Webinars
Details
Ratings
August 12, 2020
August 19, 2020
Brief, case-based webinar followed by a live Q&A to provide all the information necessary for health care providers to identify the clinical and biochemical clues for diagnosing rare pediatric neurotransmitter disorders that share overlapping clinical features with each other and other neurological conditions, such as cerebral palsy, which may result in delayed diagnosis.
August 08, 2020
International Pediatric Neuroradiology Teaching Network Series
November 19, 2020
19 November Congenital Myasthenia Syndrome - an update Sithara Ramdas Oxford University Hospitals NHS Foundation Trust John Radcliffe Hospital
October 13, 2020
Diagnostic algorithm for childhood onset chorea by Juan Dario Ortigoza-Escobar
October 06, 2020
'Treatment of spasticity in HSP and leukodystrophies' by Annemieke Buizer and laura Bonouvrié
October 01, 2020
Hereditary Spastic Paraplegia - clinical disease course by Rebecca Schüle Freyer
September 29, 2020
'How can we develop and implement evidence based rehabilitation in rare disorders' by Hortensia Gimeno
September 17, 2020
This webinar will be delivered by Annemieke Aartsma-Rus, who is a Professor of Translational Genetics, Department of Human Genetics, Leiden University Medical Center in the Netherlands.
September 15, 2020
Topic 'A challenge in neurogenetics: Huntington disease in kids' by Ferdinando Squitieri Description Joint webinar series by the European Reference Networks for Rare Neurological Diseases (ERN-RND) and Neuromuscular Diseases (ERN-EuroNMD) and the European Academy of Neurology (EAN).