Resultados globales: 9 registros encontrados en 0.03 segundos.
Artículos, Encontrados 8 registros
Documentos de investigación, Encontrados 1 registros
Artículos Encontrados 8 registros  
1.
9 p, 1.2 MB Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset / Billingsley, K.J. (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Barbosa, I.A. (Department of Medical and Molecular Genetics. King's College London School of Basic and Medical Biosciences) ; Bandrés-Ciga, S. (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Quinn, J.P. ; Bubb, V.J. ; Deshpande, C. (Clinical Genetics Unit. Guys and St. Thomas' NHS Foundation Trust) ; Botia, J.A. (Department of Neurodegenerative Disease. UCL Institute of Neurology) ; Reynolds, R.H. (Department of Neurodegenerative Disease. UCL Institute of Neurology) ; Zhang, D. (Department of Neurodegenerative Disease. UCL Institute of Neurology) ; Simpson, M.A. (Department of Medical and Molecular Genetics. King's College London School of Basic and Medical Biosciences) ; Blauwendraat, C. (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Gan-Or, Z. (Department of Human Genetics. McGill University) ; Gibbs, J.R. (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Nalls, M.A. (Data Tecnica International) ; Singleton, A. (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Noyce, A. (Preventive Neurology Unit. Wolfson Institute of Preventive Medicine. QMUL) ; Tucci, A. (Department of Molecular Neuroscience. UCL Institute of Neurology) ; Middlehurst, B. ; Kia, D. (UCL Genetics Institute; and Department of Molecular Neuroscience. UCL Institute of Neurology) ; Tan, M. (Department of Clinical Neuroscience. University College London) ; Houlden, H. (Department of Molecular Neuroscience. UCL Institute of Neurology) ; Morris, H.R. (Department of Clinical Neuroscience. University College London) ; Plun-Favreau, H. (Department of Molecular Neuroscience. UCL Institute of Neurology) ; Holmans, P. (Biostatistics & Bioinformatics Unit. Institute of Psychological Medicine and Clinical Neuroscience. MRC Centre for Neuropsychiatric Genetics & Genomics) ; Hardy, J. (Department of Molecular Neuroscience. UCL Institute of Neurology) ; Trabzuni, D. (Department of Genetics. King Faisal Specialist Hospital and Research Centre) ; Bras, J. (UK Dementia Research Institute at UCL and Department of Molecular Neuroscience. UCL Institute of Neurology) ; Mok, K. (Department of Molecular Neuroscience. UCL Institute of Neurology) ; Kinghorn, K. (Institute of Healthy Ageing. University College London) ; Wood, N. (UCL Genetics Institute; and Department of Molecular Neuroscience. UCL Institute of Neurology) ; Lewis, P. (University of Reading) ; Guerreiro, R. (UK Dementia Research Institute at UCL and Department of Molecular Neuroscience. UCL Institute of Neurology) ; Lovering, R. (University College London) ; R'Bibo, L. (Department of Molecular Neuroscience. UCL Institute of Neurology) ; Rizig, M. (Department of Molecular Neuroscience. UCL Institute of Neurology) ; Escott-Price, V. (Cardiff University School of Medicine) ; Chelban, V. (Department of Molecular Neuroscience. UCL Institute of Neurology) ; Foltynie, T. (Department of Neurodegenerative Disease. UCL Institute of Neurology) ; Williams, N. (Cardiff University School of Medicine) ; Brice, A. (Institut du Cerveau et de la Moelle épinière. ICM. Inserm U 1127. CNRS. UMR 7225. Sorbonne Universités. UPMC University Paris 06. UMR S 1127. AP-HP. Pitié-Salpêtrière Hospital) ; Danjou, F. (Institut du Cerveau et de la Moelle épinière. ICM. Inserm U 1127. CNRS. UMR 7225. Sorbonne Universités. UPMC University Paris 06. UMR S 1127. AP-HP. Pitié-Salpêtrière Hospital) ; Lesage, S. (Institut du Cerveau et de la Moelle épinière. ICM. Inserm U 1127. CNRS. UMR 7225. Sorbonne Universités. UPMC University Paris 06. UMR S 1127. AP-HP. Pitié-Salpêtrière Hospital) ; Martinez, M. (INSERM UMR 1220; and Paul Sabatier University) ; Giri, A. (DZNE. German Center for Neurodegenerative Diseases) ; Schulte, C. (DZNE. German Center for Neurodegenerative Diseases) ; Brockmann, K. (DZNE. German Center for Neurodegenerative Diseases) ; Simón-Sánchez, J. (DZNE. German Center for Neurodegenerative Diseases) ; Heutink, P. (DZNE. German Center for Neurodegenerative Diseases) ; Rizzu, P. (DZNE. German Center for Neurodegenerative Diseases) ; Sharma, M. (Centre for Genetic Epidemiology. Institute for Clinical Epidemiology and Applied Biometry. University of Tubingen) ; Gasser, T. (DZNE. German Center for Neurodegenerative Diseases) ; Nicolas, A. (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Cookson, M. (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Faghri, F. (Department of Computer Science. University of Illinois at Urbana-Champaign) ; Hernández, Dena (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Shulman, J. (Jan and Dan Duncan Neurological Research Institute. Texas Children's Hospital) ; Robak, L. (Baylor College of Medicine) ; Lubbe, S. (Ken and Ruth Davee Department of Neurology. Northwestern University Feinberg School of Medicine) ; Finkbeiner, S. (Taube/Koret Center for Neurodegenerative Disease Research) ; Mencacci, N. (Northwestern University Feinberg School of Medicine) ; Lungu, C. (National Institutes of Health Division of Clinical Research. NINDS. National Institutes of Health) ; Scholz, S. (Neurodegenerative Diseases Research Unit. National Institute of Neurological Disorders and Stroke) ; Reed, X. (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Leonard, H. (Laboratory of Neurogenetics. National Institute on Aging. National Institutes of Health) ; Rouleau, G. (Montreal Neurological Institute. McGill University) ; Krohan, L. (Department of Human Genetics. McGill University) ; van Hilten, J. (Department of Neurology. Leiden University Medical Center) ; Marinus, J. (Department of Neurology. Leiden University Medical Center) ; Adarmes-Gómez, A. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Aguilar, M. (Fundació Docència i Recerca Mútua de Terrassa and Movement Disorders Unit. Department of Neurology. University Hospital Mutua de Terrassa. Terrassa) ; Alvarez, I. (Fundació Docència i Recerca Mútua de Terrassa and Movement Disorders Unit. Department of Neurology. University Hospital Mutua de Terrassa. Terrassa) ; Alvarez, V. (Hospital Universitario Central de Asturias) ; Javier Barrero, F. (Hospital Universitario Parque Tecnologico de la Salud) ; Bergareche Yarza, J. (Instituto de Investigación Sanitaria Biodonostia) ; Bernal-Bernal, I. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Blazquez, M. (Hospital Universitario Central de Asturias) ; Bernal, M.B.T. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Boungiorno, M. (Fundació Docència i Recerca Mútua de Terrassa and Movement Disorders Unit. Department of Neurology. University Hospital Mutua de Terrassa. Terrassa) ; Buiza-Rueda, D. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Cámara, A. (Hospital Clinic de Barcelona) ; Carcel, M. (Fundació Docència i Recerca Mútua de Terrassa and Movement Disorders Unit. Department of Neurology. University Hospital Mutua de Terrassa. Terrassa) ; Carrillo, F. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Carrión-Claro, M. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Cerdan, D. (Hospital General de Segovia) ; Clarimón, J. (Institut d'Investigació Biomèdica Sant Pau) ; Compta, Y. (Hospital Clinic de Barcelona) ; Diez-Fairen, Monica. (Fundació Docència i Recerca Mútua de Terrassa and Movement Disorders Unit. Department of Neurology. University Hospital Mutua de Terrassa. Terrassa) ; Dols-Icardo, O. (Centro de Investigación Biomédica en Red en Enfermedades Neurodegenerativas (CIBERNED)) ; Duarte, J. (Hospital General de Segovia) ; Duran, R.l. (Centro de Investigacion Biomedica. Universidad de Granada) ; Escamilla-Sevilla, F. (Hospital Universitario Virgen de las Nieves. Instituto de Investigación Biosanitaria de Granada) ; Ezquerra, M. (Hospital Clinic de Barcelona) ; Fernández, M. (Hospital Clinic de Barcelona) ; Fernández-Santiago, R. (Hospital Clinic de Barcelona) ; Garcia, C. (Hospital Universitario Central de Asturias) ; García-Ruiz, P. (Instituto de Investigación Sanitaria Fundación Jiménez Díaz) ; Gómez-Garre, P. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Heredia, M.G. (Hospital Universitario Virgen de la Victoria) ; Gonzalez-Aramburu, I. (Hospital Universitario Marqués de Valdecilla-IDIVAL) ; Pagola, A.G. (Instituto de Investigación Sanitaria Biodonostia) ; Hoenicka, J. (Institut de Recerca Sant Joan de Déu) ; Infante, J. (Hospital Universitario Marqués de Valdecilla-IDIVAL) ; Jesús, S. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Jimenez-Escrig, A. (Hospital Universitario Ramón y Cajal Madrid) ; Kulisevsky, J. (Institut d'Investigació Biomèdica Sant Pau) ; Labrador-Espinosa, M. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Lopez-Sendon, J. (Hospital Universitario Ramón y Cajal Madrid) ; de Munain Arregui, A.L. (Hospital Universitario Ramón y Cajal Madrid) ; Macias, D. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Torres, I.M. (Department of Neurology. Instituto de Investigación Sanitaria La Fe. Hospital Universitario y Politécnico La Fe) ; Marín, J. (Institut d'Investigació Biomèdica Sant Pau) ; Marti, M.J. (Hospital Clinic de Barcelona) ; Martínez-Castrillo, J. (Hospital Universitario Ramón y Cajal Madrid) ; Méndez-del-Barrio, C. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Menéndez González, M. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Mínguez, A. (Hospital Universitario Virgen de las Nieves. Instituto de Investigación Biosanitaria de Granada) ; Mir, P. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Rezola, E.M. (Instituto de Investigación Sanitaria Biodonostia) ; Muñoz García, José Esteban (Hospital Clinic de Barcelona) ; Pagonabarraga, J. (Institut d'Investigació Biomèdica Sant Pau) ; Pastor, Pau (Fundació Docència i Recerca Mútua de Terrassa and Movement Disorders Unit. Department of Neurology. University Hospital Mutua de Terrassa. Terrassa) ; Errazquin, F.P. (Hospital Universitario Virgen de la Victoria) ; Periñán-Tocino, T. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Ruiz-Martínez, J. (Instituto de Investigación Sanitaria Biodonostia) ; Ruz, C. (Centro de Investigacion Biomedica. Universidad de Granada) ; Rodriguez, A.S. (Hospital Universitario Marqués de Valdecilla-IDIVAL) ; Sierra, M. (Hospital Universitario Marqués de Valdecilla-IDIVAL) ; Suarez-Sanmartin, E. (Clinical Genetics Unit. Guys and St. Thomas' NHS Foundation Trust) ; Tabernero, C. (Hospital Universitario Ramón y Cajal Madrid) ; Tartari, J.P. (Fundació Docència i Recerca Mútua de Terrassa and Movement Disorders Unit. Department of Neurology. University Hospital Mutua de Terrassa. Terrassa) ; Tejera-Parrado, C. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Tolosa, E. (Hospital Clinic de Barcelona) ; Valldeoriola, F. (Hospital Clinic de Barcelona) ; Vargas-González, L. (Instituto de Biomedicina de Sevilla (IBiS). Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla) ; Vela, L. (Department of Neurology. Hospital Universitario Fundación Alcorcón) ; Vives, F. (Centro de Investigacion Biomedica. Universidad de Granada) ; Zimprich, A. (Department of Neurology. Medical University of Vienna) ; Pihlstrom, L. (Department of Neurology. Oslo University Hospital) ; Taba, P. (Department of Neurology and Neurosurgery. University of Tartu) ; Majamaa, K. (Department of Neurology and Medical Research Center. Oulu University Hospital) ; Siitonen, A. (Institute of Clinical Medicine. Department of Neurology. University of Oulu) ; Okubadejo, N. (University of Lagos) ; Ojo, O. (University of Lagos) ; Ryten, M. (Department of Neurodegenerative Disease. UCL Institute of Neurology) ; Koks, S. (Centre for Comparative Genomics. Murdoch University) ; Universitat Autònoma de Barcelona
Mitochondrial dysfunction has been implicated in the etiology of monogenic Parkinson's disease (PD). Yet the role that mitochondrial processes play in the most common form of the disease; sporadic PD, is yet to be fully established. [...]
2019 - 10.1038/s41531-019-0080-x
NPJ Parkinson's disease, Vol. 5 Núm. 1 (january 2019) , p. 8  
2.
Association of Apolipoprotein e with Intracerebral Hemorrhage Risk by Race/Ethnicity : A Meta-analysis / Marini, S. (Massachusetts General Hospital) ; Crawford, K. (Massachusetts General Hospital) ; Morotti, A. (Fondazione Mondino IRCCS, Pavia) ; Lee, M.J. (Massachusetts General Hospital) ; Pezzini, A. (Università degli Studi di Brescia) ; Moomaw, C.J. (University of Cincinnati) ; Flaherty, M.L. (University of Cincinnati) ; Montaner, Joan (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Roquer Gonzalez, Jaume (Institut Hospital del Mar d'Investigacions Mèdiques) ; Jimenez Conde, Jordi (Institut Hospital del Mar d'Investigacions Mèdiques) ; Giralt Steinhauer, Eva (Institut Hospital del Mar d'Investigacions Mèdiques) ; Elosua, Roberto (Institut Hospital del Mar d'Investigacions Mèdiques) ; Cuadrado Godia, Elisa (Institut Hospital del Mar d'Investigacions Mèdiques) ; Soriano Tarraga, Carolina (Institut Hospital del Mar d'Investigacions Mèdiques) ; Slowik, A. (Jagiellonian University Medical College, Kraków) ; Jagiella, J.M. (Jagiellonian University Medical College, Kraków) ; Pera, J. (Jagiellonian University Medical College, Kraków) ; Urbanik, A. (Jagiellonian University Medical College, Kraków) ; Pichler, A. (Jagiellonian University Medical College, Kraków) ; Hansen, B.M. (Lund University) ; McCauley, J.L. (John P. Hussman Institute for Human Genomics, Miami) ; Tirschwell, D.L. (University of Washington) ; Selim, M. (Beth Israel Deaconess Medical Center, Boston) ; Brown, D.L. (University of Michigan) ; Silliman, S.L. (University of Florida College of Medicine) ; Worrall, B.B. (University of Virginia Health System) ; Meschia, J.F. (Mayo Clinic, Jacksonville, Florida) ; Kidwell, C.S. (University of Arizona) ; Testai, F.D. (University of Illinois) ; Kittner, S.J. (University of Maryland School of Medicine) ; Schmidt, H. (Medical University of Graz) ; Enzinger, C. (Medical University of Graz) ; Deary, I.J. (University of Edinburgh) ; Rannikmae, K. (University of Edinburgh) ; Samarasekera, N. (University of Edinburgh) ; Salman, R.A.S. (University of Edinburgh) ; Sudlow, C.L. (University of Edinburgh) ; Klijn, C.J.M. (UMC Utrecht Brain Center Rudolf Magnus) ; Van Nieuwenhuizen, K.M. (UMC Utrecht Brain Center Rudolf Magnus) ; Fernandez Cadenas, Israel (Institut d'Investigació Biomèdica Sant Pau) ; Delgado Martínez, María Pilar (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Norrving, B. (Lund University) ; Lindgren, A. (Lund University) ; Goldstein, J.N. (Massachusetts General Hospital) ; Viswanathan, A. (Massachusetts General Hospital) ; Greenberg, S.M. (Massachusetts General Hospital) ; Falcone, G.J. (Yale University) ; Biffi, A. (Massachusetts General Hospital) ; Langefeld, C.D. (Wake Forest University, Winston-Salem, North Carolina) ; Woo, D. (University of Cincinnati College of Medicine) ; Rosand, J. (Massachusetts General Hospital) ; Anderson, C.D. (Massachusetts General Hospital) ; Universitat Autònoma de Barcelona
Importance: Genetic studies of intracerebral hemorrhage (ICH) have focused mainly on white participants, but genetic risk may vary or could be concealed by differing nongenetic coexposures in nonwhite populations. [...]
2019 - 10.1001/jamaneurol.2018.4519
JAMA Neurology, Vol. 76 Núm. 4 (april 2019) , p. 480-491  
3.
7 p, 508.5 KB Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk / Figlioli, Gisella (University of Pisa. Department of Biology) ; Chen, Bowang (German Cancer Research Center (DKFZ). Molecular Genetic Epidemiology (Germany)) ; Elisei, Rossella (University of Pisa. Department of Endocrinology and Metabolism (Italy)) ; Romei, Cristina (University of Pisa. Department of Endocrinology and Metabolism (Italy)) ; Campo, Chiara (University of Pisa. Department of Biology (Italy)) ; Cipollini, Monica (University of Pisa. Department of Biology (Italy)) ; Cristaudo, Alfonso (University of Pisa. Department of Endocrinology and Metabolism (Italy)) ; Bambi, Franco (Blood Centre, Azienda Ospedaliero Universitaria A. Meyer (Italy)) ; Paolicchi, Elisa (University of Pisa. Department of Biology (Italy)) ; Hoffmann, Per (University of Basel. Department of Biomedicine (Switzerland)) ; Herms, Stefan (University of Basel. Department of Biomedicine (Switzerland)) ; Kalemba, Michał (Maria Sklodowska-Curie Memorial Cancer Center. Department of Nuclear Medicine and Endocrine Oncology (Poland)) ; Kula, Dorota (Maria Sklodowska-Curie Memorial Cancer Center. Department of Nuclear Medicine and Endocrine Oncology (Poland)) ; Pastor Benito, Susana (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Marcos Dauder, Ricardo (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Velázquez Henar, Antonia (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Jarząb, Barbara (Maria Sklodowska-Curie Memorial Cancer Center. Department of Nuclear Medicine and Endocrine Oncology (Poland)) ; Landi, Stefano (University of Pisa. Department of Biology (Italy)) ; Hemminki, Kari (Lund University. Center for Primary Health Care Research, Clinical Research Center (Sweden)) ; Gemignani, Federica (University of Pisa. Department of Biology (Italy)) ; Försti, Asta (Lund University. Center for Primary Health Care Research, Clinical Research Center (Sweden))
A genome-wide association study (GWAS) performed on a high-incidence Italian population followed by replications on low-incidence cohorts suggested a strong association of differentiated thyroid cancer (DTC) with single nucleotide polymorphisms (SNPs) at 9q22. [...]
2015 - 10.1038/srep08922
Scientific reports, Vol. 5 (March 2015) , art. 8922  
4.
10 p, 1.0 MB Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes / Mishra, Rajashree (Division of Human Genetics. The Children's Hospital of Philadelphia) ; Chesi, Alessandra (Division of Human Genetics. The Children's Hospital of Philadelphia) ; Cousminer, Diana L. (Department of Genetics, Perelman School of Medicine, University of Pennsylvania) ; Hawa, Mohammad I. (Department of Immunobiology, Barts and the London School of Medicine and Dentistry, Queen Mary University of London) ; Bradfield, Jonathan P. (Center for Applied Genomics, The Children's Hospital of Philadelphia) ; Hodge, Kenyaita M. (Division of Human Genetics. The Children's Hospital of Philadelphia) ; Guy, Vanessa C. (Division of Human Genetics. The Children's Hospital of Philadelphia) ; Hakonarson, Hakon (Division of Human Genetics. The Children's Hospital of Philadelphia) ; Mauricio, Dídac (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol. Bone Mineral Density in Childhood Study) ; Schloot, Nanette C. (German Diabetes Center, Düsseldorf) ; Yderstræde, Knud B. (Odense University Hospital) ; Voight, Benjamin F. (Department of Genetics, Perelman School of Medicine, University of Pennsylvania) ; Schwartz, Stanley (Main Line Health System, Wynnewood, PA, USA.) ; Boehm, Bernhard O. (Department of Internal Medicine I. Ulm University Medical Centre) ; Leslie, Richard David (Department of Immunobiology. Barts and the London School of Medicine and Dentistry, Queen Mary University of London) ; Grant, Struan F. A. (Division of Human Genetics. The Children's Hospital of Philadelphia)
Background: In adulthood, autoimmune diabetes can present as non-insulin-requiring diabetes, termed as 'latent autoimmune diabetes in adults' (LADA). In this study, we investigated established type 1 diabetes (T1D) and type 2 diabetes (T2D) genetic loci in a large cohort of LADA cases to assess where LADA is situated relative to these two well-characterized, classic forms of diabetes. [...]
2017
BMC Medicine, Vol. 15 Núm. 88 (2017) , p. 1-10  
5.
16 p, 352.3 KB Patient-centered care in breast cancer genetic clinics / Brédart, Anne (Univesité Paris Descartes) ; Anota, Amélie (Centre Hospitalier Régional Universitaire de Besançon) ; Dick, Julia (Cancer Center Cologne) ; Kuboth, Violetta (Cancer Center Cologne) ; Lareyre, Olivier (Institut Curie) ; De Pauw, Antoine (Institut Curie) ; Cano, Alejandra (Universitat Autònoma de Barcelona. Departament de Psicologia Bàsica, Evolutiva i de l'Educació) ; Stoppa-Lyonnet, Dominique (Institut Curie) ; Schmutzler, Rita (Cancer Center Cologne) ; Dolbeault, Sylvie (Centre de Recherche en Épidémiologie et Santé des Populations (CESP)) ; Kop, Jean-Luc (Université de Lorraine)
With advances in breast cancer (BC) gene panel testing, risk counseling has become increasingly complex, potentially leading to unmet psychosocial needs. We assessed psychosocial needs and correlates in women initiating testing for high genetic BC risk in clinics in France and Germany, and compared these results with data from a literature review. [...]
2018 - 10.3390/ijerph15020319
International journal of environmental research and public health, Vol. 15 (february 2018)  
6.
12 p, 1.2 MB Glucocorticoid Receptors, Brain-Derived Neurotrophic Factor, Serotonin and Dopamine Neurotransmission are Associated with Interferon-Induced Depression / Udina, M (Department of Psychiatry, Hospital Clínic, Institut d'Investigacions Biomèdiques de Barcelona (IDIBAPS)) ; Navinés, Ricard (Parc de Salut Mar. Secció Hepàtica) ; Egmond, E ; Oriolo, G ; Langohr, K ; Gimenez, D (Parc de Salut Mar. Secció Hepàtica) ; Valdés, M ; Gómez-Gil, E ; Grande, I ; Gratacòs i Mayora, Mònica ; Kapczinski, F ; Artigas, F ; Vieta, E ; Solà, R (Liver Section, Parc de Salut Mar, UAB) ; Martín-Santos, R ; Universitat Autònoma de Barcelona
The role of inflammation in mood disorders has received increased attention. There is substantial evidence that cytokine therapies, such as interferon alpha (IFN-alpha), can induce depressive symptoms. [...]
2015 - 10.1093/ijnp/pyv135
International journal of neuropsychopharmacology, Vol. 19 (december 2015)  
7.
8 p, 184.4 KB Parkinson's Disease : From Genetics to Clinical Practice / Clarimón, Jordi (Institut d'Investigació Biomèdica Sant Pau) ; Kulisevsky, Jaime (Institut d'Investigació Biomèdica Sant Pau) ; Universitat Autònoma de Barcelona
Breakthroughs in genetics over the last decade have radically advanced our understanding of the etiological basis of Parkinson's disease (PD). Although much research remains to be done, the main genetic causes of this neurodegenerative disorder are now partially unraveled, allowing us to feel more confident that our knowledge about the genetic architecture of PD will continue to increase exponentially. [...]
2013 - 10.2174/1389202914666131210212305
Current Genomics, Vol. 14 (december 2013) , p. 560-567  
8.
11 p, 165.4 KB Efectos de la primera visita de Consejo Genético sobre la percepción de riesgo y el malestar emocional / González, Melinda (Universitat Autònoma de Barcelona) ; Blanco Guillermo, Ignacio (Institut Català d'Oncologia) ; Blasco, Tomás (Universitat Autònoma de Barcelona)
Objetivo: Analizar los efectos que provoca la primera visita de consejo genético para cáncer hereditario sobre la percepción de riesgo, y el malestar emocional en pacientes que acuden por primera vez a la Unidad de Consejo Genético (UCG) por historia familiar de cáncer de mama, ovario o colon hereditario. [...]
Objective: To analyze how perceived risk and emotional distress were affected by the first visit to a Genetic Counseling Unit in patients with a family history of hereditarian breast cancer, ovarian cancer, or colorectal cancer. [...]

2011 - 10.5209/rev_PSIC.2011.v8.n2-3.37891
Psicooncología, Vol. 8, núm. 2-3 (2011) , p. 441-451  

Documentos de investigación Encontrados 1 registros  
1.
1 p, 455.2 KB Variation in cardiovascular risk due to polymorphisms in lipoproteins and application of nutrigenomics / Rechi Lasala, Anna ; Ordóñez, J. 1952- (Jordi), (Universitat Autònoma de Barcelona. Departament de Bioquímica i Biologia Molecular) ; Universitat Autònoma de Barcelona. Facultat de Biociències
2013
Grau en Ciències Biomèdiques [832]  

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