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Argiris Dinopoulos
Argiris Dinopoulos
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα med.uoa.gr - Αρχική σελίδα
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Έτος
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
7092006
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
2442011
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
1412011
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
1412010
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
1192006
Atypical variants of nonketotic hyperglycinemia
A Dinopoulos, Y Matsubara, S Kure
Molecular genetics and metabolism 86 (1-2), 61-69, 2005
1062005
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
922005
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
842017
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
752013
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
652011
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
622007
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
592007
Mucoepidermoid carcinoma of the bronchus
A Dinopoulos, E Lagona, I Stinios, A Konstadinidou, C Kattamis
Pediatric hematology and oncology 17 (5), 401-408, 2000
582000
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
532013
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
532002
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
412018
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
412013
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
412005
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
372016
Mycoplasma pneumoniae encephalopathy: recovery after intravenous immunoglobulin
A Attilakos, P Palaiologou, E Lagona, A Voutsioti, A Dinopoulos
Pediatric neurology 38 (5), 357-359, 2008
352008
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