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Year Number of Results
1993 1
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1998 2
2000 2
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2003 1
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2006 1
2009 1
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2019 3
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20 results

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Page 1
Levetiracetam vs Lamotrigine as First-Line Antiseizure Medication in Female Patients With Idiopathic Generalized Epilepsy.
Cerulli Irelli E, Cocchi E, Morano A, Gesche J, Caraballo RH, Lattanzi S, Strigaro G, Catania C, Ferlazzo E, Pascarella A, Casciato S, Quarato P, Pizzanelli C, Pulitano P, Giuliano L, Viola V, Mostacci B, Fortunato F, Marini C, Di Gennaro G, Gambardella A, Labate A, Operto FF, Giallonardo AT, Baykan B, Beier CP, Di Bonaventura C; Women With Epilepsy Treatment Options and Research (WETOR) Study Group. Cerulli Irelli E, et al. JAMA Neurol. 2023 Nov 1;80(11):1174-1181. doi: 10.1001/jamaneurol.2023.3400. JAMA Neurol. 2023. PMID: 37782485 Free PMC article.
Paramedian diencephalic syndrome.
Antonini G, Rasura M, Paolini S, Mercieri M, Pantano P, Gragnani F, Argentino C. Antonini G, et al. Among authors: gragnani f. Ital J Neurol Sci. 1994 Sep;15(6):285-90. doi: 10.1007/BF02339238. Ital J Neurol Sci. 1994. PMID: 7843943
Topiramate ban in women of childbearing potential with idiopathic generalized epilepsy: Does effectiveness offset the teratogenic risks?
Cerulli Irelli E, Cocchi E, Mostacci B, Orlando B, Gesche J, Caraballo RH, Lattanzi S, Strigaro G, Catania C, Pulitano P, Panzini C, Ferlazzo E, Pascarella A, Casciato S, Pizzanelli C, Giuliano L, Viola V, Fortunato F, Di Gennaro G, Gambardella A, Labate A, Operto FF, Giallonardo AT, Baykan B, Beier CP, Di Bonaventura C; Women With Epilepsy Treatment Options and Research Study Group. Cerulli Irelli E, et al. Epilepsia. 2024 Mar;65(3):e27-e34. doi: 10.1111/epi.17892. Epub 2024 Jan 31. Epilepsia. 2024. PMID: 38294338
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients.
Strafella C, Megalizzi D, Trastulli G, Proietti Piorgo E, Colantoni L, Tasca G, Monforte M, Zampatti S, Primiano G, Sancricca C, Bortolani S, Torchia E, Ravera B, Torri F, Gadaleta G, Risi B, Caria F, Gerardi F, Carraro E, Gioiosa V, Garibaldi M, Tufano L, Frezza E, Massa R, Caltagirone C, Pennisi EM, Petrucci A, Pane M, Frongia A, Gragnani F, Scutifero M, Mandich P, Grandis M, Maioli MA, Casali C, Manfroi E, Politano L, Passamano L, Petillo R, Rodolico C, Pugliese A, Previtali SC, Sansone V, Vercelli L, Mongini TE, Ricci G, Siciliano G, Filosto M, Ricci E, Cascella R, Giardina E; FSHD Italian Clinical Group. Strafella C, et al. Among authors: gragnani f. Clin Epigenetics. 2024 Oct 22;16(1):148. doi: 10.1186/s13148-024-01747-2. Clin Epigenetics. 2024. PMID: 39438900 Free PMC article.
Sensory involvement in spinal-bulbar muscular atrophy (Kennedy's disease).
Antonini G, Gragnani F, Romaniello A, Pennisi EM, Morino S, Ceschin V, Santoro L, Cruccu G. Antonini G, et al. Among authors: gragnani f. Muscle Nerve. 2000 Feb;23(2):252-8. doi: 10.1002/(sici)1097-4598(200002)23:2<252::aid-mus17>3.0.co;2-p. Muscle Nerve. 2000. PMID: 10639619 Clinical Trial.
Myasthenia gravis in the elderly: a hospital based study.
Antonini G, Morino S, Gragnani F, Fiorelli M. Antonini G, et al. Among authors: gragnani f. Acta Neurol Scand. 1996 Apr;93(4):260-2. doi: 10.1111/j.1600-0404.1996.tb00517.x. Acta Neurol Scand. 1996. PMID: 8739435
Autoantibodies to glutamic acid decarboxylase in downbeat nystagmus.
Antonini G, Nemni R, Giubilei F, Gragnani F, Ceschin V, Morino S, Bucci E, Accornero N. Antonini G, et al. Among authors: gragnani f. J Neurol Neurosurg Psychiatry. 2003 Jul;74(7):998-9. doi: 10.1136/jnnp.74.7.998. J Neurol Neurosurg Psychiatry. 2003. PMID: 12810806 Free PMC article.
Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients.
Pennisi EM, Arca M, Bertini E, Bruno C, Cassandrini D, D'amico A, Garibaldi M, Gragnani F, Maggi L, Massa R, Missaglia S, Morandi L, Musumeci O, Pegoraro E, Rastelli E, Santorelli FM, Tasca E, Tavian D, Toscano A, Angelini C; Italian NLSD Group. Pennisi EM, et al. Among authors: gragnani f. Orphanet J Rare Dis. 2017 May 12;12(1):90. doi: 10.1186/s13023-017-0646-9. Orphanet J Rare Dis. 2017. PMID: 28499397 Free PMC article.
20 results