Murat Terzi

ORCID: 0000-0002-3586-9115
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Research Areas
  • Multiple Sclerosis Research Studies
  • Peripheral Neuropathies and Disorders
  • Polyomavirus and related diseases
  • Rheumatoid Arthritis Research and Therapies
  • Autoimmune and Inflammatory Disorders Research
  • Systemic Sclerosis and Related Diseases
  • Systemic Lupus Erythematosus Research
  • Immunotherapy and Immune Responses
  • Acute Lymphoblastic Leukemia research
  • Sphingolipid Metabolism and Signaling
  • Health Systems, Economic Evaluations, Quality of Life
  • Long-Term Effects of COVID-19
  • SARS-CoV-2 and COVID-19 Research
  • Neurological disorders and treatments
  • Voice and Speech Disorders
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Restless Legs Syndrome Research
  • Mycobacterium research and diagnosis
  • Parkinson's Disease Mechanisms and Treatments
  • Migraine and Headache Studies
  • Myasthenia Gravis and Thymoma
  • Peripheral Nerve Disorders
  • Dysphagia Assessment and Management
  • Dermatological and Skeletal Disorders
  • Genomic variations and chromosomal abnormalities

Ondokuz Mayıs University
2016-2025

Biogen (Switzerland)
2024

Karolinska Institutet
2020-2024

Griffith University
2023

The University of Melbourne
2016-2023

QIMR Berghofer Medical Research Institute
2023

Barwon Health
2023

The University of Queensland
2023

University of Newcastle Australia
2023

University of Tasmania
2023

Neuromyelitis optica spectrum disorder (NMOSD) is a relapsing, autoimmune, inflammatory that typically affects the optic nerves and spinal cord. At least two thirds of cases are associated with aquaporin-4 antibodies (AQP4-IgG) complement-mediated damage to central nervous system. In previous small, open-label study involving patients AQP4-IgG–positive disease, eculizumab, terminal complement inhibitor, was shown reduce frequency relapse.

10.1056/nejmoa1900866 article EN New England Journal of Medicine 2019-05-03

<h3>Importance</h3> Within 2 decades of onset, 80% untreated patients with relapsing-remitting multiple sclerosis (MS) convert to a phase irreversible disability accrual termed secondary progressive MS. The association between disease-modifying treatments (DMTs), and this conversion has rarely been studied never using validated definition. <h3>Objective</h3> To determine the use, type of, timing DMTs risk MS diagnosed <h3>Design, Setting, Participants</h3> Cohort study prospective data from...

10.1001/jama.2018.20588 article EN JAMA 2019-01-15

Prevention of irreversible disability is currently the most important goal disease modifying therapy for multiple sclerosis. The outcomes used in clinical trials rely on progression Expanded Disability Status Scale score confirmed over 3 or 6 months. However, sensitivity and stability this metric has not been extensively evaluated. Using global MSBase cohort study, we evaluated 48 criteria progression, testing three definitions baseline disability, two magnitude, long-term irreversibility...

10.1093/brain/awv258 article EN Brain 2015-09-10

Objective In patients suffering multiple sclerosis activity despite treatment with interferon β or glatiramer acetate, clinicians often switch therapy to either natalizumab fingolimod. However, no studies have directly compared the outcomes of switching these agents. Methods Using MSBase, a large international, observational, prospectively acquired cohort study, we identified relapsing–remitting experiencing relapses disability progression within 6 months immediately preceding...

10.1002/ana.24339 article EN Annals of Neurology 2014-12-27

Background: Demyelinating lesions over 20 mm in size, referred to as tumefactive demyelinating lesions, can be misdiagnosed being either a tumor or an abscess. Although some radiological characteristics help make differential diagnosis easier, cerebral biopsy may still necessary. Objective: Our objective was assess the clinical of with without multiple sclerosis (MS), and present follow-up data for 54 patients lesions. Methods: Demographic, clinical, laboratory were gathered treatment...

10.1177/1352458512438237 article EN Multiple Sclerosis Journal 2012-03-14

Timely initiation of effective therapy is crucial for preventing disability in multiple sclerosis; however, treatment response varies greatly among patients. Comprehensive predictive models individual are lacking. Our aims were: (i) to develop algorithms using demographic, clinical and paraclinical predictors patients with (ii) evaluate accuracy, internal external validity these algorithms. This study evaluated 27 seven disease-modifying therapies MSBase, a large global cohort study....

10.1093/brain/awx185 article EN Brain 2017-06-29

After multiple sclerosis (MS) relapse while a patient is receiving an injectable disease-modifying drug, many physicians advocate therapy switch, but the relative effectiveness of different switch decisions often uncertain.To compare effect oral immunomodulator fingolimod with that all immunomodulators (interferons or glatiramer acetate) on rate, disability, and treatment persistence in patients active MS.Matched retrospective analysis data collected prospectively from MSBase, international,...

10.1001/jamaneurol.2014.4147 article EN JAMA Neurology 2015-02-09
Bruce Cree Gary Cutter Jerry S. Wolinsky Mark S. Freedman Gıancarlo Comı and 95 more Gavin Giovannoni Hans-Peter Hartung Douglas L. Arnold Jens Kühle Valerie J. Block Frederick Munschauer Frédéric Sedel Fred Lublin Stephen C. Reingold Pierre Duquette Tobias Derfuß Franz Fazekas Maria Pia Sormani Robert P. Lisak Jennifer Graves Stephen Krieger Rana Zabad Scott D. Newsome Joshua Barton Richard Macdonell Mark Marriott Nina De Klippel Guy Laureys Barbara Willekens Virginia Devonshire Mark S. Freedman J Girard Paul S. Giacomini Roger McKelvey Daniel Selchen Galina Vorobeychik Ludivine Chamard Witkowski Radek Ampapa Jana Lízrová Preiningerová Eva Meluzínová Radomír Taláb Marta Vachová Orhan Aktaş Mathias Buttmann Elias-Hamp Birte Tania Kuempfel Friedemann Paul Daniela Rau Gerd Reifschneider Piotr Sokolowski Hayrettin Tumani Mária Sátori Carlo Pozzilli Agata Klosek Jozef Koscielniak Waldemar Fryze Małgorzata Zajda Rafael Arroyo González Guillermo Izquierdo Ayuso Victoria Fernández Sánchez Celia Oreja Guevara Jose Enrique Martinez Rodriguez Xavier Montalbán Lluís Ramió‐Torrentà Lou Brundin Jan Lycke Murat Terzi Joe Guadagno Don J. Mahad Adrian Pace Klaus Schmierer Ahmed Toosy Stewart Webb Mark Agius Lilyana Amezcua Michelle Apperson Bridget Bagert Daniel S. Bandari Evanthia Bernitsas Jonathan Calkwood Jonathan Carter Bruce A. Cohen Devon Conway Joanna Cooper John R. Corboy Patricia K. Coyle Bruce Cree Mitchel Freedman Corey C. Ford Edward Fox Myla Goldman Benjamin Greenberg Mariko Kita Thomas Leist Sharon Lynch Aaron Miller Harold Moses Robert T. Naismith Mary Ann Picone Perminder Bhatia

10.1016/s1474-4422(20)30347-1 article EN The Lancet Neurology 2020-10-24

Oral immunotherapies have become a standard treatment in relapsing-remitting multiple sclerosis. Direct comparison of their effect on relapse and disability is needed.We identified all patients with sclerosis treated teriflunomide, dimethyl fumarate or fingolimod, minimum 3-month persistence follow-up the global MSBase cohort study. Patients were matched using propensity scores. Three pairwise analyses compared annualised rates hazards accumulation, improvement discontinuation (analysed...

10.1136/jnnp-2018-319831 article EN Journal of Neurology Neurosurgery & Psychiatry 2019-01-13

Radiologically isolated syndrome (RIS) represents the earliest detectable preclinical phase of multiple sclerosis (MS) punctuated by incidental magnetic resonance imaging (MRI) white matter anomalies within central nervous system.

10.1001/jamaneurol.2023.2815 article EN JAMA Neurology 2023-08-21
Izanne Roos Stella Hughes Gavin McDonnell Charles B. Malpas Sifat Sharmin and 88 more Cavit Boz Raed Alroughani Serkan Özakbaş Katherine Buzzard Olga Skibina Anneke van der Walt Helmut Butzkueven Jeannette Lechner‐Scott Jens Kühle Murat Terzi Guy Laureys Liesbeth Van Hijfte Nevin John Pierre Grammond François Grand’Maison Aysun Soysal Ana Voldsgaard Jensen Peter Vestergaard Rasmussen Kristina Bacher Svendsen Ismael Barzinji Helle Hvilsted Nielsen Tobias Sejbæk Sivagini Prakash Morten Stilund Arkadiusz Węglewski Nadia Mubder Issa Matthias Kant Finn Sellebjerg Orla Gray Melinda Magyari Tomáš Kalinčík José Antonio Cabrera-Gómez E Roullet Cees Zwanikken Leontien Den Braber‐Moerland Michael Barnett Suzanne Hodgkinson Justin Garber Mark Slee Pamela McCombe Bruce Taylor Richard Macdonell Jennifer Massey Vincent Van Pesch D. Decoo Barbara Willekens Yára Dadalti Fragoso Julie Prévost Alexandre Prat Marc Girard Pierre Grammond Catherine Larochelle Jiwon Oh Patrice H. Lalive Claudio Gobbi Dana Horáková Eva Havrdová Radek Ampapa Guillermo Izquierdo Sara Eichau José Luis Sánchez-Menoyo Cristina Ramo‐Tello Yolanda Blanco Albert Saiz Sarah Besora Vahid Shaygannejad Elisabetta Cartechini Matteo Diamanti Maria Pia Amato Daniele Spitaleri Francesco Patti Clara Grazia Chisari Emanuele D’Amico L Salvatore Bassem Yamout Samia J. Khoury Abdullah Al‐Asmi María José Sá Talal Al‐Harbi Rana Karabudak Recai Türkoğlu Trevor J. Kilpatrick John King Ai‐Lan Nguyen Chris Dwyer Mastura Monif Lisa Taylor Josephine Baker

Importance Ocrelizumab, a humanized monoclonal antibody targeted against CD20+ B cells, reduces the frequency of relapses by 46% and disability worsening 40% compared with interferon beta 1a in relapsing-remitting multiple sclerosis (MS). Rituximab, chimeric anti-CD20 agent, is often prescribed as an off-label alternative to ocrelizumab. Objective To evaluate whether effectiveness rituximab noninferior ocrelizumab MS. Design, Setting, Participants This was observational cohort study...

10.1001/jamaneurol.2023.1625 article EN JAMA Neurology 2023-06-12

Patients with pediatric-onset multiple sclerosis (POMS) typically experience higher levels of inflammation more frequent relapses, and though patients POMS usually recover from relapses better than adults, reach irreversible disability at a younger age adult-onset patients. There have been few randomized, placebo-controlled clinical trials (MS) disease-modifying therapies (DMTs) in POMS, most available data are based on observational studies off-label use DMTs approved for adults. We...

10.1212/wnl.0000000000208114 article EN Neurology 2024-03-06

<h3>Background</h3> Age at onset (AAO) in multiple sclerosis (MS) is an important marker of disease severity and may have prognostic significance. Understanding what factors can influence AAO shed light on the aetiology this complex disease, applications diagnostic process. <h3>Methods</h3> The study cohort 22 162 eligible patients from 21 countries was extracted MSBase registry. Only with MS aged ≥16 years were included. To reduce heterogeneity, only centres largely European descent...

10.1136/jnnp-2016-314013 article EN Journal of Neurology Neurosurgery & Psychiatry 2016-11-03

<h3>Objective</h3> To test the hypothesis that immunotherapy prevents long-term disability in relapsing-remitting multiple sclerosis (MS), we modeled outcomes 14,717 patients. <h3>Methods</h3> We studied patients from MSBase followed for ≥1 year, with ≥3 visits, visit per and exposed to MS therapy, a subset of ≥15-year follow-up. Marginal structural models were used compare cumulative hazards 12-month confirmed increase decrease disability, Expanded Disability Status Scale (EDSS) step 6,...

10.1212/wnl.0000000000011242 article EN Neurology 2020-12-28

Background: The risk factors for conversion from relapsing-remitting to secondary progressive multiple sclerosis remain highly contested. Objective: aim of this study was determine the demographic, clinical and paraclinical features that influence sclerosis. Methods: Patients with adult-onset relapsing–remitting at least four recorded disability scores were selected MSBase, a global observational cohort. objectively defined evaluated time points per patient using multivariable marginal Cox...

10.1177/1352458519868990 article EN Multiple Sclerosis Journal 2019-08-09

To investigate pregnancy-related disease activity in a contemporary multiple sclerosis (MS) cohort.Using data from the MSBase Registry, we included pregnancies conceived after 31 Dec 2010 women with relapsing-remitting MS or clinically isolated syndrome. Predictors of intrapartum relapse, and postpartum relapse disability progression were determined by clustered logistic regression Cox analyses.We 1998 1619 MS. Preconception annualized rate (ARR) was 0.29 (95% CI 0.27-0.32), fell to 0.19...

10.1212/wnl.0000000000012084 article EN Neurology 2021-04-21

<h3>Background and Objectives</h3> To evaluate the rate of return disease activity after cessation multiple sclerosis (MS) disease-modifying therapy. <h3>Methods</h3> This was a retrospective cohort study from 2 large observational MS registries: MSBase OFSEP. Patients with relapsing-remitting who had ceased therapy were followed up for subsequent 12 months included in analysis. The primary outcome annualized relapse discontinuation stratified by patients did, did not, commence secondary...

10.1212/wnl.0000000000201029 article EN Neurology 2022-08-17

Nutrition modulation can reduce multiple sclerosis (MS) related symptoms and fatigue severity. Mediterranean diet may be beneficial regarding anti-inflammatory components. However, previous studies are limited. This study aims to investigate the relationship between adherence MS-related severity.One hundred two adult MS patients were enrolled in this cross-sectional study. Dietary was assessed using assessment tool (MEDAS). determined symptom checklist (MS-RS), severity scale (FSS) applied....

10.1080/1028415x.2022.2034241 article EN Nutritional Neuroscience 2022-02-10
Tomáš Kalinčík Sifat Sharmin Izanne Roos Mark S. Freedman Harold Atkins and 95 more Joachim Burman Jennifer Massey Ian Sutton Barbara Withers Richard Macdonell Andrew Grigg Øivind Torkildsen Lars Bø Anne Kristine Lehmann Eva Havrdová Eva Krasulová Marek Trněný Tomáš Kozák Anneke van der Walt Helmut Butzkueven Pamela McCombe Olga Skibina Jeannette Lechner‐Scott Barbara Willekens Elisabetta Cartechini Serkan Özakbaş Raed Alroughani Jens Kühle Francesco Patti Pierre Duquette Alessandra Lugaresi Samia J. Khoury Mark Slee Recai Türkoğlu Suzanne Hodgkinson Nevin John Davide Maimone María José Sá Vincent Van Pesch Oliver Gerlach Guy Laureys Liesbeth Van Hijfte Rana Karabudak Daniele Spitaleri Tünde Csépány Riadh Gouider Tamara Castillo‐Triviño Bruce Taylor Basil Sharrack John A. Snowden Dana Horáková Katherine Buzzard Murat Terzi Alexandre Prat Marc Girard Pierre Grammond Michael Barnett Grace Stewart Marco Onofrj Guillermo Izquierdo Sara Eichau François Grand’Maison Julie Prévost Bart Van Wijmeersch Maria Pia Amato Vahid Shaygannejad Cavit Boz R. Fernandez Bolanos Aysun Soysal Cristina Ramo‐Tello Claudio Solaro Claudio Gobbi José Antonio Cabrera-Gómez E Roullet Cees Zwanikken Leontien Den Braber‐Moerland Norma Deri Maria Luisa Saladino Edgardo Cristiano Juan Ignacio Rojas Cárlos Vrech Cameron Shaw Neil Shuey Mike Boggild Ik Lin Tan Todd A. Hardy D. Decoo Fraser Moore Jiwon Oh Patrice H. Lalive Radek Ampapa Thor Petersen Celia Oreja‐Guevara Ángel Pérez Sempere José Andrés Domínguez Sarah Besora Stella Hughes Orla Gray Nikolaos Grigoriadis Piroska Imre

Autologous hematopoietic stem cell transplant (AHSCT) is available for treatment of highly active multiple sclerosis (MS).

10.1001/jamaneurol.2023.1184 article EN JAMA Neurology 2023-05-15

Patients with the 'aggressive' form of multiple sclerosis accrue disability at an accelerated rate, typically reaching Expanded Disability Status Score (EDSS) ≥ 6 within 10 years symptom onset. Several clinicodemographic factors have been associated aggressive sclerosis, but less research has focused on clinical markers that are present in first year disease. The development early predictive models is essential to optimize treatment this subtype. We evaluated whether patients who will...

10.1093/brain/awaa081 article EN Brain 2020-02-29
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