Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Andrés Augusto, Arias"'
Autor:
Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, Peng Zhang, Jeremy Manry, Yoann Seeleuthner, Yu Zhang, Alexandre Bolze, Matthieu Chaldebas, Baptiste Milisavljevic, Adrian Gervais, Paul Bastard, Takaki Asano, Lucy Bizien, Federica Barzaghi, Hassan Abolhassani, Ahmad Abou Tayoun, Alessandro Aiuti, Ilad Alavi Darazam, Luis M. Allende, Rebeca Alonso-Arias, Andrés Augusto Arias, Gokhan Aytekin, Peter Bergman, Simone Bondesan, Yenan T. Bryceson, Ingrid G. Bustos, Oscar Cabrera-Marante, Sheila Carcel, Paola Carrera, Giorgio Casari, Khalil Chaïbi, Roger Colobran, Antonio Condino-Neto, Laura E. Covill, Ottavia M. Delmonte, Loubna El Zein, Carlos Flores, Peter K. Gregersen, Marta Gut, Filomeen Haerynck, Rabih Halwani, Selda Hancerli, Lennart Hammarström, Nevin Hatipoğlu, Adem Karbuz, Sevgi Keles, Christèle Kyheng, Rafael Leon-Lopez, Jose Luis Franco, Davood Mansouri, Javier Martinez-Picado, Ozge Metin Akcan, Isabelle Migeotte, Pierre-Emmanuel Morange, Guillaume Morelle, Andrea Martin-Nalda, Giuseppe Novelli, Antonio Novelli, Tayfun Ozcelik, Figen Palabiyik, Qiang Pan-Hammarström, Rebeca Pérez de Diego, Laura Planas-Serra, Daniel E. Pleguezuelo, Carolina Prando, Aurora Pujol, Luis Felipe Reyes, Jacques G. Rivière, Carlos Rodriguez-Gallego, Julian Rojas, Patrizia Rovere-Querini, Agatha Schlüter, Mohammad Shahrooei, Ali Sobh, Pere Soler-Palacin, Yacine Tandjaoui-Lambiotte, Imran Tipu, Cristina Tresoldi, Jesus Troya, Diederik van de Beek, Mayana Zatz, Pawel Zawadzki, Saleh Zaid Al-Muhsen, Mohammed Faraj Alosaimi, Fahad M. Alsohime, Hagit Baris-Feldman, Manish J. Butte, Stefan N. Constantinescu, Megan A. Cooper, Clifton L. Dalgard, Jacques Fellay, James R. Heath, Yu-Lung Lau, Richard P. Lifton, Tom Maniatis, Trine H. Mogensen, Horst von Bernuth, Alban Lermine, Michel Vidaud, Anne Boland, Jean-François Deleuze, Robert Nussbaum, Amanda Kahn-Kirby, France Mentre, Sarah Tubiana, Guy Gorochov, Florence Tubach, Pierre Hausfater, COVID Human Genetic Effort, COVIDeF Study Group, French COVID Cohort Study Group, CoV-Contact Cohort, COVID Clinicians, Orchestra Working Group, Amsterdam UMC Covid-19 Biobank, NIAID-USUHS COVID Study Group, Isabelle Meyts, Shen-Ying Zhang, Anne Puel, Luigi D. Notarangelo, Stephanie Boisson-Dupuis, Helen C. Su, Bertrand Boisson, Emmanuelle Jouanguy, Jean-Laurent Casanova, Qian Zhang, Laurent Abel, Aurélie Cobat
Publikováno v:
Genome Medicine, Vol 16, Iss 1, Pp 1-3 (2024)
Externí odkaz:
https://doaj.org/article/8a927eb5859b43cf96c9c3e30c509b07
Autor:
Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, Peng Zhang, Jeremy Manry, Yoann Seeleuthner, Yu Zhang, Alexandre Bolze, Matthieu Chaldebas, Baptiste Milisavljevic, Adrian Gervais, Paul Bastard, Takaki Asano, Lucy Bizien, Federica Barzaghi, Hassan Abolhassani, Ahmad Abou Tayoun, Alessandro Aiuti, Ilad Alavi Darazam, Luis M. Allende, Rebeca Alonso-Arias, Andrés Augusto Arias, Gokhan Aytekin, Peter Bergman, Simone Bondesan, Yenan T. Bryceson, Ingrid G. Bustos, Oscar Cabrera-Marante, Sheila Carcel, Paola Carrera, Giorgio Casari, Khalil Chaïbi, Roger Colobran, Antonio Condino-Neto, Laura E. Covill, Ottavia M. Delmonte, Loubna El Zein, Carlos Flores, Peter K. Gregersen, Marta Gut, Filomeen Haerynck, Rabih Halwani, Selda Hancerli, Lennart Hammarström, Nevin Hatipoğlu, Adem Karbuz, Sevgi Keles, Christèle Kyheng, Rafael Leon-Lopez, Jose Luis Franco, Davood Mansouri, Javier Martinez-Picado, Ozge Metin Akcan, Isabelle Migeotte, Pierre-Emmanuel Morange, Guillaume Morelle, Andrea Martin-Nalda, Giuseppe Novelli, Antonio Novelli, Tayfun Ozcelik, Figen Palabiyik, Qiang Pan-Hammarström, Rebeca Pérez de Diego, Laura Planas-Serra, Daniel E. Pleguezuelo, Carolina Prando, Aurora Pujol, Luis Felipe Reyes, Jacques G. Rivière, Carlos Rodriguez-Gallego, Julian Rojas, Patrizia Rovere-Querini, Agatha Schlüter, Mohammad Shahrooei, Ali Sobh, Pere Soler-Palacin, Yacine Tandjaoui-Lambiotte, Imran Tipu, Cristina Tresoldi, Jesus Troya, Diederik van de Beek, Mayana Zatz, Pawel Zawadzki, Saleh Zaid Al-Muhsen, Mohammed Faraj Alosaimi, Fahad M. Alsohime, Hagit Baris-Feldman, Manish J. Butte, Stefan N. Constantinescu, Megan A. Cooper, Clifton L. Dalgard, Jacques Fellay, James R. Heath, Yu-Lung Lau, Richard P. Lifton, Tom Maniatis, Trine H. Mogensen, Horst von Bernuth, Alban Lermine, Michel Vidaud, Anne Boland, Jean-François Deleuze, Robert Nussbaum, Amanda Kahn-Kirby, France Mentre, Sarah Tubiana, Guy Gorochov, Florence Tubach, Pierre Hausfater, COVID Human Genetic Effort, COVIDeF Study Group, French COVID Cohort Study Group, CoV-Contact Cohort, COVID-STORM Clinicians, COVID Clinicians, Orchestra Working Group, Amsterdam UMC Covid-19 Biobank, NIAID-USUHS COVID Study Group, Isabelle Meyts, Shen-Ying Zhang, Anne Puel, Luigi D. Notarangelo, Stephanie Boisson-Dupuis, Helen C. Su, Bertrand Boisson, Emmanuelle Jouanguy, Jean-Laurent Casanova, Qian Zhang, Laurent Abel, Aurélie Cobat
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-25 (2023)
Abstract Background We previously reported that impaired type I IFN activity, due to inborn errors of TLR3- and TLR7-dependent type I interferon (IFN) immunity or to autoantibodies against type I IFN, account for 15–20% of cases of life-threatening
Externí odkaz:
https://doaj.org/article/86e4db2aa39842caa8f2f5c9e6d95290
Autor:
Carolina Mantilla, Mónica Toro, María Elsy Sepúlveda, Margarita Insuasty, Diana di Filippo, Juan Álvaro López, Carolina Baquero, María Cristina Navas, Andrés Augusto Arias
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 38, Iss 0, Pp 30-42 (2018)
Introduction: Type III glycogen storage disease (GSD III) is an autosomal recessive disorder in which a mutation in the AGL gene causes deficiency of the glycogen debranching enzyme. The disease is characterized by fasting hypoglycemia, hepatomegaly
Externí odkaz:
https://doaj.org/article/86cf748545b342ea8c311d1bb7948d65
Autor:
Quentin Philippot, Masato Ogishi, Jonathan Bohlen, Julia Puchan, Andrés Augusto Arias, Tina Nguyen, Marta Martin-Fernandez, Clement Conil, Darawan Rinchai, Mana Momenilandi, Seyed Alireza Mahdaviani, Mohammad Keramatipour, Jérémie Rosain, Rui Yang, Taushif Khan, Anna-Lena Neehus, Marie Materna, Ji Eun Han, Jessica Peel, Federico Mele, Marc Weisshaar, Sandra Jovic, Paul Bastard, Romain Lévy, Tom Le Voyer, Peng Zhang, Majistor Raj Luxman Maglorius Renkilaraj, Carlos A. Arango-Franco, Simon Pelham, Yoann Seeleuthner, Mathieu Pochon, Manar Mahmoud Ahmad Ata, Fatima Al Ali, Mélanie Migaud, Camille Soudée, Tatiana Kochetkov, Anne Molitor, Raphael Carapito, Seiamak Bahram, Bertrand Boisson, Claire Fieschi, Davood Mansouri, Nico Marr, Satoshi Okada, Mohammad Shahrooei, Nima Parvaneh, Zahra Chavoshzadeh, Aurélie Cobat, Dusan Bogunovic, Laurent Abel, Stuart G. Tangye, Cindy S. Ma, Vivien Béziat, Federica Sallusto, Stéphanie Boisson-Dupuis, Jacinta Bustamante, Jean-Laurent Casanova, Anne Puel
Publikováno v:
Science Immunology. 8
Patients with autosomal recessive (AR) IL-12p40 or IL-12Rβ1 deficiency display Mendelian susceptibility to mycobacterial disease (MSMD) due to impaired IFN-γ production and, less commonly, chronic mucocutaneous candidiasis (CMC) due to impaired IL-
Autor:
Masato Ogishi, Rui Yang, Rémy Rodriguez, Dominic P. Golec, Emmanuel Martin, Quentin Philippot, Jonathan Bohlen, Simon J. Pelham, Andrés Augusto Arias, Taushif Khan, Manar Ata, Fatima Al Ali, Flore Rozenberg, Xiao-Fei Kong, Maya Chrabieh, Candice Laine, Wei-Te Lei, Ji Eun Han, Yoann Seeleuthner, Zenia Kaul, Emmanuelle Jouanguy, Vivien Béziat, Leila Youssefian, Hassan Vahidnezhad, V. Koneti Rao, Bénédicte Neven, Claire Fieschi, Davood Mansouri, Mohammad Shahrooei, Sevgi Pekcan, Gulsum Alkan, Melike Emiroğlu, Hüseyin Tokgöz, Jouni Uitto, Fabian Hauck, Jacinta Bustamante, Laurent Abel, Sevgi Keles, Nima Parvaneh, Nico Marr, Pamela L. Schwartzberg, Sylvain Latour, Jean-Laurent Casanova, Stéphanie Boisson-Dupuis
Publikováno v:
Journal of Experimental Medicine. 220
Inborn errors of IFN-γ immunity can underlie tuberculosis (TB). We report three patients from two kindreds without EBV viremia or disease but with severe TB and inherited complete ITK deficiency, a condition associated with severe EBV disease that r
Autor:
Daniela, Matuozzo, Estelle, Talouarn, Astrid, Marchal, Jeremy, Manry, Yoann, Seeleuthner, Yu, Zhang, Alexandre, Bolze, Matthieu, Chaldebas, Baptiste, Milisavljevic, Peng, Zhang, Adrian, Gervais, Paul, Bastard, Takaki, Asano, Lucy, Bizien, Federica, Barzaghi, Hassan, Abolhassani, Ahmad Abou, Tayoun, Alessandro, Aiuti, Ilad Alavi, Darazam, Luis M, Allende, Rebeca, Alonso-Arias, Andrés Augusto, Arias, Gokhan, Aytekin, Peter, Bergman, Simone, Bondesan, Yenan T, Bryceson, Ingrid G, Bustos, Oscar, Cabrera-Marante, Sheila, Carcel, Paola, Carrera, Giorgio, Casari, Khalil, Chaïbi, Roger, Colobran, Antonio, Condino-Neto, Laura E, Covill, Loubna, El Zein, Carlos, Flores, Peter K, Gregersen, Marta, Gut, Filomeen, Haerynck, Rabih, Halwani, Selda, Hancerli, Lennart, Hammarström, Nevin, Hatipoğlu, Adem, Karbuz, Sevgi, Keles, Christèle, Kyheng, Rafael, Leon-Lopez, Jose Luis, Franco, Davood, Mansouri, Javier, Martinez-Picado, Ozge Metin, Akcan, Isabelle, Migeotte, Pierre-Emmanuel, Morange, Guillaume, Morelle, Andrea, Martin-Nalda, Giuseppe, Novelli, Antonio, Novelli, Tayfun, Ozcelik, Figen, Palabiyik, Qiang, Pan-Hammarström, Rebeca, Pérez de Diego, Laura, Planas-Serra, Daniel E, Pleguezuelo, Carolina, Prando, Aurora, Pujol, Luis Felipe, Reyes, Jacques G, Rivière, Carlos, Rodriguez-Gallego, Julian, Rojas, Patrizia, Rovere-Querini, Agatha, Schlüter, Mohammad, Shahrooei, Ali, Sobh, Pere, Soler-Palacin, Yacine, Tandjaoui-Lambiotte, Imran, Tipu, Cristina, Tresoldi, Jesus, Troya, Diederik, van de Beek, Mayana, Zatz, Pawel, Zawadzki, Saleh Zaid, Al-Muhsen, Hagit, Baris-Feldman, Manish J, Butte, Stefan N, Constantinescu, Megan A, Cooper, Clifton L, Dalgard, Jacques, Fellay, James R, Heath, Yu-Lung, Lau, Richard P, Lifton, Tom, Maniatis, Trine H, Mogensen, Horst, von Bernuth, Alban, Lermine, Michel, Vidaud, Anne, Boland, Jean-François, Deleuze, Robert, Nussbaum, Amanda, Kahn-Kirby, France, Mentre, Sarah, Tubiana, Guy, Gorochov, Florence, Tubach, Pierre, Hausfater, Isabelle, Meyts, Shen-Ying, Zhang, Anne, Puel, Luigi D, Notarangelo, Stephanie, Boisson-Dupuis, Helen C, Su, Bertrand, Boisson, Emmanuelle, Jouanguy, Jean-Laurent, Casanova, Qian, Zhang, Laurent, Abel, Aurélie, Cobat
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
medRxiv
Universidade de São Paulo (USP)
instacron:USP
medRxiv
BackgroundWe previously reported inborn errors of TLR3- and TLR7-dependent type I interferon (IFN) immunity in 1-5% of unvaccinated patients with life-threatening COVID-19, and auto-antibodies against type I IFN in another 15-20% of cases.MethodsWe r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c2b2b888dfa2d32ea41a056674b1215
https://doi.org/10.1101/2022.10.22.22281221
https://doi.org/10.1101/2022.10.22.22281221
Autor:
Carlos Andrés Arango-Franco, Marcela Moncada-Vélez, Alexander Franco-Gallego, Lucía Victoria Erazo, Catalina Martínez, Sebastián Gutiérrez, Jesús Armando Álvarez, Manuela Molina, Diana Arboleda, Laura Naranjo, Juan Álvaro López, Juan Fernando Alzate, Felipe Cabarcas, Claudia Milena Trujillo-Vargas, Julio César Orrego, Satoshi Okada, Anne Puel, Jacinta Bustamante, Jean-Laurent Casanova, Andrés Augusto Arias, José Luis Franco
Publikováno v:
Revista Alergia México, Vol 65 suppl 1, Pp 129-130 (2018)
Background: The genetic etiology of several primary immunodeficiency diseases (PID) remains elusive. Next generation technologies represent a cost-effective and rapid first-line genetic approach for the evaluation of diseases underlying mendelian tra
Externí odkaz:
https://doaj.org/article/c28dca86cd9a48b3acdcaca2d8e8606a
Autor:
Marcela Moncada-Vélez, Lucía Victoria Erazo-Borrás, Jesús Armando Álvarez-lvarez, Carlos Andrés Arango, Miyuki Tsumura, Satoshi Okada, Sara Daniela Osorio, Lorena Castro, Natalia González, Catalina Arango, Julio César Orrego, Lina Riaño, Juan Fernando Alzate, Felipe Cabarcas, Jean-Laurent Casanova, Jacinta Bustamante, Anne Puel, Andrés Augusto Arias, José Luis Franco
Publikováno v:
Revista Alergia México, Vol 65 suppl 1, Pp 114-115 (2018)
Background: The transcription factor STAT1 plays a critical role in the immune response against mycobacterial, viral and fungal infections. Different mutations in STAT1 result in diverse clinical phenotypes: AR complete/partial biallelic mutations ar
Externí odkaz:
https://doaj.org/article/15503ab3fb4b465a85afe9b41d45fb07
Autor:
Carlos Andrés Arango-Franco, Alejandro Nieto-Patlán, Marcela Moncada-Vélez, Jesús Armando Álvarez, Carmen Oleaga-Quinta, Caroline Deswarte, Juan Fernando Alzate, Felipe Cabarcas, Carlos Garcés, Julio César Orrego, Susana Pamela Mejía, Luz Elena Cano, Jean-Laurent Casanova, Jacinta Bustamante, José Luis Franco, Andrés Augusto Arias
Publikováno v:
Revista Alergia México, Vol 65 suppl 1, Pp 134-135 (2018)
Background: Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by susceptibility to early-onset life-threatening bacterial and fungal infections as well as dysregulated chronic inflammation. CGD results from mutations in
Externí odkaz:
https://doaj.org/article/37ef6f9f88c44eeea48b8fbb13b9428a
Autor:
Manuela Molina, Diana Marcela Arboleda, Marcela Moncada, Gabriel Vélez, Juan Fernando Alzate, Felipe Cabarcas, José Luis Franco, Andrés Augusto Arias-Sierra, Juan Álvaro López
Publikováno v:
Revista Alergia México, Vol 65 suppl 1, Pp 143-144 (2018)
Antecedentes: La enfermedad granulomatosa crónica es una inmunodeficiencia primaria producida por mutaciones en los genes que codifican para alguna de las cinco proteínas que conforman el sistema NADPH oxidasa, el cual se encarga de destruir los mi
Externí odkaz:
https://doaj.org/article/2b8f4449d74247d282d5d61a2c1d1c22