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Guillain-Barré syndrome after rtPA therapy for acute stroke.
Published in:
2010
By:
- Bersano A;
- Santoro D;
- Prelle A;
- Lanfranconi S;
- Ranieri M;
- Tadeo CS;
- Bresolin N;
- Baron PL;
- Bersano, A;
- Santoro, D;
- Prelle, A;
- Lanfranconi, S;
- Ranieri, M;
- Tadeo, C S;
- Bresolin, N;
- Baron, P L
Publication type:
Case Study
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa.
Published in:
Journal of Inherited Metabolic Disease, 1999, v. 22, n. 6, p. 762, doi. 10.1023/A:1005572906807
By:
- Hadjigeorgiou, G.;
- Comi, G.;
- Bordoni, A.;
- Shen, J.;
- Chen, Y.-T.;
- Salani, S.;
- Toscano, A.;
- Fortunato, F.;
- Lucchiari, S.;
- Bresolin, N.;
- Rodolico, C.;
- Piscaglia, M.;
- Franceschina, L.;
- Papadimitriou, A.;
- Scarlato, G.
Publication type:
Article
The genetic features of 24 patients affected by familial and sporadic hemiplegic migraine.
Published in:
Neurological Sciences, 2011, v. 32, p. 141, doi. 10.1007/s10072-011-0517-4
By:
- Gallanti, A.;
- Cardin, V.;
- Tonelli, A.;
- Bussone, G.;
- Bresolin, N.;
- Mariani, C.;
- Bassi, M.
Publication type:
Article
Guillain–Barré syndrome after rtPA therapy for acute stroke.
Published in:
Neurological Sciences, 2010, v. 31, n. 6, p. 867, doi. 10.1007/s10072-010-0259-8
By:
- Bersano, A.;
- Santoro, D.;
- Prelle, A.;
- Lanfranconi, S.;
- Ranieri, M.;
- Tadeo, C. S.;
- Bresolin, N.;
- Baron, P. L.
Publication type:
Article
Candidate gene analysis of semaphorins in patients with Alzheimer's disease.
Published in:
2010
By:
- Villa C;
- Venturelli E;
- Fenoglio C;
- De Riz M;
- Scalabrini D;
- Cortini F;
- Serpente M;
- Cantoni C;
- Bresolin N;
- Scarpini E;
- Galimberti D;
- Villa, Chiara;
- Venturelli, Eliana;
- Fenoglio, Chiara;
- De Riz, Milena;
- Scalabrini, Diego;
- Cortini, Francesca;
- Serpente, Maria;
- Cantoni, Claudia;
- Bresolin, Nereo
Publication type:
journal article
Genetics and neurobiology of frontotemporal lobar degeneration.
Published in:
Neurological Sciences, 2006, v. 27, p. s32, doi. 10.1007/s10072-006-0543-9
By:
- Scarpini, E.;
- Galimberti, D.;
- Bresolin, N.
Publication type:
Article
Retroviral vectors for gene therapy of Duchenne muscular dystrophy.
Published in:
Neurological Sciences, 2000, v. 21, p. S925, doi. 10.1007/s100720070005
By:
- Fassati, A.;
- Bresolin, N.
Publication type:
Article
Retroviral vectors for gene therapy of Duchenne muscular dystrophy.
Published in:
2000
By:
- Fassati, A;
- Bresolin, N
Publication type:
journal article
Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred.
Published in:
2011
By:
- Pietroboni AM;
- Fumagalli GG;
- Ghezzi L;
- Fenoglio C;
- Cortini F;
- Serpente M;
- Cantoni C;
- Rotondo E;
- Corti P;
- Carecchio M;
- Bassi M;
- Bresolin N;
- Galbiati D;
- Galimberti D;
- Scarpini E
Publication type:
Journal Article
Cerebrospinal fluid biomarkers in progranulin mutations carriers.
Published in:
2011
By:
- Carecchio M;
- Fenoglio C;
- Cortini F;
- Comi C;
- Benussi L;
- Ghidoni R;
- Borroni B;
- De Riz M;
- Serpente M;
- Cantoni C;
- Franceschi M;
- Albertini V;
- Monaco F;
- Rainero I;
- Binetti G;
- Padovani A;
- Bresolin N;
- Scarpini E;
- Galimberti D
Publication type:
Journal Article
Role of OLR1 and Its Regulating hsa-miR369-3p in Alzheimer's Disease: Genetics and Expression Analysis.
Published in:
2011
By:
- Serpente M;
- Fenoglio C;
- Villa C;
- Cortini F;
- Cantoni C;
- Ridolfi E;
- Clerici F;
- Marcone A;
- Benussi L;
- Ghidoni R;
- Boneschi FM;
- Gallone S;
- Cappa S;
- Binetti G;
- Franceschi M;
- Rainero I;
- Giordana MT;
- Mariani C;
- Bresolin N;
- Scarpini E
Publication type:
Journal Article
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.
Published in:
2011
By:
- Villa C;
- Ghezzi L;
- Pietroboni AM;
- Fenoglio C;
- Cortini F;
- Serpente M;
- Cantoni C;
- Ridolfi E;
- Marcone A;
- Benussi L;
- Ghidoni R;
- Jacini F;
- Arighi A;
- Fumagalli GG;
- Mandelli A;
- Binetti G;
- Cappa S;
- Bresolin N;
- Scarpini E;
- Galimberti D
Publication type:
journal article
BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease.
Published in:
2011
By:
- Venturelli E;
- Villa C;
- Fenoglio C;
- Clerici F;
- Marcone A;
- Benussi L;
- Ghidoni R;
- Gallone S;
- Cortini F;
- Serpente M;
- Cantoni C;
- Fumagalli G;
- Ridolfi E;
- Cappa S;
- Binetti G;
- Franceschi M;
- Rainero I;
- Giordana MT;
- Mariani C;
- Bresolin N
Publication type:
Journal Article
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2.
Published in:
Clinical Genetics, 2012, v. 82, n. 2, p. 157, doi. 10.1111/j.1399-0004.2011.01717.x
By:
- Crimella, C;
- Baschirotto, C;
- Arnoldi, A;
- Tonelli, A;
- Tenderini, E;
- Airoldi, G;
- Martinuzzi, A;
- Trabacca, A;
- Losito, L;
- Scarlato, M;
- Benedetti, S;
- Scarpini, E;
- Spinicci, G;
- Bresolin, N;
- Bassi, MT
Publication type:
Article
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations.
Published in:
Clinical Genetics, 2012, v. 81, n. 2, p. 150, doi. 10.1111/j.1399-0004.2011.01624.x
By:
- Arnoldi, A;
- Crimella, C;
- Tenderini, E;
- Martinuzzi, A;
- D'Angelo, MG;
- Musumeci, O;
- Toscano, A;
- Scarlato, M;
- Fantin, M;
- Bresolin, N;
- Bassi, MT
Publication type:
Article
Novel splice-site mutations and a large intragenic deletion in PLA2G6 associated with a severe and rapidly progressive form of infantile neuroaxonal dystrophy.
Published in:
Clinical Genetics, 2010, v. 78, n. 5, p. 432, doi. 10.1111/j.1399-0004.2010.01417.x
By:
- Tonelli, A.;
- Romaniello, R.;
- Grasso, R.;
- Cavallini, A.;
- Righini, A.;
- Bresolin, N.;
- Borgatti, R.;
- Bassi, M. T.
Publication type:
Article
Aberrant splicing due to a silent nucleotide change in CCM2 gene in a family with cerebral cavernous malformation.
Published in:
2009
By:
- Tonelli, A.;
- Lanfranconi, S.;
- Bersano, A.;
- Corti, S.;
- Bassi, M. T.;
- Bresolin, N.
Publication type:
Letter
First case of compound heterozygosity in ALS2 gene in infantile-onset ascending spastic paralysis with bulbar involvement.
Published in:
2008
By:
- Sztriha, L.;
- Panzeri, C.;
- Kálmánchey, R.;
- Szabó, N.;
- Endreffy, E.;
- Túria, S.;
- C Baschirotto;
- Bresolin, N.;
- Vekerdy, Z.;
- Bassi, M. T.
Publication type:
Letter
Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine.
Published in:
Clinical Genetics, 2007, v. 72, n. 6, p. 517, doi. 10.1111/j.1399-0004.2007.00892.x
By:
- Tonelli, A.;
- Gallanti, A.;
- Bersano, A.;
- Cardin, V.;
- Ballabio, E.;
- Airoldi, G.;
- Redaelli, F.;
- Candelise, L.;
- Bresolin, N.;
- Bassi, M. T.
Publication type:
Article
Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation.
Published in:
European Journal of Neurology, 2012, v. 19, n. 11, p. e127, doi. 10.1111/j.1468-1331.2012.03838.x
By:
- Tonelli, A.;
- D'Angelo, M. G.;
- Arrigoni, F.;
- Brighina, E.;
- Arnoldi, A.;
- Citterio, A.;
- Bresolin, N.;
- Bassi, M. T.
Publication type:
Article
DCUN1D1 is a risk factor for frontotemporal lobar degeneration.
Published in:
European Journal of Neurology, 2009, v. 16, n. 7, p. 870, doi. 10.1111/j.1468-1331.2009.02611.x
By:
- Villa, C.;
- Venturelli, E.;
- Fenoglio, C.;
- Clerici, F.;
- Marcone, A.;
- Benussi, L.;
- Gallone, S.;
- Scalabrini, D.;
- Cortini, F.;
- Serpente, M.;
- Martinelli Boneschi, F.;
- Cappa, S.;
- Binetti, G.;
- Mariani, C.;
- Rainero, I.;
- Giordana, M. T.;
- Bresolin, N.;
- Scarpini, E.;
- Galimberti, D.
Publication type:
Article
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.
Published in:
European Journal of Neurology, 2009, v. 16, n. 6, p. 727, doi. 10.1111/j.1468-1331.2009.02574.x
By:
- Del Bo, R.;
- Ghezzi, S.;
- Corti, S.;
- Pandolfo, M.;
- Ranieri, M.;
- Santoro, D.;
- Ghione, I.;
- Prelle, A.;
- Orsetti, V.;
- Mancuso, M.;
- Sorar, G.;
- Briani, C.;
- Angelini, C.;
- Siciliano, G.;
- Bresolin, N.;
- Comi, G. P.
Publication type:
Article
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.
Published in:
European Journal of Neurology, 2009, v. 16, n. 1, p. 37, doi. 10.1111/j.1468-1331.2008.02335.x
By:
- Venturelli, E.;
- Villa, C.;
- Fenoglio, C.;
- Clerici, F.;
- Marcone, A.;
- Ghidoni, R.;
- Cortini, F.;
- Scalabrini, D.;
- Gallone, S.;
- Rainero, I.;
- Mandelli, A.;
- Restelli, I.;
- Binetti, G.;
- Cappa, S.;
- Mariani, C.;
- Giordana, M. T.;
- Bresolin, N.;
- Scarpini, E.;
- Galimberti, D.
Publication type:
Article
Novel exon 1 progranulin gene variant in Alzheimer’s disease.
Published in:
European Journal of Neurology, 2008, v. 15, n. 10, p. 1111, doi. 10.1111/j.1468-1331.2008.02266.x
By:
- Cortini, F.;
- Fenoglio, C.;
- Guidi, I.;
- Venturelli, E.;
- Pomati, S.;
- Marcone, A.;
- Scalabrini, D.;
- Villa, C.;
- Clerici, F.;
- Dalla Valle, E.;
- Mariani, C.;
- Cappa, S.;
- Bresolin, N.;
- Scarpini, E.;
- Galimberti, D.
Publication type:
Article
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.
Published in:
European Journal of Neurology, 2008, v. 15, n. 1, p. 77, doi. 10.1111/j.1468-1331.2007.02007.x
By:
- Venturelli, E.;
- Villa, C.;
- Scarpini, E.;
- Fenoglio, C.;
- Guidi, I.;
- Lovati, C.;
- Marcone, A.;
- Cortini, F.;
- Scalabrini, D.;
- Clerici, F.;
- Bresolin, N.;
- Mariani, C.;
- Cappa, S.;
- Galimberti, D.
Publication type:
Article
IP-10 serum levels are not increased in mild cognitive impairment and Alzheimer's disease.
Published in:
2007
By:
- Galimberti, D.;
- Venturelli, E.;
- Fenoglio, C.;
- Lovati, C.;
- Guidi, I.;
- Scalabrini, D.;
- Mariani, C.;
- Bresolin, N.;
- Scarpini, E.
Publication type:
Letter
CXCL10 haplotypes and multiple sclerosis: association and correlation with clinical course.
Published in:
European Journal of Neurology, 2007, v. 14, n. 2, p. 162, doi. 10.1111/j.1468-1331.2006.01629.x
By:
- Galimberti, D.;
- Scalabrini, D.;
- Fenoglio, C.;
- Comi, C.;
- De Riz, M.;
- Venturelli, E.;
- Lovati, C.;
- Mariani, C.;
- Monaco, F.;
- Bresolin, N.;
- Scarpini, E.
Publication type:
Article
Efficacy and tolerability of eperisone and baclofen in spastic palsy: a double-blind randomized trial.
Published in:
Advances in Therapy, 2009, v. 26, n. 5, p. 563, doi. 10.1007/s12325-009-0031-8
By:
- Bresolin, N.;
- Zucca, C.;
- Pecori, A.
Publication type:
Article
Vagus nerve stimulation in treatment-resistant depression. Long-term clinical outcomes.
Published in:
European Psychiatry, 2021, v. 64, p. S492, doi. 10.1192/j.eurpsy.2021.1316
By:
- Rosson, S.;
- Bresolin, N.;
- D'Avella, D.;
- Denaro, L.;
- Landi, A.;
- Caiolo, S.;
- Lussignoli, M.;
- Toffanin, T.;
- Pigato, G.
Publication type:
Article
P01-199 - Selective DNA methylation of BDNF promoter and nociceptin gene in bipolar disorder
Published in:
2011
By:
- dell’Osso, B.;
- d’Addario, C.;
- Palazzo, M.;
- Cattaneo, E.;
- Galimberti, D.;
- Scarpini, E.;
- Bresolin, N.;
- Arosio, B.;
- Bergamaschini, L.;
- Candeletti, S.;
- Romualdi, P.;
- Altamura, A.C.
Publication type:
Abstract
Efficacy and tolerability of eperisone in patients with spastic palsy: a cross-over, placebo-controlled dose-ranging trial.
Published in:
European Review for Medical & Pharmacological Sciences, 2009, v. 13, n. 5, p. 365
By:
- BRESOLIN, N.;
- ZUCCA, C.;
- PECORI, A.
Publication type:
Article
An evolutionary history of the selectin gene cluster in humans.
Published in:
Heredity, 2012, v. 109, n. 2, p. 117, doi. 10.1038/hdy.2012.20
By:
- Fumagalli, M;
- Fracassetti, M;
- Cagliani, R;
- Forni, D;
- Pozzoli, U;
- Comi, G P;
- Marini, F;
- Bresolin, N;
- Clerici, M;
- Sironi, M
Publication type:
Article
Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males.
Published in:
Genes & Immunity, 2010, v. 11, n. 6, p. 497, doi. 10.1038/gene.2010.18
By:
- Fenoglio, C.;
- Scalabrini, D.;
- Esposito, F.;
- Comi, C.;
- Cavalla, P.;
- De Riz, M.;
- Martinelli, V.;
- Piccio, L. M.;
- Venturelli, E.;
- Fumagalli, G.;
- Capra, R.;
- Collimedaglia, L.;
- Ghezzi, A.;
- Rodegher, M. E.;
- Vercellino, M.;
- Leone, M.;
- Giordana, M. T;
- Bresolin, N.;
- Monaco, F.;
- Comi, G.
Publication type:
Article
A population genetics study of the Familial Mediterranean Fever gene: evidence of balancing selection under an overdominance regime.
Published in:
Genes & Immunity, 2009, v. 10, n. 8, p. 678, doi. 10.1038/gene.2009.59
By:
- Fumagalli, M.;
- Cagliani, R.;
- Pozzoli, U.;
- Riva, S.;
- Comi, G. P.;
- Menozzi, G.;
- Bresolin, N.;
- Sironi, M.
Publication type:
Article
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotype.
Published in:
Scientific Reports, 2016, p. 21301, doi. 10.1038/srep21301
By:
- Nizzardo, M.;
- Simone, C.;
- Rizzo, F.;
- Ulzi, G.;
- Ramirez, A.;
- Rizzuti, M.;
- Bordoni, A.;
- Bucchia, M.;
- Gatti, S.;
- Bresolin, N.;
- Comi, G. P.;
- Corti, S.
Publication type:
Article
Intra-aortic injection of myoblasts in mdx mice: genetic and technetium-99m cell labeling and biodistribution.
Published in:
1997
By:
- Bresolin, Nereo;
- Ausenda, Carlo D.;
- Casati, Rosangela;
- Torrente, Yvan;
- DeLiso, Alberto;
- D'Angelo, Maria Grazia;
- Benti, Riccardo;
- Moggio, Maurizio;
- Baldessari, Sonia;
- Comi, Giacomo P.;
- Colombo, Fabio;
- Gerundini, Paolo;
- Scarlato, Guglielmo;
- Bresolin, N;
- Ausenda, C D;
- Casati, R;
- Torrente, Y;
- DeLiso, A;
- D'Angelo, M G;
- Benti, R
Publication type:
journal article
A novel mutation in the [beta]-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance.
Published in:
2012
By:
- Romaniello R;
- Tonelli A;
- Arrigoni F;
- Baschirotto C;
- Triulzi F;
- Bresolin N;
- Bassi MT;
- Borgatti R
Publication type:
Journal Article
Novel Twinkle ( PEO1) gene mutations in mendelian progressive external ophthalmoplegia.
Published in:
Journal of Neurology, 2008, v. 255, n. 9, p. 1384, doi. 10.1007/s00415-008-0926-3
By:
- Virgilio, R.;
- Ronchi, D.;
- Hadjigeorgiou, G.;
- Bordoni, A.;
- Saladino, F.;
- Moggio, M.;
- Adobbati, L.;
- Kafetsouli, D.;
- Tsironi, E.;
- Previtali, S.;
- Papadimitriou, A.;
- Bresolin, N.;
- Comi, G.
Publication type:
Article
Transient response to immune therapies in post-irradiation lumbosacral radiculoplexopathy.
Published in:
Journal of Neurology, 2004, v. 251, n. 4, p. 488, doi. 10.1007/s00415-004-0405-4
By:
- Bersano, A.;
- Carpo, M.;
- Cappellari, A.;
- Bresolin, N.;
- Nobile-Orazio, E.
Publication type:
Article
Long-term balancing selection maintains trans-specific polymorphisms in the human TRIM5 gene.
Published in:
Human Genetics, 2010, v. 128, n. 6, p. 577, doi. 10.1007/s00439-010-0884-6
By:
- Cagliani, R.;
- Fumagalli, M.;
- Biasin, M.;
- Piacentini, L.;
- Riva, S.;
- Pozzoli, U.;
- Bonaglia, M. C.;
- Bresolin, N.;
- Clerici, M.;
- Sironi, Manuela
Publication type:
Article
Persistent inflammation, immunosuppression and catabolism syndrome (PICS) in critically ill children is associated with clinical outcomes: a prospective longitudinal study.
Published in:
Journal of Human Nutrition & Dietetics, 2021, v. 34, n. 2, p. 365, doi. 10.1111/jhn.12798
By:
- Hauschild, D. B.;
- Oliveira, L. D. A.;
- Ventura, J. C.;
- Farias, M. S.;
- Barbosa, E.;
- Bresolin, N. L.;
- Moreno, Y. M. F.
Publication type:
Article
Monogenic vessel diseases related to ischemic stroke: a clinical approach.
Published in:
Journal of Cerebral Blood Flow & Metabolism, 2007, v. 27, n. 10, p. 1649, doi. 10.1038/sj.jcbfm.9600520
By:
- Ballabio, E.;
- Bersano, A.;
- Bresolin, N.;
- Candelise, L.
Publication type:
Article
A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis.
Published in:
Molecular Biology & Evolution, 2012, v. 29, n. 6, p. 1599, doi. 10.1093/molbev/mss002
By:
- Cagliani, R.;
- Guerini, F. R.;
- Fumagalli, M.;
- Riva, S.;
- Agliardi, C.;
- Galimberti, D.;
- Pozzoli, U.;
- Goris, A.;
- Dubois, B.;
- Fenoglio, C.;
- Forni, D.;
- Sanna, S.;
- Zara, I.;
- Pitzalis, M.;
- Zoledziewska, M.;
- Cucca, F.;
- Marini, F.;
- Comi, G. P.;
- Scarpini, E.;
- Bresolin, N.
Publication type:
Article
Growth factors in ischemic stroke.
Published in:
Journal of Cellular & Molecular Medicine, 2011, v. 15, n. 8, p. 1645, doi. 10.1111/j.1582-4934.2009.00987.x
By:
- Lanfranconi, S.;
- Locatelli, F.;
- Corti, S.;
- Candelise, L.;
- Comi, G. P.;
- Baron, P. L.;
- Strazzer, S.;
- Bresolin, N.;
- Bersano, A.
Publication type:
Article
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency.
Published in:
Acta Neuropathologica, 2003, v. 105, n. 6, p. 537, doi. 10.1007/s00401-002-0654-1
By:
- Prelle, A.;
- Sciacco, M.;
- Tancredi, L.;
- Fagiolari, G.;
- Comi, G. P.;
- Ciscato, P.;
- Serafini, M.;
- Fortunato, F.;
- Zecca, C.;
- Gallanti, A.;
- Chiveri, L.;
- Bresolin, N.;
- Scarlato, G.;
- Moggio, M.
Publication type:
Article
Nomadic beekeeper movements create the potential for widespread disease in the honeybee industry.
Published in:
Australian Veterinary Journal, 2014, v. 92, n. 8, p. 283, doi. 10.1111/avj.12198
By:
- Gordon, R;
- Bresolin‐Schott, N;
- East, IJ
Publication type:
Article
Haplotype analysis in VEGF gene and increased risk of Alzheimer's disease.
Published in:
2005
By:
- Saleheen D;
- Del Bo R;
- Scarlato M;
- Boneschi FM;
- Ghezzi S;
- Bresolin N;
- Comi GP
Publication type:
Journal Article
Vascular endothelial growth factor gene variability is associated with increased risk for AD.
Published in:
2005
By:
- Del Bo R;
- Scarlato M;
- Ghezzi S;
- Boneschi FM;
- Fenoglio C;
- Galbiati S;
- Virgilio R;
- Galimberti D;
- Galimberti G;
- Crimi M;
- Ferrarese C;
- Scarpini E;
- Bresolin N;
- Comi GP
Publication type:
Journal Article
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene.
Published in:
2009
By:
- Lamperti, C.;
- Salani, S.;
- Lucchiari, S.;
- Bordoni, A.;
- Ripolone, M.;
- Fagiolari, G.;
- Fruguglietti, M.;
- Crugnola, V.;
- Colombo, C.;
- Cappellini, A.;
- Prelle, A.;
- Bresolin, N.;
- Comi, G.;
- Moggio, M.
Publication type:
Report
Neurological features of Fabry disease: clinical, pathophysiological aspects and therapy.
Published in:
Acta Neurologica Scandinavica, 2012, v. 126, n. 2, p. 77, doi. 10.1111/j.1600-0404.2012.01661.x
By:
- Bersano, A.;
- Lanfranconi, S.;
- Valcarenghi, C.;
- Bresolin, N.;
- Micieli, G.;
- Baron, P.
Publication type:
Article

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