María Rios, Rima Khabbaz, J E Kaplan, William W. Hall, Debra Kessler, Celso Bianco,
... Screened Blood Products Get access Maria Rios, Maria Rios Search for other works by this author on: Oxford Academic PubMed Google Scholar Rima F. Khabbaz, Rima F. Khabbaz Search for other ...
Tópico(s): Vector-Borne Animal Diseases
1994 - Oxford University Press | The Journal of Infectious Diseases
I. Desguerre, Marie Hully, Marlène Rio, Rima Nabbout,
Mitochondrial respiratory chain defects (RCD) often exhibit multiorgan involvement, affecting mainly tissues with high-energy requirements such as the brain. Epilepsy is frequent during the evolution of mitochondrial disorders (30%) with different presentation in childhood and adulthood in term of type of epilepsy, of efficacy of treatment and also in term of prognosis. Mitochondrial disorders can begin at any age but the diseases with early onset during childhood have generally severe or fatal outcome ...
Tópico(s): Biochemical Acid Research Studies
2014 - Elsevier BV | Revue Neurologique
Pierre‐Yves Maillard, Sarah Baer, Élise Schaefer, Béatrice Desnous, Nathalie Villeneuve, Anne Lépine, Alexandre Fabre, Caroline Lacoste, Salima El Chehadeh, Amélie Piton, Louise F. Porter, Caroline Perriard, Marie‐Thérèse Abi Wardé, Marie‐Aude Spitz, Vincent Laugel, Gaëtan Lesca, Audrey Putoux, Dorothée Ville, Cyril Mignot, Delphine Héron, Rima Nabbout, Giulia Barcia, Marlène Rio, Agathe Roubertie, Pierre Meyer, Véronique Paquis‐Flucklinger, Olivier Patat, Jérémie Lefranc, Marion Gérard, Julietta de Bellescize, Laurent Villard, Anne de Saint Martin, Mathieu Milh,
Abstract Objective γ‐Aminobutyric acid (GABA) A ‐receptor subunit variants have recently been associated with neurodevelopmental disorders and/or epilepsy. The phenotype linked with each gene is becoming better known. Because of the common molecular structure and physiological role of these phenotypes, it seemed interesting to describe a putative phenotype associated with GABA A ‐receptor–related disorders as a whole and seek possible genotype–phenotype correlations. Methods We collected clinical, ...
Tópico(s): RNA and protein synthesis mechanisms
2022 - Wiley | Epilepsia
Produção Nacional
Revisado por pares
Raquel Oliveira Santos Teixeira, Andréa Zhouri, Luana Dias Motta,
... Jequitinhonha, Minas Gerais, e da análise do EIA-RIMA de um complexo minerário na bacia do Rio Santo Antônio, sub-bacia do rio Doce, este ...
Tópico(s): Water Governance and Infrastructure
2020 - National Association of Post-Graduate Research in Social Sciences | Revista Brasileira de Ciências Sociais
Glaucilene Rodrigues dos Santos Silva Oliveira, Beatriz Brandão, Márcia de Melo Dórea, Artur Antônio Melo de Lira Brandt,
... ambiental através do produto educacional intitulado “Lixo não rima com rio”. A escolha desta proposta deve-se à demanda ...
Tópico(s): Education Pedagogy and Practices
2024 - UNIVERSIDADE FEDERAL DO PARANÁ | Divers !
C. Nascimento Silva, E.M. Carvalho Baptista,
... Mesa de Pedra (Valenca do Piaui) previstos no RIMA, em relacao a geomorfologia do rio Sambito. A metodologia constou de pesquisa bibliografica, documental ...
Tópico(s): Geography and Environmental Studies
2014 - UNIVERSIDADE FEDERAL DO AMAZONAS | Revista Geonorte
Rima Slim, Rosemary A. Fisher, Florian Milhavet, Reda Hemida, Samantha K. Rojas, Cécile Rittore, Rashmi Bagga, Mónica Aguinaga‐Ríos, Isabelle Touitou,
Hydatidiform mole (HM) is an abnormal human pregnancy characterised by excessive growth of placental trophoblasts and abnormal early embryonic development. Following a first such abnormal pregnancy, the risk for women of successive molar pregnancies significantly increases. To date variants in seven maternal-effect genes have been shown to cause recurrent HMs (RHM). NLRP7 is the major causative gene for RHM and codes for NOD-like receptor (NLR) family pyrin domain containing 7, which belongs to a family ...
Tópico(s): Polyomavirus and related diseases
2022 - Wiley | Human Mutation
Marie-Thérèse Dangles, Valérie Malan, Guillaume Dumas, Serge Romana, O Raoul, Delphine Coste‐Zeitoun, Christine Soufflet, Patricia Vignolo-Diard, Nadia Bahi‐Buisson, Christine Barnérias, Nicole Chémaly, Isabelle Desguerre, Cyril Gitiaux, Marie Hully, Marie Bourgeois, Anne Guimier, Marlène Rio, Arnold Münnich, Rima Nabbout, Anna Kamińska, Monika Eisermann,
We aimed to describe epilepsy and EEG patterns related to vigilance states and age, in chromosome15-long-arm-duplication-syndrome (dup15q) children with epilepsy, in both duplication types: interstitial (intdup15) and isodicentric (idic15). Clinical data and 70 EEGs of 12 patients (5 intdup15, 7 idic15), followed from 4.5 m.o to 17y4m (median follow-up 8y3m), were retrospectively reviewed. EEGs were analyzed visually and using power spectrum analysis. Seventy video-EEGs were analyzed (1–16 per patient, ...
Tópico(s): Congenital heart defects research
2021 - Elsevier BV | Clinical Neurophysiology
Mathilde Nizon, Joris Andrieux, Caroline Rooryck, Marie‐Christine de Blois, Emilie Bourel‐Ponchel, Béatrice Bourgois, Odile Boute, Albert David, Bruno Delobel, Bénédicte Duban‐Bedu, Fabienne Giuliano, Alice Goldenberg, Sarah Grotto, Delphine Héron, Houda Karmous‐Benailly, Boris Keren, Didier Lacombe, Jean‐Michel Lapierre, Cédric Le Caignec, Eric Le Galloudec, Martine Le Merrer, Anne‐Gaëlle Le Moing, Michèle Mathieu‐Dramard, Sylvie Nusbaum, Olivier Pichon, Lucile Pinson, O Raoul, Marlène Rio, Serge Romana, A. Roubertie, Laurence Colleaux, C Turleau, Michel Vekemans, Rima Nabbout, Valérie Malan,
Array comparative genomic hybridization (array CGH) has proven its utility in uncovering cryptic rearrangements in patients with X‐linked intellectual disability. In 2009, Giorda et al. identified inherited and de novo recurrent Xp11.23p11.22 microduplications in two males and six females from a wide cohort of patients presenting with syndromic intellectual disability. To date, 14 females and 5 males with an overlapping microduplication have been reported in the literature. To further characterize ...
Tópico(s): Glycosylation and Glycoproteins Research
2014 - Wiley | American Journal of Medical Genetics Part A
Isabelle Perrault, Fadi F. Hamdan, Marlène Rio, José‐Mario Capo‐Chichi, Nathalie Boddaert, Jean‐Claude Décarie, Bruno Maranda, Rima Nabbout, Michel Sylvain, Anne Lortie, Philippe P. Roux, Elsa Rossignol, Xavier Gérard, Giulia Barcia, Patrick Berquin, Arnold Münnich, Guy A. Rouleau, Josseline Kaplan, Jean‐Michel Rozet, Jacques L. Michaud,
Epileptic encephalopathies are increasingly thought to be of genetic origin, although the exact etiology remains uncertain in many cases. We describe here three girls from two nonconsanguineous families affected by a clinical entity characterized by dysmorphic features, early-onset intractable epilepsy, intellectual disability, and cortical blindness. In individuals from each family, brain imaging also showed specific changes, including an abnormally marked pontobulbar sulcus and abnormal signals ( ...
Tópico(s): Neuroscience and Neuropharmacology Research
2014 - Elsevier BV | The American Journal of Human Genetics
Produção Nacional
Revisado por pares
Yanick J. Crow, Diana Chase, Johanna L. Schmidt, Marcin Szynkiewicz, Gabriella Forte, Hannah Gornall, Anthony Oojageer, Beverley Anderson, Amy Pizzino, Guy Helman, Mohamed S. Abdel‐Hamid, Ghada M. H. Abdel‐Salam, Sam Ackroyd, Alec Aeby, Guillermo Agosta, Catherine S. W. Albin, Stavit A. Shalev, Montse Arellano, Giada Ariaudo, Vijay Aswani, Riyana Babul‐Hirji, Eileen Baildam, Nadia Bahi‐Buisson, Kathryn Bailey, Christine Barnérias, Magalie Barth, Roberta Battini, Michael W. Beresford, Geneviève Bernard, Marika Bianchi, Thierry Billette de Villemeur, Edward Blair, Miriam Bloom, Alberto Burlina, Maria Luisa Carpanelli, Daniel R. Carvalho, Manuel Castro‐Gago, Anna Cavallini, Cristina Cereda, Kate Chandler, David Chitayat, Abigail E. Collins, Concepción Sierra Córcoles, Nuno Cordeiro, Giovanni Crichiutti, Lyvia Dabydeen, Russell C. Dale, Stefano D’Arrigo, Christian G E L De Goede, Corinne De Laet, Liesbeth M. H. De Waele, Inés María Denzler, Isabelle Desguerre, Koenraad Devriendt, Maja Di Rocco, Michael Fahey, Elisa Fazzi, Colin D. Ferrie, António Figueiredo, Blanca Gener, Cyril Goizet, Nirmala Gowrinathan, Kalpana Gowrishankar, Donncha Hanrahan, Bertrand Isidor, Bülent Kara, Naz Khan, Mary D. King, Edwin P. Kirk, Ram Kumar, Lieven Lagae, P. Landrieu, Heinz Lauffer, Vincent Laugel, Roberta La Piana, Ming Lim, Jean‐Pierre Lin, Tarja Linnankivi, Mark T. Mackay, Daphna Marom, Charles Marques Lourenço, Shane McKee, Isabella Moroni, Jenny E.V. Morton, Marie‐Laure Moutard, Kevin Murray, Rima Nabbout, Sheela Nampoothiri, Noemí Núñez‐Enamorado, P.J. Oades, Ivana Olivieri, John R. Østergaard, Belén Pérez‐Dueñas, Julie Prendiville, Venkateswaran Ramesh, Magnhild Rasmussen, Luc Régal, Federica Ricci, Marlène Rio, Diana Rodriguez, Agathe Roubertie, E. Salvatici, Karin Segers, G Sinha, Doriette Soler, Ronen Spiegel, Tommy Stödberg, Rachel Straussberg, Kathryn J. Swoboda, Mohnish Suri, Uta Tacke, Tiong Yang Tan, Johann te Water Naudé, Keng Wee Teik, Maya Thomas, Marianne Till, Davide Tonduti, Enza Maria Valente, Rudy N. Van Coster, Marjo S. van der Knaap, Grace Vassallo, Raymon Vijzelaar, Julie Vogt, Geoffrey Wallace, Evangeline Wassmer, Hannah J. Webb, William Whitehouse, Robyn Whitney, Maha S. Zaki, Sameer M. Zuberi, John H. Livingston, Flore Rozenberg, Pierre Lebon, Adeline Vanderver, Simona Orcesi, Gillian Rice,
Aicardi–Goutières syndrome is an inflammatory disease occurring due to mutations in any of TREX1 , RNASEH2A , RNASEH2B , RNASEH2C , SAMHD1 , ADAR or IFIH1 . We report on 374 patients from 299 families with mutations in these seven genes. Most patients conformed to one of two fairly stereotyped clinical profiles; either exhibiting an in utero disease‐onset (74 patients; 22.8% of all patients where data were available), or a post‐natal presentation, usually within the first year of life (223 patients; 68.6%), characterized ...
Tópico(s): Inflammasome and immune disorders
2015 - Wiley | American Journal of Medical Genetics Part A
Maryam Rezaei, Beena Suresh, Eric Bereke, Zahra Hadipour, Mónica Aguinaga‐Ríos, Jianhua Qian, Rashmi Bagga, Majid Fardaei, Reda Hemida, Sujatha Jagadeesh, Jacek Majewski, Rima Slim,
Abstract Recurrent hydatidiform moles (RHMs) are human pregnancies with abnormal embryonic development and hyperproliferating trophoblast. Biallelic mutations in NLRP7 and KHDC3L, members of the subcortical maternal complex (SCMC), explain the etiology of RHMs in only 60% of patients. Here we report the identification of seven functional variants in a recessive state in three SCMC members, five in NLRP7 , one in NLRP5, and one in PADI6 . In NLRP5 , we report the first patient with RHMs and biallelic mutations. ...
Tópico(s): Prenatal Screening and Diagnostics
2021 - Wiley | Clinical Genetics
Pipelines are linear construction that intersect several environments, requiring integration of environmental and technical aspects in its various elaboration steps. Environmental impact assessment if made to integrate the environmental information to enable environmental characterization, possibility identify previously fragilities of environment what contributes to the safety forecast of the significant impacts. These studies shall consider superimpose of the elements and the worsening of critical ...
Tópico(s): Environmental and Social Impact Assessments
2008 - | Aleph UCLA Undergraduate Research Journal for the Humanities and Social Sciences
Carolina de la Hoz Schilling, Ahmed Diame, Alfonso Hernández Ríos, Mario Mingarro, Rima W. Jabado,
Abstract Fisheries bycatch is considered the largest threat to sea turtle populations globally. However, it has been challenging to assess the impact of bycatch on sea turtles in some regions such as Northwest Africa (i.e. Cabo Verde, Guinea, Guinea–Bissau, Mauritania, Senegal, Sierra Leone and The Gambia) owing to large data gaps. This hampers effective management actions and interferes with conservation efforts in the region. Five sea turtle species occur in Northwest Africa (i.e. green turtle Chelonia ...
Tópico(s): Ichthyology and Marine Biology
2023 - Wiley | Aquatic Conservation Marine and Freshwater Ecosystems
Jonathan E. Kaplan, Yasuhiro Yamamura, Eddy Ríos‐Olivares, Robert O. Cannon, Rima Khabbaz, Duane J. Gubler, Edmundo N. Kaiselburd, Trudie M. Hartley, Michael D. Lairmore,
Serum specimens from Puerto Rican residents were tested for antibodies to human T lymphotropic virus type I (HTLV-I) using an enzyme immunoassay, Western immunoblot, and radioimmunoprecipitation assays. Of 1,279 specimens obtained during a dengue virus surveillance program in 1986 and 1987, 3 (0.2%) tested positive; an additional 11 were indeterminate. Of 602 specimens obtained from blood donors in Ponce in 1987, 1 (0.2%) was positive; an additional specimen was indeterminate. Of 21 persons hospitalized ...
Tópico(s): Animal Disease Management and Epidemiology
1989 - American Society of Tropical Medicine and Hygiene | American Journal of Tropical Medicine and Hygiene
Produção Nacional
Silvia Cristina Martins de Souza,
Este artigo elege como locus de observação a cidade do Rio de Janeiro de fins do século XIX e início do XX. Nele busca-se analisar a produção e circulação de algumas poesias compostas por pessoas com pouca ou nenhuma educação formal e os possíveis usos e funções que seus autores conferiram a seus poemas.
Tópico(s): Sociology and Education in Brazil
2015 - UNIVERSIDADE FEDERAL DE MINAS GERAIS | Varia Historia
Giulia Barcia, Christine Barnérias, Marlène Rio, Karine Siquier-Pernet, Isabelle Desguerre, Laurence Colleaux, Arnold Münnich, Agnès Rötig, Rima Nabbout,
STXBP1 (MUNC18.1), encoding syntaxin binding protein 1, has been reported in Ohtahara syndrome, a rare epileptic encephalopathy with suppression burst pattern on EEG, in patients with infantile spasms and in a few patients with nonsyndromic mental retardation without epilepsy. We report a patient who presented late onset infantile spasms. Epilepsy was controlled but the patient developed severe mental delay. A first diagnosis of mitochondrial disease was based on clinical presentation and on a partial ...
Tópico(s): Fetal and Pediatric Neurological Disorders
2013 - Elsevier BV | European Journal of Medical Genetics
Andrés H. Rossi, Diego Ojeda, Augusto Varese, Lautaro Sánchez, María Mora González López Ledesma, Ignacio Mazzitelli, Anabel Alvarez Juliá, Santiago Oviedo Rouco, Horacio M. Pallarés, Guadalupe S. Costa Navarro, Natalí B. Rasetto, Corina García, Shirley D. Wenker, Lila Y. Ramis, Magalí G. Bialer, María José de Leone, Carlos Esteban Hernando, Santiago Sosa, Luciana Bianchimano, Antonella S. Ríos, María Soledad Treffinger Cienfuegos, Julio J. Caramelo, Yésica Longueira, Natalia Laufer, Diego E. Álvarez, Jorge Carradori, Dariana Pedrozza, Alejandra Rima, Cecilia Echegoyen, Regina Ercole, Paula Gelpi, Susana Marchetti, Martín Zubieta, Guillermo Docena, Nicolás Kreplak, Marcelo J. Yanovsky, Jorge Geffner, Marina Pífano, Andrea V. Gamarnik,
Massive vaccination offers great promise for halting the global COVID-19 pandemic. However, the limited supply and uneven vaccine distribution create an urgent need to optimize vaccination strategies. We evaluate SARS-CoV-2-specific antibody responses after Sputnik V vaccination of healthcare workers in Argentina, measuring IgG anti-spike titers and neutralizing capacity after one and two doses in a cohort of naive or previously infected volunteers. By 21 days after receiving the first dose of the ...
Tópico(s): Vaccine Coverage and Hesitancy
2021 - Elsevier BV | Cell Reports Medicine
Este trabajo intenta revalorizar el juego-rima infantil femenino, en el ambito de Rio de La Plata, como medio de supervivencia del Romancero y otras composiciones de origen hispanico, de transmision oral. El enfoque tomado apunta ...
Tópico(s): Spanish Linguistics and Language Studies
2012 - National University of La Plata | Olivar
Tri Rima Setyawati, Rio Jati Kusuma, Harry Freitag Luglio Muhammad, Neni Oktiyani, Sunarti Sunarti, Rosmala Nur, Syaiful Hendra,
BACKGROUND: Gembili or Dioscorea esculenta is a local food that is produced by several areas in Indonesia. Few studies have reported its health benefits for diabetes mellitus but a little is understood about its mechanism of action. PGC-1α is a transcriptional coactivator for genes that involved in energy metabolism and increased expression of this gene has previously been associated with improved insulin sensitivity. AIM: The objective of this study was to investigate the effect of Gembili starch ...
Tópico(s): Diet and metabolism studies
2021 - ID Design 2012/DOOEL Skopje | Open Access Macedonian Journal of Medical Sciences
Rio de Janeiro is going through a sort of unique organization of the public environment, the rising of the social segments and culture antinarrative that, somehow, suffer from marginalization and exclusion. As means of rhymes, rappers (“MCs”) are building a literary field, which creates tension on places of communication, culture, territorial appropriation, the city. It is a poetic production that requires reflection based on plural and distinct canonical tools that confronts its own concept of literature. ...
Tópico(s): Urban Development and Societal Issues
2015 - UNIVERSIDADE DO ESTADO DO RIO DE JANEIRO | Matraga - Revista do Programa de Pós-Graduação em Letras da UERJ
Yassemine Khawajkie, Nawel Mechtouf, Ngoc Minh Nguyen, Kurosh Rahimi, Magali Bréguet, Jocelyne Arseneau, Brigitte M. Ronnett, Lori Hoffner, Felicia Lazure, Marjolaine Arnaud, Fabrice Peers, L. Tan, Basam Abu Rafea, Mónica Aguinaga‐Ríos, Neil S. Horowitz, Asangla Ao, Seang Lin Tan, Richard Brown, William Buckett, Urvashi Surti, Karine Hovanes, Trilochan Sahoo, Philippe Sauthier, Rima Slim,
Hydatidiform mole (HM) is an aberrant human pregnancy characterized by excessive trophoblastic proliferation and abnormal embryonic development. HM has two morphological types, complete (CHM) and partial (PHM), and non-recurrent ones have three genotypic types, androgenetic monospermic, androgenetic dispermic, and triploid dispermic. Most available studies on risk factors predisposing to different types of HM and their malignant transformation mainly suffer from the lack of comprehensive genotypic ...
Tópico(s): Prenatal Screening and Diagnostics
2019 - Elsevier BV | Modern Pathology
Rima Rida, Paola Ríos, Alex Manzano,
Abstract A Rare Cause of Diabetes: COVID-19 Introduction: Environmental factors like viruses have been described in the mechanism of pancreatic beta cell destruction. Various viruses can trigger autoimmunity in individuals genetically predisposed to diabetes. Severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) has been shown to bind to angiotensin-converting enzyme 2 (ACE 2) which is expressed throughout the body, including pancreatic cells, leading to direct injury of the endocrine pancreas. ...
Tópico(s): Phagocytosis and Immune Regulation
2021 - Endocrine Society | Journal of the Endocrine Society
Michael Ortiz-Rios, Beshoy Agayby, Fabien Balezeau, Marcus Haag, Samy Rima, Jaime Cadena-Valencia, Michael C. Schmid,
Developing optogenetic methods for research in non-human primates (NHP) is important for translational neuroscience and for delineating brain function with unprecedented specificity. Here we assess, in macaque monkeys, the selectivity by which optogenetic stimulation of the primary visual cortex (V1) drives the local laminar and widespread cortical connectivity related to visual perception. Towards this end, we transfected neurons with light-sensitive channelrhodopsin in dorsal V1. fMRI revealed that ...
Tópico(s): Neuroscience and Neural Engineering
2023 - Elsevier BV | Current Research in Neurobiology
Nadia Bahi‐Buisson, Eva Guttierrez‐Delicado, Christine Soufflet, Marlène Rio, Valérie Cormier‐Daire, Didier Lacombe, Delphine Héron, Alain Verloès, Sameer M. Zuberi, Lydie Bürglen, Alexandra Afenjar, Marie Laure Moutard, Patrick Edery, Antonio Novelli, Laura Bernardini, Olivier Dulac, Rima Nabbout, Perrine Plouin, Agatino Battaglia,
Summary Purpose: Previous reports have summarized the seizures types occurring in 1p36 deletion syndrome. To better define the spectrum of epilepsy, we studied 91 patients (median age 7.8 years) with confirmed 1p36 deletion. Methods: Based on clinical charts, we retrospectively analyzed the evolution of both the EEG findings and seizures. Results: Epilepsy occurred in 53 patients (58.2%), with onset at a median 2.75 months. First seizures were generalized tonic (8 cases), tonic and clonic (6) or myoclonic ( ...
Tópico(s): Genomics and Rare Diseases
2007 - Wiley | Epilepsia
Nadia Bahi‐Buisson, Anna Kamińska, Nathalie Boddaert, Marlène Rio, Alexandra Afenjar, Marion Gérard, Fabienne Giuliano, Jacques Motté, Delphine Héron, Marie Ange N'Guyen Morel, Perrine Plouin, Christian Richelme, Vincent des Portes, Olivier Dulac, Christophe Philippe, Catherine Chiron, Rima Nabbout, Thierry Bienvenu,
Summary Mutations in the X‐linked cyclin‐dependent kinase‐like 5 ( CDKL5 ) gene are responsible for a severe encephalopathy with early epilepsy. So far, the electroclinical phenotype remains largely unknown and no clear genotype–phenotype correlations have been established. Purpose: To characterize the epilepsy associated with CDKL5 mutations and to look for a relationship between the genotype and the course of epilepsy. Methods : We retrospectively analyzed the electroclinical phenotypes of 12 patients ...
Tópico(s): Advanced biosensing and bioanalysis techniques
2008 - Wiley | Epilepsia
María Mora González López Ledesma, Lautaro Sánchez, Diego Ojeda, Santiago Oviedo Rouco, Andrés H. Rossi, Augusto Varese, Ignacio Mazzitelli, Carla A. Pascuale, Esteban A. Miglietta, Pamela Elizabeth Rodríguez, Horacio M. Pallarés, Guadalupe S. Costa Navarro, Julio J. Caramelo, Paul W. Rothlauf, Zhuoming Liu, Louis-Marie Bloyet, Marjorie Cornejo Pontelli, Natalí B. Rasetto, Shirley D. Wenker, Lila Y. Ramis, Magalí G. Bialer, María José de Leone, Carlos Esteban Hernando, Luciana Bianchimano, Antonella S. Ríos, María Soledad Treffinger Cienfuegos, Diana Rosa Rodríguez Garcia, Yésica Longueira, Natalia Laufer, Diego E. Álvarez, Ana Ceballos, Valeria Ochoa, Cecilia Monzani, Gariela Turk, Melina Salvatori, Jorge Carradori, Katherine Prost, Alejandra Rima, Claudia Varela, Regina Ercole, Rosana Toro, Sebastián Gutiérrez, Martín Zubieta, Dolores Acuña, Mercedes Soledad Nabaes Jodar, Carolina Torres, Laura Mojsiejczuk, Mariana Viegas, Pilar Velazquez, Clarisa Testa, Nicolás Kreplak, Marcelo J. Yanovsky, Sean P. J. Whelan, Jorge Geffner, Marina Pífano, Andrea V. Gamarnik,
Vaccines have been produced in record time for SARS-CoV-2, offering the possibility of halting the global pandemic. However, inequalities in vaccine accessibility in different regions of the world create a need to increase international cooperation.
Tópico(s): Vaccine Coverage and Hesitancy
2022 - American Society for Microbiology | mBio
Michael P. Milham, Christopher I. Petkov, Pascal Belin, Suliann Ben Hamed, HC Evrard, Damien A. Fair, Andrew S. Fox, Seán Froudist‐Walsh, Takuya Hayashi, Sabine Kästner, P. Christiaan Klink, Piotr Majka, Rogier B. Mars, Adam Messinger, Colline Poirier, Charles E. Schroeder, Amir Shmuel, Afonso C. Silva, Wim Vanduffel, David C. Van Essen, Zheng Wang, Anna Wang Roe, Melanie Wilke, Ting Xu, Mohammad Hadi Aarabi, Ralph Adolphs, Aarit Ahuja, Ashkan Alvand, Céline Amiez, Joonas A. Autio, Reza Azadi, Eunha Baeg, Ruiliang Bai, Pinglei Bao, Michele A. Basso, Austin K. Behel, Yvonne Bennett, Boris C. Bernhardt, Bharat B. Biswal, Sethu Raman Boopathy, Susann Boretius, Elena Borra, Rober Boshra, Elizabeth A. Buffalo, Long Cao, James Cavanaugh, Céline Amiez, Gianfranco Chavez, Li Min Chen, Xiaohong Chen, Luqi Cheng, François Chouinard-Decorte, Simon Clavagnier, Justine Cléry, Stanley J. Colcombe, Bevil R. Conway, Mélina Cordeau, Olivier Coulon, Yue Cui, Rakshit Dadarwal, Robert Dahnke, Theresa M. Desrochers, Deying Li, Kacie Dougherty, Hannah Doyle, Carly M. Drzewiecki, Marianne Duyck, W. M. Ediri Arachchi, Catherine Elorette, Abdelhadi Essamlali, Alan C. Evans, Alfonso Fajardo, Héctor Figueroa, Alexandre R. Franco, Guilherme Blazquez Freches, Steve Frey, Patrick Friedrich, Atsushi Fujimoto, Masaki Fukunaga, Maëva Gacoin, Guillermo Gallardo, Lixia Gao, Yang Gao, Danny Garside, Eduardo A. Garza‐Villarreal, Maxime Gaudet-Trafit, Marzio Gerbella, Steven Giavasis, Daniel Glen, Ana Rita Ribeiro Gomes, Sandra González Torrecilla, Alessandro Gozzi, Roberto A. Gulli, Suzanne N. Haber, Fadila Hadj‐Bouziane, S Hashimoto, Michael Hawrylycz, Quansheng He, Ye He, Katja Heuer, Bassem Hiba, Felix Hoffstaedter, Seok‐Jun Hong, Yuki Hori, Yujie Hou, Amy Howard, María de la Iglesia-Vayá, Takuro Ikeda, Lucija Rapan, Jorge Jaramillo, Hank P. Jedema, Hecheng Jin, Minqing Jiang, Benjamin Jung, Igor Kagan, Itamar Kahn, Gregory Kiar, Yuki Kikuchi, Bjørg Elisabeth Kilavik, Nobuyuki Kimura, Ulysse Klatzmann, Sze Chai Kwok, Hsin‐Yi Lai, Franck Lamberton, Julia F. Lehman, Pengcheng Li, Xinhui Li, Xinjian Li, Zhifeng Liang, Conor Liston, A. Roger Little, Cirong Liu, Ning Liu, Xiaojin Liu, Xinyu Liu, Haidong Lu, Kep Kee Loh, Christopher R. Madan, Loïc Magrou, Daniel S. Margulies, Mathilda Froesel, Sheyla Mejia, Yao Meng, Ravi S. Menon, David Meunier, Alex J. Mitchell, Anna S. Mitchell, Aidan J. Murphy, Towela Mvula, Michael Ortiz-Rios, Diego Emanuel Ortuzar Martinez, Marco Pagani, Nicola Palomero‐Gallagher, Vikas Pareek, Pierce Perkins, Fernanda Ponce, Mark Postans, Pierre Pouget, Meizhen Qian, Julian S.B. Ramirez, Erika P. Raven, Isabel Restrepo, Samy Rima, Kathleen S. Rockland, Nadira Yusif Rodriguez, Élise Roger, Eduardo Rojas Hortelano, Marcello G. P. Rosa, Andrew F. Rossi, Peter H. Rudebeck, Brian E. Russ, Tomoko Sakai, Kadharbatcha S. Saleem, Jérôme Sallet, Stephen J. Sawiak, David Schaeffer, Caspar M. Schwiedrzik, Jakob Seidlitz, Julien Sein, Jitendra Sharma, Kelly Shen, Wei-An Sheng, Sunhang Shi, Won Mok Shim, Luciano Simone, Nikoloz Sirmpilatze, Virginie Sivan, Xiaowei Song, Aaron Tanenbaum, Jordy Tasserie, Paul A. Taylor, Xiaoguang Tian, Roberto Toro, Lucas Trambaiolli, Nick Upright, Julien Vezoli, Sam Vickery, Julio Villalón, Xiaojie Wang, Yufan Wang, Alison R. Weiss, Charles Wilson, Ting Yat Wong, Choong‐Wan Woo, Bichan Wu, Xiao Du, Augix Guohua Xu, Dongrong Xu, Zhou Xufeng, Essa Yacoub, Ningrong Ye, Ying Zhang, Chihiro Yokoyama, Xiongjie Yu, Shasha Yue, Lu Yuheng, Xin Yumeng, D Zaldívar, Shaomin Zhang, Yuguang Zhao, Zhanguang Zuo,
Open science initiatives are creating opportunities to increase research coordination and impact in nonhuman primate (NHP) imaging. The PRIMatE Data and Resource Exchange community recently developed a collaboration-based strategic plan to advance NHP imaging as an integrative approach for multiscale neuroscience.
Tópico(s): Cell Image Analysis Techniques
2021 - Cell Press | Neuron
Rima-Maria Rahal, Hanjo Hamann, Hilmar Brohmer, Florian Pethig,
The open and transparent documentation of scientific processes has been established as a core antecedent of free knowledge. This also holds for generating robust insights in the scope of research projects. To convince academic peers and the public, the research process must be understandable and retraceable ( reproducible ), and repeatable ( replicable ) by others, precluding the inclusion of fluke findings into the canon of insights. In this contribution, we outline what reproducibility and replicability ( ...
Tópico(s): Meta-analysis and systematic reviews
2022 - Pensoft Publishers | Research Ideas and Outcomes
Chloe Durrleman, D. Grévent, Mélodie Aubart, Manoëlle Kossorotoff, Charles‐Joris Roux, Anna Kamińska, Marlène Rio, Giulia Barcia, Nathalie Boddaert, Arnold Münnich, Rima Nabbout, Isabelle Desguerre,
Stroke-like episodes (SLEs) are defined as acute onset of neurological symptoms mimicking a stroke and radiological lesions non-congruent to vascular territory. We aimed to analyze the acute clinical and radiological features of SLEs to determine their pathophysiology.We performed a monocenter retrospective analysis of 120 SLEs in 60 children over a 20-year period. Inclusion criteria were compatible clinical symptoms and stroke-like lesions on brain magnetic resonance imaging (MRI; performed for all ...
Tópico(s): Mitochondrial Function and Pathology
2023 - Wiley | European Journal of Neurology