Eduardo Nobile‐Orazio

ORCID: 0000-0003-2624-8138
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About
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Research Areas
  • Peripheral Neuropathies and Disorders
  • Hereditary Neurological Disorders
  • Myasthenia Gravis and Thymoma
  • Monoclonal and Polyclonal Antibodies Research
  • Peripheral Nerve Disorders
  • Multiple Myeloma Research and Treatments
  • Multiple Sclerosis Research Studies
  • Autoimmune Neurological Disorders and Treatments
  • Pain Mechanisms and Treatments
  • Nerve injury and regeneration
  • Long-Term Effects of COVID-19
  • Amyotrophic Lateral Sclerosis Research
  • Botulinum Toxin and Related Neurological Disorders
  • Toxin Mechanisms and Immunotoxins
  • Glycosylation and Glycoproteins Research
  • Autoimmune Bullous Skin Diseases
  • Cancer Treatment and Pharmacology
  • Chronic Lymphocytic Leukemia Research
  • SARS-CoV-2 and COVID-19 Research
  • Pharmacological Effects of Natural Compounds
  • Systemic Lupus Erythematosus Research
  • Neurogenetic and Muscular Disorders Research
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Heparin-Induced Thrombocytopenia and Thrombosis
  • Complement system in diseases

IRCCS Humanitas Research Hospital
2007-2025

Humanitas University
2015-2024

University of Milan
2015-2024

Istituti di Ricovero e Cura a Carattere Scientifico
2014-2024

Erasmus MC
2021-2023

Aarhus University Hospital
2022-2023

Mylan (South Africa)
2002-2023

Institute of Neuroimmunology of the Slovak Academy of Sciences
2020-2023

University of Michigan
2023

Daiichi Sankyo (United States)
2022

Background: Consensus guidelines on the definition, investigation, and treatment of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) have been previously published in European Journal Neurology Peripheral Nervous System . Objectives: To revise these guidelines. Methods: Disease experts, including a representative patients, considered references retrieved from MEDLINE Cochrane Systematic Reviews between August 2004 July 2009 prepared statements that were agreed an iterative...

10.1111/j.1468-1331.2009.02930.x article EN European Journal of Neurology 2010-02-23

This multicenter, randomized, double-blind, crossover trial compared a six week course of oral prednisolone tapering from 60 mg to 10 daily with intravenous immunoglobulin (IVIg) 2.0 g/kg given over one two days for treating chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Twenty-four the thirty-two randomized patients completed both treatment periods. Both treatments produced significant improvements in primary outcome measure, change an 11-point disability scale weeks...

10.1002/ana.1088 article EN Annals of Neurology 2001-07-30

To revise the 2010 consensus guideline on chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Seventeen disease experts, a patient representative, and two Cochrane methodologists constructed 12 Population/Intervention/Comparison/Outcome (PICO) questions regarding diagnosis treatment to guide literature search. Data were extracted summarized in GRADE summary of findings (for PICOs) or evidence tables diagnostic PICOs). Statements prepared according Evidence-to-Decision...

10.1111/jns.12455 article EN Journal of the Peripheral Nervous System 2021-06-04

To revise the 2010 consensus guideline on chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).Seventeen disease experts, a patient representative, and two Cochrane methodologists constructed 12 Population/Intervention/Comparison/Outcome (PICO) questions regarding diagnosis treatment to guide literature search. Data were extracted summarized in GRADE summary of findings (for PICOs) or evidence tables diagnostic PICOs).Statements prepared according Evidence-to-Decision frameworks....

10.1111/ene.14959 article EN European Journal of Neurology 2021-07-30
Alex Y. Doets Christine Verboon Bianca van den Berg Thomas Harbo David R. Cornblath and 95 more Hugh J. Willison Zhahirul Islam Shahram Attarian Fábio Barroso Kathleen Bateman Luana Benedetti Peter Van den Bergh Carlos Casasnovas Guido Cavaletti Govindsinh Chavada Kristl G. Claeys Efthimios Dardiotis Amy Davidson Pieter A. van Doorn T E Feasby Giuliana Galassi Kenneth C. Gorson Hans-Peter Hartung Sung‐Tsang Hsieh Richard AC Hughes Isabel Illa Badrul Islam Susumu Kusunoki Satoshi Kuwabara Helmar C. Lehmann James Miller Quazi Deen Mohammad Soledad Monges Eduardo Nobile‐Orazio Julio Pardo Yann Péréon Simon Rinaldi Luís Querol Stephen Reddel Ricardo Reisin Nortina Shahrizaila Søren H. Sindrup Waqar Waheed Bart C. Jacobs Bart C. Jacobs Richard AC Hughes David R. Cornblath Kenneth C. Gorson H.‐P. Hartung Susumu Kusunoki Pieter A. van Doorn Hugh J. Willison M. van Woerkom Benno van den Berg Christine Verboon Alex Y. Doets Joyce Roodbol Bart C. Jacobs Ricardo Reisin Stephen Reddel Zhahirul Islam Badrul Islam Quazi Deen Mohammad P. van den Bergh T E Feasby Thomas Harbo Yann Péréon H.‐P. Hartung Helmar C. Lehmann Efthimios Dardiotis Eduardo Nobile‐Orazio Susumu Kusunoki Nortina Shahrizaila Bart C. Jacobs Benno van den Berg Christine Verboon Alex Y. Doets Kathleen Bateman Isabel Illa Luís Querol Sung‐Tsang Hsieh Hugh J. Willison Govindsinh Chavada Amy Davidson Kenneth C. Gorson Jean Addington Senda Ajroud‐Driss Henning Andersen Giovanni Antonini Alessandra Ariatti Shahram Attarian Umesh A. Badrising Fábio Barroso Luana Benedetti Alessandro Beronio Marcelle Martim Bianco Delphine Binda Chiara Briani Carina Bunschoten Jan Bürmann

Guillain-Barré syndrome is a heterogeneous disorder regarding the clinical presentation, electrophysiological subtype and outcome. Previous single country reports indicate that may differ among regions, but no systematic comparative studies have been conducted. Comparative are required to identify factors determining disease susceptibility, variation prognosis, improve diagnostic criteria. The International Syndrome Outcome Study prospective, observational cohort study including all patients...

10.1093/brain/awy232 article EN Brain 2018-08-10
Maria Pia Sormani Matilde Inglese Irene Schiavetti Luca Carmisciano Alice Laroni and 95 more Caterina Lapucci Giorgio Da Rin Carlo Serrati Ilaria Gandoglia Tiziana Tassinari Germana Perego Giampaolo Brichetto Paola Gazzola Antonio Mannironi Maria Laura Stromillo Cinzia Cordioli Doriana Landi Marinella Clerico Elisabetta Signoriello Jessica Frau Maria Teresa Ferrò Alessia Di Sapio Livia Pasquali Monica Ulivelli F. Marinelli Graziella Callari Rosa Iodice Giuseppe Liberatore Francesca Caleri Anna Maria Repice Susanna Cordera Mario Alberto Battaglia Marco Salvetti Diego Franciotta Antonio Uccelli Alessandro Maglione Alessia Di Sapio Alessio Signori Alice Laroni Aniello Iovino Anna Maria Repice Antonio Mannironi Antonio Uccelli Carlo Serrati Carolina Gabri Nicoletti Caterina Lapucci Chiara Rosa Mancinelli Cinzia Cordioli Daiana Bezzini Daniele Carmagnini Davide Brogi Diego Franciotta Doriana Landi Eduardo Nobile‐Orazio Eleonora Cocco Elisabetta Signoriello Enri Nako Ester Assandri F. Marinelli Federica Baldi Filippo Ansaldi Francesca Bovis Francesca Caleri Gabriele Siciliano Gaia Cola Germana Perego Giacomo Lus Giampaolo Brichetto Giancarlo Icardi Gianmarco Bellucci Giorgio Da Rin Girolama Alessandra Marfia Giulia Vazzoler Giuseppe Liberatore Giuseppe Trivelli Graziella Callari Ilaria Gandoglia Ilaria Maietta Irene Schiavetti Jessica Frau Laura Sticchi Livia Pasquali Lorena Lorefice Luca Carmisciano Lucia Ruggiero M Manzino Marco Salvetti Margherita Monti Bragadin Maria Chiara Buscarinu Maria Cristina Gagliardi Maria Laura Stromillo Maria Pia Sormani Maria Teresa Ferrò Maria Teresa Rilla Marinella Clerico Mario Alberto Battaglia Marta Ponzano Marzia Fronza Massimo Del Sette Matilde Inglese

In patients with Multiple Sclerosis (pwMS) disease-modifying therapies (DMTs) affects immune response to antigens. Therefore, post-vaccination serological assessments are needed evaluate the effect of vaccine on SARS-CoV-2 antibody response.We designed a prospective multicenter cohort study enrolling pwMS who were scheduled for SARS-Cov-2 vaccination mRNA vaccines (BNT162b2, Pfizer/BioNTech,Inc or mRNA-1273, Moderna Tx,Inc). A blood collection before first dose and 4 weeks after second was...

10.1016/j.ebiom.2021.103581 article EN cc-by EBioMedicine 2021-09-22

Single cases and small series of Guillain-Barré syndrome (GBS) have been reported during the SARS-CoV-2 outbreak worldwide. We evaluated incidence clinical features GBS in a cohort patients from two regions northern Italy with highest number COVID-19.GBS diagnosed 12 referral hospitals Lombardy Veneto March April 2020 were retrospectively collected. As control population, 2019 same considered.Incidence was 0.202/100 000/month (estimated rate 2.43/100 000/year) vs 0.077/100 0.93/100 months...

10.1136/jnnp-2020-324837 article EN other-oa Journal of Neurology Neurosurgery & Psychiatry 2020-11-06

Guillain-Barré syndrome (GBS) is an acute polyradiculoneuropathy. Symptoms may vary greatly in presentation and severity. Besides weakness sensory disturbances, patients have cranial nerve involvement, respiratory insufficiency, autonomic dysfunction pain. To develop evidence-based guideline for the diagnosis treatment of GBS, using Grading Recommendations, Assessment, Development Evaluation (GRADE) methodology a Task Force (TF) European Academy Neurology (EAN) Peripheral Nerve Society (PNS)...

10.1111/ene.16073 article EN cc-by-nc-nd European Journal of Neurology 2023-10-10
Maria Pia Sormani Irene Schiavetti Matilde Inglese Luca Carmisciano Alice Laroni and 95 more Caterina Lapucci Valeria Visconti Carlo Serrati Ilaria Gandoglia Tiziana Tassinari Germana Perego Giampaolo Brichetto Paola Gazzola Antonio Mannironi Maria Laura Stromillo Cinzia Cordioli Doriana Landi Marinella Clerico Elisabetta Signoriello Eleonora Cocco Jessica Frau Maria Teresa Ferrò Alessia Di Sapio Livia Pasquali Monica Ulivelli F. Marinelli Matteo Pizzorno Graziella Callari Rosa Iodice Giuseppe Liberatore Francesca Caleri Anna Maria Repice Susanna Cordera Mario Alberto Battaglia Marco Salvetti Diego Franciotta Antonio Uccelli Alessandro Maglione Alessia Di Sapio Alessio Signori Alice Laroni Aniello Iovino Anna Maria Repice Antonio Mannironi Antonio Uccelli Carlo Serrati Carolina Gabri Nicoletti Caterina Lapucci Chiara Mancinelli Cinzia Cordioli Daiana Bezzini Daniele Carmagnini Davide Brogi Diego Franciotta Doriana Landi Eduardo Nobile‐Orazio Eleonora Cocco Elisabetta Signoriello Enri Nako Ester Assandrir F. Marinelli Federica Baldi Filippo Ansaldi Francesca Bovis Francesca Caleri Gabriele Siciliano Gaia Cola Germana Perego Giacomo Lus Giampaolo Brichetto Giancarlo Icardi Gianmarco Bellucci Giorgio Da Rin Girolama Alessandra Marfia Giulia Vazzoler Giuseppe Liberatore Giuseppe Trivelli Graziella Callari Ilaria Gandoglia Ilaria Maietta Irene Schiavetti Jessica Frau Laura Sticchi Livia Pasquali Lorena Lorefice Luca Carmisciano Lucia Ruggiero M Manzino Marco Salvetti Margherita Monti Bragadin Maria Chiara Buscarinu Maria Cristina Gagliardi Maria Laura Stromillo Maria Pia Sormani Maria Teresa Ferrò Maria Teresa Rilla Marinella Clerico Mario Alberto Battaglia Marta Ponzano Marzia Fronza

BackgroundIn this study we aimed to monitor the risk of breakthrough SARS-CoV-2 infection in patients with MS (pwMS) under different DMTs and identify correlates reduced protection.MethodsThis is a prospective Italian multicenter cohort study, long-term clinical follow-up CovaXiMS (Covid-19 vaccine Multiple Sclerosis) study. 1855 pwMS scheduled for mRNA vaccination were enrolled followed up mean time 10 months. The cumulative incidence Covid-19 cases was calculated before after December...

10.1016/j.ebiom.2022.104042 article EN cc-by-nc-nd EBioMedicine 2022-05-05

We studied the frequency and clinical correlates of different IgM specificities in 75 patients with neuropathy associated monoclonal gammopathy. Patients were tested for reactivity myelin-associated glycoprotein, P0, neurofilaments, tubulin by immunoblot; GM1, asialo-GM1, GM2, GD1a, GD1b, sulfatide, chondroitin sulfate C enzyme-linked immunosorbent assay; brain nerve glycolipids overlay high-performance thin-layer chromatography. Forty-two (56%) had high titers antibodies to MAG; 4 (5%),...

10.1002/ana.410360313 article EN Annals of Neurology 1994-09-01

Numerous sets of diagnostic criteria have sought to define chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and randomized trials systematic reviews treatment been published. The objective is prepare consensus guidelines on the definition, investigation CIDP. Disease experts a patient representative considered references retrieved from MEDLINE Cochrane Systematic Reviews in May 2004 prepared statements which were agreed an iterative fashion. Task Force good practice points...

10.1111/j.1468-1331.2006.01278.x article EN European Journal of Neurology 2006-04-01

Prognostic significance of hyperglycemia on short-term survival was evaluated in 72 patients with acute hemispheric stroke. All were admitted within 48 hours onset, and the neurologic deficit assessed by means a standardized score. A computed tomogram taken all cases admission. Mortality higher hyperglycemic no history diabetes mellitus (78%) than diabetic (45%) normoglycemic nondiabetic (29%) patients. In patients, glucose level correlated score lesion size tomogram. Reactive due to major...

10.1001/archneur.1985.04060070051014 article EN Archives of Neurology 1985-07-01

Many data point to a pathogenetic role for IgM antibodies the myelin-associated glycoprotein (MAG) in neuropathy associated with monoclonal gammopathy, supporting use of immune therapies affected patients. Almost 50% patients have been reported improve these therapies, but effect treatment on long-term prognosis remains unclear. We analysed outcome 25 26 (mean age at entry 65 years, range 45–85 years) and high anti-MAG IgM, first examined by us between 1984 1994. By January 1999, after mean...

10.1093/brain/123.4.710 article EN Brain 2000-04-01

In order to clarify the role of angiogenic factors in polyneuropathy POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, skin changes) syndrome, we measured serum concentrations vascular endothelial growth factor (VEGF) and erythropoietin (EPO) 11 patients correlated these with VEGF EPO peripheral nerve expression degree endoneurial vessel involvement. We found that syndrome was associated high levels and, conversely, low EPO. Similarly, nerves highly expressed blood...

10.1093/brain/awh519 article EN Brain 2005-06-23

We investigated the role of complement in pathogenesis demyelinating polyneuropathy that occurs some patients with IgM monoclonal gammopathy. Seven chronic sensorimotor and gammopathy were examined. In six patients, protein recognized an epitope shared by myelin-associated glycoprotein two peripheral-nerve glycolipids, whereas one patient, bound to unidentified myelin antigen. Direct indirect immunofluorescence immunoperoxidase assays showed colocalization along sheaths fibers components...

10.1056/nejm199003083221002 article EN New England Journal of Medicine 1990-03-08

Peripheral neuropathy was found in 12 (46%) of 26 patients with macroglobulinemia. The subclinical two. Anti-myelin-associated glycoprotein (MAG) activity six (50%) neuropathy. Sural nerve biopsies showed demyelination and IgM deposits on the myelin sheath. In one patient who had no anti-MAG activity, serum bound to peripheral by indirect immunofluorescence several protein bands other tissues immunoblot. five neuropathy, we binding M proteins components, but three there were endoneurial...

10.1212/wnl.37.9.1506 article EN Neurology 1987-09-01

Some patients with neuropathy have IgM M-proteins that bind to myelin and myelin-associated glycoprotein (MAG). We compared the binding properties of a human anti-MAG M-protein three mouse monoclonal antibodies (GEN-S1, GEN-S3, GEN-S8) antibody (HNK-1) binds both MAG natural killer cells. The GEN-S1, GEN-S8 bound different epitopes in polypeptide portion as shown by peptide mapping, deglycosylation competitive studies. M protein HNK-1 CNS PNS several additional bands 70K, 30K, 26K, 23K...

10.1212/wnl.34.10.1336 article EN Neurology 1984-10-01

In an unselected series of patients with monoclonal gammopathy undetermined significance (MGUS) we found neuropathy in 2 34 IgG (6%), 14 IgA (14%), and 8 26 IgM MGUS (31%). The was subclinical 6 (1 IgG, 1 IgA, 4 IgM). Patients or had a prominent motor impairment electrophysiologic morphologic findings suggestive predominant axonal degeneration. No deposit the M-protein sural nerve no reactivity detected these patients. sensory evidence demyelination. reacted myelin-associated glycoprotein...

10.1111/j.1600-0404.1992.tb06033.x article EN Acta Neurologica Scandinavica 2009-01-29

Objectives A few variants of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) have been described, but their frequency and evolution to typical CIDP remain unclear. To determine the characteristics variants, possible CIDP, treatment response. Methods We applied a set diagnostic criteria 460 patients included in database Italian with CIDP. Clinical response were reviewed for each patient. The Kaplan-Meier curve was used estimate progression rate from atypical Results At time...

10.1136/jnnp-2018-318714 article EN Journal of Neurology Neurosurgery & Psychiatry 2018-10-08

Objectives: We performed responsiveness comparison between the patient-reported Inflammatory Rasch-built Overall Disability Scale (I-RODS) and widely used clinician-reported Neuropathy Cause Treatment–Overall Limitation (INCAT-ONLS) in patients with Guillain-Barré syndrome (GBS), chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), immunoglobulin M–monoclonal gammopathy of undetermined significance related polyneuropathy (IgM-MGUSP). Methods: One hundred thirty-seven (GBS: 55,...

10.1212/wnl.0000000000001044 article EN Neurology 2014-11-07
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