Showing results (71-80 of 4,787) with videos related to
Sort By:
Pageof 479
Brain & Development|September 17, 2019
Recent treatment patterns and variations for pediatric acute encephalopathy in JapanItaru Hayakawa, Yusuke Okubo, Hiroki Nariai, et al.Brain & Development|September 8, 2019
Clinical features of early myoclonic encephalopathy caused by a CDKL5 mutationKanako Takeda, Yusaku Miyamoto, Hisako Yamamoto, et al.Brain & Development|September 11, 2019
Early infantile-onset Leigh syndrome complicated with infantile spasms associated with the m.9185 T > C variant in the MT-ATP6 gene: Expanding the clinical spectrumRei Takada, Takenori Tozawa, Hidehito Kondo, et al.Brain & Development|September 29, 2019
High-frequency component in flash visual evoked potentials in type 3 Gaucher diseaseMasayoshi Oguri, Yoshiaki Saito, Tohru Okanishi, et al.Brain & Development|January 16, 2021
Rapid-onset dystonia-parkinsonism with ATP1A3 mutation and left lower limb paroxysmal dystoniaShohei Nomura, Mitsuru Kashiwagi, Takuya Tanabe, et al.Brain & Development|January 29, 2021
Prognostic factors for relapse and outcome in pediatric acute transverse myelitisJelte Helfferich, Arlette L Bruijstens, Yu Yi M Wong, et al.Brain & Development|January 4, 2022
Clinical and molecular characteristics of tectonic (TCTN1) gene-related Joubert syndrome in a Saudi boyBader H Shirah, Nahla M Alshaikh, Ayman Shawli, et al.Brain & Development|January 16, 2022
Short-term clinical outcomes of onasemnogene abeparvovec treatment for spinal muscular atrophySeungbok Lee, Yun Jeong Lee, Juhyun Kong, et al.Brain & Development|January 3, 2022
Cerebral creatine deficiency disorders - A clinical, genetic and follow up study from IndiaGouri Rao Passi, Swati Pandey, Akella Radha Rama Devi, et al.Brain & Development|January 3, 2022
Spinal muscular atrophy with predominant lower extremity (SMA-LED) with no signs other than pure motor symptoms at the intersection of multiple overlap syndromeHande Gazeteci Tekin, Pinar Edem, Berk ÖzyılmazPageof 479