Resultados globales: 5 registros encontrados en 0.02 segundos.
Artículos, Encontrados 4 registros
Documentos de investigación, Encontrados 1 registros
Artículos Encontrados 4 registros  
1.
10 p, 1.6 MB Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course / Gil-Varea, Elia (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Urcelay, Elena (Hospital Clinico San Carlos, Instituto de Investigacion Sanitaria San Carlos (IdISSC). Immunology Department) ; Vilariño-Güell, Carles (University of British Columbia. Department of Medical Genetics) ; Costa, Carme (Hospital Universitari Vall d'Hebron. Institut de Recerca ) ; Midaglia, Luciana (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Matesanz, Fuencisla (Instituto de Parasitología y Biomedicina "López Neyra", Consejo Superior de Investigaciones Científicas (IPBLN-CSIC). Department of Cell Biology and Immunology) ; Rodríguez-Antigüedad, Alfredo (Hospital Universitario Basurto-Osakidetza. Servicio de Neurología) ; Oksenberg, Jorge (University of California. Department of Neurology) ; Espino-Paisan, Laura (Hospital Clinico San Carlos, Instituto de Investigacion Sanitaria San Carlos (IdISSC). Immunology Department) ; Dessa Sadovnick, A. (University of British Columbia. Department of Medical Genetics) ; Saiz, Albert (Hospital Clinic and Institut d'Investigació Biomèdica Pi i Sunyer (IDIBAPS). Neurology Service) ; Villar, Luisa M. (Hospital Ramon y Cajal, (IRYCIS). Departments of Immunology and Neurology, Multiple Sclerosis Unit) ; García-Merino, Juan Antonio (Puerta de Hierro University Hospital and Research Institute, Universidad Autónoma de Madrid. Neuroimmunology Unit) ; Ramió-Torrentà, Lluís (Neuroimmunology and Multiple Sclerosis Unit, Department of Neurology, Hospital Dr Josep Trueta, IDIBGI, University of Girona, Girona, Spain) ; Triviño, Juan Carlos (Genomic Systems, Valencia, Spain) ; Quintana, Ester (Neuroimmunology and Multiple Sclerosis Unit, Department of Neurology, Hospital Dr Josep Trueta, IDIBGI, University of Girona, Girona, Spain) ; Robles, René (Neuroimmunology and Multiple Sclerosis Unit, Department of Neurology, Hospital Dr Josep Trueta, IDIBGI, University of Girona, Girona, Spain) ; Sánchez-López, Antonio (Puerta de Hierro University Hospital and Research Institute, Universidad Autónoma de Madrid. Neuroimmunology Unit) ; Arroyo, Rafael (Hospital Universitario Quirón Salud. Servicio de Neurología) ; Alvarez-Cermeño, Jose C. (Hospital Ramon y Cajal, (IRYCIS). Departments of Immunology and Neurology, Multiple Sclerosis Unit) ; Vidal-Jordana, Angela (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Malhotra, Sunny (Hospital Universitari Vall d'Hebron. Institut de Recerca ) ; Fissolo, Nicolas (Hospital Universitari Vall d'Hebron. Institut de Recerca ) ; Montalban, Xavier (Hospital Universitari Vall d'Hebron. Institut de Recerca ) ; Comabella, Manuel (Hospital Universitari Vall d'Hebron. Institut de Recerca ) ; Universitat Autònoma de Barcelona
It remains unclear whether disease course in multiple sclerosis (MS) is influenced by genetic polymorphisms. Here, we aimed to identify genetic variants associated with benign and aggressive disease courses in MS patients. [...]
2018 - 10.1186/s12974-018-1307-1
Journal of neuroinflammation, Vol. 15 (september 2018)  
2.
7 p, 1018.1 KB Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients / Sadovnick, A. Dessa (Division of Neurology, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, V6T 1Z3, Canada) ; Traboulsee, Anthony L. (Division of Neurology, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, V6T 1Z3, Canada) ; Bernales, Cecily Q. (Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, V6T 1Z3, Canada) ; Ross, Jay P. (Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, V6T 1Z3, Canada) ; Forwell, Amanda L. (Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, V6T 1Z3, Canada) ; Yee, Irene M. (Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, V6T 1Z3, Canada) ; Guillot-Noel, Lena (Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, France) ; Fontaine, Bertrand (Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, France) ; Cournu-Rebeix, Isabelle (Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM, France) ; Alcina, Antonio (Department of Cell Biology and Immunology, Instituto de Parasitología y Biomedicina López Neyra (IPBLN), CSIC, 18100 Granada, Spain) ; Fedetz, Maria (Unidad de Esclerosis Múltiple, Hospital Universitario Virgen Macarena, 41071 Sevilla, Spain) ; Izquierdo, Guillermo (Unidad de Esclerosis Múltiple, Hospital Universitario Virgen Macarena, 41071 Sevilla, Spain) ; Matesanz, Fuencisla (Department of Cell Biology and Immunology, Instituto de Parasitología y Biomedicina López Neyra (IPBLN), CSIC, 18100 Granada, Spain) ; Hilven, Kelly (Laboratory for Neuroimmunology, Neurosciences, University of Leuven, 1022, Belgium) ; Dubois, Bénédicte (Department of Neurology, University Hospitals Leuven, University of Leuven, Belgium) ; Goris, An (Laboratory for Neuroimmunology, Neurosciences, University of Leuven, 1022, Belgium) ; Astobiza, Ianire (Achucarro Basque Center for Neuroscience, 48170 Spain) ; Alloza, Iraide (IKERBASQUE, Basque Foundation for Science, 48011 Spain) ; Antigüedad, Alfredo (Servicio de Neurología, Hospital Universitario Basurto-Osakidetza, 48940 Bilbao, Spain) ; Vandenbroeck, Koen (IKERBASQUE, Basque Foundation for Science, 48011 Spain) ; Akkad, Denis A. (Department of Human Genetics, Ruhr University, 44801 Bochum, Germany) ; Aktas, Orhan (Department of Neurology, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany) ; Blaschke, Paul (Department of Neurology, University of Rostock, 18059 Germany) ; Buttmann, Mathias (Department of Neurology, University of Würzburg, 97080 Würzburg, Germany) ; Chan, Andrew (Department of Neurology, University Hospital Bern and University of Bern, 3010 Bern, Switzerland) ; Epplen, Joerg T. (Department of Human Genetics, Ruhr University, 44801 Bochum, Germany) ; Gerdes, Lisa-Ann (Institute for Clinical Neuroimmunology, Ludwig Maximilian University, 80539 Munich, Germany) ; Kroner, Antje (Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI 53226) ; Kubisch, Christian (Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany) ; Kümpfel, Tania (Institute for Clinical Neuroimmunology, Ludwig Maximilian University, 80539 Munich, Germany) ; Lohse, Peter (Institute of Laboratory Medicine and Human Genetics, 78224 Singen, Germany) ; Rieckmann, Peter (Department of Neurology, Sozialstiftung Bamberg Hospital, 96049 Germany) ; Zettl, Uwe K. (Department of Neurology, University of Rostock, 18059 Germany) ; Zipp, Frauke (Department of Neurology, Focus Program Translational Neuroscience, University Medical Center of the Johannes Gutenberg-University Mainz, 55122 Germany) ; Bertram, Lars (School of Public Health, Medicine, Imperial College London, SW7 2AZ, UK) ; Lill, Christina M (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Fernandez, Oscar (Department of Neurology, UGC Neurociencias Clínicas. IBIMA-Hospital Regional Universitario de Málaga, 29010 Spain) ; Urbaneja, Patricia (Department of Neurology, UGC Neurociencias Clínicas. IBIMA-Hospital Regional Universitario de Málaga, 29010 Spain) ; Leyva, Laura (Research Laboratory, UGC Neurociencias Clínicas. IBIMA-Hospital Regional Universitario de Málaga, 29010 Spain) ; Alvarez-Cermeño, Jose Carlos (Immunology and Neurology Service, Multiple Sclerosis Unit, Ramón y Cajal University Hospital-IRYCIS, 28034 Madrid, Spain) ; Arroyo, Rafael (Department of Neurology, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos-IdISSC, 28040 Madrid, Spain) ; Garagorri, Aroa M. (Department of Immunology, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos-IdISSC, Madrid, Spain) ; García-Martínez, Angel (Department of Immunology, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos-IdISSC, Madrid, Spain) ; Villar, Luisa M. (Immunology and Neurology Service, Multiple Sclerosis Unit, Ramón y Cajal University Hospital-IRYCIS, 28034 Madrid, Spain) ; Urcelay, Elena (Department of Immunology, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos-IdISSC, Madrid, Spain) ; Malhotra, Sunny (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Montalban, Xavier (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Comabella, Manuel (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Berger, Thomas (Department of Clinical Neurology, Medical University of Innsbruck, 6020 Austria) ; Fazekas, Franz (Department of Neurology, Medical University of Graz, 8010 Austria) ; Reindl, Markus (Department of Clinical Neurology, Medical University of Innsbruck, 6020 Austria) ; Schmied, Mascha C. (Department of Neurology, Medical University of Vienna, 1090 Austria) ; Zimprich, Alexander (Department of Neurology, Medical University of Vienna, 1090 Austria) ; Vilariño-Güell, Carles (Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, V6T 1Z3, Canada) ; Universitat Autònoma de Barcelona
Multiple sclerosis (MS) is a prevalent neurological disease of complex etiology. Here, we describe the characterization of a multi-incident MS family that nominated a rare missense variant (p. G420D) in plasminogen (PLG) as a putative genetic risk factor for MS. [...]
2016 - 10.1534/g3.116.030841
G3, enomes  
3.
5 p, 393.0 KB Role of high mobility group box protein 1 (HMGB1) in peripheral blood from patients with multiple sclerosis / Malhotra, Sunny (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Fissolo, Nicolas (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Tintoré, Mar (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Wing, Ana Cristina (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Castilló, Joaquin (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Vidal-Jordana, Angela (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Montalban, Xavier (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Comabella, Manuel (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Universitat Autònoma de Barcelona
High mobility group box protein 1 (HMGB1) is a transcriptional regulator that is receiving increasing attention in autoimmune disorders including multiple sclerosis (MS). Here, we investigated the role of HMGB1 in the peripheral blood compartment from MS patients. [...]
2015 - 10.1186/s12974-015-0269-9
Journal of neuroinflammation, Vol. 12 (march 2015)  
4.
5 p, 320.8 KB Natalizumab-related anaphylactoid reactions in MS patients are associated with HLA class II alleles / de la Hera, Belén (Hospital Clínico San Carlos (IdISSC), Madrid) ; Urcelay, Elena (Hopital Purpan, Toulouse) ; Brassat, David (Ruhr University, Bochum) ; Chan, Andrew ; Vidal-Jordana, Angela (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Salmen, Anke (St. Josef-Hospital) ; Villar, Luisa Maria (Hospital Universitario Ramón y Cajal) ; Álvarez-Cermeño, José Carlos (Hospital Universitario Ramón y Cajal) ; Izquierdo, Guillermo (Hospital Universitario Virgen Macarena) ; Fernández, Oscar (Hospital Universitario Regional de Málaga) ; Oliver, Begoña (Instituto de Biomedicina de Málaga (IBIMA)) ; Saiz, Albert (Hospital Clínic de Barcelona) ; Ara, Jose Ramón (Universidad de Zaragoza) ; Vigo, Ana G. ; Arroyo, Rafael ; Meca, Virginia (Hospital Universitario de la Princesa) ; Malhotra, Sunny (Hospital Universitari Vall d'Hebron) ; Fissolo, Nicolás (Hospital Universitari Vall d'Hebron) ; Horga, Alejandro ; Montalban, Xavier (Hospital Universitari Vall d'Hebron) ; Comabella, Manuel (Hospital Universitari Vall d'Hebron) ; Universitat Autònoma de Barcelona
We aimed to investigate potential associations between human leukocyte antigen (HLA) class I and class II alleles and the development of anaphylactic/anaphylactoid reactions in patients with multiple sclerosis (MS) treated with natalizumab. [...]
2014 - 10.1212/NXI.0000000000000047
Neurology® neuroimmunology & neuroinflammation, Vol. 1 (december 2014)  

Documentos de investigación Encontrados 1 registros  
1.
244 p, 4.1 MB Búsqueda de variantes genéticas causales y estudio de sus implicaciones funcionales en pacientes con esclerosis múltiple / Gil Varea, Elia ; Comabella, Manuel, dir. ; Malhotra, Sunny, 1984-, dir. ; Montalbán Gairín, Xavier, dir. ; Selva O'Callaghan, Albert, dir. ; Universitat Autònoma de Barcelona. Departament de Medicina
Varios estudios de asociación del genoma completo (GWAS) han contribuido a la caracterización del componente genético de la esclerosis múltiple (EM). Estos estudios examinan cientos de miles o millones de polimorfismos de un solo nucleótido (SNPs) distribuidos por todo el genoma. [...]
Several genome-wide association studies (GWAS) have contributed to the characterization of the genetic component of multiple sclerosis (MS). These studies examine hundreds of thousands or millions of single nucleotide polymorphisms (SNPs) distributed throughout the whole genome. [...]

[Barcelona] : Universitat Autònoma de Barcelona, 2019.  

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