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Neurology|September 30, 2022
Child Neurology: Maternal Transmission of Congenital Myotonic Dystrophy Type 2: Case ReportAlide A Tieleman, Manon J Damen, Aad Verrips, et al.Journal of Neurology|April 5, 2011
High disease impact of myotonic dystrophy type 2 on physical and mental functioningAlide A Tieleman, Kathleen M Jenks, Joke S Kalkman, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 28, 2010
Poor sleep quality and fatigue but no excessive daytime sleepiness in myotonic dystrophy type 2Alide A Tieleman, Hans Knoop, Anne-Els van de Logt, et al.Journal of Neuromuscular Diseases|September 6, 2024
Life expectancy and causes of death in patients with Myotonic Dystrophy Type 2Manon J Damen, Otto G Muilwijk, Tom Bg Olde Dubbelink, et al.Neuromuscular Disorders : NMD|July 8, 2008
Gastrointestinal involvement is frequent in Myotonic Dystrophy type 2Alide A Tieleman, Judith van Vliet, Jan B M J Jansen, et al.Neuromuscular Disorders : NMD|September 22, 2019
High incidence of falls in patients with myotonic dystrophy type 1 and 2: A prospective studyJoost Berends, Alide A Tieleman, Corinne G C Horlings, et al.European Journal of Human Genetics : EJHG|January 13, 2011
Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotypeMarieke J H Coenen, Alide A Tieleman, Mascha M V A P Schijvenaars, et al.The Journal of Pain|March 31, 2018
Qualitative and Quantitative Aspects of Pain in Patients With Myotonic Dystrophy Type 2Judith van Vliet, Alide A Tieleman, Aad Verrips, et al.Neurology|January 19, 2018
Hearing impairment in patients with myotonic dystrophy type 2Judith van Vliet, Alide A Tieleman, Baziel G M van Engelen, et al.Genome Research|March 20, 2025
Optical genome mapping enables accurate testing of large repeat expansionsBart van der Sanden, Kornelia Neveling, Syukri Shukor, et al.Pageof 1