of Denosumab Therapy for Osteogenesis Imperfecta Patients with Osteoporosis-Case SeriesTsukasa Kobayashi, Yukio Nakamura, Takako Suzuki, et al.
Chemosphere|May 9, 2002
Effect of 17beta-estradiol on the reproduction of Japanese medaka (Oryzias latipes)Ik Joon Kang, Hirofumi Yokota, Yuji Oshima, et al.
Diagnostic Cytopathology|July 28, 2021
Direct next-generation sequencing analysis using endometrial liquid-based cytology specimens for rapid cancer genomic profilingToshiaki Akahane, Ikumi Kitazono, Yusuke Kobayashi, et al.
International Journal of Clinical and Experimental Pathology|April 5, 2024
Prognostic impact of tumor-associated neutrophils in breast cancerAkinari Kakumoto, Tsengelmaa Jamiyan, Hajime Kuroda, et al.
International Journal of Hematology|March 24, 2021
A novel germline GATA2 frameshift mutation with a premature stop codon in a family with congenital sensory hearing loss and myelodysplastic syndromeHideyuki Nakazawa, Tomomi Yamaguchi, Hitoshi Sakai, et al.
Therapeutics and Clinical Risk Management|July 25, 2018
Efficacy of denosumab therapy for neurofibromatosis type 1 with osteoporosis and history of fractures: a case reportMasashi Uehara, Yukio Nakamura, Jun Takahashi, et al.
DEN Open|December 22, 2025
Adalimumab-responsive Monogenic Inflammatory Bowel Disease With Pseudopolyposis Characteristic of TGFBR2 Variant in Loeys-Dietz SyndromeTomomitsu Sado, Satoshi Ukai, Shingo Kurasawa, et al.
Interventional Neuroradiology : Journal of Peritherapeutic Neuroradiology, Surgical Procedures and Related Neurosciences|October 20, 2020
Intracranial and extracranial multiple arterial dissecting aneurysms in rheumatoid arthritis: A case reportKen Uekawa, Yasuyuki Kaku, Toshihiro Amadatsu, et al.
Internal Medicine (Tokyo, Japan)|September 20, 2017
Mobile Cecum in a Young Woman with Ehlers-Danlos Syndrome Hypermobility type: A Case Report and Review of the LiteratureYoshihisa Fukuda, Yusuke Higuchi, Kanae Shinozaki, et al.
Human Genome Variation|October 31, 2017
A novel frameshift mutation of SYNE1 in a Japanese family with autosomal recessive cerebellar ataxia type 8Tsuneaki Yoshinaga, Katsuya Nakamura, Masumi Ishikawa, et al.
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