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Human Molecular Genetics|January 6, 2026
An R83W mutation in Rab3A causes autosomal-dominant cerebellar ataxiaRyosuke Miyamoto, Ayuko Sakane, Hiroyuki Morino, et al.
Biomedicines|June 24, 2022
From SGAP-Model to SGAP-Score: A Simplified Predictive Tool for Post-Surgical Recurrence of PheochromocytomaMirko Parasiliti-Caprino, Fabio Bioletto, Chiara Lopez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 4, 2009
LRRK2 mutations and risk variants in Japanese patients with Parkinson's diseaseCyrus P Zabetian, Mitsutoshi Yamamoto, Alexis N Lopez, et al.
Biochemical and Biophysical Research Communications|March 16, 2020
Optineurin regulates osteoblastogenesis through STAT1Noriyoshi Mizuno, Tomoyuki Iwata, Ryosuke Ohsawa, et al.
Journal of Neurology|May 14, 2025
Ravulizumab for generalized Myasthenia Gravis: a multicenter real-life experienceElena Rossini, Vincenzo Di Stefano, Raffaele Iorio, et al.
Eurointervention : Journal of Europcr in Collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology|November 9, 2016
Impact of lesion calcification on angiographic outcomes after Absorb everolimus-eluting bioresorbable vascular scaffold implantation: an observation from the ABSORB Japan trialMasanobu Ohya, Kazushige Kadota, Yohei Sotomi, et al.
Journal of the Peripheral Nervous System : JPNS|August 3, 2023
Quantitative sensory testing and skin biopsy findings in late-onset ATTRv presymptomatic carriers: Relationships with predicted time of disease onset (PADO)Luca Leonardi, Rocco Costanzo, Francesca Forcina, et al.
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