Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Teresa Espanol"'
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 3, Iss 4 (2004)
HIV infection by maternal transmission is increasing in the world due to the increase in infected women who are not receiving appropriate antiretroviral therapy. Prognosis of HIV infection in children is poor because the newborn has an immature immun
Externí odkaz:
https://doaj.org/article/a283e5de00cd457b8ec7a7fdd4bbe8e6
Autor:
Hassan Abolhassani, Asghar Aghamohammadi, Pilar Llobet Agulló, Hamid Ahanchian, Soheila Alyasin, Saba Arshi, Gholamreza Azizi, Mohamed-Ridha Barbouche, Mohammad Hassan Bemanian, Aziz Bousfiha, Zahra Chavoshzadeh, Taher Cheraghi, Romina Dieli Crimi, Charlotte Cunningham-Rundles, Abbas Dabbaghzadeh, Sepideh Darougar, Rainer Doffinger, Anne Durandy, Mohammad Ehlayel, Hermann Eibel, Mohammad Hossein Eslamian, Hossein Esmaeilzadeh, Teresa Espanol, Morteza Fallahpour, Saba Fekrvand, Andrew R Gennery, Javad Ghaffari, Negar Ghaffari, Sudhir Gupta, Lennart Hammarström, Marzieh Heydrzadeh, Arash Kalantari, Rasoul Nasiri Kalmarzi, Hirokazu Kanegane, Negar Khalighi, Abbas Khalili, Martin Lavin, Alireza Mahdaviani, Tooba Momen, Mohammad Nabavi, Tim Niehues, Hans D. Ochs, Peter Olbrich, Alessandro Plebani, Nima Rezaei, Farhad Seif, Mikko Seppänen, Mahnaz Sadeghi Shabestari, Alireza Shafiei, Mansoureh Shariat, Deepti Suri, Marzieh Tavakol, Mirjam van der Burg, Menno van Zelm, Ahmad Vosoughi Motlagh, Reza Yazdani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b9c97f6b84cbcb6dd734523a60abefa
https://doi.org/10.1016/b978-0-12-821028-4.09989-9
https://doi.org/10.1016/b978-0-12-821028-4.09989-9
Autor:
Hassan Abolhassani, Negar Khalighi, Tim Niehues, Teresa Espanol, Abbas Dabbaghzadeh, Javad Ghaffari, Hamid Ahanchian, Mohammad S. Ehlayel, Pilar Llobet Agulló, Romina Dieli Crimi
Primary immunodeficiency disorders (PIDs) are often associated with autoimmune disease due to the dysregulation of the immune system and distributed central and peripheral tolerance. In many inborn immune deficiencies, lymphocytes may be present but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f2834d723e86c9a767ec7c3ab9e5b29
https://doi.org/10.1016/b978-0-12-821028-4.00005-1
https://doi.org/10.1016/b978-0-12-821028-4.00005-1
Autor:
I. Celine Hanson, Nedim Hadzic, Gustavo Kusminsky, Francesca Ferrua, Matías Oleastro, Isabelle Meyts, Giorgia Bucciol, Jacques Pirenne, Paola Quarello, M. Teresa de la Morena, Andrzej Lange, Marek Stefanowicz, Nizar Mahlaoui, Francesco Tandoi, Z Nademi, Pier Luigi Calvo, Elena Soncini, Fulvio Porta, Troy R. Torgerson, Andrew J. Cant, Teresa Espanol, Marcelo Silva, Andrew R. Gennery, Sarah K. Nicholas, Benedicte Neven, Beata Wolska-Kuśnierz, Katja G. Weinacht, Paul Veys, Fanny Lanternier, Miguel Galicchio, Despina Moshous, J. David M. Edgar, Mary Slatter, Mikołaj Teisseyre
Liver disease in X-linked hyper IgM syndrome (XHIGM) is an important predictor of mortality. In case liver transplantation (LT) is required, a survival benefit is observed when LT is combined with HSCT. ispartof: JOURNAL OF ALLERGY AND CLINICAL IMMUN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47b33dc1fa6504d7faeb91aa6bf94066
https://lirias.kuleuven.be/handle/123456789/633572
https://lirias.kuleuven.be/handle/123456789/633572
Autor:
Vojtech Thon, Bénédicte Neven, Frank L. van de Veerdonk, Anna Villa, Mario Abinun, Jean Donadieu, Christoph Klein, Hans D. Ochs, Despina Moshous, Geneviève de Saint Basile, Klaus Warnatz, Alain Fischer, Sofia Grigoriadou, Nizar Mahlaoui, Raphael Scheible, Dominique Stoppa-Lyonnet, Nicolette Moes, Shen-Yin Zhang, Reinhard Seger, Isabelle Meyts, Sarah Beaussant Cohen, Andrew J. Cant, Bodo Grimbacher, Markus G. Seidel, Frédéric Rieux-Laucat, Michael H. Albert, Lukas M. Gasteiger, Stephan Ehl, David Edgar, Joris M. van Montfrans, Ania Manson, Maria Kanariou, Richard Gatti, Capucine Picard, Teresa Espanol, Beata Wolska, Amos Etzioni, Anne Durandy, Stephan Rusch, Jacinta Bustamante, Gerhard Kindle, Esther de Vries, Andrew R. Gennery, Annarosa Soresina, Benjamin Gathmann, Helen Chapel, Isabella Quinti, Steven M. Holland, Helen J. Lachmann, Adrian J. Thrasher, Inderjeet Dokal, Ellen D. Renner, Gritta Janka, Natalia Martinez, Bobby Gaspar, Desa Lilic, Matthew Buckland, Jean-Laurent Casanova, Corry M.R. Weemaes
Publikováno v:
The Journal of Allergy and Clinical Immunology. In Practice, 7(6), 1763-1770. Elsevier
Journal of Allergy and Clinical Immunology. In Practice, 7, 1763-1770
Journal of Allergy and Clinical Immunology: In Practice, 7(6), 1763. Elsevier
Journal of Allergy and Clinical Immunology. In Practice, 7, 6, pp. 1763-1770
Journal of Allergy and Clinical Immunology. In Practice, 7, 1763-1770
Journal of Allergy and Clinical Immunology: In Practice, 7(6), 1763. Elsevier
Journal of Allergy and Clinical Immunology. In Practice, 7, 6, pp. 1763-1770
Item does not contain fulltext Patient registries are instrumental for clinical research in rare diseases. They help to achieve a sufficient sample size for epidemiological and clinical research and to assess the feasibility of clinical trials. The E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a70466cd03f2576a9c2a054c6a955faf
https://research.tilburguniversity.edu/en/publications/117b1dbb-c5a6-45b4-b69f-962fb05c06f7
https://research.tilburguniversity.edu/en/publications/117b1dbb-c5a6-45b4-b69f-962fb05c06f7
Autor:
Isabelle Meyts, Christopher C. Dvorak, Morna J. Dorsey, Antonio Condino-Neto, Hassan Abolhassani, Rongras Damrongwatanasuk, Reinhard Seger, John M. Routes, Trudy N. Small, Hans D. Ochs, Maria Kanariou, Carsten Speckmann, Beatriz Tavares Costa Carvalho, J. David M. Edgar, Luis Ignacio Gonzalez-Granado, Andrew R. Gennery, Victor M. Aquino, M. Teresa de la Morena, Ramsay Fuleihan, Gisela Seminario, Nancy Bunin, Neena Kapoor, Chaim M. Roifman, Alan P. Knutsen, Helen Chapel, Jiri Litzman, Lisa Kobrynski, Liliana Bezrodnik, Anna Shcherbina, Teresa Espanol, Paul Gray, Francisco A. Bonilla, Janet Chou, Andrew J. Cant, Imelda C. Hanson, Luis Murguia-Favela, Troy R. Torgerson, Christian A. Wysocki, Fatima Dhalla, Mary Slatter, Eyal Grunebaum, Andrea C. Gómez Raccio, Necil Kutukculer, Jordan K. Abbott, David Leonard, Evangelia Farmaki, Joris M. van Montfrans, Srdjan Pasic, Sharat Chandra, Ales Janda, Luigi D. Notarangelo, Melanie Wong, Otavio Cabral-Marques, M.J. Cowan, Caroline Y. Kuo, Alexandra H. Filipovich, Asghar Aghamohammadi, John W. Sleasman, Darko Richter, Karin Chen, Suranjith L. Seneviratne, Charlotte Cunningham-Rundles, Daniela DiGiovanni
Publikováno v:
The Journal of allergy and clinical immunology, vol 139, iss 4
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Journal of Allergy and Clinical Immunology, 139(4), 1282. Mosby Inc.
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Journal of Allergy and Clinical Immunology, 139(4), 1282. Mosby Inc.
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
WOS: 000398771800023
PubMed ID: 27697500
Background: X-linked hyper-IgM syndrome (XHIGM) is a primary immunodeficiency with high morbidity and mortality compared with those seen in healthy subjects. Hematopoietic cell transplantation (HCT)
PubMed ID: 27697500
Background: X-linked hyper-IgM syndrome (XHIGM) is a primary immunodeficiency with high morbidity and mortality compared with those seen in healthy subjects. Hematopoietic cell transplantation (HCT)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9332ffae746e556d7530bfa4b4ec3a6
https://ora.ox.ac.uk/objects/uuid:d6d75a9e-d449-4450-a6c7-97227d89d44a
https://ora.ox.ac.uk/objects/uuid:d6d75a9e-d449-4450-a6c7-97227d89d44a
Autor:
P. Martin van Hagen, Patrice Debré, Gonke Poerksen, Christian Schmitt, Claudia Wehr, Jiri Litzman, John R Jones, E. Bateman, Ulrich Baumann, Mauno Vihinen, Michael Schlesier, Magali Le Garff, Alessandro Plebani, Torsten Witte, Florence Bergeron-van der Cruyssen, Horst von Bernuth, A. David B. Webster, Sigune Goldacker, Berne Ferry, Teresa Espanol, Reinhold E. Schmidt, Hans-Hartmut Peter, Philip R. Bos, Isabella Quinti, Teemu Kivioja, Roland Jacobs, M. Hernández, Vojtech Thon, Efrem Eren, Marcela Vlková, Drahomíra Detková, Sylvia Gutenberger, Eric Oksenhendler, Helen Chapel, Klaus Warnatz
Publikováno v:
Blood, 111(1), 77-85. American Society of Hematology
The heterogeneity of common variable immunodeficiency (CVID) calls for a classification addressing pathogenic mechanisms as well as clinical relevance. This European multicenter trial was initiated to develop a consensus of 2 existing classification
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a324debb931a89c3f5f585babb336b2
https://ora.ox.ac.uk/objects/uuid:9232fb39-5f08-4162-b96b-096eb5a50c80
https://ora.ox.ac.uk/objects/uuid:9232fb39-5f08-4162-b96b-096eb5a50c80
Autor:
Ma Pilar Llobet, Pere Soler-Palacín, Drahomíra Detková, I. Caragol, Teresa Espanol, M. Hernández
Publikováno v:
Pediatric Allergy and Immunology. 20:113-118
Common variable immunodeficiency (CVID) is the most common symptomatic primary immunodeficiency. It can present at any age in patients with a history of recurrent bacterial infections, with or without a family history of other primary immunodeficienc
Autor:
Giulia Casorati, Jiri Litzman, Maria Grazia Roncarolo, Teresa Espanol, Paolo Dellabona, Marita Bosticardo, Caterina Cancrini, László Maródi, Ansgar Schulz, Elena Draghici, Anna Villa, Marco Catucci, Francesco Marangoni, Michela Locci, Robbert G. M. Bredius, Adrian J. Thrasher, Alessandro Aiuti
Publikováno v:
The Journal of Experimental Medicine
The Journal of experimental medicine, vol 206, iss 4
The Journal of experimental medicine, vol 206, iss 4
The Wiskott-Aldrich syndrome (WAS) protein (WASp) is a regulator of actin cytoskeleton in hematopoietic cells. Mutations of the WASp gene cause WAS. Although WASp is involved in various immune cell functions, its role in invariant natural killer T (i
Autor:
Javad Mohammadi, Teresa Espanol, Nima Rezaei, Asghar Aghamohammadi, Nima Parvaneh, Lennart Hammarström, Mostafa Moin
Publikováno v:
International Archives of Allergy and Immunology. 147:87-92
Selective IgA deficiency (IgAD) is the most common primary immunodeficiency in Caucasians. Although it is often asymptomatic, selected patients show an increased frequency of infections, allergies and autoimmune manifestations. Common variable immuno