Rapamycin causes regression of astrocytomas in tuberous sclerosis complex DN Franz, J Leonard, C Tudor, G Chuck, M Care, G Sethuraman, ... Annals of neurology 59 (3), 490-498, 2006 | 709 | 2006 |
GFAP mutations, age at onset, and clinical subtypes in Alexander disease M Prust, J Wang, H Morizono, A Messing, M Brenner, E Gordon, T Hartka, ... Neurology 77 (13), 1287-1294, 2011 | 244 | 2011 |
Genetic spectrum of hereditary neuropathies with onset in the first year of life J Baets, T Deconinck, E De Vriendt, M Zimoń, L Yperzeele, ... Brain 134 (9), 2664-2676, 2011 | 141 | 2011 |
GENETIC SPECTRUM OF HEREDITARY NEUROPATHIES WITH ONSET IN THE FIRST YEAR OF LIFE J Baets, M Zimoń, E De Vriendt, T Deconinck, R Spiegel, Y Parman, ... Journal of the Peripheral Nervous System 515 (3), 248-249, 2010 | 141 | 2010 |
Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia S Kure, K Kato, A Dinopoulos, C Gail, TJ DeGrauw, J Christodoulou, ... Human mutation 27 (4), 343-352, 2006 | 119 | 2006 |
Atypical variants of nonketotic hyperglycinemia A Dinopoulos, Y Matsubara, S Kure Molecular genetics and metabolism 86 (1-2), 61-69, 2005 | 106 | 2005 |
Brain MRI and proton MRS findings in infants and children with respiratory chain defects A Dinopoulos, KM Cecil, MB Schapiro, A Papadimitriou, ... Neuropediatrics 36 (05), 290-301, 2005 | 92 | 2005 |
ADCY5-related movement disorders: frequency, disease course and phenotypic variability in a cohort of paediatric patients M Carecchio, NE Mencacci, A Iodice, R Pons, C Panteghini, G Zorzi, ... Parkinsonism & related disorders 41, 37-43, 2017 | 84 | 2017 |
Levodopa‐induced dyskinesias in tyrosine hydroxylase deficiency R Pons, D Syrengelas, S Youroukos, I Orfanou, A Dinopoulos, B Cormand, ... Movement Disorders 28 (8), 1058-1063, 2013 | 75 | 2013 |
Novel mutations affecting LRP5 splicing in patients with osteoporosis-pseudoglioma syndrome (OPPG) CM Laine, BD Chung, M Susic, T Prescott, O Semler, T Fiskerstrand, ... European Journal of Human Genetics 19 (8), 875-881, 2011 | 65 | 2011 |
Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology MS Van der Knaap, T Linnankivi, A Paetau, A Feigenbaum, K Wakusawa, ... Neurology 69 (2), 166-171, 2007 | 62 | 2007 |
MLC1 is associated with the dystrophin-glycoprotein complex at astrocytic endfeet I Boor, M Nagtegaal, W Kamphorst, P van der Valk, JC Pronk, ... Acta neuropathologica 114 (4), 403-410, 2007 | 59 | 2007 |
Mucoepidermoid carcinoma of the bronchus A Dinopoulos, E Lagona, I Stinios, A Konstadinidou, C Kattamis Pediatric hematology and oncology 17 (5), 401-408, 2000 | 58 | 2000 |
Homovanillic acid in cerebrospinal fluid of 1388 children with neurological disorders M Molero‐Luis, M Serrano, A Ormazábal, B Pérez‐Dueñas, ... Developmental Medicine & Child Neurology 55 (6), 559-566, 2013 | 53 | 2013 |
Reversible MR imaging and MR spectroscopy abnormalities in association with metronidazole therapy KM Cecil, MJ Halsted, M Schapiro, A Dinopoulos, BV Jones Journal of computer assisted tomography 26 (6), 948-951, 2002 | 53 | 2002 |
Postherpes simplex encephalitis: a case series of viral-triggered autoimmunity, synaptic autoantibodies and response to therapy H Alexopoulos, S Akrivou, S Mastroyanni, M Antonopoulou, A Dinopoulos, ... Therapeutic Advances in Neurological Disorders 11, 1756286418768778, 2018 | 41 | 2018 |
De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy I Mademan, T Deconinck, A Dinopoulos, T Voit, U Schara, K Devriendt, ... Neurology 81 (22), 1953-1958, 2013 | 41 | 2013 |
Glycine decarboxylase mutations: a distinctive phenotype of nonketotic hyperglycinemia in adults A Dinopoulos, S Kure, G Chuck, K Sato, DL Gilbert, Y Matsubara, ... Neurology 64 (7), 1255-1257, 2005 | 41 | 2005 |
A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings AA Polymeris, A Tessa, K Anagnostopoulou, A Rubegni, D Galatolo, ... Journal of neurology 263 (8), 1604-1611, 2016 | 37 | 2016 |
Mycoplasma pneumoniae encephalopathy: recovery after intravenous immunoglobulin A Attilakos, P Palaiologou, E Lagona, A Voutsioti, A Dinopoulos Pediatric neurology 38 (5), 357-359, 2008 | 35 | 2008 |