Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Maria G Kanariou"'
Autor:
Vasiliki Kalotychou, Demetrios Mermigkis, Maria G. Kanariou, Marianna Tzanoudaki, Vasiliki Epameinondas Georgakopoulou, Irene Kourbeti, George L. Daikos
Publikováno v:
IDCases, Vol 26, Iss , Pp e01323- (2021)
The X-chromosome linked (XL) female carriers of chronic granulomatous disease (CGD) are considered to have no risk for infection. Herein we present a female CGD XL-carrier who developed Pneumocystis jirovecii pneumonia and Serratia marcescens infecti
Externí odkaz:
https://doaj.org/article/e2a9e8b844824171b445878cfe691c80
Autor:
Chen Wang, Bijun Sun, Kevin Wu, Jocelyn Farmer, Boglarka Ujhazi, Christoph B. Geier, Sumai Gordon, Emma Westermann-Clark, Sinisa Savic, Sargur Ravishankar, Karin Chen, Cullen M Dutmer, Maria G Kanariou, Mehdi Adeli, Paolo Palma, Carmem Bonfim, Evangelia Lycopoulou, Beata Wolska-Kusnierz, Dbaibo Ghassan, Jack Bleesing, Despina Moshous, Benedicte Neven, Catharina Schuetz, Geha Raif, Luigi D. Notarangelo, Maurizio Miano, David K. Buchbinder, Krisztian Csomos, Wenjie Wang, Ji-Yang Wang, Xiaochuan Wang, Jolan E. Walter
Publikováno v:
Blood. 140:2448-2450
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16324698f68790ed34c744c5d29ec07b
https://doi.org/10.1182/blood-2022-162845
https://doi.org/10.1182/blood-2022-162845
Autor:
Kerry Dobbs, Giovanna Tabellini, Enrica Calzoni, Ornella Patrizi, Paula Martinez, Silvia Clara Giliani, Daniele Moratto, Waleed Al-Herz, Caterina Cancrini, Morton Cowan, Jacob Bleesing, Claire Booth, David Buchbinder, Siobhan O. Burns, Talal A. Chatila, Janet Chou, Vanessa Daza-Cajigal, Lisa M. Ott de Bruin, Maite Teresa de la Morena, Gigliola Di Matteo, Andrea Finocchi, Raif Geha, Rakesh K. Goyal, Anthony Hayward, Steven Holland, Chiung-Hui Huang, Maria G. Kanariou, Alejandra King, Blanka Kaplan, Anastasiya Kleva, Taco W. Kuijpers, Bee Wah Lee, Vassilios Lougaris, Michel Massaad, Isabelle Meyts, Megan Morsheimer, Benedicte Neven, Sung-Yun Pai, Nima Parvaneh, Alessandro Plebani, Susan Prockop, Ismail Reisli, Jian Yi Soh, Raz Somech, Troy R. Torgerson, Yae-Jean Kim, Jolan E. Walter, Andrew R. Gennery, Sevgi Keles, John P. Manis, Emanuela Marcenaro, Alessandro Moretta, Silvia Parolini, Luigi D. Notarangelo
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
Externí odkaz:
https://doaj.org/article/4d51d92b2058445c88fe2aadfd3afece
Autor:
Kerry Dobbs, Giovanna Tabellini, Enrica Calzoni, Ornella Patrizi, Paula Martinez, Silvia Clara Giliani, Daniele Moratto, Waleed Al-Herz, Caterina Cancrini, Morton Cowan, Jacob Bleesing, Claire Booth, David Buchbinder, Siobhan O. Burns, Talal A. Chatila, Janet Chou, Vanessa Daza-Cajigal, Lisa M. Ott de Bruin, Maite Teresa de la Morena, Gigliola Di Matteo, Andrea Finocchi, Raif Geha, Rakesh K. Goyal, Anthony Hayward, Steven Holland, Chiung-Hui Huang, Maria G. Kanariou, Alejandra King, Blanka Kaplan, Anastasiya Kleva, Taco W. Kuijpers, Bee Wah Lee, Vassilios Lougaris, Michel Massaad, Isabelle Meyts, Megan Morsheimer, Benedicte Neven, Sung-Yun Pai, Nima Parvaneh, Alessandro Plebani, Susan Prockop, Ismail Reisli, Jian Yi Soh, Raz Somech, Troy R. Torgerson, Yae-Jaen Kim, Jolan E. Walter, Andrew R. Gennery, Sevgi Keles, John P. Manis, Emanuela Marcenaro, Alessandro Moretta, Silvia Parolini, Luigi D. Notarangelo
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
Mutations of the recombinase-activating genes 1 and 2 (RAG1 and RAG2) in humans are associated with a broad range of phenotypes. For patients with severe clinical presentation, hematopoietic stem cell transplantation (HSCT) represents the only curati
Externí odkaz:
https://doaj.org/article/882eccf644f04a0a9df352439dfff1bd
Autor:
Amy E O'Connell, Stefano eVolpi, Kerry eDobbs, Claudia eFiorini, Erdyni eTsitsikov, Helen ede Boer, Isil B Barlan, Jenny M Despotovic, Francisco J Espinosa-Rosales, Celine eHanson, Maria G Kanariou, Roxana eMartinez-Beckerat, Alvaro eMayorga-Sirera, Carmen eMeija-Carvajal, Nesrine eRadwan, Aaron R Weiss, Yu Nee eLee, Sung-Yun ePai, Luigi Daniele Notarangelo
Publikováno v:
Frontiers in Immunology, Vol 5 (2014)
The Wiskott Aldrich syndrome (WAS) is due to mutations of the WAS gene encoding for the cytoskeletal WAS protein (WASp), leading to abnormal downstream signaling from the T cell and B cell antigen receptors (TCR, BCR). We hypothesized that the impair
Externí odkaz:
https://doaj.org/article/f8b96d5993654915a40dd38504003158
Publikováno v:
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology. 21(3)
Although many children develop frequent infections, only a few have an underlying immune disorder. Children with dysfunction of the immune system develop frequent infections and/or recurrent, persistent, severe, and rare infections. The aim of this r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54b6311d7e53703ded35e3fae087f300
https://pubmed.ncbi.nlm.nih.gov/19922449
https://pubmed.ncbi.nlm.nih.gov/19922449
Autor:
Milito, Cinzia, Pulvirenti, Federica, Garzi, Giulia, Sculco, Eleonora, Cinetto, Francesco, Firinu, Davide, Lagnese, Gianluca, Punziano, Alessandra, Discardi, Claudia, Costanzo, Giulia, Felice, Carla, Spadaro, Giuseppe, Ferrari, Simona, Quinti, Isabella
Publikováno v:
Frontiers in Immunology; 2023, p1-8, 8p
Autor:
Cassimos, Dimitrios C.1,2, Liatsis, Manolis1, Stogiannidou, Anastasia2, Kanariou, Maria G.1 mkanariou@hol.gr
Publikováno v:
Pediatric Allergy & Immunology. May2010, Vol. 21 Issue 3, p463-473. 11p. 1 Diagram, 8 Charts.
Publikováno v:
Autoimmunity; 1997, Vol. 26 Issue 4, p209-214, 6p