Showing results (351-360 of 3,396) with videos related to
Sort By:
Pageof 340
Neuromuscular Disorders : NMD|January 29, 2010
The role of patient advocacy organisations in neuromuscular disease R&D--The case of the Dutch neuromuscular disease association VSNWouter Boon, Ria BroekgaardenNeuromuscular Disorders : NMD|August 21, 2016
Identifying evidence of cardio-renal syndrome in patients with Duchenne muscular dystrophy using cystatin CChet R Villa, Ahmad Kaddourah, Jacob Mathew, et al.Neuromuscular Disorders : NMD|August 22, 2016
Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patientsGyorgy Mate Milley, Edina Timea Varga, Zoltan Grosz, et al.Neuromuscular Disorders : NMD|August 23, 2016
A novel neuromuscular form of glycogen storage disease type IV with arthrogryposis, spinal stiffness and rare polyglucosan bodies in muscleEdoardo Malfatti, Christine Barnerias, Carola Hedberg-Oldfors, et al.Neuromuscular Disorders : NMD|July 12, 2017
First clinical and genetic description of a family diagnosed with late-onset Pompe disease from Costa RicaGabriel Torrealba-Acosta, María Consuelo Rodríguez-Roblero, Sixto Bogantes-Ledezma, et al.Neuromuscular Disorders : NMD|February 4, 2010
Microvasculopathic neuromuscular diseases: lessons from hypoxia-inducible factorsStefan Probst-Cousin, Bernhard Neundörfer, Dieter HeussNeuromuscular Disorders : NMD|July 19, 2018
A new case expanding the mutation and phenotype spectrum of TMEM5-related alpha-dystroglycanopathyAnn-Kathrin Zaum, Konstantinos Kolokotronis, Wolfram Kress, et al.Neuromuscular Disorders : NMD|July 14, 2018
Ketoacidosis in Duchenne muscular dystrophy: A report on 4 casesT E Doris, A Bowron, A Armstrong, et al.Neuromuscular Disorders : NMD|January 1, 1992
Molecular analysis for the myotonic dystrophy mutation in neuromuscular disordersJ C MacMillan, J Myring, H G Harley, et al.Neuromuscular Disorders : NMD|December 9, 2003
Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD geneChristophe Béroud, Alain Carrié, Chérif Beldjord, et al.Pageof 340