Zobrazeno 1 - 6 of 6 pro vyhledávání: '"Maria G, Kanariou"'
1
Akademický článek
Pneumocystis jirovecii pneumonia in a X-linked chronic granulomatous disease female carrier
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
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4
Akademický článek
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content
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
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5
Akademický článek
Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with Wiskott Aldrich syndrome
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
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6
Children with frequent infections: a proposal for a stepwise assessment and investigation of the immune system
Autor: Dimitrios C, Cassimos, Manolis, Liatsis, Anastasia, Stogiannidou, Maria G, Kanariou
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
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