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British Journal of Clinical Pharmacology|October 6, 2018
The journey of metformin from glycaemic control to mTOR inhibition and the suppression of tumour growthSam Amin, Andrew Lux, Finbar O'CallaghanSAGE Open Medical Case Reports|April 15, 2021
Hereditary geniospasm in a mother and son treated with botulinum toxin injection: A case reportClare Perkins, Wei Jia, James Rainsbury, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 24, 2019
Quality of life in patients with Tuberous Sclerosis Complex (TSC)Sam Amin, Andrew A Mallick, Andrew Lux, et al.Journal of Child Neurology|June 5, 2020
Recurrence of First Afebrile Unprovoked Seizure and Parental Consanguinity: A Hospital-Based StudyMiral A Al Momani, Basima Almomani, Salar Bani Hani, et al.Developmental Medicine and Child Neurology|December 10, 2016
Causes of mortality in individuals with tuberous sclerosis complexSam Amin, Andrew Lux, Nuala Calder, et al.Developmental Medicine and Child Neurology|December 31, 2017
'Leukodystrophy-like' phenotype in children with myelin oligodendrocyte glycoprotein antibody-associated diseaseYael Hacohen, Thomas Rossor, Kshitij Mankad, et al.Trials|April 28, 2017
Ketogenic diet in the treatment of epilepsy in children under the age of 2 years: study protocol for a randomised controlled trialSiobhan Titre-Johnson, Natasha Schoeler, Christin Eltze, et al.Journal of Neurology|September 12, 2014
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotypeKathryn J Peall, Manju A Kurian, Mark Wardle, et al.Brain : a Journal of Neurology|February 1, 2013
SGCE mutations cause psychiatric disorders: clinical and genetic characterizationKathryn J Peall, Daniel J Smith, Manju A Kurian, et al.Pageof 1