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Magnesium-enriched deep-sea water inhibits NLRP3 inflammasome activation and dampens inflammation

Heliyon 2024年第15期10卷 e35136页

作者： Wang, Hsueh-Hsiao Huang, Chi-Ruei Lin, Hsin-Chung Lin, Hsin-An Chen, Yu-Jen Tsai, Kuen-Jou Shih, Chieh-Tien Huang, Kuo-Yang Ojcius, David M. Tsai, Ming-Hang Tseng, Kuang-Wen Chen, Lih-Chyang Department of Medicine MacKay Medical College Master Program in Biomedicine College of Science and Engineering National Taitung University Biomedicine Agriculture and Food Sciences Research Center College of Science and Engineering National Taitung University Graduate Institute of Pathology and Parasitology National Defense Medical Center Division of Clinical Pathology Department of Pathology Tri-Service General Hospital National Defense Medical Center Division of Infection Department of Medicine Tri-Service General Hospital SongShan Branch National Defense Medical Center Department of Health Promotion and Health Education National Taiwan Normal University Department of Medical Research MacKay Memorial Hospital Department of Radiation Oncology MacKay Memorial Hospital Department of Artificial Intelligence and Medical Application MacKay Junior College of Medicine Nursing and Management Department of Medical Research China Medical University Hospital Department of Laboratory Medicine MacKay Memorial Hospital Department of Nursing MacKay Medical College Department of Biomedical Sciences University of the Pacific Arthur Dugoni School of Dentistry Department of Medicine Tri-Service General Hospital SongShan Branch National Defense Medical Center

The NLRP3 inflammasome is an essential component of the innate immune system, but excessive activation can lead to inflammatory diseases. Ion fluxes across the plasma membrane or from intracellular stores are known to regulate NLRP3 inflammasome activation. Deep-sea water (DSW) contains high concentrations of many mineral ions, which could potentially influence NLRP3 inflammasome activation. However, the impact of DSW on NLRP3 inflammasome activation has not been investigated. Here, we demonstrated that DSW with water hardness levels up to 500 mg/L did not affect cell viability or the expression of NLRP3 inflammasome components in macrophages derived from THP-1 cells. However, the DSW significantly inhibited IL-1β secretion and caspase-1 activation in response to NLRP3 activators such as nigericin, ATP, or monosodium urate (MSU) crystals. Mechanically, it was discovered that the presence of 5 mM magnesium ions (Mg2⁺), equivalent to the Mg2⁺ concentration found in the DSW with a water hardness of 500 mg/L, inhibits NLRP3 inflammasome activation. This indicates that Mg2⁺ contributes to the mechanism by which DSW mitigates NLRP3 inflammasome activation. Moreover, DSW administration effectively lessens MSU-triggered peritonitis in mice, a commonly used model for examining the impacts of NLRP3 inflammasome activation. These results show that DSW enriched with Mg²⁺ could potentially be beneficial in modulating NLRP3 inflammasome-associated diseases. © 2024 The Authors

关键词： Deep-sea water Macrophages Magnesium NLRP3 inflammasome

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MetaMOPE: a web service for mobile phase determination and fast chromatography peaks evaluation for metabolomics

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Bioinformatics Advances 2023年第1期3卷

作者： Tsai, Dong-Ming Chang, Ching-Yao Lin, Shih-Ming Kuo, Tien-Chueh Wang, San-Yuan Chen, Guan-Yuan Kuo, Ching-Hua Tseng, Yufeng Jane Graduate Institute of Biomedical Electronics and Bioinformatics National Taiwan University Taipei 106216 Taiwan The Metabolomics Core Laboratory Centers of Genomic and Precision Medicine National Taiwan University Taipei 100225 Taiwan Department of Computer Science and Information Engineering National Taiwan University Taipei 106216 Taiwan Master Program for Clinical Pharmacogenomics and Pharmacoproteomics School of Pharmacy Taipei Medical University Taipei 110301 Taiwan Forensic Medicine College of Medicine National Taiwan University Taipei 100225 Taiwan School of Pharmacy College of Medicine National Taiwan University Taipei 100225 Taiwan

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Optimization of hybrid PVA/hFDM scaffold preparation

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AIP Conference Proceedings 2021年第1期2344卷

作者： Rizqa Inayati Muhammad Suhaeri Nuzli Fahdia Melinda Remelia Radiana Dhewayani Antarianto 1Master Program in Biomedical Science Faculty of Medicine Universitas Indonesia Jl. Salemba Raya No. 6 Central Jakarta DKI Jakarta 10430 Indonesia 2Rumah Sakit Universitas Indonesia Kampus Universitas Indonesia Depok West Java 16424 Indonesia 3Stem cell and Tissue Engineering Research Cluster Indonesian Medical Education and Research Institute (IMERI) Universitas Indonesia Salemba Raya Jakarta West Java 10430 Indonesia 4Doctoral Program in Biomedical Science Faculty of Medicine Universitas Indonesia Jl. Salemba Raya No. 6 Central Jakarta DKI Jakarta 10430 Indonesia 5Department of Basic Biomedicine Faculty of Medicine Universitas Kristen Indonesia Jl Mayjen Sutoyo No 2 DKI Jakarta 13630 Indonesia 6Department of Histology Faculty of Medicine Universitas Indonesia Jl. Salemba Raya No. 6 Central Jakarta DKI Jakarta 10430 Indonesia

Osteogenic differentiation from Mesenchymal Stem Cell (MSC) to osteoblast has a clinical significance which is very important for treating bone injuries, in the form of femoral fractures with the most cases in Indonesia. Various studies have been conducted to find the best scaffold that can improve osteogenic differentiation, one of which is the development of a hybrid scaffold made from natural biomaterials in the form of the extracellular matrix, and from synthetic biomaterials. The discovery of the best scaffold is not only focused on the source of the scaffold but also requires optimization of the method in making the scaffold. Therefore, the aim of this study is to find out the optimum method for making hybrid scaffolds that support osteogenic differentiation from MSC. Materials and methods: human Fibroblast-derived Matrix (hFDM) as a hybrid scaffold material collected from decellularized fibroblasts cultures from post-cleft-surgery reconstruction palatal skin. Fibroblast cell cultures were divided into two groups of cultures, cultures without Platelet Rich Plasma (PRP), and cultures with the addition of PRP. For decellularization, we performed optimization at the preparation stage of the decellularization solution, and the time of culture for decellularization. In the preparation of the decellularization solution, we divided it into two groups, NH4OH as material from the decellularization solution was diluted with PBS before mixing with 0.25% Triton X-100, and NH4OH was diluted directly in 0.25% Triton X-100. In optimizing the culture time for decellularization, we divided it into three groups, decellularization on the day when cell growth reached 100% confluent, decellularization on the 3rd day after 100% confluent (H + 3) cells, and decellularization on the 4th day after 100% confluent (H + 4) cells. Next, the hFDM matrix is collected and added Polyvinyl Alcohol (PVA) solutions to form a hybrid PVA / hFDM scaffold in the form of a hydrogel. Observations on h

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Hypoxia-responsive circular RNA circAAGAB reduces breast cancer malignancy by activating p38 MAPK and sponging miR-378 h

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Cancer cell international 2023年第1期23卷 45页

作者： Kuan-Yi Lee Chia-Ming Liu Li-Han Chen Chien-Yueh Lee Tzu-Pin Lu Li-Ling Chuang Liang-Chuan Lai Graduate Institute of Physiology College of Medicine National Taiwan University Taipei Taiwan. Institute of Fisheries Science College of Life Science National Taiwan University Taipei Taiwan. Department of Life Science College of Life Science National Taiwan University Taipei Taiwan. Master Program for Biomedical Engineering College of Biomedical Engineering China Medical University Taichung Taiwan. Institute of Epidemiology and Preventive Medicine Department of Public Health National Taiwan University Taipei Taiwan. School of Physical Therapy and Graduate Institute of Rehabilitation Science College of Medicine Chang Gung University Taoyuan Taiwan. lchuang@gap.cgu.edu.tw. Department of Physical Medicine and Rehabilitation Chang Gung Memorial Hospital at Linkou Taoyuan Taiwan. lchuang@gap.cgu.edu.tw. Graduate Institute of Physiology College of Medicine National Taiwan University Taipei Taiwan. llai@ntu.edu.tw. Bioinformatics and Biostatistics Core Center of Genomic and Precision Medicine National Taiwan University Taipei Taiwan. llai@ntu.edu.tw.

BACKGROUND:Breast cancer is a prevalent disease in women, with high prevalence worldwide. The hypoxic microenvironment of solid tumors develops during the progress of carcinogenesis and leads to greater malignancy and treatment resistance. Recently, accumulating evidence indicates that non-coding RNAs, such as circular RNAs (circRNAs), play a pivotal role in altering cellular functions. However, the underlying mechanisms of circRNAs in breast cancer are still unclear. Therefore, the purpose of this study was to investigate the role of a tumor-suppressive circRNA, circAAGAB, in breast cancer by assuming down-regulation of circAAGAB under hypoxia and the properties of a tumor suppressor. METHODS:Firstly, circAAGAB was identified from expression profiling by next generation sequencing. Next, the stability of circAAGAB increased by interacting with the RNA binding protein FUS. Moreover, cellular and nuclear fractionation showed that most circAAGAB resided in the cytoplasm and that it up-regulated KIAA1522, NKX3-1, and JADE3 by sponging miR-378 h. Lastly, the functions of circAAGAB were explored by identifying its down-stream genes using Affymetrix microarrays and validated by in vitro assays. RESULTS:The results showed that circAAGAB reduced cell colony formation, cell migration, and signaling through p38 MAPK pathway, as well as increased radiosensitivity. CONCLUSION:These findings suggest that the oxygen-responsive circAAGAB acts as a tumor suppressor in breast cancer, and may contribute to the development of a more specific therapeutic regimen for breast cancer.

关键词： Breast cancer Hypoxia Radiosensitivity Tumor suppressor circAAGAB miRNA sponge p38 MAPK

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Decellularization of liver cubes using multiple site syringe injection for generating native liver scaffold: Preliminary report

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AIP Conference Proceedings 2019年第1期2193卷

作者： Radiana D. Antarianto A. A. Ayu Asri Prima Dewi Adrian Pragiwaksana Jeanne Adiwinata Pawitan 1Department of Histology Faculty of Medicine Universitas Indonesia Jl Salemba Raya No 6 Senen Central Jakarta 10430 Indonesia 2Stem Cell and Tissue Engineering Research Cluster Indonesian Medical Education and Research Institute Faculty of Medicine Universitas Indonesia Jl Salemba Raya No 6 Senen Central Jakarta 10430 Indonesia 3Master Program in Biomedical Science Faculty of Medicine Universitas Indonesia Jl Salemba Raya No 6 Senen Central Jakarta 10430 Indonesia 4Department of Histology Faculty of Medicine Warmadewa University Jl. Terompong 24 Tanjung Bungkak Denpasar Bali Indonesia 5Integrated Stem Cell Technology Service Unit Cipto Mangunkusumo National General Hospital Jl. Diponegoro No.71 Salemba Jakarta Indonesia

Scaffold is one of the important parts of tissue engineering. Liver scaffolds are obtained by decellularization of native liver. Frequently used decellularization methods include immersion or peristaltic pump perfusion techniques. Immersion technique requires longer duration and risk of tissue decay in the tissue core. Limited laboratory facilities have a peristaltic pump, thus limiting the usage of perfusion decellularization techniques. Therefore, the aim of this study was to develop a technique of simple liver decellularization with multiple site syringe injection. Material and methods: Isolated rat livers were freeze-thawed and cut into cubical form with a size of 1.5 cm × 1.5 cm × 0.7 cm up to 1 cm. The liver cubes were incubated in EGTA solution for 30 minutes and followed by multiple site syringe injection with increasing SDS concentration (0.1 %, 0.25%, 0.5%, 0.75%, and 1%) until appeared transparent (± 6 hours). The decellularized liver cubes were processed histologically and stained with hematoxylin-eosin. Result and discussion: Decellularized liver cubes using multiple site syringe injection compared to undecellularized liver showed removal of cells and structurally intact extracellular matrix as observed from histological specimens. Conclusions: Multiple site syringe injection is a simple technique to decellularized liver cubes for preparation of native liver scaffold for tissue engineering.

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Metadata Correction: Importance-Performance Analysis of Personal Health Records in Taiwan: A Web-Based Survey

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Journal of medical Internet research 2017年第6期19卷 e209页

作者： Hsiao-Hsien Rau Yi-Syuan Wu Chi-Ming Chu Fu-Chung Wang Min-Huei Hsu Chi-Wen Chang Kang-Hua Chen Yen-Liang Lee Senyeong Kao Yu-Lung Chiu Hsyien-Chia Wen Anis Fuad Chien-Yeh Hsu Hung-Wen Chiu Graduate Institute of Biomedical Informatics Taipei Medical University Taipei Taiwan. Administration Department Healthconn Corp Taipei Taiwan. Institute of Medical Informatics Department of Computer Science of Information Engineering National Cheng Kung University Tainan Taiwan. School Of Public Health National Defense Medical Center Taiepi Taiwan. National Health Insurance Administration Ministry of Health and Welfare Taiepi Taiwan. School of Nursing College of Medicine Chang Gung University Linkou Taiwan. Division of Endocrinology Department of Pediatrics Linkou Chang Gung Memorial Hospital Linkou Taiwan. Internet of Things Laboratory Chunghwa Telecom Laboratories TaoYuen Taiwan. School of Health Care Administration Taipei Medical University Taipei Taiwan. Department of Biostatistics Epidemiology and Population Health Faculty of Medicine Universitas Gadjah Mada Yogyakarta Indonesia. Department of Information Management National Taipei University of Nursing and Health Sciences Taipei Taiwan. Master Program in Global Health and Development Taipei Medical University Taipei Taiwan.

[This corrects the article DOI: .].

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The pathogenicity of COVID-19 and the role of pentraxin-3: An updated review study

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Pathology - Research and Practice 2022年 238卷

作者： Ria Margiana Satish Kumar Sharma Bilal Irshad Khan Ameer A. Alameri Maria Jade Catalan Opulencia Ali Thaeer Hammid Thulfeqar Ahmed Hamza Sharaf Khamrakulovich Babakulov Walid Kamal Abdelbasset Zanko Hassan Jawhar Department of Anatomy Faculty of Medicine Universitas Indonesia Jakarta Indonesia Master's Programme Biomedical Sciences Faculty of Medicine Universitas Indonesia Jakarta Indonesia Andrology Program Faculty of Medicine Universitas Airlangga Surabaya Indonesia Dr. Soetomo General Academic Hospital Surabaya Indonesia Department of Pharmacology Glocal School of Pharmacy The Glocal University Saharanpur India Mbbs Rawalpindi Medical University Rawalpindi Pakistan Department of Chemistry University of Babylon Iraq College of Business Administration Ajman University Ajman United Arab Emirates Computer Engineering Techniques Department Faculty of Information Technology Imam Ja’afar Al-Sadiq University Baghdad Iraq Medical laboratory techniques department Al-Mustaqbal University College Babylon Iraq Tashkent State Dental Institute Makhtumkuli Street 103 Tashkent 100047 Uzbekistan Research scholar Department of Scientific affairs Samarkand State Medical Institute Amir Temur Street 18 Samarkand Uzbekistan Department of Health and Rehabilitation Sciences College of Applied Medical Sciences Prince Sattam bin Abdulaziz University Al Kharj Saudi Arabia Department of Physical Therapy Kasr Al-Aini Hospital Cairo University Giza Egypt Department of Medical Laboratory Science College of Health Science Lebanese French University Kurdistan Region Iraq

In recent years, the COVID-19 pandemic has become one of the most crucial scientific issues in the world, and efforts to eradicate the disease are still ongoing. The acute inflammatory reaction associated with this disease is associated with several complications such as cytokine storm, multiple organ damage, lung fibrosis, and blood clots. PTX3, as part of the humoral innate immune systems, is one of the acute-phase proteins that perform various functions, such as modulating inflammation, repairing tissue, and recruiting immune cells. PTX3 is increased in people with SARS-CoV-2, and its level decreases with proper treatment. Therefore, it can be regarded as a suitable marker for the prognosis of the COVID-19 and evaluating the effectiveness of the treatment method applied. However, some studies have shown that PTX3 can be a double-edged sword and develop tumors by providing an immunosuppressive environment.

关键词： COVID-19 SARS-CoV-2 Pentraxin-3 Acute-phase proteins

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The Broad Institute-Six Years Later

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CHEMISTRY & BIOLOGY 2010年第4期17卷 311-312页

作者： McCarthy, Alice Main Text “In June 2003 the scientific and medical communities at MIT Harvard University and its affiliated hospitals and the Whitehead Institute banded together as collaborating partners to form the Eli and Edythe L. Broad Institute based in Cambridge MA. The Broad Institute established with initial funding from a $100 million philanthropic donation from the Los Angeles-based Broad family was primarily viewed as a marriage between the Whitehead Institute's Center for Genome Research (WICGR) and the Harvard Institute of Chemistry and Cell Biology (ICCB). Eli Broad founder and chairman of AIG SunAmerica Inc. explained “the purpose of the Broad Institute is to create a new type of research institute to build on the accomplishments of the human genome project and to move to clinical applications to both prevent and cure diseases.” Every Thursday morning we meet with perhaps 20 faculty members and 100 other researchers to discuss what we're all doing and should be doing next. -David Altschuler This paragraph was written five years ago when the Broad Institute was in its very earliest days as a life science research community (McCarthy 2005). Since that time “the Broad” as it's known has kept true to Eli Broad's vision having attracted a talented group of researchers faculty trainees and professional staff. This 1600 person research community known internally as “Broadies” includes faculty staff and students from throughout the MIT and Harvard biomedical research communities and beyond with collaborations spanning over a hundred private and public institutions in more than 40 countries worldwide. “What is special about the Broad is that we have people from Harvard MIT and the Harvard hospitals come together and work on problems of shared interest that could not be solved in their own individuals labs” explains David Altshuler M.D. Ph.D. Deputy Director and one of the Broad's six core faculty members. “These problems require expertise beyond any one principal investigator and in

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Novel cancer treatment paradigm targeting hypoxia-induced factor in conjunction with current therapies to overcome resistance

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Journal of experimental & clinical cancer research : CR 2023年第1期42卷 171页

作者： Ting-Wan Kao Geng-Hao Bai Tian-Li Wang Ie-Ming Shih Chi-Mu Chuang Chun-Liang Lo Meng-Chen Tsai Li-Yun Chiu Chu-Chien Lin Yao-An Shen Department of Pathology School of Medicine College of Medicine Taipei Medical University Taipei 110301 Taiwan. Graduate Institute of Clinical Medicine College of Medicine Taipei Medical University Taipei 110301 Taiwan. Department of Internal Medicine National Taiwan University Hospital College of Medicine National Taiwan University Taipei City 100225 Taiwan. Departments of Pathology Oncology and Gynecology and Obstetrics Johns Hopkins Medical Institutions 1550 Orleans StreetRoom 306 Baltimore MD CRB221231 USA. Sidney Kimmel Comprehensive Cancer Center Johns Hopkins University School of Medicine Baltimore MD USA. Faculty of Medicine School of Medicine National Yang-Ming Chiao Tung University Taipei 112304 Taiwan. Department of Obstetrics and Gynecology Taipei Veterans General Hospital Taipei 112201 Taiwan. Department of Midwifery and Women Health Care National Taipei University of Nursing and Health Sciences Taipei 112303 Taiwan. Department of Biomedical Engineering National Yang-Ming Chiao Tung University Taipei 112304 Taiwan. Medical Device Innovation and Translation Center National Yang Ming Chiao Tung University Taipei 112304 Taiwan. Department of General Medicine Taipei Medical University Hospital Taipei 110301 Taiwan. Department of General Medicine Mackay Memorial Hospital Taipei 104217 Taiwan. School of Medicine College of Medicine Taipei Medical University Taipei City 110301 Taiwan. Department of Pathology School of Medicine College of Medicine Taipei Medical University Taipei 110301 Taiwan. shen1202@tmu.edu.tw. Graduate Institute of Clinical Medicine College of Medicine Taipei Medical University Taipei 110301 Taiwan. shen1202@tmu.edu.tw. International Master/Ph.D. Program in Medicine College of Medicine Taipei Medical University Taipei 110301 Taiwan. shen1202@tmu.edu.tw.

Chemotherapy, radiotherapy, targeted therapy, and immunotherapy are established cancer treatment modalities that are widely used due to their demonstrated efficacy against tumors and favorable safety profiles or tolerability. Nevertheless, treatment resistance continues to be one of the most pressing unsolved conundrums in cancer treatment. Hypoxia-inducible factors (HIFs) are a family of transcription factors that regulate cellular responses to hypoxia by activating genes involved in various adaptations, including erythropoiesis, glucose metabolism, angiogenesis, cell proliferation, and apoptosis. Despite this critical function, overexpression of HIFs has been observed in numerous cancers, leading to resistance to therapy and disease progression. In recent years, much effort has been poured into developing innovative cancer treatments that target the HIF pathway. Combining HIF inhibitors with current cancer therapies to increase anti-tumor activity and diminish treatment resistance is one strategy for combating therapeutic resistance. This review focuses on how HIF inhibitors could be applied in conjunction with current cancer treatments, including those now being evaluated in clinical trials, to usher in a new era of cancer therapy.

关键词： Chemotherapy Combination therapy HIF-1 HIF-2 Hypoxia Immunotherapy Metabolic therapy Radiotherapy Target therapy Therapeutic resistance

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Author Correction: Brain clocks capture diversity and disparities in aging and dementia across geographically diverse populations

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Nature medicine 2024年第12期30卷 3779页

作者： Sebastian Moguilner Sandra Baez Hernan Hernandez Joaquín Migeot Agustina Legaz Raul Gonzalez-Gomez Francesca R Farina Pavel Prado Jhosmary Cuadros Enzo Tagliazucchi Florencia Altschuler Marcelo Adrián Maito María E Godoy Josephine Cruzat Pedro A Valdes-Sosa Francisco Lopera John Fredy Ochoa-Gómez Alfredis Gonzalez Hernandez Jasmin Bonilla-Santos Rodrigo A Gonzalez-Montealegre Renato Anghinah Luís E d'Almeida Manfrinati Sol Fittipaldi Vicente Medel Daniela Olivares Görsev G Yener Javier Escudero Claudio Babiloni Robert Whelan Bahar Güntekin Harun Yırıkoğulları Hernando Santamaria-Garcia Alberto Fernández Lucas David Huepe Gaetano Di Caterina Marcio Soto-Añari Agustina Birba Agustin Sainz-Ballesteros Carlos Coronel-Oliveros Amanuel Yigezu Eduar Herrera Daniel Abasolo Kerry Kilborn Nicolás Rubido Ruaridh A Clark Ruben Herzog Deniz Yerlikaya Kun Hu Mario A Parra Pablo Reyes Adolfo M García Diana L Matallana José Alberto Avila-Funes Andrea Slachevsky María I Behrens Nilton Custodio Juan F Cardona Pablo Barttfeld Ignacio L Brusco Martín A Bruno Ana L Sosa Ortiz Stefanie D Pina-Escudero Leonel T Takada Elisa Resende Katherine L Possin Maira Okada de Oliveira Alejandro Lopez-Valdes Brian Lawlor Ian H Robertson Kenneth S Kosik Claudia Duran-Aniotz Victor Valcour Jennifer S Yokoyama Bruce Miller Agustin Ibanez Latin American Brain Health Institute Universidad Adolfo Ibañez Santiago de Chile Chile. Cognitive Neuroscience Center Universidad de San Andrés Buenos Aires Argentina. Department of Neurology Massachusetts General Hospital and Harvard Medical School Boston MA USA. Universidad de los Andes Bogota Colombia. Global Brain Health Institute (GBHI) University of California San Francisco CA USA. Global Brain Health Institute (GBHI) Trinity College Dublin Dublin Ireland. The University of California Santa Barbara (UCSB) Santa Barbara CA USA. Escuela de Fonoaudiología Universidad San Sebastián Santiago de Chile Chile. Grupo de Bioingeniería Decanato de Investigación Universidad Nacional Experimental del Táchira San Cristóbal Venezuela. Advanced Center for Electrical and Electronic Engineering Universidad Técnica Federico Santa María Valparaíso Chile. University of Buenos Aires Buenos Aires Argentina. The Clinical Hospital of Chengdu Brain Sciences Institute University of Electronic Sciences and Technology of China Chengdu China. Technology of China Chengdu China. Cuban Neuroscience Center La Habana Cuba. Grupo de Neurociencias de Antioquia (GNA) University of Antioquia Medellín Colombia. Department of Psychology Master Program of Clinical Neuropsychology Universidad Surcolombiana Neiva Neiva Colombia. Department of Psychology Universidad Cooperativa de Colombia Arauca Colombia. Neurocognition and Psychophysiology Laboratory Universidad Surcolombiana Neiva Colombia. Reference Center of Behavioural Disturbances and Dementia School of Medicine University of Sao Paulo Sao Paulo Brazil. Traumatic Brain Injury Cognitive Rehabilitation Out-Patient Center University of Sao Paulo Sao Paulo Brazil. Center for Social and Cognitive Neuroscience School of Psychology Universidad Adolfo Ibáñez Santiago Chile. Neuropsychology and Clinical Neuroscience Laboratory (LANNEC) Physiopathology Program-Institute of Biomedical Sciences (ICBM) Neuroscience and East Neuroscience Dep

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