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Items: 1 to 50 of 1545

1.

Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature.

Gagliardi D, Mauri E, Magri F, Velardo D, Meneri M, Abati E, Brusa R, Faravelli I, Piga D, Ronchi D, Triulzi F, Peverelli L, Sciacco M, Bresolin N, Comi GP, Corti S, Govoni A.

Front Neurol. 2019 Jan 31;10:38. doi: 10.3389/fneur.2019.00038. eCollection 2019.

PMID:
30766507
2.

Assessing seasonal dynamics of Guillain-Barré syndrome with search engine query data.

Giordano A, Vabanesi M, Dalla Costa G, Cerri F, Comi G, Martinelli V, Fazio R.

Neurol Sci. 2019 Feb 14. doi: 10.1007/s10072-019-03757-y. [Epub ahead of print]

PMID:
30762168
3.

Serum neurofilaments increase at PML onset in natalizumab-treated MS patients.

Dalla Costa G, Martinelli V, Moiola L, Sangalli F, Colombo B, Finardi A, Cinque P, Kolb EM, Haghikia A, Gold R, Furlan R, Comi G.

Ann Neurol. 2019 Feb 13. doi: 10.1002/ana.25437. [Epub ahead of print]

PMID:
30761586
4.

Muscle pain in mitochondrial diseases: a picture from the Italian network.

Filosto M, Cotti Piccinelli S, Lamperti C, Mongini T, Servidei S, Musumeci O, Tonin P, Santorelli FM, Simoncini C, Primiano G, Vercelli L, Rubegni A, Galvagni A, Moggio M, Comi GP, Carelli V, Toscano A, Padovani A, Siciliano G, Mancuso M.

J Neurol. 2019 Feb 2. doi: 10.1007/s00415-019-09219-x. [Epub ahead of print]

PMID:
30710167
5.

Imaging correlates of hand motor performance in multiple sclerosis: A multiparametric structural and functional MRI study.

Cordani C, Meani A, Esposito F, Valsasina P, Colombo B, Pagani E, Preziosa P, Comi G, Filippi M, Rocca MA.

Mult Scler. 2019 Jan 18:1352458518822145. doi: 10.1177/1352458518822145. [Epub ahead of print]

PMID:
30657011
6.

Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons.

Rizzo F, Nizzardo M, Vashisht S, Molteni E, Melzi V, Taiana M, Salani S, Santonicola P, Di Schiavi E, Bucchia M, Bordoni A, Faravelli I, Bresolin N, Comi GP, Pozzoli U, Corti S.

Brain. 2019 Feb 1;142(2):276-294. doi: 10.1093/brain/awy330.

7.

Brain and cord imaging features in neuromyelitis optica spectrum disorders.

Cacciaguerra L, Meani A, Mesaros S, Radaelli M, Palace J, Dujmovic-Basuroski I, Pagani E, Martinelli V, Matthews L, Drulovic J, Leite MI, Comi G, Filippi M, Rocca MA.

Ann Neurol. 2019 Jan 11. doi: 10.1002/ana.25411. [Epub ahead of print]

PMID:
30635936
8.

Functional and morphological changes of the retinal vessels in Alzheimer's disease and mild cognitive impairment.

Querques G, Borrelli E, Sacconi R, De Vitis L, Leocani L, Santangelo R, Magnani G, Comi G, Bandello F.

Sci Rep. 2019 Jan 11;9(1):63. doi: 10.1038/s41598-018-37271-6.

9.

Prognostic value of serum neurofilaments in patients with clinically isolated syndromes.

Dalla Costa G, Martinelli V, Sangalli F, Moiola L, Colombo B, Radaelli M, Leocani L, Furlan R, Comi G.

Neurology. 2019 Feb 12;92(7):e733-e741. doi: 10.1212/WNL.0000000000006902. Epub 2019 Jan 11.

PMID:
30635483
10.

Structural connectivity in multiple sclerosis and modeling of disconnection.

Pagani E, Rocca MA, De Meo E, Horsfield MA, Colombo B, Rodegher M, Comi G, Filippi M.

Mult Scler. 2019 Jan 9:1352458518820759. doi: 10.1177/1352458518820759. [Epub ahead of print]

PMID:
30625050
11.

MicroRNAs as regulators of cell death mechanisms in amyotrophic lateral sclerosis.

Gagliardi D, Comi GP, Bresolin N, Corti S.

J Cell Mol Med. 2019 Jan 4. doi: 10.1111/jcmm.13976. [Epub ahead of print] Review.

12.

Added value of multimodal MRI to the clinical diagnosis of primary progressive aphasia variants.

Canu E, Agosta F, Imperiale F, Fontana A, Caso F, Spinelli EG, Magnani G, Falini A, Comi G, Filippi M.

Cortex. 2018 Dec 8;113:58-66. doi: 10.1016/j.cortex.2018.11.025. [Epub ahead of print]

PMID:
30605869
13.

Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eye.

Mauri E, Dilena R, Boccazzi A, Ronchi D, Piga D, Triulzi F, Gagliardi D, Brusa R, Faravelli I, Bresolin N, Magri F, Corti S, Comi GP.

BMC Neurol. 2018 Dec 27;18(1):220. doi: 10.1186/s12883-018-1227-9.

14.

Central Nervous System Involvement in Common Variable Immunodeficiency: A Case of Acute Unilateral Optic Neuritis in a 26-Year-Old Italian Patient.

Abati E, Faravelli I, Magri F, Govoni A, Velardo D, Gagliardi D, Mauri E, Brusa R, Bresolin N, Fabio G, Comi GP, Carrabba M, Corti S.

Front Neurol. 2018 Nov 30;9:1031. doi: 10.3389/fneur.2018.01031. eCollection 2018.

15.

Safety and efficacy of nabiximols on spasticity symptoms in patients with motor neuron disease (CANALS): a multicentre, double-blind, randomised, placebo-controlled, phase 2 trial.

Riva N, Mora G, Sorarù G, Lunetta C, Ferraro OE, Falzone Y, Leocani L, Fazio R, Comola M, Comi G; CANALS Study Group.

Lancet Neurol. 2019 Feb;18(2):155-164. doi: 10.1016/S1474-4422(18)30406-X. Epub 2018 Dec 13.

PMID:
30554828
16.

Severe disease activity in a patient with multiple sclerosis after daclizumab discontinuation.

Martinelli V, Dalla Costa G, Sangalli F, Colombo B, Robotti M, Moiola L, Comi G.

Mult Scler Relat Disord. 2018 Dec 1;28:57-59. doi: 10.1016/j.msard.2018.11.034. [Epub ahead of print]

PMID:
30554038
17.

Acquired haemophilia A as a secondary autoimmune disease after alemtuzumab treatment in multiple sclerosis: A case report.

Pisa M, Della Valle P, Coluccia A, Martinelli V, Comi G, D'Angelo A, Moiola L.

Mult Scler Relat Disord. 2019 Jan;27:403-405. doi: 10.1016/j.msard.2018.11.029. Epub 2018 Nov 29.

PMID:
30513503
18.

Fibrosis Rescue Improves Cardiac Function in Dystrophin-Deficient Mice and Duchenne Patient-Specific Cardiomyocytes by Immunoproteasome Modulation.

Farini A, Gowran A, Bella P, Sitzia C, Scopece A, Castiglioni E, Rovina D, Nigro P, Villa C, Fortunato F, Comi GP, Milano G, Pompilio G, Torrente Y.

Am J Pathol. 2019 Feb;189(2):339-353. doi: 10.1016/j.ajpath.2018.10.010. Epub 2018 Nov 16.

PMID:
30448404
19.

The Italian multiple sclerosis register.

Trojano M, Bergamaschi R, Amato MP, Comi G, Ghezzi A, Lepore V, Marrosu MG, Mosconi P, Patti F, Ponzio M, Zaratin P, Battaglia MA; Italian Multiple Sclerosis Register Centers Group.

Neurol Sci. 2019 Jan;40(1):155-165. doi: 10.1007/s10072-018-3610-0. Epub 2018 Nov 13.

20.

Letter to the Editor Regarding: A Comprehensive Review on Copemyl®.

Comi G, Nicoletti F, Canonico PL, Centonze D.

Neurol Ther. 2018 Dec;7(2):385-390. doi: 10.1007/s40120-018-0115-y. Epub 2018 Nov 10. No abstract available.

21.

Elucidating the role of Agl in bladder carcinogenesis by generation and characterization of genetically engineered mice.

Sottnik JL, Mallaredy V, Chauca-Diaz A, Ritterson Lew C, Owens C, Dancik GM, Pagliarani S, Lucchiari S, Moggio M, Ripolone M, Comi GP, Frierson HF Jr, Clouthier D, Theodorescu D.

Carcinogenesis. 2018 Nov 7. doi: 10.1093/carcin/bgy139. [Epub ahead of print]

PMID:
30403777
22.

Stormorken Syndrome Caused by a p.R304W STIM1 Mutation: The First Italian Patient and a Review of the Literature.

Borsani O, Piga D, Costa S, Govoni A, Magri F, Artoni A, Cinnante CM, Fagiolari G, Ciscato P, Moggio M, Bresolin N, Comi GP, Corti S.

Front Neurol. 2018 Oct 15;9:859. doi: 10.3389/fneur.2018.00859. eCollection 2018.

23.

Copy Number Variants Account for a Tiny Fraction of Undiagnosed Myopathic Patients.

Giugliano T, Savarese M, Garofalo A, Picillo E, Fiorillo C, D'Amico A, Maggi L, Ruggiero L, Vercelli L, Magri F, Fattori F, Torella A, Ergoli M, Rubegni A, Fanin M, Musumeci O, Bleecker J, Peverelli L, Moggio M, Mercuri E, Toscano A, Mora M, Santoro L, Mongini T, Bertini E, Bruno C, Minetti C, Comi GP, Santorelli FM, Angelini C, Politano L, Piluso G, Nigro V.

Genes (Basel). 2018 Oct 26;9(11). pii: E524. doi: 10.3390/genes9110524.

24.

The Multiple Sclerosis Care Unit.

Soelberg Sorensen P, Giovannoni G, Montalban X, Thalheim C, Zaratin P, Comi G.

Mult Scler. 2018 Oct 23:1352458518807082. doi: 10.1177/1352458518807082. [Epub ahead of print]

PMID:
30351211
25.

Mitochondrial Dysregulation and Impaired Autophagy in iPSC-Derived Dopaminergic Neurons of Multiple System Atrophy.

Monzio Compagnoni G, Kleiner G, Samarani M, Aureli M, Faustini G, Bellucci A, Ronchi D, Bordoni A, Garbellini M, Salani S, Fortunato F, Frattini E, Abati E, Bergamini C, Fato R, Tabano S, Miozzo M, Serratto G, Passafaro M, Deleidi M, Silipigni R, Nizzardo M, Bresolin N, Comi GP, Corti S, Quinzii CM, Di Fonzo A.

Stem Cell Reports. 2018 Nov 13;11(5):1185-1198. doi: 10.1016/j.stemcr.2018.09.007. Epub 2018 Oct 18.

26.

Optic nerve involvement in experimental autoimmune encephalomyelitis to homologous spinal cord homogenate immunization in the dark agouti rat.

Castoldi V, Marenna S, Santangelo R, d'Isa R, Cursi M, Chaabane L, Quattrini A, Comi G, Leocani L.

J Neuroimmunol. 2018 Dec 15;325:1-9. doi: 10.1016/j.jneuroim.2018.09.009. Epub 2018 Sep 25.

PMID:
30340030
27.

The role of clinical and neuroimaging features in the diagnosis of CADASIL.

Bersano A, Bedini G, Markus HS, Vitali P, Colli-Tibaldi E, Taroni F, Gellera C, Baratta S, Mosca L, Carrera P, Ferrari M, Cereda C, Grieco G, Lanfranconi S, Mazucchelli F, Zarcone D, De Lodovici ML, Bono G, Boncoraglio GB, Parati EA, Calloni MV, Perrone P, Bordo BM, Motto C, Agostoni E, Pezzini A, Padovani A, Micieli G, Cavallini A, Molini G, Sasanelli F, Sessa M, Comi G, Checcarelli N, Carmerlingo M, Corato M, Marcheselli S, Fusi L, Grampa G, Uccellini D, Beretta S, Ferrarese C, Incorvaia B, Tadeo CS, Adobbati L, Silani V, Faragò G, Trobia N, Grond-Ginsbach C, Candelise L; Lombardia GENS-group.

J Neurol. 2018 Dec;265(12):2934-2943. doi: 10.1007/s00415-018-9072-8. Epub 2018 Oct 11.

PMID:
30311053
28.

Functioning and quality of life in patients with neuropathy associated with anti-MAG antibodies.

Falzone YM, Campagnolo M, Bianco M, Dacci P, Martinelli D, Ruiz M, Bocci S, Cerri F, Quattrini A, Comi G, Benedetti L, Giannini F, Lauria G, Nobile-Orazio E, Briani C, Fazio R, Riva N.

J Neurol. 2018 Dec;265(12):2927-2933. doi: 10.1007/s00415-018-9081-7. Epub 2018 Oct 10.

29.

Mitochondrial dysfunction in fibroblasts of Multiple System Atrophy.

Monzio Compagnoni G, Kleiner G, Bordoni A, Fortunato F, Ronchi D, Salani S, Guida M, Corti C, Pichler I, Bergamini C, Fato R, Pellecchia MT, Vallelunga A, Del Sorbo F, Elia A, Reale C, Garavaglia B, Mora G, Albanese A, Cogiamanian F, Ardolino G, Bresolin N, Corti S, Comi GP, Quinzii CM, Di Fonzo A.

Biochim Biophys Acta Mol Basis Dis. 2018 Dec;1864(12):3588-3597. doi: 10.1016/j.bbadis.2018.09.018. Epub 2018 Sep 19.

PMID:
30254015
30.

Preconditioning and Cellular Engineering to Increase the Survival of Transplanted Neural Stem Cells for Motor Neuron Disease Therapy.

Abati E, Bresolin N, Comi GP, Corti S.

Mol Neurobiol. 2018 Aug 17. doi: 10.1007/s12035-018-1305-4. [Epub ahead of print] Review.

PMID:
30120734
31.

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature.

Gagliardi D, Faravelli I, Villa L, Pero G, Cinnante C, Brusa R, Mauri E, Tresoldi L, Magri F, Govoni A, Bresolin N, Comi GP, Corti S.

Front Neurol. 2018 Aug 2;9:619. doi: 10.3389/fneur.2018.00619. eCollection 2018.

32.

Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1.

Ripolone M, Lucchini V, Ronchi D, Fagiolari G, Bordoni A, Fortunato F, Mondello S, Bonato S, Meregalli M, Torrente Y, Corti S, Comi GP, Moggio M, Sciacco M.

J Neurosci Res. 2018 Sep;96(9):1576-1585. doi: 10.1002/jnr.24263.

PMID:
30113722
33.

Visual Evoked Potentials as a Biomarker in Multiple Sclerosis and Associated Optic Neuritis.

Leocani L, Guerrieri S, Comi G.

J Neuroophthalmol. 2018 Sep;38(3):350-357. doi: 10.1097/WNO.0000000000000704.

PMID:
30106802
34.

Functional and structural plasticity following action observation training in multiple sclerosis.

Rocca MA, Meani A, Fumagalli S, Pagani E, Gatti R, Martinelli-Boneschi F, Esposito F, Preziosa P, Cordani C, Comi G, Filippi M.

Mult Scler. 2018 Aug 7:1352458518792771. doi: 10.1177/1352458518792771. [Epub ahead of print]

PMID:
30084706
35.

Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III mice.

Pagliarani S, Lucchiari S, Ulzi G, Ripolone M, Violano R, Fortunato F, Bordoni A, Corti S, Moggio M, Bresolin N, Comi GP.

Biochim Biophys Acta Mol Basis Dis. 2018 Oct;1864(10):3407-3417. doi: 10.1016/j.bbadis.2018.07.031. Epub 2018 Aug 1.

36.

Neuromyelitis optica spectrum disorder and multiple sclerosis in a Sardinian family.

Gelibter S, Mazzi B, Tassara M, Colombo B, Guerrieri S, Giordano A, Preziosa P, Comola M, Esposito F, Martinelli V, Rocca MA, Comi G, Leocani L, Martinelli-Boneschi F.

Mult Scler Relat Disord. 2018 Oct;25:73-76. doi: 10.1016/j.msard.2018.07.017. Epub 2018 Jul 24.

PMID:
30053751
37.

R-Loops in Motor Neuron Diseases.

Perego MGL, Taiana M, Bresolin N, Comi GP, Corti S.

Mol Neurobiol. 2018 Jul 25. doi: 10.1007/s12035-018-1246-y. [Epub ahead of print] Review.

PMID:
30047099
38.

Efficacy and safety of ozanimod in multiple sclerosis: Dose-blinded extension of a randomized phase II study.

Cohen JA, Comi G, Arnold DL, Bar-Or A, Selmaj KW, Steinman L, Havrdová EK, Cree BA, Montalbán X, Hartung HP, Huang V, Frohna P, Skolnick BE, Kappos L; RADIANCE Trial Investigators.

Mult Scler. 2018 Jul 25:1352458518789884. doi: 10.1177/1352458518789884. [Epub ahead of print]

PMID:
30043658
39.

Assessing the role of innovative therapeutic paradigm on multiple sclerosis treatment response.

Romeo MAL, Martinelli V, Dalla Costa G, Colombo B, De Feo D, Esposito F, Ferrè L, Guaschino C, Guerrieri S, Liberatore G, Martinelli Boneschi F, Merlini A, Messina M, Messina R, Nuara A, Preziosa P, Radaelli M, Rocca MA, Rodegher M, Sangalli F, Strambo D, Moiola L, Comi G.

Acta Neurol Scand. 2018 Nov;138(5):447-453. doi: 10.1111/ane.12999. Epub 2018 Jul 22.

PMID:
30033621
40.

Secondary prevention of cryptogenic stroke in patients with patent foramen ovale: a systematic review and meta-analysis.

Fiorelli EM, Carandini T, Gagliardi D, Bozzano V, Bonzi M, Tobaldini E, Comi GP, Scarpini EA, Montano N, Solbiati M.

Intern Emerg Med. 2018 Dec;13(8):1287-1303. doi: 10.1007/s11739-018-1909-8. Epub 2018 Jul 21.

PMID:
30032341
41.

MicroRNA expression analysis identifies a subset of downregulated miRNAs in ALS motor neuron progenitors.

Rizzuti M, Filosa G, Melzi V, Calandriello L, Dioni L, Bollati V, Bresolin N, Comi GP, Barabino S, Nizzardo M, Corti S.

Sci Rep. 2018 Jul 4;8(1):10105. doi: 10.1038/s41598-018-28366-1.

42.

Progressive visual function impairment as the predominant symptom of the transition phase to secondary progressive multiple sclerosis: A case report.

Giordano A, Colombo B, Spinelli EG, Gelibter S, Guerrieri S, Leocani L, Comi G, Martinelli V.

Mult Scler Relat Disord. 2018 Aug;24:69-71. doi: 10.1016/j.msard.2018.06.011. Epub 2018 Jun 20.

PMID:
29957351
43.

The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel.

Altamura C, Lucchiari S, Sahbani D, Ulzi G, Comi GP, D'Ambrosio P, Petillo R, Politano L, Vercelli L, Mongini T, Dotti MT, Cardani R, Meola G, Lo Monaco M, Matthews E, Hanna MG, Carratù MR, Conte D, Imbrici P, Desaphy JF.

Hum Mutat. 2018 Sep;39(9):1273-1283. doi: 10.1002/humu.23581. Epub 2018 Jul 4.

PMID:
29935101
44.

The MELAS mutation m.3243A>G promotes reactivation of fetal cardiac genes and an epithelial-mesenchymal transition-like program via dysregulation of miRNAs.

Meseguer S, Panadero J, Navarro-González C, Villarroya M, Boutoual R, Comi GP, Armengod ME.

Biochim Biophys Acta Mol Basis Dis. 2018 Sep;1864(9 Pt B):3022-3037. doi: 10.1016/j.bbadis.2018.06.014. Epub 2018 Jun 19.

45.

Clinical Features of Headache in Patients With Diagnosis of Definite Vestibular Migraine: The VM-Phenotypes Projects.

Teggi R, Colombo B, Albera R, Asprella Libonati G, Balzanelli C, Batuecas Caletrio A, Casani AP, Espinosa-Sanchez JM, Gamba P, Lopez-Escamez JA, Lucisano S, Mandalà M, Neri G, Nuti D, Pecci R, Russo A, Martin-Sanz E, Sanz R, Tedeschi G, Torelli P, Vannucchi P, Comi G, Bussi M.

Front Neurol. 2018 Jun 5;9:395. doi: 10.3389/fneur.2018.00395. eCollection 2018.

46.

Laser capture microdissection for transcriptomic profiles in human skin biopsies.

Santoro S, Lopez ID, Lombardi R, Zauli A, Osiceanu AM, Sorosina M, Clarelli F, Peroni S, Cazzato D, Marchi M, Quattrini A, Comi G, Calogero RA, Lauria G, Martinelli Boneschi F.

BMC Mol Biol. 2018 Jun 19;19(1):7. doi: 10.1186/s12867-018-0108-5.

47.

Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis.

Jia X, Madireddy L, Caillier S, Santaniello A, Esposito F, Comi G, Stuve O, Zhou Y, Taylor B, Kilpatrick T, Martinelli-Boneschi F, Cree BAC, Oksenberg JR, Hauser SL, Baranzini SE.

Ann Neurol. 2018 Jul;84(1):51-63. doi: 10.1002/ana.25263. Epub 2018 Jul 3.

PMID:
29908077
48.

Pediatric sporadic hemiplegic migraine (ATP1A2 gene): a case report and brief literature review.

Schwarz G, Anzalone N, Baldoli C, Impellizzeri M, Minicucci F, Comi G, Colombo B.

Neurol Sci. 2018 Jun;39(Suppl 1):69-71. doi: 10.1007/s10072-018-3405-3. Review. No abstract available.

PMID:
29904856
49.

Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease.

Savarese M, Torella A, Musumeci O, Angelini C, Astrea G, Bello L, Bruno C, Comi GP, Di Fruscio G, Piluso G, Di Iorio G, Ergoli M, Esposito G, Fanin M, Farina O, Fiorillo C, Garofalo A, Giugliano T, Magri F, Minetti C, Moggio M, Passamano L, Pegoraro E, Picillo E, Sampaolo S, Santorelli FM, Semplicini C, Udd B, Toscano A, Politano L, Nigro V.

Neuromuscul Disord. 2018 Jul;28(7):586-591. doi: 10.1016/j.nmd.2018.03.011. Epub 2018 Apr 9.

PMID:
29880332
50.

Rhabdomyolysis-Associated Acute Kidney Injury.

Esposito P, Estienne L, Serpieri N, Ronchi D, Comi GP, Moggio M, Peverelli L, Bianzina S, Rampino T.

Am J Kidney Dis. 2018 Jun;71(6):A12-A14. doi: 10.1053/j.ajkd.2018.03.009. No abstract available. Erratum in: Am J Kidney Dis. 2018 Sep;72(3):468.

PMID:
29801551

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