Showing results (21-30 of 33) with videos related to
Sort By:
Pageof 4
Journal of the Neurological Sciences|September 1, 2024
Tissue plasminogen activator for acute branch atheromatous disease exhibits transient improvement and worseningYuya Kobayashi, Yasufumi Kondo, Kanji Yamamoto, et al.Journal of Human Genetics|March 10, 2017
Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patientsKiyoshiro Nagamatsu, Yoshiki Sekijima, Katsuya Nakamura, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 16, 2026
Atrial natriuretic peptide can be biomarker for predicting atrial fibrillation in embolic stroke of undetermined sourceYuya Kobayashi, Chinami Yuzawa, Minori Kurashina, et al.IJU Case Reports|December 17, 2025
A Case of Acquired Factor V Deficiency in a Hemodialysis Patient: A Case Report With Literature ReviewAkihiko Sugino, Yoshiyuki Miyazawa, Shugo Harashima, et al.AJOG Global Reports|August 1, 2026
Preoperative prediction of the need for postoperative adjuvant therapy in stage IB cervical cancer using tumor size measured on magnetic resonance imaging and serum squamous cell carcinoma antigen levelsMichihide Maeda, Miho Kitai, Masashi Akada, et al.Journal of Nutritional Science and Vitaminology|November 8, 2023
Resveratrol Upregulates Senescence Marker Protein 30 by Activating AMPK/Sirt1-Foxo1 Signals and Attenuating H2O2-Induced Damage in FAO Rat Liver CellsHirofumi Inoue, Yusaku Shimizu, Hiroto Yoshikawa, et al.Journal of Human Genetics|March 20, 2010
Cerebral hemorrhage in Fabry's diseaseKatsuya Nakamura, Yoshiki Sekijima, Kimitoshi Nakamura, et al.Journal of Atherosclerosis and Thrombosis|August 12, 2025
Combined Use of Statin and PCSK9 Inhibitor in a Pregnant Woman with Possible Familial Hypercholesterolemia and Coronary Artery StenosisYusaku Shimizu, Tae Yokouchi-Konishi, Chizuko Aoki-Kamiya, et al.Cerebellum (London, England)|November 11, 2016
Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective StudyKatsuya Nakamura, Kunihiro Yoshida, Akira Matsushima, et al.Journal of Human Genetics|April 15, 2006
A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in NaganoTakako Ohata, Kunihiro Yoshida, Haruya Sakai, et al.Pageof 4