受强制性开放获取政策约束的文章 - Stanislav Groppa了解详情
可在其他位置公开访问的文章：22 篇
Global impact of COVID-19 on stroke care and IV thrombolysis
RG Nogueira, MM Qureshi, M Abdalkader, SO Martins, H Yamagami, ...
Neurology 96 (23), e2824-e2838, 2021
强制性开放获取政策： US National Institutes of Health
Deep brain stimulation and L-DOPA therapy: concepts of action and clinical applications in Parkinson's disease
M Muthuraman, N Koirala, D Ciolac, B Pintea, M Glaser, S Groppa, ...
Frontiers in neurology 9, 711, 2018
强制性开放获取政策： German Research Foundation
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation
V Chelban, MP Wilson, J Warman Chardon, J Vandrovcova, MN Zanetti, ...
Annals of neurology 86 (2), 225-240, 2019
强制性开放获取政策： Canadian Institutes of Health Research, Genome Canada, Dunhill Medical Trust …
Bi-allelic JAM2 variants lead to early-onset recessive primary familial brain calcification
LV Schottlaender, R Abeti, Z Jaunmuktane, C Macmillan, V Chelban, ...
The American Journal of Human Genetics 106 (3), 412-421, 2020
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination
S Efthymiou, V Salpietro, N Malintan, M Poncelet, Y Kriouile, S Fortuna, ...
Brain 142 (10), 2948-2964, 2019
强制性开放获取政策： German Research Foundation, Dunhill Medical Trust, UK, UK Medical Research …
Global impact of the COVID-19 pandemic on stroke volumes and cerebrovascular events: a 1-year follow-up
TN Nguyen, MM Qureshi, P Klein, H Yamagami, R Mikulik, ...
Neurology 100 (4), e408-e421, 2023
强制性开放获取政策： US National Institutes of Health, European Commission
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants
C Neuray, R Maroofian, M Scala, T Sultan, GS Pai, M Mojarrad, ...
Brain 143 (8), 2388-2397, 2020
强制性开放获取政策： Dunhill Medical Trust, UK, UK Medical Research Council, National Institute …
Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia
V Chelban, A Tucci, DS Lynch, JM Polke, L Santos, H Jonvik, S Groppa, ...
Journal of Neurology, Neurosurgery & Psychiatry 88 (8), 681-687, 2017
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Breakdown of Thalamo-Cortical Connectivity Precedes Spike Generation in Focal Epilepsies
C Vitalie, G Stanislav A, C Dumitru, K Nabin, M Liudmila, W Yaroslav, ...
Brain Connectivity 7 (5), 309-320, 2017
强制性开放获取政策： German Research Foundation
Successful surgical resection in non-lesional operculo-insular epilepsy without intracranial monitoring
V Chiosa, C Granziera, L Spinelli, C Pollo, E Roulet-Perez, S Groppa, ...
Epileptic disorders 15 (2), 148-157, 2013
强制性开放获取政策： Swiss National Science Foundation
Genetic and phenotypic characterization of NKX6‐2‐related spastic ataxia and hypomyelination
V Chelban, M Alsagob, K Kloth, A Chirita‐Emandi, J Vandrovcova, ...
European journal of neurology 27 (2), 334-342, 2020
强制性开放获取政策： US National Institutes of Health, Dunhill Medical Trust, UK, UK Medical …
Large-scale network architecture and associated structural cortico-subcortical abnormalities in patients with sleep/awake-related seizures
V Chiosa, D Ciolac, S Groppa, N Koirala, B Pintea, A Vataman, Y Winter, ...
Sleep 42 (4), zsz006, 2019
强制性开放获取政策： German Research Foundation
MYORG-related disease is associated with central pontine calcifications and atypical parkinsonism
V Chelban, M Carecchio, G Rea, A Bowirrat, S Kirmani, L Magistrelli, ...
Neurology: Genetics 6 (2), e399, 2020
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
IL-34 exacerbates pathogenic features of Alzheimer’s disease and calvaria osteolysis in triple transgenic (3x-Tg) female mice
H Anny, N Bidii, Y Chiaki, G Christopher, D Carolina, G Stanislav, ...
Biomedicine & Pharmacotherapy 166, 1-10, 2023
强制性开放获取政策： US National Institutes of Health
Dynamic flexibility and controllability of network communities in juvenile myoclonic epilepsy
A Vataman, D Ciolac, V Chiosa, D Aftene, P Leahu, Y Winter, SA Groppa, ...
Neurobiology of Disease 179, 106055, 2023
强制性开放获取政策： German Research Foundation
Characterisation of the antibody response in sinopharm (BBIBP-CorV) recipients and COVID-19 Convalescent Sera from the Republic of Moldova
M Ulinici, A Suljič, M Poggianella, R Milan Bonotto, K Resman Rus, ...
Vaccines 11 (3), 637, 2023
强制性开放获取政策： Fondazione Cariplo
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease
E Calì, SJ Lin, C Rocca, Y Sahin, A Al Shamsi, S El Chehadeh, ...
Genetics in Medicine 24 (10), 2194-2203, 2022
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Altered grey matter integrity and network vulnerability relate to epilepsy occurrence in patients with multiple sclerosis
D Ciolac, G Gonzalez‐Escamilla, Y Winter, N Melzer, F Luessi, A Radetz, ...
European journal of neurology 29 (8), 2309-2320, 2022
强制性开放获取政策： German Research Foundation
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome
V Salpietro, R Maroofian, MS Zaki, J Wangen, A Ciolfi, S Barresi, ...
The American Journal of Human Genetics 111 (1), 200-210, 2024
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Indicatorii de calitate ai atacului cerebral în Republica Moldova–registrul RES-Q
E Manole, C Tiu, A Vilionskis, A Tsiskaridze, E Zota, A Grecu, R Mikulik, ...
Revista de Ştiinţe ale Sănătăţii din Moldova 27 (1), 32-44, 2022
强制性开放获取政策： European Commission
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