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Rare, inherited disorders of neuromuscular transmission
31 octobre 2019 @ 12:00 - 13:00 EDT
Crédit image : www.medicalgraphics.de
Rare, inherited disorders of neuromuscular transmission
Le Pr Hanns Lochmuller, professeur au CHEO Research Institute à Ottawa, sera l’invité du Pr Jean-François Côté, membre régulier du CERMO-FC, le Jeudi 31 octobre 2019 à 12h00 au SB-1115.
En savoir plus sur les recherches du Pr Lochmuller (anglais).
Rare, inherited disorders of neuromuscular transmission
Pr Hanns Lochmuller, a professor at CHEO Research Institute at Ottawa, will be the guest of Pr Nicolas Pilon, director of CERMO-FC, on Thursday October 31 at 12:00 in SB-1115.
Learn more about Pr Lochmuller ‘s research.
Biography
Hanns is a neurologist and clinical academic specializing in genetic neuromuscular disorders and rare disease. He is a Senior Scientist at the Children’s Hospital of Eastern Ontario (CHEO) Research Institute. He also holds appointments as Professor of Neurology in the University of Ottawa Faculty of Medicine and the Department of Medicine, Division of Neurology at The Ottawa Hospital. Dr Lochmuller has recently been awarded a tier 1 Canada Research Chair in Neuromuscular Genomics and Health
Hanns trained as a neurologist in Munich, Germany and in Montreal, Canada. From 2007 to 2017, he held the chair of experimental myology at the Institute of Genetic Medicine at Newcastle University in the UK. He continues to hold a scientific appointment at the Department of Neuropediatrics and Muscle Disorders of the Medical Center – University of Freiburg in Germany and as visiting scientist at the Centro Nacional de Análisis Genómico (CNAG), Centre for Genomic Regulation, Barcelona in Spain.
His research interests include molecular therapies of neuromuscular disorders; molecular pathogenesis of muscle and neuromuscular junction disorders; neurogenetics and translational research; data sharing and -omics in neuromuscular and rare diseases; and genomics and systems medicine. In addition to his scientific and clinical research interests, he is internationally active in rare disease science policy and research collaborations. He chaired the Interdisciplinary Scientific Committee of the International Rare Diseases Research Consortium (IRDiRC) and the Executive Committee of the TREAT-NMD Alliance. He initiated and coordinated the highly successful “RD-Connect” international infrastructure for rare disease data and biosample sharing and analysis, is co-founder and former coordinator of the German muscular dystrophy network (MD-NET), and former scientific coordinator of EuroBioBank, a European (and Canadian) network of biobanks for rare disorders.
Hanns’ clinical activities focus on clinical research and care of patients with rare neuromuscular disorders, including myotonic dystrophy (DM1), spinal muscular atrophy (SMA), muscular dystrophy and congenital myasthenic syndromes (CMS). He has a strong commitment to working with patients and patient organizations in Canada, as he has with organizations in Europe for many years.
Un évènement organisé dans le cadre des Pause-conférences du CERMO-FC et soutenu par :
An event organized as part of the Pause-conférences of CERMO-FC, and support by :
