Showing results (101-110 of 122) with videos related to
Sort By:
Pageof 13
Neuroscience Letters|August 28, 2007
The wolframin His611Arg polymorphism influences medication overuse headacheC Di Lorenzo, G Sances, G Di Lorenzo, et al.Annals of Neurology|June 1, 1996
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patientsF M Santorelli, M Sciacco, K Tanji, et al.Neurology|May 1, 1997
Mitochondrial encephalomyopathy with coenzyme Q10 deficiencyC Sobreira, M Hirano, S Shanske, et al.Journal of the Neurological Sciences|February 19, 2019
Clinical and neuroimaging features of the m.10197G>A mtDNA mutation: New case reports and expansion of the phenotype variabilityD Tolomeo, A Rubegni, M Severino, et al.Neurology|March 29, 2001
Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish familyC Casali, V Bonifati, F M Santorelli, et al.European Journal of Neurology|October 2, 2019
The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian familiesM Lieto, V Riso, D Galatolo, et al.Neurology|April 26, 2006
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic studyC Criscuolo, L Chessa, S Di Giandomenico, et al.The Journal of Pediatrics|August 4, 1999
The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathyC Bruno, D M Kirby, Y Koga, et al.Molecular Genetics and Metabolism|June 28, 2005
Molecular studies in Portuguese patients with Smith-Lemli-Opitz syndrome and report of three new mutations in DHCR7M L Cardoso, A Balreira, E Martins, et al.Journal of Neurology|July 14, 2021
Adult-onset mitochondrial movement disorders: a national picture from the Italian NetworkV Montano, D Orsucci, V Carelli, et al.Pageof 13