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Journal of the Neurological Sciences|January 15, 2008
Familial amyotrophic lateral sclerosis with Gly93Ser mutation in Cu/Zn superoxide dismutase: a clinical and neuropathological studyMegumi Suzuki, Togo Irie, Takeshi Watanabe, et al.
Animal Science Journal = Nihon Chikusan Gakkaiho|June 26, 2014
Proteomic analysis of Nipponia nippon (ID#162)Mitsuru Oyanagi, Kentaro Kaneko, Yoshinori Kaneko, et al.
The Tohoku Journal of Experimental Medicine|April 1, 1987
Clinical, biochemical and enzymatic studies in type I hyperprolinemia associated with chromosomal abnormalityK Oyanagi, A Tsuchiyama, Y Itakura, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 6, 2021
Oral sodium phenylbutyrate for hyperammonemia associated with congenital portosystemic shunt: a case reportTakeshi Sato, Tomohiro Ishii, Mototoshi Kato, et al.
Journal of Clinical Ultrasound : JCU|February 7, 2001
Congenital ileal atresia presenting as a single cyst-like lesion on prenatal sonographyA Kubota, T Nakayama, T Yonekura, et al.
Journal of Neuropathology and Experimental Neurology|July 20, 2000
Alpha-synuclein inclusions in amygdala in the brains of patients with the parkinsonism-dementia complex of GuamM Yamazaki, Y Arai, M Baba, et al.
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