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Course and outcome of a voltage-gated potassium channel antibody negative Morvan's syndrome.
Published in:
2009
By:
- Rinaldi C;
- Russo CV;
- Filla A;
- De Michele G;
- Marano E;
- Rinaldi, Carlo;
- Russo, Cinzia Valeria;
- Filla, Alessandro;
- De Michele, Giuseppe;
- Marano, Enrico
Publication type:
journal article
Dementia, ataxia, extrapyramidal features, and epilepsy: phenotype spectrum in two Italian families with spinocerebellar ataxia type 17.
Published in:
2003
By:
- De Michele, G.;
- Maltecca, F.;
- Carella, M.;
- Volpe, G.;
- Orio, M.;
- De Falco, A.;
- Gombia, S.;
- Servadio, A.;
- Casari, G.;
- Filla, A.;
- Bruni, A.
Publication type:
journal article
PARK6 is a common cause of familial parkinsonism.
Published in:
2002
By:
- Valente, E.M.;
- Brancati, F.;
- Caputo, V.;
- Graham, E.A.;
- Davis, M.B.;
- Ferraris, A.;
- Breteler, M.M.B.;
- Gasser, T.;
- Bonifati, V.;
- Bentivoglio, A.R.;
- De Michele, G.;
- Durr, A.;
- Cortelli, P.;
- Filla, A.;
- Meco, G.;
- Oostra, B.A.;
- Brice, A.;
- Albanese, A.;
- Wood, N.W.;
- Dürr, A
Publication type:
journal article
Friedreich's ataxia: from the patient to the gene.
Published in:
Neurological Sciences, 2001, v. 22, p. S21, doi. 10.1007/s100720170005
By:
- Filla, A.;
- Cocozza, S.;
- De Michele, G.
Publication type:
Article
The parkin gene and its phenotype.
Published in:
Neurological Sciences, 2001, v. 22, n. 1, p. 51, doi. 10.1007/s100720170042
By:
- Bonifati, V.;
- De Michele, G.;
- Lücking, C. B.;
- Dürr, A.;
- Fabrizio, E.;
- Ambrosio, G.;
- Vanacore, N.;
- De Mari, M.;
- Marconi, R.;
- Capus, L.;
- Breteler, M. M. B.;
- Gasser, T.;
- Oostra, B.;
- Wood, N.;
- Agid, Y.;
- Filla, A.;
- Meco, G.;
- Brice, A.
Publication type:
Article
Epidemiology of multiple system atrophy. ESGAP Consortium. European Study Group on Atypical Parkinsonisms.
Published in:
2001
By:
- Vanacore, N;
- Bonifati, V;
- Fabbrini, G;
- Colosimo, C;
- De Michele, G;
- Marconi, R;
- Nicholl, D;
- Locuratolo, N;
- Talarico, G;
- Romano, S;
- Stocchi, F;
- Bonuccelli, U;
- De Mari, M;
- Vieregge, P;
- Meco, G;
- European Study Group on Atypical Parkinsonism (ESGAP)
Publication type:
journal article
Epidemiology of progressive supranuclear palsy. ESGAP Consortium. European Study Group on Atypical Parkinsonisms.
Published in:
2001
By:
- Vanacore, N;
- Bonifati, V;
- Colosimo, C;
- Fabbrini, G;
- De Michele, G;
- Marconi, R;
- Nicholl, D;
- Locuratolo, N;
- Romano, S;
- Talarico, G;
- Stocchi, F;
- Bonuccelli, U;
- Lamberti, P;
- Vieregge, P;
- Meco, G;
- European Study Group on Atypical Parkinsonism (ESGAP)
Publication type:
journal article
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Published in:
2001
By:
- Bonifati, V;
- De Michele, G;
- Lücking, C B;
- Dürr, A;
- Fabrizio, E;
- Ambrosio, G;
- Vanacore, N;
- De Mari, M;
- Marconi, R;
- Capus, L;
- Breteler, M M;
- Gasser, T;
- Oostra, B;
- Wood, N;
- Agid, Y;
- Filla, A;
- Meco, G;
- Brice, A;
- Italian PD Genetics Study Group, French PD Genetics Study Group, European Consortium on Genetic Susceptibility in PD
Publication type:
journal article
Stimulation of growth hormone release in multiple system atrophy, Parkinson's disease and idiopathic cerebellar ataxia.
Published in:
2001
By:
- Pellecchia, M. T.;
- Salvatore, E.;
- Pivonello, R.;
- Faggiano, A.;
- Barone, P.;
- De Michele, G.;
- Colao, A. M.;
- Filla, A.
Publication type:
journal article
Epidemiology of multiple system atrophy.
Published in:
Neurological Sciences, 2001, v. 22, n. 1, p. 97, doi. 10.1007/s100720170064
By:
- Vanacore, N.;
- Bonifati, V.;
- Fabbrini, G.;
- Colosimo, C.;
- De Michele, G.;
- Marconi, R.;
- Nicholl, D.;
- Locuratolo, N.;
- Talarico, G.;
- Romano, S.;
- Stocchi, F.;
- Bonuccelli, U.;
- De Mari, M.;
- Vieregge, P.;
- Meco, G.
Publication type:
Article
Epidemiology of progressive supranuclear palsy.
Published in:
Neurological Sciences, 2001, v. 22, n. 1, p. 101, doi. 10.1007/s100720170065
By:
- Vanacore, N.;
- Bonifati, V.;
- Colosimo, C.;
- Fabbrini, G.;
- De Michele, G.;
- Marconi, R.;
- Nicholl, D.;
- Locuratolo, N.;
- Romano, S.;
- Talarico, G.;
- Stocchi, F.;
- Bonuccelli, U.;
- Lamberti, P.;
- Vieregge, P.;
- Meco, G.
Publication type:
Article
Relationship between apathy and cognitive dysfunctions in de novo untreated Parkinson's disease: a prospective longitudinal study.
Published in:
European Journal of Neurology, 2015, v. 22, n. 2, p. 253, doi. 10.1111/ene.12467
By:
- Santangelo, G.;
- Vitale, C.;
- Trojano, L.;
- Picillo, M.;
- Moccia, M.;
- Pisano, G.;
- Pezzella, D.;
- Cuoco, S.;
- Erro, R.;
- Longo, K.;
- Pellecchia, M. T.;
- Amboni, M.;
- De Rosa, A.;
- De Michele, G.;
- Barone, P.
Publication type:
Article
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa and cataracts ( PHARC) screening in an Italian population.
Published in:
European Journal of Neurology, 2013, v. 20, n. 4, p. e60, doi. 10.1111/ene.12056
By:
- Criscuolo, C.;
- Guacci, A.;
- Carbone, R.;
- Lieto, M.;
- Salsano, E.;
- Nanetti, L.;
- De Michele, G.;
- Filla, A.
Publication type:
Article
Long-term clinical experience with weekly interferon beta-1a in relapsing multiple sclerosis.
Published in:
European Journal of Neurology, 2006, v. 13, n. 9, p. 1014, doi. 10.1111/j.1468-1331.2006.01422.x
By:
- Coppola, G.;
- Lanzillo, R.;
- Florio, C.;
- Orefice, G.;
- Vivo, P.;
- Ascione, S.;
- Schiavone, V.;
- Pagano, A.;
- Vacca, G.;
- De Michele, G.;
- Morra, V. Brescia
Publication type:
Article
Hemodynamic and Ventilatory Effects of Intravenous Salbutamol in Patients Affected by COLD.
Published in:
Respiration, 1980, v. 40, n. 5, p. 272, doi. 10.1159/000194294
By:
- Iodice, F.;
- Rufolo, L.;
- Piscione, F.;
- De Michele, G.
Publication type:
Article
19Neurophysiological study in a Spanish family with recessive spastic ataxia of charlevoix-saguenay.
Published in:
2008
By:
- García A;
- Criscuolo C;
- de Michele G;
- Berciano J
Publication type:
Journal Article
Low-dose idebenone treatment in Friedreich’s ataxia with and without cardiac hypertrophy.
Published in:
Journal of Neurology, 2009, v. 256, n. 9, p. 1434, doi. 10.1007/s00415-009-5130-6
By:
- Rinaldi, C.;
- Tucci, T.;
- Maione, S.;
- Giunta, A.;
- De Michele, G.;
- Filla, A.
Publication type:
Article
Screening for POLG1 mutations in a Southern Italian ataxia population.
Published in:
Journal of Neurology, 2008, v. 255, n. 3, p. 454, doi. 10.1007/s00415-007-0736-z
By:
- Criscuolo, C.;
- Mancini, P.;
- Ammendola, S.;
- Cicala, D.;
- Banfi, S.;
- De Michele, G.;
- Filla, A.
Publication type:
Article
Environmental and genetic risk factors in Parkinson's disease: A case-control study in southern italy.
Published in:
Movement Disorders, 1996, v. 11, n. 1, p. 17, doi. 10.1002/mds.870110105
By:
- De Michele, G.;
- Filla, A.;
- Volpe, G.;
- De Marco, V.;
- Gogliettino, A.;
- Ambrosio, G.;
- Marconi, R.;
- Castellano, A. E.;
- Campanella, G.
Publication type:
Article
Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines.
Published in:
Acta Neurologica Scandinavica, 2001, v. 103, n. 4, p. 261, doi. 10.1034/j.1600-0404.2001.103004261.x
By:
- Colosimo, C.;
- Vanacore, N.;
- Bonifati, V.;
- Fabbrini, G.;
- Rum, A.;
- De Michele, G.;
- De Mari, M.;
- Bonuccelli, U.;
- Nicholl, D. J.;
- Meco, G.
Publication type:
Article
Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa.
Published in:
2006
By:
- Ibáñez P;
- Lesage S;
- Lohmann E;
- Thobois S;
- De Michele G;
- Borg M;
- Agid Y;
- Dürr A;
- Brice A;
- French Parkinson's Disease Genetics Study Group;
- Ibáñez, Pablo;
- Lesage, Suzanne;
- Lohmann, Ebba;
- Thobois, Stéphane;
- De Michele, Giuseppe;
- Borg, Michel;
- Agid, Yves;
- Dürr, Alexandra;
- Brice, Alexis
Publication type:
journal article
Parkin mutations are frequent in patients with isolated early-onset parkinsonism.
Published in:
2003
By:
- Periquet M;
- Latouche M;
- Lohmann E;
- Rawal N;
- De Michele G;
- Ricard S;
- Teive H;
- Fraix V;
- Vidaihet M;
- Nicholl D;
- Barone P;
- Wood NW;
- Raskin S;
- Deleuze J;
- Agid Y;
- Dürr A;
- Brice A;
- French Parkinson's Disease Genetics Study Group;
- European Consortium on Genetic Susceptibility in Parkinson's Disease;
- Periquet, Magali
Publication type:
journal article
Parkin mutations are frequent in patients with isolated early-onset parkinsonism.
Published in:
Brain: A Journal of Neurology, 2003, v. 126, n. 6, p. 1271
By:
- D. Nicholl;
- M. Periquet;
- P. Barone;
- M. Latouche;
- N.W. Wood;
- E. Lohmann;
- S. Raskin;
- N. Rawal;
- G. de Michele;
- J-F. Deleuze;
- S. Ricard;
- Y. Agid;
- H. Teive;
- A. Dürr;
- V. Fraix;
- A. Brice;
- M. Vidailhet
Publication type:
Article
Static Magnetic Fields Effects on Polysaccharides Production by Different Microalgae Strains.
Published in:
Applied Sciences (2076-3417), 2021, v. 11, n. 11, p. 5299, doi. 10.3390/app11115299
By:
- Deamici, Kricelle M.;
- de Morais, Michele G.;
- Santos, Lucielen O.;
- Muylaert, Koenraad;
- Gardarin, Christine;
- Costa, Jorge Alberto V.;
- Laroche, Céline
Publication type:
Article
Very late onset in ataxia oculomotor apraxia type I.
Published in:
2005
By:
- Criscuolo C;
- Mancini P;
- Menchise V;
- Saccà F;
- De Michele G;
- Banfi S;
- Filla A
Publication type:
Journal Article
Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.
Published in:
2003
By:
- Marconi R;
- De Fusco M;
- Aridon P;
- Plewnia K;
- Rossi M;
- Carapelli S;
- Ballabio A;
- Morgante L;
- Musolino R;
- Epifanio A;
- Micieli G;
- De Michele G;
- Casari G
Publication type:
Journal Article
Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay.
Published in:
Journal of Neurology, 2015, v. 262, n. 12, p. 2755, doi. 10.1007/s00415-015-7911-4
By:
- Criscuolo, Chiara;
- Procaccini, C.;
- Meschini, M.;
- Cianflone, A.;
- Carbone, R.;
- Doccini, S.;
- Devos, D.;
- Nesti, C.;
- Vuillaume, I.;
- Pellegrino, M.;
- Filla, A.;
- De Michele, G.;
- Matarese, G.;
- Santorelli, F.
Publication type:
Article
SPG5 and multiple sclerosis: clinical and genetic overlap?
Published in:
Acta Neurologica Scandinavica, 2016, v. 133, n. 6, p. 410, doi. 10.1111/ane.12476
By:
- Criscuolo, C.;
- Carbone, R.;
- Lieto, M.;
- Peluso, S.;
- Guacci, A.;
- Filla, A.;
- Quarantelli, M.;
- Lanzillo, R.;
- Brescia Morra, V.;
- De Michele, G.
Publication type:
Article
The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families.
Published in:
European Journal of Neurology, 2020, v. 27, n. 3, p. 498, doi. 10.1111/ene.14094
By:
- Lieto, M.;
- Riso, V.;
- Galatolo, D.;
- De Michele, G.;
- Rossi, S.;
- Barghigiani, M.;
- Cocozza, S.;
- Pontillo, G.;
- Trovato, R.;
- Saccà, F.;
- Salvatore, E.;
- Tessa, A.;
- Filla, A.;
- Santorelli, F. M.;
- Silvestri, G.
Publication type:
Article
Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q.
Published in:
1995
By:
- Palau, Francisco;
- de Michele, Giuseppe;
- Vilchez, Juan J.;
- Pandolfo, Massimo;
- Monrós, Eugègnia;
- Cocozza, Sergio;
- Smeyers, Patricia;
- Lopez-Arlandis, José;
- Campanella, Giuseppe;
- di Donato, Stefano;
- Filla, Alessandro;
- Palau, F;
- De Michele, G;
- Vilchez, J J;
- Pandolfo, M;
- Monrós, E;
- Cocozza, S;
- Smeyers, P;
- Lopez-Arlandis, J;
- Campanella, G
Publication type:
journal article
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.
Published in:
Neurogenetics, 2004, v. 5, n. 1, p. 49, doi. 10.1007/s10048-003-0167-7
By:
- Muglia, M.;
- Criscuolo, C.;
- Magariello, A.;
- de Michele, G.;
- Scarano, V.;
- D'Adamo, P.;
- Ambrosio, G.;
- Gabriele, A. L.;
- Patitucci, A.;
- Mazzei, R.;
- Conforti, F. L.;
- Sprovieri, T.;
- Morgante, L.;
- Epifanio, A.;
- La Spina, P.;
- Valentino, P.;
- Gasparini, P.;
- Filla, A.;
- Quattrone, A.
Publication type:
Article
PRICKLE1 progressive myoclonus epilepsy in Southern Italy.
Published in:
Movement Disorders, 2010, v. 25, n. 15, p. 2686, doi. 10.1002/mds.23350
By:
- Criscuolo, C.;
- de Leva, M.F.;
- Sorrentino, P.;
- Piro, R.;
- Carbone, R.;
- Guacci, A.;
- De Michele, G.;
- Filla, A.
Publication type:
Article
Accuracy of clinical diagnostic criteria for Friedreich's ataxia.
Published in:
Movement Disorders, 2000, v. 15, n. 6, p. 1255, doi. 10.1002/1531-8257(200011)15:6<1255::AID-MDS1031>3.0.CO;2-C
By:
- Filla, A.;
- De Michele, G.;
- Coppola, G.;
- Federico, A.;
- Vita, G.;
- Toscano, A.;
- Uncini, A.;
- Pisanelli, P.;
- Barone, P.;
- Scarano, V.;
- Perretti, A.;
- Santoro, L.;
- Monticelli, A.;
- Cavalcanti, F.;
- Caruso, G.;
- Cocozza, S.
Publication type:
Article
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.
Published in:
2004
By:
- Muglia, M.;
- Criscuolo, C;
- Magariello, A;
- De Michele, G;
- Scarano, V;
- D’Adamo, P;
- Ambrosio, G;
- Gabriele, AL;
- Patitucci, A;
- Mazzei, R;
- Conforti, FL;
- Sprovieri, T;
- Morgante, L;
- Epifanio, A;
- La Spina, P;
- Valentino, P;
- Gasparini, P;
- Filla, A;
- Quattrone, A
Publication type:
Abstract
Genotype–phenotype correlation in some autosomal recessive hereditary spastic paraplegias.
Published in:
2004
By:
- Manganelli, F.;
- Criscuolo, C;
- Scarano, V;
- Perretti, A;
- De Michele, G;
- Filla, A;
- Santoro, L
Publication type:
Abstract
Cervico-Oculo-Acoustic Syndrome in a Male with Consanguineous Parents.
Published in:
Canadian Journal of Neurological Sciences, 2006, v. 33, n. 2, p. 237, doi. 10.1017/S0317167100005059
By:
- Di Maio, L.;
- Marcelli, V.;
- Vitale, C.;
- Menzione, M.;
- De Giorgio, A.;
- Briganti, F.;
- Perretti, A.;
- Marciano, E.;
- Filla, A.;
- De Michele, G.
Publication type:
Article

Found: 36