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Frontiers in Human Neuroscience|November 26, 2019
Corrigendum: Altered Brain Microstate Dynamics in Adolescents With NarcolepsyNatasha M Drissi, Attila Szakács, Suzanne T Witt, et al.Frontiers in Human Neuroscience|August 19, 2016
Altered Brain Microstate Dynamics in Adolescents with NarcolepsyNatasha M Drissi, Attila Szakács, Suzanne T Witt, et al.JIMD Reports|November 20, 2019
Diagnostic pitfalls in vitamin B6-dependent epilepsy caused by mutations in the <i>PLPBP</i> geneKristian Vestergaard Jensen, Maria Frid, Tommy Stödberg, et al.Pediatric Neurology|July 6, 2013
Cerebrospinal fluid brain injury biomarkers in children: a multicenter studyPashtun Shahim, Niklas Darin, Ulf Andreasson, et al.Mitochondrion|January 24, 2015
Broad phenotypic variability in patients with complex I deficiency due to mutations in NDUFS1 and NDUFV1Kristoffer Björkman, Kalliopi Sofou, Niklas Darin, et al.Molecular Genetics and Metabolism|February 5, 2008
The in-depth evaluation of suspected mitochondrial disease, Richard H Haas, Sumit Parikh, et al.JIMD Reports|September 9, 2016
Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic CounsellingSabine Grønborg, Niklas Darin, Maria J Miranda, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 6, 2009
SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degenerationHanna Orlén, Atle Melberg, Raili Raininko, et al.Pediatric Research|October 6, 2017
Oxygen consumption in platelets as an adjunct diagnostic method for pediatric mitochondrial diseaseEmil Westerlund, Sigurður E Marelsson, Johannes K Ehinger, et al.Journal of Inherited Metabolic Disease|August 29, 2020
Diagnostic value of serum biomarkers FGF21 and GDF15 compared to muscle sample in mitochondrial diseaseJenni M Lehtonen, Mari Auranen, Niklas Darin, et al.Pageof 10