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Journal of Clinical Medicine|September 14, 2024
Esophageal Dysmotility in Multiple System Atrophy: A Retrospective Cross-Sectional StudyRumi Ueha, Misaki Koyama, Akiko Seto, et al.
Rinsho Shinkeigaku = Clinical Neurology|December 1, 2004
[An autopsy case of systemic vasculitis associated with hepatitis C virus-related mixed cryoglobulinemia presenting severe peripheral neuropathy]Mari Tada, Satoshi Naruse, Aki Arai, et al.
Journal of the Neurological Sciences|November 11, 2009
Prominent cauda equina involvement in patients with chronic inflammatory demyelinating polyradiculoneuropathyHideyuki Matsumoto, Ritsuko Hanajima, Yasuo Terao, et al.
Archives of Neurology|December 17, 2003
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gammaIchiro Yabe, Hidenao Sasaki, Dong-Hui Chen, et al.
Pediatric Nephrology (Berlin, Germany)|October 22, 2016
Decreased urinary excretion of the ectodomain form of megalin (A-megalin) in children with OCRL gene mutationsChikushi Suruda, Shoji Tsuji, Sohsaku Yamanouchi, et al.
Frontiers in Aging Neuroscience|April 7, 2023
Early detection of cognitive decline in Alzheimer's disease using eye trackingShin-Ichi Tokushige, Hideyuki Matsumoto, Shun-Ichi Matsuda, et al.
American Journal of Human Genetics|August 14, 2012
The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvementHiroyuki Ishiura, Wataru Sako, Mari Yoshida, et al.
Annals of Clinical and Translational Neurology|September 23, 2025
INF2-Related Charcot-Marie-Tooth Disease in a Japanese Cohort: Genetic and Clinical InsightsChikashi Yano, Masahiro Ando, Yujiro Higuchi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 1, 2009
TRPM7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the Kii peninsula of JapanKenju Hara, Yasumasa Kokubo, Hiroyuki Ishiura, et al.
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