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Items: 1 to 50 of 152

1.

LGI1 and CASPR2 autoimmunity in children: Systematic literature review and report of a young girl with Morvan syndrome.

Nosadini M, Toldo I, Tascini B, Bien CG, Parmeggiani L, De Gaspari P, Zuliani L, Sartori S.

J Neuroimmunol. 2019 Jul 18;335:577008. doi: 10.1016/j.jneuroim.2019.577008. [Epub ahead of print] Review.

PMID:
31352183
2.

Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly.

Domingues FS, König E, Schwienbacher C, Volpato CB, Picard A, Cantaloni C, Mascalzoni D, Lackner P, Heimbach A, Hoffmann P, Stanzial F, Hicks AA, Parmeggiani L, Benedicenti F, Pellegrin S, Casara G, Pramstaller PP.

Seizure. 2019 Mar;66:81-85. doi: 10.1016/j.seizure.2018.12.021. Epub 2018 Dec 23.

3.

Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study.

Trivisano M, Pietrafusa N, Terracciano A, Marini C, Mei D, Darra F, Accorsi P, Battaglia D, Caffi L, Canevini MP, Cappelletti S, Cesaroni E, de Palma L, Costa P, Cusmai R, Giordano L, Ferrari A, Freri E, Fusco L, Granata T, Martino T, Mastrangelo M, Bova SM, Parmeggiani L, Ragona F, Sicca F, Striano P, Specchio LM, Tondo I, Zambrelli E, Zamponi N, Zanus C, Boniver C, Vecchi M, Avolio C, Dalla Bernardina B, Bertini E, Guerrini R, Vigevano F, Specchio N.

Epilepsia. 2018 Dec;59(12):2260-2271. doi: 10.1111/epi.14600. Epub 2018 Nov 19.

PMID:
30451291
4.

Clinical features and outcome of 6 new patients carrying de novo KCNB1 gene mutations.

Marini C, Romoli M, Parrini E, Costa C, Mei D, Mari F, Parmeggiani L, Procopio E, Metitieri T, Cellini E, Virdò S, De Vita D, Gentile M, Prontera P, Calabresi P, Guerrini R.

Neurol Genet. 2017 Dec 11;3(6):e206. doi: 10.1212/NXG.0000000000000206. eCollection 2017 Dec.

5.

A thicker intima-media carotid wall was found in a cohort of children with recent onset migraine.

Parmeggiani L, Salandin M, Egger F, Lupi F, Primerano M, Radetti G.

Acta Paediatr. 2016 Dec;105(12):e577-e581. doi: 10.1111/apa.13611.

PMID:
27686570
6.

Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy.

Marini C, Darra F, Specchio N, Mei D, Terracciano A, Parmeggiani L, Ferrari A, Sicca F, Mastrangelo M, Spaccini L, Canopoli ML, Cesaroni E, Zamponi N, Caffi L, Ricciardelli P, Grosso S, Pisano T, Canevini MP, Granata T, Accorsi P, Battaglia D, Cusmai R, Vigevano F, Dalla Bernardina B, Guerrini R.

Epilepsia. 2012 Dec;53(12):2111-9. doi: 10.1111/j.1528-1167.2012.03649.x. Epub 2012 Sep 4.

7.

Protocadherin 19 mutations in girls with infantile-onset epilepsy.

Marini C, Mei D, Parmeggiani L, Norci V, Calado E, Ferrari A, Moreira A, Pisano T, Specchio N, Vigevano F, Battaglia D, Guerrini R.

Neurology. 2010 Aug 17;75(7):646-53. doi: 10.1212/WNL.0b013e3181ed9e67.

PMID:
20713952
8.

Evaluation of carisbamate, a novel antiepileptic drug, in photosensitive patients: an exploratory, placebo-controlled study.

Trenité DG, French JA, Hirsch E, Macher JP, Meyer BU, Grosse PA, Abou-Khalil BW, Rosenfeld WE, van Gerven J, Novak GP, Parmeggiani L, Schmidt B, Gibson D, Guerrini R.

Epilepsy Res. 2007 May;74(2-3):193-200. Epub 2007 Apr 19.

PMID:
17448639
9.

Adenosine A1 receptor expression during the transition from compensated pressure overload hypertrophy to heart failure.

Perlini S, Arosio B, Parmeggiani L, Santambrogio D, Palladini G, Tozzi R, Gatti C, Annoni G, Meyer TE, Ferrari AU.

J Hypertens. 2007 Feb;25(2):449-54.

PMID:
17211253
10.

Topiramate and its clinical applications in epilepsy.

Guerrini R, Parmeggiani L.

Expert Opin Pharmacother. 2006 Apr;7(6):811-23. Review.

PMID:
16556095
11.

Practitioner review: use of antiepileptic drugs in children.

Guerrini R, Parmeggiani L.

J Child Psychol Psychiatry. 2006 Feb;47(2):115-26. Review.

PMID:
16423142
12.

Nonconvulsive status epilepticus precipitated by carbamazepine presenting as dissociative and affective disorders in adolescents.

Marini C, Parmeggiani L, Masi G, D'Arcangelo G, Guerrini R.

J Child Neurol. 2005 Aug;20(8):693-6.

PMID:
16225818
13.

Pallister-Killian syndrome: an unusual cause of epileptic spasms.

Sánchez-Carpintero R, McLellan A, Parmeggiani L, Cockwell AE, Ellis RJ, Cross JH, Eckhardt S, Guerrini R.

Dev Med Child Neurol. 2005 Nov;47(11):776-9.

14.

Autosomal dominant cortical myoclonus and epilepsy (ADCME) with linkage to chromosome 2p11.1-q12.2.

Guerrini R, Parmeggiani L, Marini C, Brovedani P, Bonanni P.

Adv Neurol. 2005;95:273-9. No abstract available.

PMID:
15508930
15.

Pathophysiology of myoclonic epilepsies.

Guerrini R, Bonanni P, Parmeggiani L, Hallett M, Oguni H.

Adv Neurol. 2005;95:23-46. Review. No abstract available.

PMID:
15508912
16.
17.

Epilepsy and malformations of the cerebral cortex.

Guerrini R, Sicca F, Parmeggiani L.

Epileptic Disord. 2003 Sep;5 Suppl 2:S9-26. Review.

PMID:
14617417
18.

Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutations.

Guerrini R, Moro F, Andermann E, Hughes E, D'Agostino D, Carrozzo R, Bernasconi A, Flinter F, Parmeggiani L, Volzone A, Parrini E, Mei D, Jarosz JM, Morris RG, Pratt P, Tortorella G, Dubeau F, Andermann F, Dobyns WB, Das S.

Ann Neurol. 2003 Jul;54(1):30-7.

PMID:
12838518
19.

Abnormal corticomuscular and intermuscular coupling in high-frequency rhythmic myoclonus.

Grosse P, Guerrini R, Parmeggiani L, Bonanni P, Pogosyan A, Brown P.

Brain. 2003 Feb;126(Pt 2):326-42.

PMID:
12538401
20.

Early-onset absence epilepsy and paroxysmal dyskinesia.

Guerrini R, Sanchez-Carpintero R, Deonna T, Santucci M, Bhatia KP, Moreno T, Parmeggiani L, Bernardina BD.

Epilepsia. 2002 Oct;43(10):1224-9.

21.
22.

Epilepsy and paroxysmal dyskinesia: co-occurrence and differential diagnosis.

Guerrini R, Parmeggiani L, Casari G.

Adv Neurol. 2002;89:433-41. Review. No abstract available.

PMID:
11968467
23.

[The Debye-Scherrer method in the analysis of silicon in industrial dust. 1951].

Parmeggiani L.

Med Lav. 2001 Nov-Dec;92(6):415-8. Italian. No abstract available.

PMID:
11899930
24.

Autosomal recessive polymicrogyria with infantile spasms and limb deformities.

Ciardo F, Zamponi N, Specchio N, Parmeggiani L, Guerrini R.

Neuropediatrics. 2001 Dec;32(6):325-9.

PMID:
11870589
25.

Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2.

Guerrini R, Bonanni P, Patrignani A, Brown P, Parmeggiani L, Grosse P, Brovedani P, Moro F, Aridon P, Carrozzo R, Casari G.

Brain. 2001 Dec;124(Pt 12):2459-75.

PMID:
11701600
26.

Aloe-Emodin quinone pretreatment reduces acute liver injury induced by carbon tetrachloride.

Arosio B, Gagliano N, Fusaro LM, Parmeggiani L, Tagliabue J, Galetti P, De Castri D, Moscheni C, Annoni G.

Pharmacol Toxicol. 2000 Nov;87(5):229-33.

PMID:
11129503
27.

Add-on lamotrigine treatment in children and young adults with severe partial epilepsy: an open, prospective, long-term study.

Parmeggiani L, Belmonte A, Ferrari AR, Perucca E, Guerrini R.

J Child Neurol. 2000 Oct;15(10):671-4.

PMID:
11063081
28.

Locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.

Guerrini R, Parmeggiani L, Bonanni P, Carrozzo R, Casari G.

Neurology. 2000 Sep 12;55(5):738-9. No abstract available.

PMID:
10980756
30.

Myoclonic status epilepticus following high-dosage lamotrigine therapy.

Guerrini R, Belmonte A, Parmeggiani L, Perucca E.

Brain Dev. 1999 Sep;21(6):420-4.

PMID:
10487478
31.

Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.

Guerrini R, Bonanni P, Nardocci N, Parmeggiani L, Piccirilli M, De Fusco M, Aridon P, Ballabio A, Carrozzo R, Casari G.

Ann Neurol. 1999 Mar;45(3):344-52.

PMID:
10072049
32.

Cortical reflex myoclonus in Rett syndrome.

Guerrini R, Bonanni P, Parmeggiani L, Santucci M, Parmeggiani A, Sartucci F.

Ann Neurol. 1998 Apr;43(4):472-9.

PMID:
9546328
33.

Induction of partial seizures by visual stimulation. Clinical and electroencephalographic features and evoked potential studies.

Guerrini R, Bonanni P, Parmeggiani L, Thomas P, Mattia D, Harvey AS, Duchowny MS.

Adv Neurol. 1998;75:159-78. Review. No abstract available.

PMID:
9385420
34.

Adolescent onset of idiopathic photosensitive occipital epilepsy after remission of benign rolandic epilepsy.

Guerrini R, Bonanni P, Parmeggiani L, Belmonte A.

Epilepsia. 1997 Jul;38(7):777-81.

35.

Electroclinical features of idiopathic generalised epilepsy with persisting absences in adult life.

Michelucci R, Rubboli G, Passarelli D, Riguzzi P, Volpi L, Parmeggiani L, Rizzi R, Gardella E, Tassinari CA.

J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):471-7.

36.

Dipole-modeling of the visual evoked P300.

Goto Y, Brigell MG, Parmeggiani L.

J Psychosom Res. 1996 Jul;41(1):71-9.

PMID:
8887821
37.

The effects of luminance and chromatic background flicker on the human visual evoked potential.

Brigell M, Strafella A, Parmeggiani L, DeMarco PJ Jr, Celesia GG.

Vis Neurosci. 1996 Mar-Apr;13(2):265-75.

PMID:
8737277
38.

Frontal inhibitory spike component associated with epileptic negative myoclonus.

Rubboli G, Parmeggiani L, Tassinari CA.

Electroencephalogr Clin Neurophysiol. 1995 Sep;95(3):201-5.

PMID:
7555910
39.

Epileptic negative myoclonus.

Tassinari CA, Rubboli G, Parmeggiani L, Valzania F, Plasmati R, Riguzzi P, Michelucci R, Volpi L, Passarelli D, Meletti S, et al.

Adv Neurol. 1995;67:181-97. Review.

PMID:
8848969
40.

Locating VEP equivalent dipoles in magnetic resonance images.

Towle VL, Cakmur R, Cao Y, Brigell M, Parmeggiani L.

Int J Neurosci. 1995;80(1-4):105-16.

PMID:
7775043
41.

Dipole source localization in a case of epilepsia partialis continua without premyoclonic EEG spikes.

Celesia GG, Parmeggiani L, Brigell M.

Electroencephalogr Clin Neurophysiol. 1994 Apr;90(4):316-9.

PMID:
7512914
42.

Slowly progressive familial dementia with recurrent strokes and white matter hypodensities on CT scan.

Salvi F, Michelucci R, Plasmati R, Parmeggiani L, Zonari P, Mascalchi M, Tassinari CA.

Ital J Neurol Sci. 1992 Mar;13(2):135-40.

PMID:
1592574
43.

Liver system. V. Activation-extinction line of cyclic hepatocyte activities.

Dioguardi N, Brambilla F, Dell'Oca M, Arosio E, Parmeggiani L.

Ric Clin Lab. 1991 Jan-Mar;21(1):69-78.

PMID:
1866576
44.

Caudal migration of the Günther vena caval filter.

Schneider PA, Parmeggiani L, Piguet JC, Bounameaux H.

Radiology. 1989 Nov;173(2):465-6.

PMID:
2678258
45.

An international viewpoint on exposure limits.

Parmeggiani L.

Am J Ind Med. 1988;14(2):213-4. No abstract available.

PMID:
3207107
46.

Survey on resources for occupational health research in European Community countries.

Vanhoorne M, Parmeggiani L, Harrington M, Hunter W, Aresini G, Vuylsteek K.

Med Lav. 1988 Jan-Feb;79(1):3-18. No abstract available.

PMID:
3173220
47.

Alpha interferon in the treatment of symptomatic myelofibrosis with myeloid metaplasia.

Parmeggiani L, Ferrant A, Rodhain J, Michaux JL, Sokal G.

Eur J Haematol. 1987 Sep;39(3):228-32.

PMID:
3678474
48.

From the PCIAOH to the ICOH: continuity and development.

Parmeggiani L.

Med Lav. 1986 Nov-Dec;77(6):586-92. No abstract available.

PMID:
3550398
49.

Occupational carcinogens: standards issued by the International Labour Organization.

Parmeggiani L.

Med Lav. 1986 Jul-Aug;77(4):449-56. No abstract available.

PMID:
3784957
50.

[Recent trends in radiation protection].

Parmeggiani L.

Med Lav. 1986 Mar-Apr;77(2):149-53. Italian. No abstract available.

PMID:
3724642

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