Results overview: Found 21 records in 0.02 seconds.
Articles, 16 records found
Research literature, 4 records found
Course materials, 1 records found
Articles 16 records found  1 - 10next  jump to record:
1.
12 p, 772.4 KB Clock/Sleep-Dependent Learning and Memory in Male 3xTg-AD Mice at Advanced Disease Stages and Extrinsic Effects of Huprine X and the Novel Multitarget Agent AVCRI104P3 / Giménez Llort, Lydia (Universitat Autònoma de Barcelona. Departament de Psiquiatria i de Medicina Legal) ; Santana-Santana, Mikel (Universitat Autònoma de Barcelona. Departament de Psiquiatria i de Medicina Legal) ; Ratia, Míriam (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia) ; Pérez, Belén (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia) ; Camps García, Pelayo (Universitat de Barcelona. Laboratori de Química Farmacèutica) ; Muñoz-Torrero López-Ibarra, Diego (Universitat de Barcelona. Laboratori de Química Farmacèutica) ; Badia Sancho, Albert (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia) ; Clos, Victòria (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia)
A new hypothesis highlights sleep-dependent learning/memory consolidation and regards the sleep-wake cycle as a modulator of β-amyloid and tau Alzheimer's disease (AD) pathologies. Sundowning behavior is a common neuropsychiatric symptom (NPS) associated with dementia. [...]
2021 - 10.3390/brainsci11040426
Brain sciences, Vol. 11 Núm. 4 (2021) , p. 426  
2.
795.1 KB Genetic and phenotypic spectrum associated with IFIH1 gain-of-function / Rice, Gillian I. (University of Manchester) ; Park, Sehoon (Boston Children's Hospital) ; Gavazzi, Francesco (Children's Hospital of Philadelphia) ; Adang, Laura A. (Children's Hospital of Philadelphia) ; Ayuk, Loveline A. (Dumfries and Galloway Royal Infirmary) ; Eyck, Lien Van (Institut Imagine (Paris, França)) ; Seabra, Luis (Institut Imagine (Paris, França)) ; Barrea, Christophe (Université de Liège) ; Battini, Roberta (IRCCS Fondazione Stella Maris) ; Belot, Alexandre (Université de Lyon) ; Berg, Stefan (The Queen Silvia Children's Hospital) ; de Villemeur, Thierry Billette (Sorbonne Université) ; Bley, Annette E. (University Children's Hospital) ; Blumkin, Lubov (Tel-Aviv University) ; Boespflug-Tanguy, Odile (Centre de Référence Maladies Rares "Leucodystrophies") ; Briggs, Tracy A. (St Mary's Hospital) ; Brimble, Elise (Stanford University School of Medicine) ; Dale, Russell C. (University of Sydney) ; Darin, Niklas (The Queen Silvia Children's Hospital) ; Debray, François-Guillaume (Université de Liège) ; De Giorgis, Valentina (IRCCS Mondino Foundation) ; Denecke, Jonas (University Medical Center Hamburg Eppendorf) ; Doummar, Diane (Hôpital Armand Trousseau) ; Hagelsrum, Gunilla Drake af (PeThe Queen Silvia Children's Hospital) ; Eleftheriou, Despina (University College London (UCL)) ; Estienne, Margherita (Istituto Neurologico Carlo Besta) ; Fazzi, Elisa (University of Brescia. Department of Experimental and Clinical Sciences) ; Feillet, François (Centre de Référence des maladies métaboliques de Nancy (França)) ; Galli, Jessica (University of Brescia. Department of Experimental and Clinical Sciences) ; Hartog, Nicholas (Michigan State University College of Human Medicine) ; Harvengt, Julie (University of Liège. Department of Medical Genetics) ; Heron, Bénédicte (Hôpital Trousseau (París, França). Centre Référence des Maladies Lysosomales) ; Heron, Delphine (Groupe Hospitalier Pitié-Salpêtrière (París, França). UF Génétique Médicale et Centre de Référence "Déficiences Intellectuelles) ; Kelly, Diedre A. (Birmingham Women's and Children's Hospital (Regne Unit)) ; Lev, Dorit (The Rina Mor Institute of Medical Genetics (Holon, Israel)) ; Levrat, Virginie (Centre Hospitalier Annecy Genevois (Pringy, França)) ; Livingston, John H. (Leeds General Infirmary (Leeds, Regne Unit)) ; Marti, Itxaso (Universidad del País Vasco. Hospital Universitario Donostia) ; Mignot, Cyril (GH Pitié-Sapêtrière (París, França). Departement de Génétique & Centre de Référence Déficience Intellectuelle de cause rare) ; Mochel, Fanny (Sorbonne Universités. Institut du Cerveau et de la Moelle épinière) ; Nougues, Marie-Christine (Hôpital Armand Trousseau (París, França)) ; Oppermann, Ilena (University Medical Center Hamburg Eppendorf) ; Pérez-Dueñas, Belén (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Popp, Bernt (Friedrich-Alexander-Universität Erlangen-Nürnberg. Institute of Human Genetics) ; Rodero, Mathieu P. (Institut Imagine (París, França). Laboratory of Neurogenetics and Neuroinflammation) ; Rodriguez, Diana (Hôpital Trousseau (París, França). Centre Référence des Maladies Lysosomales) ; Saletti, Veronica (Fondazione IRCCS Istituto Neurologico Carlo Besta (Milà, Itàlia)) ; Sharpe, Cia (Paediatric Neurology, Starship Children's Hospital, Auckland, New Zealand) ; Tonduti, Davide (V. Buzzi Children's Hospital (Milà, Itàlia)) ; Vadlamani, Gayatri (Leeds General Infirmary (Leeds, Regne Unit)) ; Haren, Keith Van (Stanford University School of Medicine. Department of Neurology) ; Vila, Miguel Tomas (Hospital Universitari i Pôlitecnic La Fe (València)) ; Vogt, Julie (West Midlands Regional Clinical Genetics Service (Regne Unit)) ; Wassmer, Evangeline (Birmingham Women's and Children's Hospital (Regne Unit)) ; Wiedemann, Arnaud (Centre de Référence des maladies métaboliques de Nancy (França)) ; Wilson, Callum J. (Starship Children's Hospital (Auckland, Nova Zelanda)) ; Zerem, Ayelet (Tel-Aviv Universitym. Sackler Faculty of Medicine) ; Zweier, Christiane (Friedrich-Alexander-Universität Erlangen-Nürnberg) ; Zuberi, Sameer M. (University of Glasgow. School of Medicine) ; Orcesi, Simona (University of Pavia. Department of Brain and Behavioural Sciences) ; Vanderver, Adeline L. (Children's Hospital of Philadelphia) ; Hur, Sun (Boston Children's Hospital) ; Crow, Yanick J. (University of Edinburgh. Institute of Genetics and Molecular Medicine) ; Universitat Autònoma de Barcelona
IFIH1 gain-of-function has been reported as a cause of a type I interferonopathy encompassing a spectrum of autoinflammatory phenotypes including Aicardi-Goutières syndrome and Singleton Merten syndrome. [...]
2020 - 10.1002/humu.23975
Human mutation, Vol. 41 (january 2020) , p. 837-849  
3.
3 p, 169.2 KB NR4A2 Mutations Can Cause Intellectual Disability and Language Impairment With Persistent Dystonia-Parkinsonism / Jesús, Silvia (Instituto de Biomedicina de Sevilla (IBiS)) ; Hinarejos, Isabel (Centro de Investigación Príncipe Felipe (València)) ; Carrillo, Fátima (Instituto de Biomedicina de Sevilla (IBiS)) ; Martínez-Rubio, Dolores (Centro de Investigación Príncipe Felipe (València)) ; Macías-García, Daniel (Instituto de Biomedicina de Sevilla (IBiS)) ; Sánchez-Monteagudo, Ana (Centro de Investigación Príncipe Felipe (València)) ; Adarmes-Gómez, A.D. (Instituto de Biomedicina de Sevilla (IBiS)) ; Lupo, Vincenzo (Centro de Investigación Príncipe Felipe (València)) ; Pérez-Dueñas, Belén (Hospital Universitari Vall d'Hebron) ; Mir, Pablo (Instituto de Biomedicina de Sevilla (IBiS)) ; Espinós, Carmen (Centro de Investigación Príncipe Felipe (València))
2021 - 10.1212/NXG.0000000000000543
Neurology: Genetics, Vol. 7 (january 2021)  
4.
7 p, 396.4 KB Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect / Correa-Vela, Marta (Universitat Autònoma de Barcelona) ; Lupo, Vincenzo (Centro de Investigación Príncipe Felipe (CIPF)) ; Montpeyó, Marta (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Sancho, Paula (Centro de Investigación Príncipe Felipe (CIPF)) ; Marcé-Grau, Anna (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Hernández-Vara, Jorge (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Darling, Alejandra (Hospital Sant Joan de Déu) ; Jenkins, Alison (Centro de Investigación Príncipe Felipe (CIPF)) ; Fernández-Rodríguez, Sandra (Centro de Investigación Príncipe Felipe (CIPF)) ; Tello, Cristina (Centro de Investigación Príncipe Felipe (CIPF)) ; Ramírez-Jiménez, Laura (Centro de Investigación Príncipe Felipe (CIPF)) ; Pérez, Belén (Instituto de Investigación Sanitaria Hospital La Paz (IdiPaz)) ; Sánchez-Montáñez, Ángel (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Macaya Ruiz, Alfons (Universitat Autònoma de Barcelona) ; Sobrido, María J. (Centro de Investigación Biomédica en Red de Enfermedades Raras) ; Martinez-Vicente, Marta (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Pérez-Dueñas, Belén (Universitat Autònoma de Barcelona) ; Espinós, Carmen (Centro de Investigación Príncipe Felipe (CIPF)) ; Universitat Autònoma de Barcelona
FBXO7 is implicated in the ubiquitin-proteasome system and parkin-mediated mitophagy. FBXO7defects cause a levodopa-responsive parkinsonian-pyramidal syndrome(PPS). Methods: We investigated the disease molecular bases in a child with PPS and brain iron accumulation. [...]
2020 - 10.1002/acn3.51095
Annals of Clinical and Translational Neurology, Vol. 7 (august 2020) , p. 1436-1442  
5.
16 p, 3.4 MB AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders / Salpietro, V. (Department of Neurosciences. Rehabilitation. Ophthalmology. Genetics. Maternal and Child Health. University of Genoa) ; Dixon, C.L. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Guo, H. (Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics. School of Life Sciences. Central South University) ; Bello, O.D. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Vandrovcova, J. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Efthymiou, S. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Maroofian, R. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Heimer, G. (Pediatric Neurology Unit. Safra Children's Hospital. Sheba Medical Center and Sackler Faculty of Medicine. Tel Aviv University) ; Burglen, L. (Centre de Référence des Malformations et Maladies Congénitales du Cervelet. Département de Génétique et Embryologie Médicale. APHP. Hôpital Trousseau) ; Valence, S. (Centre de Référence des Malformations et Maladies Congénitales du Cervelet. Service de Neurologie Pédiatrique. APHP. Hôpital Trousseau) ; Torti, E. (GeneDx) ; Hacke, M. (Biochemistry Center. Heidelberg University) ; Rankin, J. (Royal Devon and Exeter NHS Foundation Trust) ; Tariq, H. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Colin, E. (MitoLab. UMR CNRS 6015-INSERM U1083. MitoVasc Institute. Angers University) ; Procaccio, V. (MitoLab. UMR CNRS 6015-INSERM U1083. MitoVasc Institute. Angers University) ; Striano, P. (Department of Neurosciences. Rehabilitation. Ophthalmology. Genetics. Maternal and Child Health. University of Genoa) ; Mankad, K. (Great Ormond Street Hospital for Children) ; Lieb, A. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Chen, S. (Division of Medical Genetics. Northwell Health/Hofstra University SOM) ; Pisani, L. (Division of Medical Genetics. Northwell Health/Hofstra University SOM) ; Bettencourt, C. (Department of Clinical and Movement Neurosciences and Queen Square Brain Bank for Neurological Disorders. UCL Queen Square Institute of Neurology) ; Männikkö, R. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Manole, A. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Brusco, A. (Department of Medical Sciences. Medical Genetics Unit. University of Torino) ; Grosso, E. (Department of Medical Sciences. Medical Genetics Unit. University of Torino) ; Ferrero, G.B. (Department of Public Health and Pediatrics. University of Torino) ; Armstrong-Moron, J. (Unit of Medical and Molecular Genetics. University Hospital Sant Joan de Deu Barcelona) ; Gueden, S. (Unit of Neuropediatrics. University Hospital) ; Bar-Yosef, O. (Pediatric Neurology Unit. Safra Children's Hospital. Sheba Medical Center and Sackler Faculty of Medicine. Tel Aviv University) ; Tzadok, M. (Pediatric Neurology Unit. Safra Children's Hospital. Sheba Medical Center and Sackler Faculty of Medicine. Tel Aviv University) ; Monaghan, K.G. (GeneDx) ; Santiago-Sim, T. (GeneDx) ; Person, R.E. (GeneDx) ; Cho, M.T. (GeneDx) ; Willaert, R. (GeneDx) ; Yoo, Y. (Department of Biomedical Sciences. Seoul National University) ; Chae, J.H. (Department of Pediatrics. Seoul National University) ; Quan, Y. (Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics. School of Life Sciences. Central South University) ; Wu, H. (Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics. School of Life Sciences. Central South University) ; Wang, T. (Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics. School of Life Sciences. Central South University) ; Bernier, R.A. (Department of Psychiatry. University of Washington) ; Xia, K. (Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics. School of Life Sciences. Central South University) ; Blesson, A. (Center for Autism and Related Disorders. Kennedy Krieger Institute) ; Jain, M. (Center for Autism and Related Disorders. Kennedy Krieger Institute) ; Motazacker, M.M. (Department of Clinical Genetics. University of Amsterdam) ; Jaeger, B. (Department of Pediatric Neurology. Amsterdam UMC) ; Schneider, A.L. (Epilepsy Research Centre. Department of Medicine. University of Melbourne. Austin Health) ; Boysen, K. (Epilepsy Research Centre. Department of Medicine. University of Melbourne. Austin Health) ; Muir, A.M. (Department of Pediatrics. University of Washington) ; Myers, C.T. (Department of Pediatrics. Division of Genetic Medicine. University of Washington) ; Gavrilova, R.H. (Department of Clinical Genomics. Mayo Clinic) ; Gunderson, L. (Department of Clinical Genomics. Mayo Clinic) ; Schultz-Rogers, L. (Department of Clinical Genomics. Mayo Clinic) ; Klee, E.W. (Department of Clinical Genomics. Mayo Clinic) ; Dyment, D. (Children's Hospital of Eastern Ontario Research Institute. University of Ottawa) ; Osmond, M. (Genome Québec Innovation Center) ; Parellada, M. (Hospital General Universitario Gregorio Marañón) ; Llorente, C. (Institute of Psychiatry and Mental Health. Hospital General Universitario Gregorio Maranon. Universidad Complutense. CIBERSAM) ; Gonzalez-Peñas, J. (Hospital Gregorio Marañón (Madrid)) ; Carracedo, A. (Fundación Pública Galega de Medicina Xenómica- IDIS- Servicio Galego de Saúde (SERGAS). 15706) ; Van Haeringen, A. (Department of Clinical Genetics. Leiden University Medical Center) ; Ruivenkamp, C. (Department of Clinical Genetics. Leiden University Medical Center) ; Nava, Caroline. (Department of Genetics. Assistance Publique - Hôpitaux de Paris. University Hôpital Pitié-Salpêtrière) ; Heron, D. (Department of Genetics. Assistance Publique - Hôpitaux de Paris. University Hôpital Pitié-Salpêtrière) ; Nardello, R. (Department of Health Promotion,Mother and Child Care. Internal Medicine and Medical Specialities "G. D'Alessandro". University of Palermo) ; Iacomino, M. (Laboratory of Neurogenetics and Neuroscience. IRCCS Istituto "Giannina Gaslini") ; Minetti, C. (Department of Neurosciences. Rehabilitation. Ophthalmology. Genetics. Maternal and Child Health. University of Genoa) ; Skabar, A. (Institute for Maternal and Child Health. IRCCS "Burlo Garofolo". University of Trieste) ; Fabretto, A. (Institute for Maternal and Child Health. IRCCS "Burlo Garofolo". University of Trieste) ; Hanna, M.G. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Bugiardini, E. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Hostettler, I. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; O'Callaghan, B. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Khan, A. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Cortese, A. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; O'Connor, E. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Yau, W.Y. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Bourinaris, T. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Kaiyrzhanov, R. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Chelban, V. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Madej, M. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Diana, M.C. (Pediatric Neurology and Muscular Diseases Unit. IRCCS Istituto "Giannina Gaslini") ; Vari, M.S. (Pediatric Neurology and Muscular Diseases Unit. IRCCS Istituto "Giannina Gaslini") ; Pedemonte, M. (Pediatric Neurology and Muscular Diseases Unit. IRCCS Istituto "Giannina Gaslini") ; Bruno, C. (Pediatric Neurology and Muscular Diseases Unit. IRCCS Istituto "Giannina Gaslini") ; Balagura, G. (Department of Neurosciences. Rehabilitation. Ophthalmology. Genetics. Maternal and Child Health. University of Genoa) ; Scala, M. (Department of Neurosciences. Rehabilitation. Ophthalmology. Genetics. Maternal and Child Health. University of Genoa) ; Fiorillo, C. (Department of Neurosciences. Rehabilitation. Ophthalmology. Genetics. Maternal and Child Health. University of Genoa) ; Nobili, L. (Department of Neurosciences. Rehabilitation. Ophthalmology. Genetics. Maternal and Child Health. University of Genoa) ; Malintan, N.T. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Zanetti, M.N. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Krishnakumar, S.S. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Lignani, G. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Jepson, J.E.C. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Broda, P. (Laboratory of Neurogenetics and Neuroscience. IRCCS Istituto "Giannina Gaslini") ; Baldassari, S. (Laboratory of Neurogenetics and Neuroscience. IRCCS Istituto "Giannina Gaslini") ; Rossi, P. (Laboratory of Neurogenetics and Neuroscience. IRCCS Istituto "Giannina Gaslini") ; Fruscione, F. (Laboratory of Neurogenetics and Neuroscience. IRCCS Istituto "Giannina Gaslini") ; Madia, F. (Laboratory of Neurogenetics and Neuroscience. IRCCS Istituto "Giannina Gaslini") ; Traverso, M. (Laboratory of Neurogenetics and Neuroscience. IRCCS Istituto "Giannina Gaslini") ; De-Marco, P. (Laboratory of Neurogenetics and Neuroscience. IRCCS Istituto "Giannina Gaslini") ; Pérez-Dueñas, Belén (Hospital Universitari Vall d'Hebron) ; Munell Casadesus, Francina (Hospital Universitari Vall d'Hebron) ; Kriouile, Y. (Children's Hospital of Rabat. University of Rabat) ; El-Khorassani, M. (Children's Hospital of Rabat. University of Rabat) ; Karashova, B. (Department of Paediatrics. Medical University of Sofia) ; Avdjieva, D. (Department of Paediatrics. Medical University of Sofia) ; Kathom, H. (Department of Paediatrics. Medical University of Sofia) ; Tincheva, R. (Department of Paediatrics. Medical University of Sofia) ; Van-Maldergem, L. (Centre of Human Genetics. University Hospital Liege) ; Nachbauer, W. (Department of Neurology. Medical University Innsbruck) ; Boesch, S. (Department of Neurology. Medical University Innsbruck) ; Gagliano, A. (Ospedale Pediatrico "A. Cao". Department of Biomedical Sciences. University of Cagliari) ; Amadori, E. (Child and Adolescent Neuropsychiatry. University of Campania "Luigi Vanvitelli") ; Goraya, J.S. (Division of Paediatric Neurology. Dayanand Medical College & Hospital) ; Sultan, T. (Department of Paediatric Neurology. Children's Hospital of Lahore) ; Kirmani, S. (Department of Medical Genetics. Aga Khan University Hospital. Karachi) ; Ibrahim, S. (Department of Paediatric Neurology. Aga Khan University Hospital. Karachi) ; Jan, F. (Department of Paediatric Neurology. Aga Khan University Hospital. Karachi) ; Mine, J. (Department of Pediatrics. Shimane University School of Medicine) ; Banu, S. (Institute of Child Health and Shishu Shastho Foundation Hospital) ; Veggiotti, P. (Vittore Buzzi Children's Hospital) ; Zuccotti, G.V. (Vittore Buzzi Children's Hospital) ; Ferrari, M.D. (Leiden University Medical Center) ; Van Den Maagdenberg, A.M.J. (Leiden University Medical Center) ; Verrotti, A. (Paediatric Department. San Salvatore Hospital. University of L'Aquila) ; Marseglia, G.L. (Department of Pediatrics. University of Pavia. IRCCS Policlinico "San Matteo") ; Savasta, S. (Department of Pediatrics. University of Pavia. IRCCS Policlinico "San Matteo") ; Soler, M.A. (Computational Modelling of Nanoscale and Biophysical systems Laboratory. Italian Institute of Technology) ; Scuderi, C. (Laboratorio di Neuropatologia Clinica. U.O.S. Malattie. Neuromuscolari Associazione OASI Maria SS. ONLUS - IRCCS) ; Borgione, E. (Laboratorio di Neuropatologia Clinica. U.O.S. Malattie. Neuromuscolari Associazione OASI Maria SS. ONLUS - IRCCS) ; Chimenz, R. (Department of Pediatrics. University Hospital "Gaetano Martino". University of Messina) ; Gitto, E. (Department of Pediatrics. University Hospital "Gaetano Martino". University of Messina) ; Dipasquale, V. (Department of Pediatrics. University Hospital "Gaetano Martino". University of Messina) ; Sallemi, A. (Department of Pediatrics. University Hospital "Gaetano Martino". University of Messina) ; Fusco, M. (Department of Pediatrics. University Hospital "Gaetano Martino". University of Messina) ; Cuppari, C. (Department of Pediatrics. University Hospital "Gaetano Martino". University of Messina) ; Cutrupi, M.C. (Department of Pediatrics. University Hospital "Gaetano Martino". University of Messina) ; Ruggieri, M. (Department of Clinical and Experimental Medicine. Section of Pediatrics and Child Neuropsychiatry. University of Catania) ; Cama, A. (Department of Neurosurgery. IRCCS Istituto Giannina Gaslini) ; Capra, V. (Department of Neurosurgery. IRCCS Istituto Giannina Gaslini) ; Mencacci, N.E. (Department of Neurology. Northwestern University Feinberg School of Medicine) ; Boles, R. (Courtagen Life Sciences) ; Gupta, N. (Division of Genetics. Department of Pediatrics. All India Institute of Medical Sciences (AIIMS)) ; Kabra, M. (Division of Genetics. Department of Pediatrics. All India Institute of Medical Sciences (AIIMS)) ; Papacostas, S. (The Cyprus Institute of Neurology and Genetics) ; Zamba-Papanicolaou, E. (The Cyprus Institute of Neurology and Genetics) ; Dardiotis, E. (University Hospital of Larissa. Department of Neurology) ; Maqbool, S. (Department of Developmental and Behavioral Pediatrics. Children Hospital Complex and Institute of Child Health) ; Rana, N. (Department of Pediatric Neurology. Children Hospital Complex and Institute of Child Health) ; Atawneh, O. (Hilal Pediatric Hospital Hebron. Hebron. West Bank) ; Lim, S.Y. (Department of Biomedical Science. Faculty of Medicine. University of Malaysia) ; Shaikh, F. (Jeffrey Cheah School of Medicine and Health Sciences. Monash University Malaysia) ; Koutsis, G. (Neurogenetics Unit. Neurology Department. Eginition Hospital. National and Kapodistrian University) ; Breza, M. (Neurogenetics Unit. Neurology Department. Eginition Hospital. National and Kapodistrian University) ; Coviello, D.A. (Laboratorio di Genetica Umana. IRCCS Istituto Giannina Gaslini) ; Dauvilliers, Y.A. (University Hospital Montpellier) ; AlKhawaja, I. (Albashir University Hospital) ; AlKhawaja, M. (Prince Hamzah Hospital. Ministry of Health) ; Al-Mutairi, F. (King Saud University) ; Stojkovic, T. (Institute of Myology. Hôpital La Pitié Salpêtrière) ; Ferrucci, V. (CEINGE. Biotecnologie Avanzate S.c.a.rl.) ; Zollo, M. (CEINGE. Biotecnologie Avanzate S.c.a.rl.) ; Alkuraya, F.S. (King Faisal Specialist Hospital and Research Center) ; Kinali, M. (The Portland Hospital) ; Sherifa, H. (Assiut University Hospital) ; Benrhouma, H. (Research Unit UR12 SP24. Department of Child and Adolescent Neurology. National Institute Mongi Ben Hmida of Neurology) ; Turki, I.B.Y. (Research Unit UR12 SP24. Department of Child and Adolescent Neurology. National Institute Mongi Ben Hmida of Neurology) ; Tazir, M. (Laboratoire de Recherche en Neurosciences. Service de Neurologie) ; Obeid, M. (Department of Anatomy. Cell Biology and Physiology. American University of Beirut Medical Center) ; Bakhtadze, S. (Department of Child Neurology. Tbilisi State Medical University) ; Saadi, N.W. (Baghdad College of Medicine. Children Welfare Teaching Hospital) ; Zaki, M.S. (Human Genetics and Genome Research Division. National Research Centre) ; Triki, C.C. (Child Neurology Department. Hedi Chaker hospital- Sfax Tunisia) ; Benfenati, F. (Istituto Italiano di Tecnologia) ; Gustincich, S. (Istituto Italiano di Tecnologia) ; Kara, M. (Paediatric Neurology Unit. Department of Pediatrics. University of Tripoli) ; Belcastro, V. (Neurology Unit. S. Anna Hospital) ; Specchio, N. (Child Neurology Unit. "Bambino Gesù" Pediatric Hospital) ; Capovilla, G. (Child Neuropsychiatry Department. Epilepsy Center. C. Poma Hospital) ; Karimiani, E.G. (Genetics Research Centre. Molecular and Clinical Sciences Institute. St George's. University of London. Cranmer Terrace) ; Salih, A.M. (Medical University of Duhok) ; Okubadejo, N.U. (College of Medicine. University of Lagos (CMUL) & Lagos University Teaching Hospital) ; Ojo, O.O. (College of Medicine. University of Lagos (CMUL) & Lagos University Teaching Hospital) ; Oshinaike, O.O. (College of Medicine. University of Lagos (CMUL) & Lagos University Teaching Hospital) ; Oguntunde, O. (College of Medicine. University of Lagos (CMUL) & Lagos University Teaching Hospital) ; Wahab, K. (University of Ilorin Teaching Hospital (UITH)) ; Bello, A.H. (University of Ilorin Teaching Hospital (UITH)) ; Abubakar, S. (Ahmadu Bello University) ; Obiabo, Y. (Delta State University Teaching Hospital) ; Nwazor, E. (Federal Medical Centre) ; Ekenze, O. (University of Nigeria Teaching Hospital) ; Williams, U. (University of Calabar Teaching Hospital) ; Iyagba, A. (University of Port Harcourt Teaching Hospital) ; Taiwo, L. (Babcock University. Ilishan. Remo & Federal Medical Centre) ; Komolafe, M. (Obafemi Awolowo University Teaching Hospital (OAUTH)) ; Senkevich, K. (Almazov Medical Research Centre and Pavlov First Saint Petersburg State Medical University) ; Shashkin, C. (Kazakh National State University) ; Zharkynbekova, N. (Shymkent Medical Academy) ; Koneyev, K. (Kazakh National State University) ; Manizha, G. (Avicenna Tajik State Medical University) ; Isrofilov, M. (Avicenna Tajik State Medical University) ; Guliyeva, U. (Mediclub clinic) ; Salayev, K. (Azerbaijan State Medical University) ; Khachatryan, S. ("Somnus" Neurology Clinic Sleep and Movement Disorders Center) ; Rossi, S. (Department of Neurology. Università Cattolica del Sacro Cuore) ; Silvestri, G. (Department of Neurology. Università Cattolica del Sacro Cuore) ; Haridy, N. (Department of Neurology and Psychiatry. Assuit University Hospital) ; Ramenghi, L.A. (Neonatal Intensive Care Unit. Istituto Giannina Gaslini) ; Xiromerisiou, G. (Department of Neurology. Medical School. University of Thessaly) ; David, E. (Radiology Unit. Papardo Hospital. Viale Ferdinando Stagno d'Alcontres. Contrada Papardo) ; Aguennouz, M. (Unit of Neurology and Neuromuscular Diseases. Department of Clinical and Experimental Medicine. University of Messina) ; Fidani, L. (Department of Biology. Medical School. Aristotle University) ; Spanaki, C. (Department of Neurology. Medical School. University of Crete) ; Tucci, A. (William Harvey Research Institute. The NIHR Biomedical Research Centre at Barts. Queen Mary University London) ; Raspall-Chaure, Miquel (Hospital Universitari Vall d'Hebron) ; Chez, M. (Neuroscience Medical Group. 1625 Stockton Boulevard. Suite 104) ; Tsai, A. (Department of Genetics and Inherited Metabolic diseases. Children's Hospital Colorado) ; Fassi, E. (Department of Pediatrics. Washington University School of Medicine) ; Shinawi, M. (Department of Pediatrics. Washington University School of Medicine) ; Constantino, J.N. (William Greenleaf Eliot Division of Child & Adolescent Psychiatry. Department of Psychiatry. Washington University School of Medicine) ; De Zorzi, R. (Department of Chemical and Pharmaceutical Sciences. University of Trieste) ; Fortuna, S. (Department of Chemical and Pharmaceutical Sciences. University of Trieste) ; Kok, F. (Mendelics Genomic Analysis) ; Keren, B. (Department of Genetics. Assistance Publique - Hôpitaux de Paris. University Hôpital Pitié-Salpêtrière) ; Bonneau, D. (MitoLab. UMR CNRS 6015-INSERM U1083. MitoVasc Institute. Angers University) ; Choi, M. (Department of Biomedical Sciences. Seoul National University) ; Benzeev, B. (Pediatric Neurology Unit. Safra Children's Hospital. Sheba Medical Center and Sackler Faculty of Medicine. Tel Aviv University) ; Zara, F. (Laboratory of Neurogenetics and Neuroscience. IRCCS Istituto "Giannina Gaslini") ; Mefford, H.C. (Department of Pediatrics. University of Washington) ; Scheffer, I.E. (Epilepsy Research Centre. Department of Medicine. University of Melbourne. Austin Health) ; Clayton-Smith, J. (Division of Evolution and Genomic Sciences. School of Biological Sciences. University of Manchester) ; Macaya Ruiz, Alfons (Hospital Universitari Vall d'Hebron) ; Rothman, J.E. (Department of Cell Biology. Yale University School of Medicine) ; Eichler, E.E. (Howard Hughes Medical Institute. University of Washington) ; Kullmann, D.M. (Department of Clinical and Experimental Epilepsy. UCL Queen Square Institute of Neurology) ; Houlden, H. (Department of Neuromuscular Disorders. UCL Queen Square Institute of Neurology) ; Universitat Autònoma de Barcelona
AMPA receptors (AMPARs) are tetrameric ligand-gated channels made up of combinations of GluA1-4 subunits encoded by GRIA1-4 genes. GluA2 has an especially important role because, following post-transcriptional editing at the Q607 site, it renders heteromultimeric AMPARs Ca-impermeable, with a linear relationship between current and trans-membrane voltage. [...]
2019 - 10.1038/s41467-019-10910-w
Nature communications, Vol. 10 Núm. 1 (january 2019) , p. 3094  
6.
2 p, 188.6 KB Synthesis, in vitro profiling, and in vivo efficacy studies of a new family of multitarget antiAlzheimer compounds / Pérez-Areales, Francisco Javier (Universitat de Barcelona) ; Garrido, María (Instituto de Química Avanzada de) ; Catalunya (IQAC-CSIC) ; Aso, Ester (Universitat de Barcelona) ; Bartolini, Manuela (Department of Pharmacy and Biotechnology. Alma Mater Studiorum University of Bologna) ; De Simone, Angela (University of Bologna. Department for Life Quality Studies) ; Espargaró Colomé, Alba (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular) ; Ginex, Tiziana (Universitat de Barcelona) ; Sabate, Raimon (Universitat de Barcelona) ; Pérez, Belén (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia) ; Andrisano, Vincenza (University of Bologna. Department for Life Quality Studies) ; Luque, Francisco Javier (Universitat de Barcelona) ; Ferrer, Isidro (Universitat de Barcelona. Unitat de Neuropatologia Experimental) ; Ciruela, Francisco (Universitat de Barcelona) ; Messeguer, Àngel (Instituto de Química Avanzada de) ; Catalunya (IQAC-CSIC) ; Muñoz-Torrero López-Ibarra, Diego (Universitat de Barcelona. Laboratori de Química Farmacèutica)
Simultaneous modulation of several targets or athological events with a key pathogenic role is a promising strategy to tackle thus far difficult-to-cure or incurable multifactorial diseases, such as Alzheimer's disease (AD). [...]
2019 - 10.3390/proceedings2019022071
Proceedings, Vol. 22 (2019) , p. 1-2  
7.
1 p, 134.6 KB Dibenzylxanthines as PPEPCK-M inhibitors for cancer therapy / Aragó, Marc (University of Barcelona. Department of Physiological Sciences, Faculty of Medicine) ; Rodríguez-Arévalo , Sergio (Universitat de Barcelona. Institut de Biomedicina) ; Moreno, Juan (University of Barcelona. Faculty of Medicine) ; Abás, Sònia (Universitat de Barcelona. Institut de Biomedicina) ; Figueras, Agnès (Institut d'Investigació Biomèdica de Bellvitge) ; Pérez, Belén (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia) ; Viñals, Francesc (Institut d'Investigació Biomèdica de Bellvitge) ; Carmen Escolano, María (University of Barcelona. Institute of Biomedicine(IBUB)) ; Carlos Perales, José (University of Barcelona. Faculty of Medicine)
Phosphoenolpyruvate carboxykinase (PEPCK) is the key enzyme in gluconeogenesis/glyceroneogenesis, which catalyzes the decarboxylation of oxaloacetate to phosphoenolpyruvate. In eukaryotes, there are two isozymes present either in the cytosol (PEPCKC, PCK1) or the mitochondria (PEPCK-M, PCK2). [...]
2019 - 10.3390/proceedings2019022079
Proceedings, Vol. 22 (2019) , p. 1  
8.
17 p, 941.9 KB Locura, crimen y revolución como resistencia discursiva en Los siete locos y Los lanzallamas de Roberto Arlt / Pérez Barreiro, Ana Belén (Universidad Iberoamericana (Mèxic))
Los siete locos y Los lanzallamas han sido consideradas como las novelas más importantes de la producción narrativa de Roberto Arlt. Por medio del delito y la simulación, los personajes pretenden llevar a cabo una revolución e instaurar un nuevo orden social. [...]
Los siete locos i Los lanzallamas han estat considerades com les novel·les més importants de la producció narrativa de Roberto Arlt. Per mitjà del delicte i la simulació, els personatges pretenen dur a terme una revolució i instaurar un nou ordre social. [...]
Los siete locos and Los lanzallamas have been considered as the most important novels of the narrative production of Roberto Arlt. Through crime and simulation, the characters intend to carry out a revolution and establish a new social order. [...]

2019 - 10.5565/rev/mitologias.635
Mitologías hoy, Vol. 20 (2019) , p. 311-327 (Miscelánea)  
9.
8 p, 812.8 KB Tetrasubstituted imidazolium salts as potent antiparasitic agents against African and American trypanosomiases / Ghashghaei, Ouldouz (Universitat de Barcelona. Laboratori de Química Orgànica) ; Kielland, Nicola (Universitat de Barcelona. Laboratori de Química Orgànica) ; Revés, Marc (Universitat de Barcelona. Laboratori de Química Orgànica) ; Taylor, Martin C. (Department of Pathogen Molecular Biology. London School of Hygiene and Tropical Medicine) ; Kelly, John M. (Department of Pathogen Molecular Biology. London School of Hygiene and Tropical Medicine) ; Pietro, Ornella Di (Universitat de Barcelona. Laboratori de Química Farmacèutica) ; Muñoz-Torrero López-Ibarra, Diego (Universitat de Barcelona. Laboratori de Química Farmacèutica) ; Pérez, Belén. (Universitat Autònoma de Barcelona. Institut de Neurociències) ; Lavilla, Rodolfo (Universitat de Barcelona. Laboratori de Química Orgànica)
Imidazolium salts are privileged compounds in organic chemistry, and have valuable biological properties. Recent studies show that symmetric imidazolium salts with bulky moieties can display antiparasitic activity against T. [...]
2018 - 10.3390/molecules23010177
Molecules, Vol. 23 Núm. 1 (2018) , p. 177  
10.
19 p, 3.9 MB Increasing polarity in tacrine and huprine derivatives : Potent anticholinesterase agents for the treatment of myasthenia gravis / Galdeano, Carles (Universitat de Barcelona. Laboratori de Química Farmacèutica) ; Coquelle, Nicolas (Large-Scale Structures Group. Institut Laue-Langevin) ; Cieslikiewicz-Bouet, Monika (Laboratory COBRA (UMR 6014). Normandie Université. UNIROUEN. Institut National des Sciences Appliquées (INSA) Rouen. CNRS) ; Bartolini, Manuela (Department of Pharmacy and Biotechnology. Alma Mater Studiorum University of Bologna) ; Pérez, Belén (Universitat Autònoma de Barcelona. Institut de Neurociències) ; Clos, Victòria (Universitat Autònoma de Barcelona. Institut de Neurociències) ; Silman, Israel (Department of Neurobiology. Weizmann Institute of Science) ; Jean, Ludovic (Laboratory COBRA (UMR 6014). Normandie Université. UNIROUEN. Institut National des Sciences Appliquées (INSA) Rouen. CNRS) ; Colletier, Jacques Phillippe (Institut de Biologie Structurale. Université Grenoble Alpes. Centre National de la Recherche Scientifique (CNRS). Commissariat à l'Énergie Atomique (CEA) (UMR 5075)) ; Renard, Pierre Yves (Laboratory COBRA (UMR 6014). Normandie Université. UNIROUEN. Institut National des Sciences Appliquées (INSA) Rouen. CNRS) ; Muñoz-Torrero López-Ibarra, Diego (Universitat de Barcelona. Laboratori de Química Farmacèutica)
Symptomatic treatment of myasthenia gravis is based on the use of peripherally-acting acetylcholinesterase (AChE) inhibitors that, in some cases, must be discontinued due to the occurrence of a number of side-effects. [...]
2018 - 10.3390/molecules23030634
Molecules, Vol. 23 Núm. 3 (2018) , p. 634  

Articles : 16 records found   1 - 10next  jump to record:
Research literature 4 records found  
1.
226 p, 5.1 MB Efecte dels anticolinesteràsics huprina x i avcri104p3 en els processos neurodegeneratius i d'envelliment / Relat Pardo, Júlia ; Clos Guillén, Mª Victòria, dir. ; Pérez Fernández, Belén, dir. ; Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia
Entre els diferents trastorns neurodegeneratius, la malaltia d'Alzheimer (MA) es caracteritza per la pèrdua progressiva de les funcions cognitives i l'alteració del comportament, essent el sistema colinèrgic central el principal sistema afectat. [...]
Among the different neurodegenerative disorders, Alzheimer's disease (AD) is characterized by the progressive loss of cognitive function and the altered behaviour, being the central cholinergic system the main affected. [...]

[Barcelona] : Universitat Autònoma de Barcelona, 2015  
2.
225 p, 1.8 MB Utilidad de marcadores genéticos en el seguimiento de pacientes con antecedentes de carcinoma urotelial no músculo infiltrante / Galván Pérez, Ana Belén ; Gelabert Mas, Antonio, dir. (Universitat Autònoma de Barcelona. Departament de Cirurgia) ; Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia
El carcinoma de células uroteliales no músculo infiltrante (CCUNMI) se asocia con una alta tasa de recurrencia (60-85%) y de progresión a lesiones de alto grado (10-30%) y por lo tanto, estos pacientes deben ser monitorizados regularmente. [...]
Non muscle-invasive urothelial cell carcinoma (NMIUCC) is associated with a high rate of recurrence (60-85%) and progression to high-grade lesions (10-30%) and therefore these patients must be monitored regularly. [...]

[Barcelona] : Universitat Autònoma de Barcelona, 2014  
3.
226 p, 840.4 KB Comportament farmacocinètic i depleció tisular de la tilosina en vedells i porcs / Prats Fuxet, Carme ; Arboix Arzo, Margarita, dir. (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia) ; Pérez Fernández, Belén, dir. (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia)
Pendent.
Bellaterra : Universitat Autònoma de Barcelona, 2004  
4.
192 p, 1.7 MB Farmacocinética y eficacia de oxitetraciclina tras su administración intramuscular en bovino : : depleción tisular / El Korchi, Ghizlane ; Arboix Arzo, Margarita, dir. (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia) ; Pérez Fernández, Belén, dir. (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia)
El amplio uso de antibióticos en producción animal ha aportado sin duda un importante beneficio para la sanidad y el bienestar de los animales. Aunque, en los últimos años este uso ha sido objeto de duras críticas y presiones legales debido a la controversia originada entre el riesgo y el efecto beneficioso de estas sustancias. [...]
The wide use of antibiotics in animal production has contributed an important benefit for the health and the well-being of animals. However, the use of antibiotics has been recently criticized and there have been legal pressures to avoid it, due to the lack of a clear relation between its beneficial effects and its risk. [...]

Bellaterra : Universitat Autònoma de Barcelona, 2007  

Course materials 1 records found  
1.
7 p, 245.2 KB Farmacologia II [21265] / Clos Guillén, Victoria (Universitat Autònoma de Barcelona. Departament de Farmacologia, de Terapèutica i de Toxicologia) ; Alfón, José ; Mora, Fernando de ; Puigdemont, Anna ; Peréz, Belen ; Castells, Gloria ; Universitat Autònoma de Barcelona. Facultat de Veterinària
2008-09
Llicenciat en Veterinària [35]  

See also: similar author names
6 Perez, B.
1 Perez, Bernardo
11 Peréz, Belen
6 Pérez, B.
1 Pérez, B. A.
1 Pérez, Begoña
11 Pérez, Belen
11 Pérez, Belen
11 Pérez, Belén
1 Pérez, Belén.
1 Pérez, Briza
Interested in being notified about new results for this query?
Set up a personal email alert or subscribe to the RSS feed.