Breza, Marianthi; Hirst, Jennifer; Chelban, Viorica; Banneau, Guillaume; Tissier, Laurene; Kol, Bophara; Bourinaris, Thomas; Said, Samia A.; Pereon, Yann; Heinzmann, Anna; Debs, Rabab; Juntas-Morales, Raul; Martinez, Victoria G.; Camdessanche, Jean P.; Scherer-Gagou, Clarisse; Zola, Jean-Medard; Athanasiou-Fragkouli, Alkyoni; Efthymiou, Stephanie; Vavougios, George; Velonakis, Georgios; Stamelou, Maria; Tzartos, John; Potagas, Constantin; Zambelis, Thomas; Mariotti, Caterina; Blackstone, Craig; Vandrovcova, Jana; Mavridis, Theodoros; Kartanou, Chrisoula; Stefanis, Leonidas; Wood, Nicholas; Karadima, Georgia; LeGuern, Eric; Koutsis, Georgios; Houlden, Henry; Stevanin, Giovanni

Validation of differentially expressed brain-enriched microRNAs in the plasma of PD patients

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY

IF3.9

2020-08-2948

OAAI

Wide range of reduced penetrance alleles in spinal and bulbar muscular atrophy: a model-based approach

JOURNAL OF MEDICAL GENETICS

IF3.7

2020-06-227

PREAI

A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia

BRAIN

IF11.7

2020-05-185

OAAI

Deciphering anti-MOG IgG antibodies: Clinical and radiological spectrum, and comparison of antibody detection assays

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2020-03-0113

PREAI

Tzartos, John S.; Karagiorgou, Katerina; Tzanetakos, Dimitrios; Breza, Marianthi; Evangelopoulos, Maria Eleftheria; Pelidou, Sygkliti-Henrietta; Bakirtzis, Christos; Nikolaidis, Ioannis; Koutsis, Georgios; Notas, Konstantinos; Chroni, Elisabeth; Markakis, Ioannis; Grigoriadis, Nikolaos C.; Anagnostouli, Maria; Orologas, Anastasios; Parisis, Dimitrios; Karapanayiotides, Theodoros; Papadimitriou, Dimitra; Kostadima, Vasiliki; Elloul, John; Xidakis, Iosif; Maris, Thomas; Zisimopoulou, Paraskevi; Tzartos, Socrates; Kilidireas, Costas

A longitudinal study of cognitive function in multiple sclerosis: is decline inevitable?

JOURNAL OF NEUROLOGY

IF4.6

2020-02-0114

PREAI

Evidence for Cognitive Deficits in X-Linked Charcot-Marie-Tooth Disease

JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY

IF2.6

2020-01-174

OAAI

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

AMPA受体GluA2亚基缺陷是神经发育障碍的一个原因

NATURE COMMUNICATIONS

IF15.7

2019-07-12159

OAAI

Salpietro, Vincenzo; Dixon, Christine L.; Guo, Hui; Bello, Oscar D.; Vandrovcova, Jana; Efthymiou, Stephanie; Maroofian, Reza; Heimer, Gali; Burglen, Lydie; Valence, Stephanie; Torti, Erin; Hacke, Moritz; Rankin, Julia; Tariq, Huma; Colin, Estelle; Procaccio, Vincent; Striano, Pasquale; Mankad, Kshitij; Lieb, Andreas; Chen, Sharon; Pisani, Laura; Bettencourt, Conceicao; Mannikko, Roope; Manole, Andreea; Brusco, Alfredo; Grosso, Enrico; Ferrero, Giovanni Battista; Armstrong-Moron, Judith; Gueden, Sophie; Bar-Yosef, Omer; Tzadok, Michal; Monaghan, Kristin G.; Santiago-Sim, Teresa; Person, Richard E.; Cho, Megan T.; Willaert, Rebecca; Yoo, Yongjin; Chae, Jong-Hee; Quan, Yingting; Wu, Huidan; Wang, Tianyun; Bernier, Raphael A.; Xia, Kun; Blesson, Alyssa; Jain, Mahim; Motazacker, Mohammad M.; Jaeger, Bregje; Schneider, Amy L.; Boysen, Katja; Muir, Alison M.; Myers, Candace T.; Gavrilova, Ralitza H.; Gunderson, Lauren; Schultz-Rogers, Laura; Klee, Eric W.; Dyment, David; Osmond, Matthew; Parellada, Mara; Llorente, Cloe; Gonzalez-Penas, Javier; Carracedo, Angel; Van Haeringen, Arie; Ruivenkamp, Claudia; Nava, Caroline; Heron, Delphine; Nardello, Rosaria; Iacomino, Michele; Minetti, Carlo; Skabar, Aldo; Fabretto, Antonella; Chez, Michael; Tsai, Anne; Fassi, Emily; Shinawi, Marwan; Constantino, John N.; De Zorzi, Rita; Fortuna, Sara; Kok, Fernando; Keren, Boris; Bonneau, Dominique; Choi, Murim; Benzeev, Bruria; Zara, Federico; Mefford, Heather C.; Scheffer, Ingrid E.; Clayton-Smith, Jill; Macaya, Alfons; Rothman, James E.; Eichler, Evan E.; Kullmann, Dimitri M.; Houlden, Henry; Raspall-Chaure, Miquel; Hanna, Michael G.; Bugiardini, Enrico; Hostettler, Isabel; O'Callaghan, Benjamin; Khan, Alaa; Cortese, Andrea; O'Connor, Emer; Yau, Wai Y.; Bourinaris, Thomas; Kaiyrzhanov, Rauan; Chelban, Viorica; Madej, Monika; Diana, Maria C.; Vari, Maria S.; Pedemonte, Marina; Bruno, Claudio; Balagura, Ganna; Scala, Marcello; Fiorillo, Chiara; Nobili, Lino; Malintan, Nancy T.; Zanetti, Maria N.; Krishnakumar, Shyam S.; Lignani, Gabriele; Jepson, James E. C.; Broda, Paolo; Baldassari, Simona; Rossi, Pia; Fruscione, Floriana; Madia, Francesca; Traverso, Monica; De-Marco, Patrizia; Perez-Duenas, Belen; Munell, Francina; Kriouile, Yamna; El-Khorassani, Mohamed; Karashova, Blagovesta; Avdjieva, Daniela; Kathom, Hadil; Tincheva, Radka; Van-Maldergem, Lionel; Nachbauer, Wolfgang; Boesch, Sylvia; Gagliano, Antonella; Amadori, Elisabetta; Goraya, Jatinder S.; Sultan, Tipu; Kirmani, Salman; Ibrahim, Shahnaz; Jan, Farida; Mine, Jun; Banu, Selina; Veggiotti, Pierangelo; Zuccotti, Gian, V; Ferrari, Michel D.; Van Den Maagdenberg, Arn M. J.; Verrotti, Alberto; Marseglia, Gian L.; Savasta, Salvatore; Soler, Miguel A.; Scuderi, Carmela; Borgione, Eugenia; Chimenz, Roberto; Gitto, Eloisa; Dipasquale, Valeria; Sallemi, Alessia; Fusco, Monica; Cuppari, Caterina; Cutrupi, Maria C.; Ruggieri, Martino; Cama, Armando; Capra, Valeria; Mencacci, Niccolo E.; Boles, Richard; Gupta, Neerja; Kabra, Madhulika; Papacostas, Savvas; Zamba-Papanicolaou, Eleni; Dardiotis, Efthymios; Maqbool, Shazia; Rana, Nuzhat; Atawneh, Osama; Lim, Shen Y.; Shaikh, Farooq; Koutsis, George; Breza, Marianthi; Coviello, Domenico A.; Dauvilliers, Yves A.; AlKhawaja, Issam; AlKhawaja, Mariam; Al-Mutairi, Fuad; Stojkovic, Tanya; Ferrucci, Veronica; Zollo, Massimo; Alkuraya, Fowzan S.; Kinali, Maria; Sherifa, Hamed; Benrhouma, Hanene; Turki, Ilhem B. Y.; Tazir, Meriem; Obeid, Makram; Bakhtadze, Sophia; Saadi, Nebal W.; Zaki, Maha S.; Triki, Chahnez C.; Benfenati, Fabio; Gustincich, Stefano; Kara, Majdi; Belcastro, Vincenzo; Specchio, Nicola; Capovilla, Giuseppe; Karimiani, Ehsan G.; Salih, Ahmed M.; Okubadejo, Njideka U.; Ojo, Oluwadamilola O.; Oshinaike, Olajumoke O.; Oguntunde, Olapeju; Wahab, Kolawole; Bello, Abiodun H.; Abubakar, Sanni; Obiabo, Yahaya; Nwazor, Ernest; Ekenze, Oluchi; Williams, Uduak; Iyagba, Alagoma; Taiwo, Lolade; Komolafe, Morenikeji; Senkevich, Konstantin; Shashkin, Chingiz; Zharkynbekova, Nazira; Koneyev, Kairgali; Manizha, Ganieva; Isrofilov, Maksud; Guliyeva, Ulviyya; Salayev, Kamran; Khachatryan, Samson; Rossi, Salvatore; Silvestri, Gabriella; Haridy, Nourelhoda; Ramenghi, Luca A.; Xiromerisiou, Georgia; David, Emanuele; Aguennouz, Mhammed; Fidani, Liana; Spanaki, Cleanthe; Tucci, Arianna

Screening for spinocerebellar ataxia type 36 (SCA36) in the Greek population

在希腊人群中筛查脊髓小脑性共济失调36型 (SCA36)

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2019-07-017

PREAI

Mutational screening of the SH3TC2 gene in Greek patients with suspected demyelinating recessive Charcot-Marie-Tooth disease reveals a varied and unusual phenotypic spectrum

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

IF3.2

2019-02-0611

PREAI

Ocular flutter as presenting manifestation of pediatric MOG antibody-associated demyelination: A case report