Vedrana Milić Rašić
University Children's Hospital, Belgrade(RS)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Genetic Neurodegenerative Diseases, Hereditary Neurological Disorders, Neurogenetic and Muscular Disorders Research, Mitochondrial Function and Pathology
Most-Cited Works
- → The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations(2015)733 cited
- → Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database(2017)180 cited
- → Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes(2008)159 cited
- → Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia(2012)129 cited
- → Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2(2014)108 cited
- → The TREAT-NMD Duchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia(2013)108 cited
- → Mapping the differences in care for 5,000 Spinal Muscular Atrophy patients, a survey of 24 national registries in North America, Australasia and Europe(2013)105 cited
- → ANO10 mutations cause ataxia and coenzyme Q10 deficiency(2014)83 cited
- → Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy(2017)71 cited
- → Genotype–phenotype analysis in patients with giant axonal neuropathy (GAN)(2007)31 cited