Ángel Pérez Sempere

ORCID: 0000-0002-0195-2834
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Research Areas
  • Multiple Sclerosis Research Studies
  • Peripheral Neuropathies and Disorders
  • Polyomavirus and related diseases
  • Epilepsy research and treatment
  • Rheumatoid Arthritis Research and Therapies
  • Health Systems, Economic Evaluations, Quality of Life
  • Neurological disorders and treatments
  • Parkinson's Disease Mechanisms and Treatments
  • Pharmacological Effects and Toxicity Studies
  • Patient-Provider Communication in Healthcare
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Neurology and Historical Studies
  • Systemic Lupus Erythematosus Research
  • Migraine and Headache Studies
  • Glycogen Storage Diseases and Myoclonus
  • Healthcare Systems and Technology
  • Neurological and metabolic disorders
  • Clinical Reasoning and Diagnostic Skills
  • Parkinson's Disease and Spinal Disorders
  • Metabolism and Genetic Disorders
  • Pharmaceutical studies and practices
  • Trigeminal Neuralgia and Treatments
  • Traumatic Brain Injury and Neurovascular Disturbances
  • Botulinum Toxin and Related Neurological Disorders
  • Genetic Neurodegenerative Diseases

Universitat de Miguel Hernández d'Elx
2020-2024

Instituto de investigación sanitaria y biomédica de Alicante
2021-2024

Hospital General Universitario de Alicante Doctor Balmis
2015-2024

Instituto de Neurociencias
2023

Hospital Marina Baixa
2016

University of Alicante
2015

Hospital Vega Baja
1996-2011

Centro de Investigación Biomédica en Red
2009

Instituto de Salud Carlos III
2009

Centre for Biomedical Network Research on Rare Diseases
2008-2009

María Sepúlveda Thaís Armangué Núria Solà‐Valls Georgina Arrambide José Meca-Lallana and 79 more Celia Oreja‐Guevara Mar Mendibe Bilbao Amaya Álvarez de Arcaya Yolanda Aladro Bonaventura Casanova Javier Olascoaga Adolfo Jiménez‐Huete Mireya Fernández-Fournier Lluı́s Ramió-Torrentà Álvaro Cobo‐Calvo Montserrat Viñals Clara de Andrés Virginia Meca‐Lallana A Cervelló Carmen Calles Manuel Barón Rubio Cristina Ramo‐Tello Ana B. Caminero Elvira Munteis Alfredo Rodríguez Antigüedad Yolanda Blanco Pablo Villoslada Xavier Montalbán Francesc Graus Albert Saiz Laura Borrego Francisco José Julián Villaverde Ángel Pérez Sempere Luís Brieva Macarena Bonet Montserrat González-Platas Delón La Puma Sara Llufriú Eugenia H. Martínez Sabas Boyero Julián Benito‐León Juan Carlos López René Carlos Calderón Robles Jesús Foronda Laura Navarro-Cantó Tomás Millán Miguel Hervás Antonio Tallón Inmaculada Puertas Nuria Huertas Laura Rodríguez Redondo Sônia Santos Itziar Palmí Mônica Santos Salgado José E. Martínez Miguel A. Rubio Agustı́n Oterino Ramón Ara R Villaverde Teresa Ayuso Elena Erro M Di Marco Luisa María Villar José C. Álvarez‐Cermeño Eduardo Agüera Enrique Bescansa Isabel Yugüeros Miguel A. Tola Aida Orviz-García Tomás del Haro M Bestué Monserrat Gómez Luís Querol Elena Rodríguez Jordi Ballabriga Mar Tintoré Joaquín Castilló Jordi Río Delicias Muñoz Luciana Midaglia Ester Carreón Guarnizo José L. Casado Antonio Uclés Rosa García-Montero

To (1) determine the value of recently proposed criteria neuromyelitis optica (NMO) spectrum disorder (NMOSD) that unify patients with NMO and those limited forms (NMO/LF) aquaporin-4 immunoglobulin G (AQP4-IgG) antibodies; (2) investigate clinical significance serologic status in NMO.This was a retrospective, multicenter study 181 fulfilling 2006 (n = 127) or NMO/LF AQP4-IgG 54). myelin oligodendrocyte glycoprotein (MOG-IgG) antibodies were tested using cell-based assays.Patients mainly...

10.1212/nxi.0000000000000225 article EN cc-by-nc-nd Neurology Neuroimmunology & Neuroinflammation 2016-04-15
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

<h3>Objective</h3> To evaluate the safety and efficacy of cladribine tablets in patients still experiencing active relapsing MS despite interferon (IFN)-β treatment. <h3>Methods</h3> A 96-week phase II study, randomizing treated with IFN-β to 3.5 mg/kg/IFN-β or placebo/IFN-β. Patients were receive placebo/IFN-β a 2:1 ratio (n = 172) exploratory outcomes being assessed. <h3>Results</h3> Adverse events (AEs) serious AEs similar across treatment groups, except lymphopenia. Fifty 124 (40.3%)...

10.1212/nxi.0000000000000477 article EN cc-by-nc-nd Neurology Neuroimmunology & Neuroinflammation 2018-07-12

Multiple sclerosis patients who discontinue using natalizumab are at risk of a rebound in disease activity. However, the optimal alternative therapy is not currently known.We report on clinical and MRI data patient safety group relapsing-remitting multiple tested seropositive for JC virus have switched from to fingolimod because concerns regarding PML risks.The test antibodies was performed 18 were being treated with more than 1 year. Eight while seronegative continued natalizumab.After...

10.1111/ane.12082 article EN Acta Neurologica Scandinavica 2013-01-22

Background: Therapeutic inertia (TI) in multiple sclerosis (MS) is defined as the lack of treatment escalation when there evidence disease activity. Limited information available on physician-related factors influencing TI MS. The aim study was to evaluate whether physicians' risk preferences are associated with management MS by applying concepts from behavioral economics. Methods: A neurologists managing patients conducted Spain. Participants answered questions regarding 20 case-scenarios...

10.3389/fneur.2017.00065 article EN cc-by Frontiers in Neurology 2017-03-01

Abstract A questionnaire designed to screen Parkinson's disease (PD) in literate populations has been developed. It consists of nine questions, self‐administered at medical facilities or by mail, and a scale weights for ascribing scores specific questions when the answer is positive. The were chosen be symptom PD determined from answers provided 37 patients neurological outpatient clinic. sensitivity was tested on different population same clinic−50 individuals‐and specificity group 100...

10.1002/mds.870100518 article EN Movement Disorders 1995-09-01

Abstract We assessed the prevalence of Parkinson's disease in Cantalejo, Spain. In 1994, we screened 1,579 persons (age ≥ 40 years) using a high‐sensitivity method. Cases fulfilling established clinical criteria were followed for minimum 3 years. Prevalences compared with those from other door‐to‐door surveys. detected 27 individuals parkinsonism, 20 whom had disease. The increased age and, when age‐adjusted to European standards, was 9.01 per 1,000 years and over; 10.78 men 5.23 women). Of...

10.1002/mds.10087 article EN Movement Disorders 2002-02-20

The objective in this paper is to compare the cumulative incidence and density of therapy-related acute myeloid leukaemia two cohorts patients with multiple sclerosis treated mitoxantrone, previously reported data literature. Six new cases were observed by prospectively following Spanish series 142 88 worsening relapsing secondary-progressive disease mitoxantrone. A literature review shows 32 further reported, 65.6% which are promyelocytic leukaemia. Five fulfilled diagnostic criteria for...

10.1177/1352458509107015 article EN Multiple Sclerosis Journal 2009-10-13

The management of multiple sclerosis (MS) is rapidly changing by the introduction new and more effective disease-modifying agents. importance risk stratification was confirmed results on disease progression predicted different score systems. Despite these advances, we know very little about medical decisions under uncertainty in MS. goal this study to i) identify whether overconfidence, tolerance risk/uncertainty, herding influence decisions, ii) evaluate frequency therapeutic inertia...

10.1186/s12883-016-0577-4 article EN cc-by BMC Neurology 2016-05-04

Abstract Objective Pivotal trial have shown that patients with multiple sclerosis (MS) receiving ocrelizumab had better outcomes. However, data on in clinical practice are limited. The aim of this study was to evaluate the preliminary safety profile and effectiveness treatment for a real‐world setting. Methods We conducted retrospective including consecutive from nine public hospitals south‐eastern Spain who received after it approved. Results A total 228 MS were included (144...

10.1002/acn3.51282 article EN Annals of Clinical and Translational Neurology 2020-12-25
Izanne Roos Emmanuelle Leray Federico Frascoli Romain Casey J William L Brown and 95 more Dana Horáková Eva Havrdová Maria Trojano Francesco Patti Guillermo Izquierdo Sara Eichau Marco Onofrj Alessandra Lugaresi Alexandre Prat Marc Girard Pierre Grammond Patrizia Sola Diana Ferraro Serkan Özakbaş Roberto Bergamaschi María José Sá Elisabetta Cartechini Cavit Boz Franco Granella Raymond Hupperts Murat Terzi Jeannette Lechner‐Scott Daniele Spitaleri Vincent Van Pesch Aysun Soysal Javier Olascoaga Julie Prévost Eduardo Agüera Mark Slee Tünde Csépány Recai Türkoğlu Youssef Sidhom Riadh Gouider Bart Van Wijmeersch Pamela McCombe Richard Macdonell Alasdair Coles Charles B. Malpas Helmut Butzkueven Sandra Vukusic Tomáš Kalinčík Pierre Duquette François Grand’Maison Gerardo Iuliano Cristina Ramo‐Tello Claudio Solaro José Antonio Cabrera-Gómez Maria Edite Rio R. Fernandez Bolanos Vahid Shaygannejad Celia Oreja‐Guevara José Luis Sánchez-Menoyo Thor Petersen Ayşe Altıntaş Michael Barnett Shlomo Flechter Yára Dadalti Fragoso Maria Pia Amato Fraser Moore Radek Ampapa Freek Verheul Suzanne Hodgkinson Edgardo Cristiano Bassem Yamout Guy Laureys José Andrés Domínguez Cees Zwanikken Norma Deri Enikő Dobos Cárlos Vrech Ernest Butler Csilla Rózsa Tatjana Petkovska‐Boskova Rana Karabudak Cecília Rajda Jabir Alkhaboori Maria Luisa Saladino Cameron Shaw Neil Shuey Steve Vucic Ángel Pérez Sempere Jamie Campbell Piroska Imre Bruce Taylor Anneke van der Walt Ludwig Kappos E Roullet Orla Gray Magdolna Simó Carmen Adella Sîrbu Bruno Brochet François Cotton de Sèze Armelle Dion Pascal Douek

Abstract In multiple sclerosis, treatment start or switch is prompted by evidence of disease activity. Whilst immunomodulatory therapies reduce activity, the time required to attain maximal effect unclear. this study we aimed develop a method that allows identification manifest fully and clinically sclerosis treatments (‘therapeutic lag’) on clinical activity represented relapses progression-of-disability events. Data from two registries, MSBase (multinational) OFSEP (French), were used....

10.1093/brain/awaa231 article EN Brain 2020-06-24

<h3>Objective</h3> To understand COVID-19 characteristics in people with multiple sclerosis (MS) and identify high-risk individuals due to their immunocompromised state resulting from the use of disease-modifying treatments. <h3>Methods</h3> Retrospective multicenter registry patients MS suspected or confirmed diagnosis available disease course (mild = ambulatory; severe hospitalization; critical intensive care unit/death). Cases were analyzed for associations between identifying risk...

10.1212/nxi.0000000000001024 article EN cc-by-nc-nd Neurology Neuroimmunology & Neuroinflammation 2021-06-24

A prospective study of 98 consecutive adults with a first seizure to determine the most important etiological factors and optimum diagnostics. 27 were thought have cryptogenic seizures. Main causes symptomatic seizures were: cerebral infarction, alcohol-withdrawal, CNS infections, tumors, vascular malformations, traumatism miscellanea. Eight infected by human immunodeficiency virus (HIV-1) representing 8.2% all patients 20% 15-45-year age group. CT disclosed structural lesions in 33 cases....

10.1111/j.1600-0404.1992.tb05054.x article EN Acta Neurologica Scandinavica 1992-08-01

Objective: The aim of this study is to report the clinical profile and outcome longitudinally extensive transverse myelitis (LETM). Methods: We prospectively studied adult patients who presented with LETM from January 2008 December 2011. Information on demographic, course, magnetic resonance imaging (MRI) was collected. HLA-DRB1 genotype compared those 225 normal controls MS (228) neuromyelitis optica (NMO) (22). Results: In total, 23 (16 female) a median age 44.5 years (range: 20–77 years)...

10.1177/1352458512461968 article EN Multiple Sclerosis Journal 2012-10-04

Objective To assess patients’ preferences for a range of disease-modifying therapy (DMT) attributes in multiple sclerosis (MS). Design A cross-sectional observational study. Setting The data reported were from 17 MS units throughout Spain. Participants Adult patients with relapsing-remitting MS. Main outcome conjoint analysis was applied to preferences. total 221 completed survey 10 hypothetical DMT profiles developed using an orthogonal design and rating 1 (most acceptable) (least...

10.1136/bmjopen-2016-014433 article EN cc-by-nc BMJ Open 2017-03-01

Geographical variations in the incidence and prevalence of multiple sclerosis have been reported globally. Latitude as a surrogate for exposure to ultraviolet radiation but also other lifestyle environmental factors are regarded drivers this variation. No previous studies evaluated geographical variation risk secondary progressive sclerosis, an advanced form that is characterized by steady accrual irreversible disability. We differences relation latitude country residence, modified...

10.1093/brain/awad218 article EN cc-by-nc Brain 2023-06-25
Cyrus Daruwalla Vahid Shaygannejad Serkan Özakbaş Eva Havrdová Dana Horáková and 87 more Raed Alroughani Cavit Boz Francesco Patti Marco Onofrj Alessandra Lugaresi Sara Eichau Marc Girard Alexandre Prat Pierre Duquette Bassem Yamout Samia J. Khoury Seyed Aidin Sajedi Recai Türkoğlu Ayşe Altıntaş Olga Skibina Katherine Buzzard Pierre Grammond Rana Karabudak Anneke van der Walt Helmut Butzkueven Davide Maimone Jeannette Lechner‐Scott Aysun Soysal Nevin John Julie Prévost Daniele Spitaleri Cristina Ramo‐Tello Oliver Gerlach Gerardo Iuliano Matteo Foschi Radek Ampapa Vincent Van Pesch Michael Barnett Nevin Shalaby Marie D’hooghe Jens Kühle María José Sá Marzena J. Fabis‐Pedrini Allan G. Kermode Saloua Mrabet Riadh Gouider Suzanne Hodgkinson Guy Laureys Liesbeth Van Hijfte Richard Macdonell Celia Oreja‐Guevara Edgardo Cristiano Pamela McCombe José Luis Sánchez-Menoyo Bhim Singhal Yolanda Blanco Stella Hughes Justin Garber Claudio Solaro Chris McGuigan Bruce Taylor Koen de Gans Mario Habek Abdullah Al‐Asmi Simu Mihaela Tamara Castillo‐Triviño Talal Al‐Harbi Juan Ignacio Rojas Orla Gray Dheeraj Khurana Bart Van Wijmeersch Nikolaos Grigoriadis Jihad Inshasi Jiwon Oh Eduardo Agüera Yára Dadalti Fragoso Fraser Moore Cameron Shaw Seyed Mohammad Baghbanian Neil Shuey Barbara Willekens Todd A. Hardy D. Decoo Ángel Pérez Sempere Deborah Field Ray Wynford–Thomas Nick Cunniffe Izanne Roos Charles B. Malpas Alasdair Coles Tomáš Kalinčík J William L Brown

Background: The prognostic significance of non-disabling relapses in people with relapsing-remitting multiple sclerosis (RRMS) is unclear. Objective: To determine whether early predict disability accumulation RRMS. Methods: We redefined mild MSBase as ‘non-disabling’, and moderate or severe ‘disabling’. used mixed-effects Cox models to compare 90-day confirmed events exclusively within 2 years RRMS diagnosis those no relapses; any disabling relapses. Analyses were stratified by...

10.1177/13524585231151951 article EN cc-by Multiple Sclerosis Journal 2023-02-27

Background and Purpose The aim of this study was to determine the incidence transient ischemic attacks (TIAs) minor strokes (MISs) in Segovia, Spain. Methods A 2-year prospective community-based register TIAs MISs established Segovia from February 16, 1992, 15, 1994. Every patient underwent a complete clinical evaluation cranial CT scan. Sex- age-specific rates with 95% confidence intervals (CIs) were calculated for all ages. Results total series included 235 patients; 103 suffered 132 MISs....

10.1161/01.str.27.4.667 article EN Stroke 1996-04-01

Objective To study the molecular genetic and clinical features of cerebral cavernous malformations (CCM) in a cohort Spanish patients. Methods We analyzed CCM1, CCM2, CCM3 genes by MLPA direct sequencing exons intronic boundaries 94 familial forms 41 sporadic cases CCM patients extraction. When available, RNA studies were performed seeking for alternative or cryptic splicing. Results A total 26 pathogenic mutations, 22 which predict truncated proteins, identified 29 three cases. The...

10.1371/journal.pone.0086286 article EN cc-by PLoS ONE 2014-01-23

Objectives: The aim of this study was to describe the tolerability, safety, and effectiveness ocrelizumab for primary progressive multiple sclerosis (PPMS) relapsing (RMS) in a clinical practice setting. Methods: In retrospective observational study, we analyzed MRI data all patients with PPMS RMS who had received at least one infusion two health areas south-eastern Spain. Patients involved any trial those follow-up shorter than 6 months were excluded. Results: cohort included 70 (42 women)...

10.3389/fneur.2020.592304 article EN cc-by Frontiers in Neurology 2021-01-15

SYNOPSIS Twenty‐seven patients with acute severe headache of recent onset were prospectively recruited in the Emergency Room. Mean duration was 61 hours. CT scan disclosed subarachnoid bleeding 4 and spinal tap revealed hemorrhage (SAH) 5 normal scan. In most SAH cases pain bilateral, very intense involving occipital region. Four these had doubtful or no nuchal rigidity one, improved while every case an (if normal) a lumbar puncture are warranted to help rule out SAH.

10.1111/j.1526-4610.1994.hed3403172.x article EN Headache The Journal of Head and Face Pain 1994-03-01
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