1.1 Articolo in rivista: [13148] Home page tipologia

Sfoglia
Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 481 a 500 di 13.148
Titolo Data di pubblicazione Autore(i) File
Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNA(Cys) gene 1-gen-2007 Scuderi, C; Borgione, E; Musumeci, S; Elia, M; Castello, F; Fichera, M; Davidzon, G; Dimauro, S
Chromosome abnormalities and epilepsy 1-gen-2001 Elia, M; Musumeci, Sa; Ferri, R; Ayala, Gf
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression 1-gen-2009 Lintas, C; Sacco, R; Garbett, K; Mirnics, K; Militerni, R; Bravaccio, C; Curatolo, P; Manzi, B; Schneider, C; Melmed, R; Elia, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, Kl; Persico, Am
Analysis of the gastrin-releasing peptide receptor gene in Italian patients with autism spectrum disorders 1-gen-2008 Seidita, G; Mirisola, M; D'Anna, Rp; Gallo, A; Jensen, Rt; Mantey, Sa; Gonzalez, N; Falco, M; Zingale, M; Elia, M; Cucina, L; Chiavetta, V; Romano, V; Cali, F
Lennox-Gastaut syndrome with late-onset and prominent reflex seizures in trisomy 21 patients 1-gen-2009 Ferlazzo, E; Adjien, Ck; Guerrini, R; Calarese, T; Crespel, A; Elia, M; Striano, P; Gelisse, P; Bramanti, P; di Bella, P; Genton, P
Cyclic alternating pattern and spectral analysis of heart rate variability during normal sleep 1-gen-2000 Ferri, R; Parrino, L; Smerieri, A; Terzano, Mg; Elia, M; Musumeci, Sa; Pettinato, S
Novel deletion of the E3A ubiquitin protein ligase gene detected by multiplex ligation-dependent probe amplification in a patient with Angelman syndrome 1-gen-2010 Cali, F; Ragalmuto, A; Chiavetta, V; Calabrese, G; Fichera, M; Vinci, M; Ruggeri, G; Schinocca, P; Sturnio, M; Romano, S; Romano, V; Elia, M
Epilepsy and EEG findings in males with fragile X syndrome 1-gen-1999 Musumeci, Sa; Hagerman, Rj; Ferri, R; Bosco, P; Dalla Bernardina, B; Tassinari, Ca; De Sarro, Gb; Elia, M
Seizures in Klinefelter's syndrome 1-gen-1998 Tatum, Wo; Passaro, Ea; Elia, M; Guerrini, R; Gieron, M; Genton, P
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability 1-gen-2015 Miceli, Francesco; Striano, Pasquale; Soldovieri Maria, Virginia; Fontana, Antonina; Nardello, Rosaria; Robbiano, Angela; Bellini, Giulia; Elia, M; Zara, Federico; Taglialatela, Maurizio; Mangano, Salvatore
Seizures and epileptiform EEG abnormalities in FRAXE syndrome 1-gen-2001 Musumeci, Sa; Ferri, R; Scuderi, C; Bosco, P; Elia, M
Sleep polygraphy in Angelman syndrome 1-gen-2004 Miano, S; Bruni, O; Leuzzi, V; Elia, M; Verrillo, E; Ferri, R
Sleep breathing and periodic leg movement pattern in Angelman Syndrome: A polysomnographic study 1-gen-2005 Miano, S; Bruni, O; Elia, M; Musumeci, Sa; Verrillo, E; Ferri, R
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1 1-gen-2010 Palmieri, L; Papaleo, V; Porcelli, V; Scarcia, P; Gaita, L; Sacco, R; Hager, J; Rousseau, F; Curatolo, P; Manzi, B; Militerni, R; Bravaccio, C; Trillo, S; Schneider, C; Melmed, R; Elia, M; Lenti, C; Saccani, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, Kl; Persico, Am
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy 1-gen-2007 Striano, P; Coppola, A; Pezzella, M; Ciampa, C; Specchio, N; Ragona, F; Mancardi, Mm; Gennaro, E; Beccaria, F; Capovilla, G; Rasmini, P; Besana, D; Coppola, Gg; Elia, M; Granata, T; Vecchi, M; Vigevano, F; Viri, M; Gaggero, R; Striano, S; Zara, F
Polysomnographic assessment of sleep disturbances in children with developmental disabilities and seizures 1-gen-2010 Miano, S; Bruni, O; Arico, D; Elia, M; Ferri, R
SEIZURES IN KLINEFELTERS-SYNDROME - A CLINICAL AND EEG STUDY OF 5 PATIENTS 1-gen-1995 Elia, M; Musumeci, Sa; Ferri, R; Scuderi, C; Delgracco, S; Stefanini, Mc
Saethre-Chotzen syndrome: A clinical, EEG and neuroradiological study 1-gen-1996 Elia, M; Musumeci, Sa; Ferri, R; Greco, D; Romano, C; Delgracco, S; Stefanini, Mc
GIANT SOMATOSENSORY-EVOKED POTENTIALS AND PATHOPHYSIOLOGY OF HYPEREKPLEXIA - NEUROPHYSIOLOGICAL STUDY OF ONE PATIENT 1-gen-1994 Ferri, R; Elia, M; Musumeci, Sa; Colamaria, V; Dallabernardina, B; Delgracco, S; Bergonzi, P
Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua 1-gen-1996 Elia, M; Musumeci, Sa; Ferri, R; Colamaria, V; Azan, G; Greco, D; Stefanini, Mc
Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 481 a 500 di 13.148
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile

Scopri
Tipologia
  • 1 Contributo su Rivista13145
  • 2 Contributo in Volume1
  • 4 Contributo in Atti di Convegno ...1
Autore
  • BARBANTI, MARCO416
  • DOMINGUEZ RODRIGUEZ, LIGIA JULIANA329
  • PAPPALARDO, FEDERICO327
  • GEBBIA, VITTORIO320
  • TUMINO, AURORA310
  • GULINO, MARISA283
  • MANIACI, ANTONINO231
  • ELIA, MAURIZIO223
  • LANZALONE, GAETANO217
  • SCHIMMENTI, ADRIANO208
Data di pubblicazione
  • In corso di stampa18
  • 2020 - 20255444
  • 2010 - 20195394
  • 2000 - 20091818
  • 1990 - 1999416
  • 1980 - 198956
  • 1979 - 19791
Editore
  • Trans Tech Publications1
Rivista
  • INTERNATIONAL JOURNAL OF MOLECULA...143
  • JOURNAL OF CLINICAL MEDICINE108
  • INTERNATIONAL JOURNAL OF ENVIRONM...106
  • CANCERS98
  • LNS. ACTIVITY REPORT85
  • PHD KORE REVIEW78
  • RIVISTA DELLA COOPERAZIONE GIURID...72
  • DIAGNOSTICS69
  • SUSTAINABILITY64
  • JACC: CARDIOVASCULAR INTERVENTIONS60
Serie
  • ADVANCED MATERIALS RESEARCH1
  • WORKING PAPERS RES1
Keyword
  • COVID-19220
  • Humans212
  • Female111
  • Male107
  • SARS-CoV-292
  • Italy66
  • inflammation59
  • Adult52
  • Epilepsy52
  • Middle Aged51
Lingua
  • eng9216
  • ita2402
  • fre66
  • spa60
  • lat12
  • ger9
  • por6
  • ara3
  • cat3
  • enm2
Accesso al fulltext
  • no fulltext13147