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Neuromuscular Disorders : NMD|July 25, 2022
Cognitive assessment in patients with myotonic dystrophy type 2Stojan Peric, Ilija Gunjic, Neda Delic, et al.Neurogenetics|March 19, 2024
Whole exome sequencing in Serbian patients with hereditary spastic paraplegiaMarija Brankovic, Vukan Ivanovic, Ivana Basta, et al.Annals of Neurology|October 24, 2024
Recessive Variants in PIGG Cause a Motor Neuropathy with Variable Conduction Block, Childhood Tremor, and Febrile Seizures: Expanding the PhenotypeChristopher J Record, Antoinette O'Connor, Nienke E Verbeek, et al.Journal of Neuromuscular Diseases|February 20, 2025
International collaboration to improve knowledge on myotonic dystrophy type 2Stojan Peric, Vukan Ivanovic, Emma-Jayne Ashley, et al.European Journal of Human Genetics : EJHG|June 4, 2025
Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell modelsBarbara Tedesco, Stojan Peric, Goknur Selen Kocak, et al.Pageof 2