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Items: 1 to 50 of 587

1.

A Model to Study Myelinated Fiber Degeneration and Regeneration in Human Skin.

Provitera V, Piscosquito G, Manganelli F, Mozzillo S, Caporaso G, Stancanelli A, Borreca I, Di Caprio G, Santoro L, Nolano M.

Ann Neurol. 2019 Dec 17. doi: 10.1002/ana.25662. [Epub ahead of print]

PMID:
31849107
2.

In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C.

Esposito M, Dubbioso R, Tozza S, Iodice R, Aiello M, Nicolai E, Cavaliere C, Salvatore M, Santoro L, Manganelli F.

Heliyon. 2019 Nov 14;5(11):e02776. doi: 10.1016/j.heliyon.2019.e02776. eCollection 2019 Nov.

3.

Different cortical excitability profiles in hereditary brain iron and copper accumulation.

Dubbioso R, Ruggiero L, Esposito M, Tarantino P, De Angelis M, Aruta F, Pappatà S, Ugga L, Piperno A, Iorio R, Santoro L, Iodice R, Manganelli F.

Neurol Sci. 2019 Nov 26. doi: 10.1007/s10072-019-04147-0. [Epub ahead of print]

PMID:
31773358
4.

Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCs.

Manganelli F, Parisi S, Nolano M, Miceli F, Tozza S, Pisciotta C, Iodice R, Provitera V, Cicatiello R, Zuchner S, Taglialatela M, Russo T, Santoro L.

J Peripher Nerv Syst. 2019 Dec;24(4):330-339. doi: 10.1111/jns.12357. Epub 2019 Nov 24.

PMID:
31707753
5.

Infantile inflammatory myofibroblastic tumors: clinicopathological and molecular characterization of 12 cases.

Lopez-Nunez O, John I, Panasiti RN, Ranganathan S, Santoro L, Grélaud D, Wu T, Buccoliero AM, Casanova M, Alaggio R, Surrey LF.

Mod Pathol. 2019 Nov 5. doi: 10.1038/s41379-019-0406-6. [Epub ahead of print]

PMID:
31690781
6.

Mutational and Immunophenotypic Profiling of a Series of 8 Tubo-ovarian Carcinosarcomas Revealed a Monoclonal Origin of the Disease.

Trento M, Munari G, Carraro V, Lanza C, Salmaso R, Pizzi S, Santoro L, Chiarelli S, Dal Santo L, Nardelli GB, Saccardi C, Nicoletto O, Baldoni A, Rugge M, Fassan M.

Int J Gynecol Pathol. 2019 Nov 1. doi: 10.1097/PGP.0000000000000645. [Epub ahead of print]

PMID:
31688243
7.

Patient-derived organoids (PDOs) as a novel in vitro model for neuroblastoma tumours.

Fusco P, Parisatto B, Rampazzo E, Persano L, Frasson C, Di Meglio A, Leslz A, Santoro L, Cafferata B, Zin A, Cimetta E, Basso G, Esposito MR, Tonini GP.

BMC Cancer. 2019 Oct 21;19(1):970. doi: 10.1186/s12885-019-6149-4.

8.

Cardiac and Neuromuscular Features of Patients with LMNA-Related Cardiomyopathy.

Peretto G, Di Resta C, Perversi J, Forleo C, Maggi L, Politano L, Barison A, Previtali SC, Carboni N, Brun F, Pegoraro E, D'Amico A, Rodolico C, Magri F, Manzi RC, Palladino A, Isola F, Gigli L, Mongini TE, Semplicini C, Calore C, Ricci G, Comi GP, Ruggiero L, Bertini E, Bonomo P, Nigro G, Resta N, Emdin M, Favale S, Siciliano G, Santoro L, Sinagra G, Limongelli G, Ambrosi A, Ferrari M, Golzio PG, Bella PD, Benedetti S, Sala S; Italian Network for Laminopathies (NIL).

Ann Intern Med. 2019 Sep 3. doi: 10.7326/M18-2768. [Epub ahead of print]

PMID:
31476771
9.

Subclinical atherosclerosis and endothelial dysfunction in patients with polymyalgia rheumatica: a pilot study.

Santoro L, Birra D, Bosello S, Nesci A, Di Giorgio A, Peluso G, Giupponi B, Zaccone V, Gasbarrini A, Zoli A, Santoliquido A.

Scand J Rheumatol. 2020 Jan;49(1):68-74. doi: 10.1080/03009742.2019.1628297. Epub 2019 Aug 16.

PMID:
31418315
10.

Neonatal asymmetrical vulvar hypertrophy: a neonatal manifestation of 'classic' prepubertal vulvar fibroma?

Tessari A, Santoro L, De Corti F, Valerio E, Cutrone M.

Arch Dis Child Fetal Neonatal Ed. 2019 Jul 30. pii: fetalneonatal-2019-316869. doi: 10.1136/archdischild-2019-316869. [Epub ahead of print] No abstract available.

PMID:
31362939
11.

Risk factors for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): antecedent events, lifestyle and dietary habits. Data from the Italian CIDP Database.

Doneddu PE, Bianchi E, Cocito D, Manganelli F, Fazio R, Filosto M, Mazzeo A, Cosentino G, Cortese A, Jann S, Clerici AM, Antonini G, Siciliano G, Luigetti M, Marfia GA, Briani C, Lauria G, Rosso T, Cavaletti G, Carpo M, Benedetti L, Beghi E, Liberatore G, Santoro L, Peci E, Tronci S, Cotti Piccinelli S, Toscano A, Piccolo L, Verrengia EP, Leonardi L, Schirinzi E, Mataluni G, Ruiz M, Dacci P, Nobile-Orazio E; Italian CIDP Database Study Group.

Eur J Neurol. 2020 Jan;27(1):136-143. doi: 10.1111/ene.14044. Epub 2019 Aug 9.

PMID:
31325350
12.

Benign cephalic histiocytosis: an atypical case with plaque-like presentation.

Orlando G, Todesco A, Santoro L, Belloni Fortina A.

G Ital Dermatol Venereol. 2019 Jul 12. doi: 10.23736/S0392-0488.19.06309-0. [Epub ahead of print] No abstract available.

PMID:
31302975
13.

A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family.

Cotti Piccinelli S, Bassi MT, Citterio A, Manganelli F, Tozza S, Santorelli FM, Gallo Cassarino S, Caria F, Baldelli E, Galvagni A, Santoro L, Padovani A, Filosto M.

Front Neurol. 2019 Jun 5;10:580. doi: 10.3389/fneur.2019.00580. eCollection 2019.

14.

Spinocerebellar ataxia type 2-neuronopathy or neuropathy?

Pelosi L, Iodice R, Antenora A, Kilfoyle D, Mulroy E, Rodrigues M, Roxburgh R, Iovino A, Filla A, Manganelli F, Santoro L.

Muscle Nerve. 2019 Sep;60(3):271-278. doi: 10.1002/mus.26613. Epub 2019 Jul 5.

PMID:
31228263
15.

RYR1 Sequence Variants in Myopathies: Expression and Functional Studies in Two Families.

Zullo A, Perrotta G, D'Angelo R, Ruggiero L, Gravino E, Del Vecchio L, Santoro L, Salvatore F, Carsana A.

Biomed Res Int. 2019 Apr 21;2019:7638946. doi: 10.1155/2019/7638946. eCollection 2019.

16.

Stakeholder value judgments in decision-making on the incorporation, financing, and allocation of new health technologies in limited-resource settings: a potential Brazilian approach.

Santoro L, Lessa F, Nardi EP, Ferraz MB.

Rev Panam Salud Publica. 2018 Aug 10;42:e102. doi: 10.26633/RPSP.2018.102. eCollection 2018.

17.

A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs).

Pareyson D, Stojkovic T, Reilly MM, Leonard-Louis S, Laurà M, Blake J, Parman Y, Battaloglu E, Tazir M, Bellatache M, Bonello-Palot N, Lévy N, Sacconi S, Guimarães-Costa R, Attarian S, Latour P, Solé G, Megarbane A, Horvath R, Ricci G, Choi BO, Schenone A, Gemelli C, Geroldi A, Sabatelli M, Luigetti M, Santoro L, Manganelli F, Quattrone A, Valentino P, Murakami T, Scherer SS, Dankwa L, Shy ME, Bacon CJ, Herrmann DN, Zambon A, Tramacere I, Pisciotta C, Magri S, Previtali SC, Bolino A.

Ann Neurol. 2019 Jul;86(1):55-67. doi: 10.1002/ana.25500. Epub 2019 May 27.

PMID:
31070812
18.

Combined Effects of Isokinetic Training and Botulinum Toxin Type A on Spastic Equinus Foot in Patients with Chronic Stroke: A Pilot, Single-blind, Randomized Controlled Trial.

Cinone N, Letizia S, Santoro L, Facciorusso S, Armiento R, Picelli A, Ranieri M, Santamato A.

Toxins (Basel). 2019 Apr 8;11(4). pii: E210. doi: 10.3390/toxins11040210.

19.

Are novel outcome measures for Charcot-Marie-Tooth disease sensitive to change? The 6-minute walk test and StepWatch™ Activity Monitor in a 12-month longitudinal study.

Pazzaglia C, Padua L, Pareyson D, Schenone A, Aiello A, Fabrizi GM, Cavallaro T, Santoro L, Manganelli F, Coraci D, Gemignani F, Vitetta F, Quattrone A, Mazzeo A, Russo M, Vita G; CMT-TRIAAL Group.

Neuromuscul Disord. 2019 Apr;29(4):310-316. doi: 10.1016/j.nmd.2019.01.009. Epub 2019 Feb 2.

PMID:
30926199
20.

A novel family with axonal Charcot-Marie-Tooth disease caused by a mutation in the EGR2 gene.

Tozza S, Magri S, Pennisi EM, Schirinzi E, Pisciotta C, Balistreri F, Severi D, Ricci G, Siciliano G, Taroni F, Santoro L, Manganelli F.

J Peripher Nerv Syst. 2019 Jun;24(2):219-223. doi: 10.1111/jns.12314. Epub 2019 Mar 28.

PMID:
30843326
21.

Molecular diagnosis of patients affected by mucopolysaccharidosis: a multicenter study.

Zanetti A, D'Avanzo F, Rigon L, Rampazzo A, Concolino D, Barone R, Volpi N, Santoro L, Lualdi S, Bertola F, Scarpa M, Tomanin R.

Eur J Pediatr. 2019 May;178(5):739-753. doi: 10.1007/s00431-019-03341-8. Epub 2019 Feb 26.

22.

Effects of a New Combination of Medical Food on Endothelial Function and Lipid Profile in Dyslipidemic Subjects: A Pilot Randomized Trial.

Landi F, Martone AM, Salini S, Zazzara B, Calvani R, Marzetti E, Nesci A, Di Giorgio A, Giupponi B, Santoro L, Santoliquido A.

Biomed Res Int. 2019 Jan 6;2019:1970878. doi: 10.1155/2019/1970878. eCollection 2019.

23.

Six-minute walk test is reliable and sensitive in detecting response to therapy in CIDP.

Spina E, Topa A, Iodice R, Tozza S, Ruggiero L, Dubbioso R, Esposito M, Dolce P, Santoro L, Manganelli F.

J Neurol. 2019 Apr;266(4):860-865. doi: 10.1007/s00415-019-09207-1. Epub 2019 Feb 5.

PMID:
30721354
24.

Botulinum Toxin Type A for the Treatment of Lower Limb Spasticity after Stroke.

Santamato A, Cinone N, Panza F, Letizia S, Santoro L, Lozupone M, Daniele A, Picelli A, Baricich A, Intiso D, Ranieri M.

Drugs. 2019 Feb;79(2):143-160. doi: 10.1007/s40265-018-1042-z. Review.

PMID:
30623347
25.

Comparison of the effect of beclometasone/formoterol in asthma patients after methacholine-induced bronchoconstriction: A noninferiority study using metered dose vs. dry powder inhaler.

Singh D, van den Berg F, Leaker B, Corradi M, Jabbal S, Collarini S, Mongelli V, Santoro L, Piccinno A, Biondaro S, Lipworth B.

Br J Clin Pharmacol. 2019 Apr;85(4):729-736. doi: 10.1111/bcp.13847. Epub 2019 Feb 3.

26.

One-year follow up of three Italian patients with Duchenne muscular dystrophy treated with ataluren: is earlier better?

Ruggiero L, Iodice R, Esposito M, Dubbioso R, Tozza S, Vitale F, Santoro L, Manganelli F.

Ther Adv Neurol Disord. 2018 Nov 3;11:1756286418809588. doi: 10.1177/1756286418809588. eCollection 2018.

27.

Implementation of patient dosimetry in the clinical practice after targeted radiotherapy using [177Lu-[DOTA0, Tyr3]-octreotate.

Santoro L, Mora-Ramirez E, Trauchessec D, Chouaf S, Eustache P, Pouget JP, Kotzki PO, Bardiès M, Deshayes E.

EJNMMI Res. 2018 Nov 29;8(1):103. doi: 10.1186/s13550-018-0459-4.

28.

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.

29.

Atypical CIDP: diagnostic criteria, progression and treatment response. Data from the Italian CIDP Database.

Doneddu PE, Cocito D, Manganelli F, Fazio R, Briani C, Filosto M, Benedetti L, Mazzeo A, Marfia GA, Cortese A, Fierro B, Jann S, Beghi E, Clerici AM, Carpo M, Schenone A, Luigetti M, Lauria G, Antonini G, Rosso T, Siciliano G, Cavaletti G, Liberatore G, Santoro L, Peci E, Tronci S, Ruiz M, Cotti Piccinelli S, Toscano A, Mataluni G, Piccolo L, Cosentino G, Sabatelli M, Nobile-Orazio E; Italian CIDP Database study group.

J Neurol Neurosurg Psychiatry. 2019 Feb;90(2):125-132. doi: 10.1136/jnnp-2018-318714. Epub 2018 Oct 8.

30.

Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise".

Grandis M, Geroldi A, Gulli R, Manganelli F, Gotta F, Lamp M, Origone P, Trevisan L, Gemelli C, Fabbri S, Schenone A, Tozza S, Santoro L, Bellone E, Mandich P.

Orphanet J Rare Dis. 2018 Oct 4;13(1):177. doi: 10.1186/s13023-018-0917-0.

31.

Generalized anhidrosis as first clinical presentation of systemic lupus erythematosus.

Provitera V, Lubrano E, Piscosquito G, Manganelli F, Santoro L, Nolano M.

Lupus. 2018 Dec;27(14):2296-2297. doi: 10.1177/0961203318804887. Epub 2018 Oct 3. No abstract available.

PMID:
30282559
32.

Artificial nutrition in patients with cancer has no impact on tumour glucose metabolism: Results of the PETANC Study.

Deshayes E, de Forges H, Fraisse J, Eberlé MC, Guillemard S, Fallières A, Pouget JP, Tétreau R, Kotzki PO, Santoro L, Senesse P, Flori N.

Clin Nutr. 2019 Oct;38(5):2121-2126. doi: 10.1016/j.clnu.2018.08.033. Epub 2018 Aug 31.

PMID:
30209026
33.

False positive screen test for mucopolysaccharidoses in healthy female newborns.

Monachesi C, Zampini L, Padella L, Marchesiello RL, Galeazzi T, Santoro L, Catassi C, Gasparrini E, Carnielli VP, Volpi N, Fiumara A, Concolino D, Tomanin R, Coppa GV, Gabrielli O.

Clin Chim Acta. 2018 Nov;486:221-223. doi: 10.1016/j.cca.2018.08.016. Epub 2018 Aug 12.

PMID:
30110607
34.

microRNAs as biomarkers in Pompe disease.

Tarallo A, Carissimo A, Gatto F, Nusco E, Toscano A, Musumeci O, Coletta M, Karali M, Acampora E, Damiano C, Minopoli N, Fecarotta S, Della Casa R, Mongini T, Vercelli L, Santoro L, Ruggiero L, Deodato F, Taurisano R, Bembi B, Dardis A, Banfi S, Pijnappel WWP, van der Ploeg AT, Parenti G.

Genet Med. 2019 Mar;21(3):591-600. doi: 10.1038/s41436-018-0103-8. Epub 2018 Jul 12.

PMID:
29997386
35.

Intra-articular injection of botulinum toxin type A for shoulder pain in glenohumeral osteoarthritis: a case series summary and review of the literature.

Cinone N, Letizia S, Santoro L, Gravina M, Amoruso L, Molteni F, Ranieri M, Santamato A.

J Pain Res. 2018 Jun 25;11:1239-1245. doi: 10.2147/JPR.S159700. eCollection 2018.

36.

A novel SCN9A splicing mutation in a compound heterozygous girl with congenital insensitivity to pain, hyposmia and hypogeusia.

Marchi M, Provitera V, Nolano M, Romano M, Maccora S, D'Amato I, Salvi E, Gerrits M, Santoro L, Lauria G.

J Peripher Nerv Syst. 2018 Sep;23(3):202-206. doi: 10.1111/jns.12280. Epub 2018 Jul 23.

37.

Prevalence of dyslipidaemia and awareness of blood cholesterol levels among community-living people: results from the Longevity check-up 7+ (Lookup 7+) cross-sectional survey.

Marzetti E, Calvani R, Picca A, Sisto A, Tosato M, Martone AM, Ortolani E, Salini S, Pafundi T, Santoliquido A, Santoro L, Bernabei R, Landi F.

BMJ Open. 2018 Jun 30;8(6):e021627. doi: 10.1136/bmjopen-2018-021627.

38.

Small fiber pathology parallels disease progression in Parkinson disease: a longitudinal study.

Nolano M, Provitera V, Stancanelli A, Saltalamacchia AM, Caporaso G, Lullo F, Borreca I, Piscosquito G, Mozzillo S, Esposito M, Manganelli F, Lanzillo B, Santoro L.

Acta Neuropathol. 2018 Sep;136(3):501-503. doi: 10.1007/s00401-018-1876-1. Epub 2018 Jun 18. No abstract available.

PMID:
29916036
39.

Muscle pain syndromes and fibromyalgia: the role of muscle biopsy.

Ruggiero L, Manganelli F, Santoro L.

Curr Opin Support Palliat Care. 2018 Sep;12(3):382-387. doi: 10.1097/SPC.0000000000000355. Review.

PMID:
29912728
40.

Association between peripheral arterial disease and cardiovascular risk factors: role of ultrasonography versus ankle-brachial index.

Santoro L, Flex A, Nesci A, Ferraro PM, De Matteis G, Di Giorgio A, Giupponi B, Saviano L, Gambaro G, Franceschi F, Gasbarrini A, Landolfi R, Santoliquido A.

Eur Rev Med Pharmacol Sci. 2018 May;22(10):3160-3165. doi: 10.26355/eurrev_201805_15076.

41.

Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes.

Bernasconi P, Carboni N, Ricci G, Siciliano G, Politano L, Maggi L, Mongini T, Vercelli L, Rodolico C, Biagini E, Boriani G, Ruggiero L, Santoro L, Schena E, Prencipe S, Evangelisti C, Pegoraro E, Morandi L, Columbaro M, Lanzuolo C, Sabatelli P, Cavalcante P, Cappelletti C, Bonne G, Muchir A, Lattanzi G.

Nucleus. 2018 Jan 1;9(1):292-304. doi: 10.1080/19491034.2018.1467722.

42.

Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs.

Schiavo G, Bertolini F, Utzeri VJ, Ribani A, Geraci C, Santoro L, Óvilo C, Fernández AI, Gallo M, Fontanesi L.

Anim Genet. 2018 Aug;49(4):321-325. doi: 10.1111/age.12665. Epub 2018 Apr 19.

PMID:
29672877
43.

The effect of long-term treatment with coenzyme Q10 on nucleic acid modifications by oxidation in children with Down syndrome.

Larsen EL, Padella L, Bergholdt HKM, Henriksen T, Santoro L, Gabrielli O, Poulsen HE, Littarru GP, Orlando P, Tiano L.

Neurobiol Aging. 2018 Jul;67:159-161. doi: 10.1016/j.neurobiolaging.2018.03.001. Epub 2018 Mar 15.

PMID:
29665577
44.

Breast milk oligosaccharides: effects of 2'-fucosyllactose and 6'-sialyllactose on the adhesion of Escherichia coli and Salmonella fyris to Caco-2 cells.

Facinelli B, Marini E, Magi G, Zampini L, Santoro L, Catassi C, Monachesi C, Gabrielli O, Coppa GV.

J Matern Fetal Neonatal Med. 2019 Sep;32(17):2950-2952. doi: 10.1080/14767058.2018.1450864. Epub 2018 Mar 21.

PMID:
29562795
45.

Long-term therapy with miglustat and cognitive decline in the adult form of Niemann-Pick disease type C: a case report.

Tozza S, Dubbioso R, Iodice R, Topa A, Esposito M, Ruggiero L, Spina E, De Rosa A, Saccà F, Santoro L, Manganelli F.

Neurol Sci. 2018 Jun;39(6):1015-1019. doi: 10.1007/s10072-018-3314-5. Epub 2018 Mar 13.

PMID:
29536386
46.

Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2.

Lassuthova P, Rebelo AP, Ravenscroft G, Lamont PJ, Davis MR, Manganelli F, Feely SM, Bacon C, Brožková DŠ, Haberlova J, Mazanec R, Tao F, Saghira C, Abreu L, Courel S, Powell E, Buglo E, Bis DM, Baxter MF, Ong RW, Marns L, Lee YC, Bai Y, Isom DG, Barro-Soria R, Chung KW, Scherer SS, Larsson HP, Laing NG, Choi BO, Seeman P, Shy ME, Santoro L, Zuchner S.

Am J Hum Genet. 2018 Mar 1;102(3):505-514. doi: 10.1016/j.ajhg.2018.01.023.

47.

The role of skin biopsy in differentiating small-fiber neuropathy from ganglionopathy.

Provitera V, Gibbons CH, Wendelschafer-Crabb G, Donadio V, Vitale DF, Loavenbruck A, Stancanelli A, Caporaso G, Liguori R, Wang N, Santoro L, Kennedy WR, Nolano M.

Eur J Neurol. 2018 Jun;25(6):848-853. doi: 10.1111/ene.13608. Epub 2018 Apr 6. Erratum in: Eur J Neurol. 2019 Jan;26(1):202.

PMID:
29493845
48.

Hypofractionated postmastectomy radiotherapy with helical tomotherapy in patients with immediate breast reconstruction: dosimetric results and acute/intermediate toxicity evaluation.

Orecchia R, Rojas DP, Cattani F, Ricotti R, Santoro L, Morra A, Cambria R, Luraschi R, Dicuonzo S, Ronchi S, Surgo A, Dell' Acqua V, Veronesi P, De Lorenzi F, Fodor C, Leonardi MC, Jereczek-Fossa BA.

Med Oncol. 2018 Feb 13;35(3):39. doi: 10.1007/s12032-018-1095-6.

PMID:
29442173
49.

Interpreting Genetic Variants in Titin in Patients With Muscle Disorders.

Savarese M, Maggi L, Vihola A, Jonson PH, Tasca G, Ruggiero L, Bello L, Magri F, Giugliano T, Torella A, Evilä A, Di Fruscio G, Vanakker O, Gibertini S, Vercelli L, Ruggieri A, Antozzi C, Luque H, Janssens S, Pasanisi MB, Fiorillo C, Raimondi M, Ergoli M, Politano L, Bruno C, Rubegni A, Pane M, Santorelli FM, Minetti C, Angelini C, De Bleecker J, Moggio M, Mongini T, Comi GP, Santoro L, Mercuri E, Pegoraro E, Mora M, Hackman P, Udd B, Nigro V.

JAMA Neurol. 2018 May 1;75(5):557-565. doi: 10.1001/jamaneurol.2017.4899. Erratum in: JAMA Neurol. 2018 Nov 1;75(11):1443.

50.

Atherosclerosis and cardiovascular involvement in celiac disease: the role of autoimmunity and inflammation.

Santoro L, De Matteis G, Fuorlo M, Giupponi B, Martone AM, Landi F, Landolfi R, Santoliquido A.

Eur Rev Med Pharmacol Sci. 2017 Dec;21(23):5437-5444. doi: 10.26355/eurrev_201712_13932. Review.

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