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Autoimmune Diseases|November 24, 2011
Juvenile myasthenia gravis: a paediatric perspectiveMaria F Finnis, Sandeep JayawantArchives of Disease in Childhood|March 23, 2007
Outcome following subdural haemorrhages in infancySandeep Jayawant, Jeremy ParrNeuromuscular Disorders : NMD|March 23, 2010
WITHDRAWN: Nemaline myopathy presenting as a stiff babyRakesh Kumar Jain, Sandeep JayawantHandbook of Clinical Neurology|April 30, 2013
Autoimmune myasthenia gravisSandeep Jayawant, Jeremy Parr, Angela VincentInternational Journal of Pediatric Otorhinolaryngology|September 14, 2016
Symptomatic stroke complicating central skull base osteomyelitis following otitis media in a 2-year old boy: Case report and review of the literatureEliz Kilich, Reena Dwivedi, Shelley Segal, et al.The Turkish Journal of Pediatrics|July 3, 2023
Expanding the phenotype of DYNC1H1-associated diseases with a rare variant resulting in spinal muscular atrophy with lower extremity predominance (SMA-LED) and upper motor neuron signsJessica Lee, Philip Millington, Kavinda Dayasiri, et al.Developmental Medicine and Child Neurology|September 15, 2009
A novel ARX phenotype: rapid neurodegeneration with Ohtahara syndrome and a dyskinetic movement disorderMichael Absoud, Jeremy R Parr, Dorothy Halliday, et al.Archives of Disease in Childhood|February 7, 2014
How common is childhood myasthenia? The UK incidence and prevalence of autoimmune and congenital myastheniaJeremy Ross Parr, Morag Jane Andrew, Maria Finnis, et al.Neurology|August 23, 2015
Salbutamol and ephedrine in the treatment of severe AChR deficiency syndromesPedro M Rodríguez Cruz, Jacqueline Palace, Hayley Ramjattan, et al.Neuromuscular Disorders : NMD|September 24, 2011
Clinical features in a series of fast channel congenital myasthenia syndromeJacqueline Palace, Daniel Lashley, Stephen Bailey, et al.Pageof 5