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Clinical Nephrology|March 27, 2012
GSTT1 gene abnormality in minimal change nephrotic syndrome with elevated serum immunoglobulin EKohei Miyazaki, Keisuke Sugimoto, Shoji Tsuji, et al.
Journal of Neurophysiology|October 17, 2008
Double-pulse magnetic brain stem stimulation: mimicking successive descending volleysHideyuki Matsumoto, Ritsuko Hanajima, Masashi Hamada, et al.
Internal Medicine (Tokyo, Japan)|August 6, 2010
A case of atypical amyloid polyneuropathy with predominant upper-limb involvement with the diagnosis unexpectedly found at lung operationYuichiro Shirota, Atsushi Iwata, Hiroyuki Ishiura, et al.
American Journal of Nephrology|April 4, 2013
A novel nuclear factor κB inhibitor, dehydroxymethylepoxyquinomicin, ameliorates puromycin aminonucleoside-induced nephrosis in miceTomohiko Shimo, Yasushi Adachi, Sohsaku Yamanouchi, et al.
Journal of Neurology|April 17, 2013
Progressive apraxic agraphia with micrographia presenting as corticobasal syndrome showing extensive Pittsburgh compound B uptakeYasuhisa Sakurai, Kenji Ishii, Masahiro Sonoo, et al.
Muscle & Nerve|February 6, 2013
Far-field potentials in hypothenar motor unit number estimationMana Higashihara, Masahiro Sonoo, Tomotaka Yamamoto, et al.
Human Molecular Genetics|October 9, 2013
Altered CpG methylation in sporadic Alzheimer's disease is associated with APP and MAPT dysregulationAtsushi Iwata, Kenichi Nagata, Hiroyuki Hatsuta, et al.
Epilepsia|April 6, 2023
Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansionsMark A Corbett, Christel Depienne, Liana Veneziano, et al.
Journal of Human Genetics|September 6, 2021
Chédiak-Higashi syndrome presenting as a hereditary spastic paraplegiaKishin Koh, Mai Tsuchiya, Hiroyuki Ishiura, et al.
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