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Neurology|July 8, 2024
Evolution of Movement Disorders in Patients With CLN2-Batten Disease Treated With Enzyme Replacement TherapyRobert Spaull, Audrey K Soo, Spyros Batzios, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 17, 2020
Transitional Care for Young People with Neurological Disorders: A Scoping Review with A Focus on Patients with Movement DisordersEavan McGovern, Tamara Pringsheim, Alex Medina, et al.
Neuroscience and Biobehavioral Reviews|May 22, 2017
A review of psychiatric co-morbidity described in genetic and immune mediated movement disordersK J Peall, M S Lorentzos, I Heyman, et al.
Molecular Psychiatry|October 15, 2021
The dopamine transporter gene SLC6A3: multidisease risksMaarten E A Reith, Sandhya Kortagere, Corinde E Wiers, et al.
Biochimica Et Biophysica Acta|March 21, 2016
The novel R347g pathogenic mutation of aromatic amino acid decarboxylase provides additional molecular insights into enzyme catalysis and deficiencyRiccardo Montioli, Alessandro Paiardini, Manju A Kurian, et al.
Developmental Medicine and Child Neurology|April 2, 2014
Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrumAdeline Ngoh, Amy McTague, Ingrid M Wentzensen, et al.
Neuropediatrics|November 10, 2004
Short-chain acyl-CoA dehydrogenase deficiency associated with early onset severe axonal neuropathyM A Kurian, L Hartley, Z Zolkipli, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|April 15, 2006
Correlating nanoscale titania structure with toxicity: a cytotoxicity and inflammatory response study with human dermal fibroblasts and human lung epithelial cellsChristie M Sayes, Rajeev Wahi, Preetha A Kurian, et al.
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