| Tipo Producción |
Título |
Autor |
Año de Producción |
DOI |
Revista |
Fuente |
Cuartil de ScimagoJR o JCR* |
|
Artículo en revista científica
|
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
|
Matuozzo D.
|
2023
|
10.1186/S13073-023-01173-8
|
Genome Medicine
|
|
2023: No disponible**, 2020: Q1
|
|
Journal - Article
|
Successful desensitization to colistin in a Peruvian patient with cystic fibrosis
|
Veramendi-Espinoza, Liz | Espinoza-Ildefonso, Vladimir | Herrera, Joel Calero | Becerra, Juan Carlos Aldave
|
2023
|
10.35434/RCMHNAAA.2023.162.1706
|
REVISTA DEL CUERPO MEDICO DEL HOSPITAL NACIONAL ALMANZOR AGUINAGA ASENJO
|
|
S/C***
|
|
Artículo en revista científica
|
Allergic manifestations of inborn errors of immunity and their impact on the diagnosis: A worldwide study
|
El-Sayed Z.A.
|
2022
|
10.1016/J.WAOJOU.2022.100657
|
World Allergy Organization Journal
|
|
Q1
|
|
Artículo en revista científica
|
Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths
|
Bastard P.
|
2021
|
10.1126/SCIIMMUNOL.ABL4340
|
Science immunology
|
|
Q1
|
|
Artículo en revista científica
|
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19
|
Asano T.
|
2021
|
10.1126/SCIIMMUNOL.ABL4348
|
Science immunology
|
|
Q1
|
|
Artículo en revista científica
|
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
|
Zhang Q.
|
2020
|
10.1126/SCIENCE.ABD4570
|
Science
|
|
Q1
|
|
Artículo en revista científica
|
Autoantibodies against type I IFNs in patients with life-threatening COVID-19
|
Bastard P.
|
2020
|
10.1126/SCIENCE.ABD4585
|
Science
|
|
Q1
|
|
Journal-article
|
COVID-19 y oftalmología: rol del sistema inmunitario
|
|
2020
|
10.15381/ANALES.V81I2.17807
|
|
Crossref a través de ORCID
|
|
|
Other
|
The first patient reported with X-linked severe combined immunodeficiency in Peru
|
|
2020
|
10.21203/RS.3.RS-47002/V1
|
|
Crossref a través de ORCID
|
|
|
Editorial
|
U100: An innovative usern platform for education and research without borders
|
Momtazmanesh S.
|
2020
|
|
Acta Medica Iranica
|
|
No Aplica
|
|
Journal - Review
|
Latin American consensus on the supportive management of patients with severe combined immunodeficiency
|
Bustamante Ogando, Juan Carlos | Partida Gaytan, Armando | Aldave Becerra, Juan Carlos | Alvarez Cardona, Aristoteles | Bezrodnik, Liliana | Borzutzky, Arturo | Galicia, Lizbeth Blancas | Cabanillas, Diana | Condino-Neto, Antonio | Ranero, Agustin De Colsa | Padilla, Sara Espinosa | Fernandes, Juliana Folloni | Garcia Campos, Jorge Alberto | Tello, Hector Gomez | Gonzalez Serrano, Maria Edith | Gutierrez Hernandez, Alonso | Hernandez Bautista, Victor Manuel | Escoto, Gabriele Ivankovich | King, Alejandra | Mazzucchelli, Juliana Lessa | Llamas Guillen, Beatriz Adriana | Lugo Reyes, Saul Oswaldo | Moreno Espinosa, Sarbelio | Oleastro, Matias | Mendoza, Francisco Otero | Poli Harlowe, Maria Cecilia | Porras, Oscar | Ramirez Uribe, Nideshda | Regairaz, Lorean | Larrauri, Francisco Rivas | Saracho Weber, Federico Jose | Grumach, Anete S. | Boone, Tamara Staines | Costa-Carvalho, Beatriz Tavares | Yamazaki Nakashimada, Marco Antonio | Espinosa Rosales, Francisco Javier
|
2019
|
10.1016/J.JACI.2019.08.002
|
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
|
|
Q1
|
|
Artículo en revista científica
|
Latin American consensus on the supportive management of patients with severe combined immunodeficiency
|
Bustamante Ogando J.C.
|
2019
|
10.1016/J.JACI.2019.08.002
|
Journal of Allergy and Clinical Immunology
|
|
Q1
|
|
Journal-article
|
Latin American consensus on the supportive management of patients with severe combined immunodeficiency
|
|
2019
|
10.1016/J.JACI.2019.08.002
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Journal - Article
|
X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world
|
El-Sayed, Zeinab A. | Abramova, Irina | Carlos Aldave, Juan | Al-Herz, Waleed | Bezrodnik, Liliana | Boukari, Rachida | Bousfiha, Ahmed Aziz | Cancrini, Caterina | Condino-Neto, Antonio | Dbaibo, Ghassan | Derfalvi, Beata | Dogu, Figen | Edgar, J. David M. | Eley, Brian | El-Owaidy, Rasha Hasan | Elva Espinosa-Padilla, Sara | Galal, Nermeen | Haerynck, Filomeen | Hanna-Wakim, Rima | Hossny, Elham | Ikinciogullari, Aydan | Kamal, Ebtihal | Kanegane, Hirokazu | Kechout, Nadia | Lau, Yu Lung | Morio, Tomohiro | Moschese, Viviana | Neves, Joao Farela | Ouederni, Monia | Paganelli, Roberto | Paris, Kenneth | Pignata, Claudio | Plebani, Alessandro | Qamar, Farah Naz | Qureshi, Sonia | Radhakrishnan, Nita | Rezaei, Nima | Rosario, Nelson | Routes, John | Sanchez, Berta | Sediva, Anna | Seppanen, Mikko R. J. | Serrano, Edith Gonzalez | Shcherbina, Anna | Singh, Surjit | Siniah, Sangeetha | Spadaro, Guiseppe | Tang, Mimi | Maria Vinet, Ana | Volokha, Alla | Sullivan, Kathleen E.
|
2019
|
10.1016/J.WAOJOU.2019.100018
|
World Allergy Organization Journal
|
|
Q2
|
|
Journal-article
|
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world
|
|
2019
|
10.1016/J.WAOJOU.2019.100018
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Artículo en revista científica
|
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world
|
El-Sayed Z.A.
|
2019
|
10.1016/J.WAOJOU.2019.100018
|
World Allergy Organization Journal
|
|
Q1
|
|
Journal-article
|
Lentiviral gene therapy combined with low-dose busulfan in infants with SCID-X1
|
|
2019
|
10.1056/NEJMOA1815408
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Artículo en revista científica
|
Lentiviral gene therapy combined with low-dose busulfan in infants with SCID-X1
|
Mamcarz E.
|
2019
|
10.1056/NEJMOA1815408
|
New England Journal of Medicine
|
|
Q1
|
|
Journal - Article
|
Lentiviral Gene Therapy Combined with Low-Dose Busulfan in Infants with SCID-X1
|
Mamcarz, Ewelina | Zhou, Sheng | Lockey, Timothy | Abdelsamed, Hossam | Cross, Shane J. | Kang, Guolian | Ma, Zhijun | Condori, Jose | Dowdy, Jola | Triplett, Brandon | Li, Chen | Maron, Gabriela | Aldave Becerra, Juan C. | Church, Joseph A. | Dokmeci, Elif | Love, James T. | da Matta Ain, Ana C. | van der Watt, Hedi | Tang, Xing | Janssen, William | Ryu, Byoung Y. | De Ravin, Suk See | Weiss, Mitchell J. | Youngblood, Benjamin | Long-Boyle, Janel R. | Gottschalk, Stephen | Meagher, Michael M. | Malech, Harry L. | Puck, Jennifer M. | Cowan, Morton J. | Sorrentino, Brian P.
|
2019
|
10.1056/NEJMOA1815408
|
NEW ENGLAND JOURNAL OF MEDICINE
|
|
Q1
|
|
Journal-article
|
Genetic diagnosis of patients with primary agammaglobulinemia treated at third level peruvian centers
|
|
2019
|
10.17843/RPMESP.2019.364.4311
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Artículo en revista científica
|
Genetic diagnosis of patients with primary agammaglobulinemia treated at third level peruvian centers
|
Matos-Benavides E.
|
2019
|
10.17843/RPMESP.2019.364.4311
|
Revista Peruana de Medicina de Experimental y Salud Publica
|
|
Q3
|
|
Journal - Article
|
Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations
|
Leiding, Jennifer W. | Okada, Satoshi | Hagin, David | Abinun, Mario | Shcherbina, Anna | Balashov, Dmitry N. | Kim, Vy H. D. | Ovadia, Adi | Guthery, Stephen L. | Pulsipher, Michael | Lilic, Desa | Devlin, Lisa A. | Christie, Sharon | Depner, Mark | Fuchs, Sebastian | van Royen-Kerkhof, Annet | Lindemans, Caroline | Petrovic, Aleksandra | Sullivan, Kathleen E. | Bunin, Nancy | Kilic, Sara Sebnem | Arpaci, Fikret | de la Calle-Martin, Oscar | Martinez-Martinez, Laura | Aldave, Juan Carlos | Kobayashi, Masao | Ohkawa, Teppei | Imai, Kohsuke | Iguchi, Akihiro | Roifman, Chaim M. | Gennery, Andrew R. | Slatter, Mary | Ochs, Hans D. | Morio, Tomohiro | Torgerson, Troy R.
|
2018
|
10.1016/J.JACI.2017.03.049
|
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
|
|
Q1
|
|
Journal-article
|
Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations
|
|
2018
|
10.1016/J.JACI.2017.03.049
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Artículo en revista científica
|
Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations
|
Leiding J.W.
|
2018
|
10.1016/J.JACI.2017.03.049
|
Journal of Allergy and Clinical Immunology
|
|
Q1
|
|
Artículo en revista científica
|
Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis
|
Chinn I.K.
|
2018
|
10.1182/BLOOD-2017-11-814244
|
Blood
|
|
Q1
|
|
Journal - Article
|
Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis
|
Chinn, Ivan K. | Eckstein, Olive S. | Peckham-Gregory, Erin C. | Goldberg, Baruch R. | Forbes, Lisa R. | Nicholas, Sarah K. | Mace, Emily M. | Vogel, Tiphanie P. | Abhyankar, Harshal A. | Diaz, Maria I. | Heslop, Helen E. | Krance, Robert A. | Martinez, Caridad A. | Nguyen, Trung C. | Bashir, Dalia A. | Goldman, Jordana R. | Stray-Pedersen, Asbjorg | Pedroza, Luis A. | Poli, M. Cecilia | Aldave-Becerra, Juan C. | McGhee, Sean A. | Al-Herz, Waleed | Chamdin, Aghiad | Coban-Akdemir, Zeynep H. | Jhangiani, Shalini N. | Muzny, Donna M. | Cao, Tram N. | Hong, Diana N. | Gibbs, Richard A. | Lupski, James R. | Orange, Jordan S. | McClain, Kenneth L. | Allen, Carl E.
|
2018
|
10.1182/BLOOD-2017-11-814244
|
BLOOD
|
|
Q1
|
|
Journal-article
|
Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis
|
|
2018
|
10.1182/BLOOD-2017-11-814244
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Letter
|
Registration of patients with primary immunodeficiencies in the three main reference centers in Peru
|
García-Gomero D.S.
|
2018
|
10.17843/RPMESP.2018.353.3317
|
Revista Peruana de Medicina de Experimental y Salud Publica
|
|
No Aplica
|
|
Journal-article
|
Registration of patients with primary immunodeficiencies in the three main reference centers in Peru,Registro de pacientes con inmunodeficiencias primarias en los tres principales centros de referencia del Perú
|
|
2018
|
10.17843/RPMESP.2018.353.3317
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Artículo en revista científica
|
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
|
Stray-Pedersen A.
|
2017
|
10.1016/J.JACI.2016.05.042
|
Journal of Allergy and Clinical Immunology
|
|
Q1
|
|
Journal - Article
|
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
|
Stray-Pedersen, Asbjorg | Sorte, Hanne Sormo | Samarakoon, Pubudu | Gambin, Tomasz | Chinn, Ivan K. | Akdemir, Zeynep H. Coban | Erichsen, Hans Christian | Forbes, Lisa R. | Gu, Shen | Yuan, Bo | Jhangiani, Shalini N. | Muzny, Donna M. | Rodningen, Olaug Kristin | Sheng, Ying | Nicholas, Sarah K. | Noroski, Lenora M. | Seeborg, Filiz O. | Davis, Carla M. | Canter, Debra L. | Mace, Emily M. | Vece, Timothy J. | Allen, Carl E. | Abhyankar, Harshal A. | Boone, Philip M. | Beck, Christine R. | Wiszniewski, Wojciech | Fevang, Borre | Aukrust, Pal | Tjonnfjord, Geir E. | Gedde-Dahl, Tobias | Hjorth-Hansen, Henrik | Dybedal, Ingunn | Nordoy, Ingvild | Jorgensen, Silje F. | Abrahamsen, Tore G. | Overland, Torstein | Bechensteen, Anne Grete | Skogen, Vegard | Osnes, Liv T. N. | Kulseth, Mari Ann | Prescott, Trine E. | Rustad, Cecilie F. | Heimdal, Ketil R. | Belmont, John W. | Rider, Nicholas L. | Chinen, Javier | Cao, Tram N. | Smith, Eric A. | Soledad Caldirola, Maria | Bezrodnik, Liliana | Lugo Reyes, Saul Oswaldo | Espinosa Rosales, Francisco J. | Guerrero-Cursaru, Nina Denisse | Pedroza, Luis Alberto | Poli, Cecilia M. | Franco, Jose L. | Trujillo Vargas, Claudia M. | Aldave Becerra, Juan Carlos | Wright, Nicola | Issekutz, Thomas B. | Issekutz, Andrew C. | Abbott, Jordan | Caldwell, Jason W. | Bayer, Diana K. | Chan, Alice Y. | Aiuti, Alessandro | Cancrini, Caterina | Holmberg, Eva | West, Christina | Burstedt, Magnus | Karaca, Ender | Yesil, Gozde | Artac, Hasibe | Bayram, Yavuz | Atik, Mehmed Musa | Eldomery, Mohammad K. | Ehlayel, Mohammad S. | Jolles, Stephen | Flato, Berit | Bertuch, Alison A. | Hanson, I. Celine | Zhang, Victor W. | Wong, Lee-Jun | Hu, Jianhong | Walkiewicz, Magdalena | Yang, Yaping | Eng, Christine M. | Boerwinkle, Eric | Gibbs, Richard A. | Shearer, William T. | Lyle, Robert | Orange, Jordan S. | Lupski, James R.
|
2017
|
10.1016/J.JACI.2016.05.042
|
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
|
|
Q1
|
|
Journal-article
|
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
|
|
2017
|
10.1016/J.JACI.2016.05.042
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Journal-article
|
A 3-year-old girl with recurrent infections and autoimmunity due to a STAT1 gain-of-function mutation: The expanding clinical presentation of primary immunodeficiencies
|
|
2017
|
10.3389/FPED.2017.00055
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Artículo en revista científica
|
A 3-year-old girl with recurrent infections and autoimmunity due to a STAT1 gain-of-function mutation: The expanding clinical presentation of primary immunodeficiencies
|
Becerra J.
|
2017
|
10.3389/FPED.2017.00055
|
Frontiers in Pediatrics
|
|
2017: No disponible**, 2020: Q1
|
|
Journal - Article
|
A 3-Year-Old Girl with Recurrent Infections and Autoimmunity due to a STAT1 Gain-of-Function Mutation: The Expanding Clinical Presentation of Primary Immunodeficiencies
|
Aldave Becerra, Juan Carlos | Cachay Rojas, Enrique
|
2017
|
10.3389/FPED.2017.00055
|
Frontiers in Pediatrics
|
|
Q2
|
|
Journal - Article
|
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
|
Toubiana, Julie | Okada, Satoshi | Hiller, Julia | Oleastro, Matias | Lagos Gomez, Macarena | Aldave Becerra, Juan Carlos | Ouachee-Chardin, Marie | Fouyssac, Fanny | Girisha, Katta Mohan | Etzioni, Amos | Van Montfrans, Joris | Camcioglu, Yildiz | Kerns, Leigh Ann | Belohradsky, Bernd | Blanche, Stephane | Bousfiha, Aziz | Rodriguez-Gallego, Carlos | Meyts, Isabelle | Kisand, Kai | Reichenbach, Janine | Renner, Ellen D. | Rosenzweig, Sergio | Grimbacher, Bodo | van de Veerdonk, Frank L. | Traidl-Hoffmann, Claudia | Picard, Capucine | Marodi, Laszlo | Morio, Tomohiro | Kobayashi, Masao | Lilic, Desa | Milner, Joshua D. | Holland, Steven | Casanova, Jean-Laurent | Puel, Anne | Cypowyj, Sophie | Thumerelle, Caroline | Toulon, Antoine | Bustamante, Jacinta | Tahuil, Natalia | Salhi, Aicha | Boiu, Sorina | Chopra, Charu | Di Giovanni, Daniela | Bezrodnik, Liliana | Boutros, Jeannette | Thomas, Caroline | Lacuesta, Gina | Jannier, Sarah | Korganow, Anne-Sophie | Paillard, Catherine | Boutboul, David | Bue, Melanie | Marie-Cardine, Aude | Bayart, Sophie | Migaud, Melanie | Weiss, Laurence | Karmochkine, Marina | Garcia-Martinez, Juan-Miguel | Stephan, Jean-Louis | Bensaid, Philippe | Jaennoel, Guy-Patrick | Witte, Torsten | Baumann, Ulrich | Harrer, Thomas | Navarrete, Carmen | Benjamin, Antony Terance | Firinu, Davide | Pignata, Claudio | Picco, Paolo | Mendoza, David | Reyes, Saul Oswaldo Lugo | Lozano, Carlos Torres | Ortega-Cisneros, Margarita | Cortina, Mariana | Mesdaghi, Mehrnaz | Nabavi, Mohammad | Espanol, Teresa | Martinez-Saavedra, Maia Teresa | Rezaei, Nima | Zoghi, Samaneh | Pac, Malgorzata | Barlogis, Vincent | Revon-Riviere, Gabriel | Haimi-Cohen, Yishai | Spiegel, Ronen | Miron, Dan | Bouchaib, Jabir | Blancas-Galicia, Lizbeth | Toth, Beata | Drexel, Barbara | Rohrlich, Pierre Simon | Lesens, Olivier | Hoernes, Miriam | Drewe, Elizabeth | Abinum, Mario | Sawalle-Belohradsky, Julie | Kindle, Gerhard | Depner, Mark | Milani, Lili | Nikopensius, Tiit | Remm, Maido | Talas, Ulvi Gerst | Tucker, Mark | Willis, Mary | Leonard, Stephanie | Meuwissen, Hilaire | Ferdman, Ronald M. | Wallace, Mark | Desai, Mukesh M. | Taur, Prasad | Badolato, Raffaele | Soltesz, Beata | Schnopp, Christina | Jansson, Annette F. | Ayvaz, Deniz | Shabashova, Nadejda | Chernyshova, Liudmyla | Bondarenko, Anastasia | Moshous, Despina | Neven, Benedicte | Boubidi, Chahinez | Ailal, Fatima | Giardino, Giuliana | Del Giacco, Stefano | Bougnoux, Marie-Elisabeth | Imai, Kohsuke | Okawa, Teppei | Mizoguchi, Yoko | Ozaki, Yusuke | Takeuchi, Masato | Hayakawa, Akira | Logering, Birgit | Reich, Kristian | Buhl, Timo | Eyerich, Kilian | Schaller, Martin | Arkwright, Peter D. | Gennery, Andrew R. | Cant, Andrew J. | Warris, Adilia | Henriet, Stefanie | Mekki, Najla | Barbouche, Ridha | Ben Mustapha, Imen | Bodemer, Christine | Polak, Michel | Grimprel, Emmanuel | Burgel, Pierre-Regis | Fischer, Alain | Hermine, Olivier | Debre, Marianne | Kocacyk, Dilara | Dhalla, Fatima | Patel, Smita Y. | Moens, Leen | Haerynck, Filomeen | Dullaers, Melissa | Hoste, Levi | Sanal, Ozden | Kilic, Sara Sebnem | Roesler, Joachim | Lanternier, Fanny | Lortholary, Olivier | Fieschi, Claire | Church, Joseph A. | Roifman, Chaim | Yuenyongviwat, Araya | Peterson, Part | Boisson-Dupuis, Stephanie | Abel, Laurent | Marciano, Beatriz E. | Netea, Mihai G.
|
2016
|
10.1182/BLOOD-2015-11-679902
|
BLOOD
|
|
Q1
|
|
Journal-article
|
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
|
|
2016
|
10.1182/BLOOD-2015-11-679902
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Artículo en revista científica
|
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
|
Toubiana J.
|
2016
|
10.1182/BLOOD-2015-11-679902
|
Blood
|
|
Q1
|
|
Journal - Article
|
International survey on skin patch test procedures, attitudes and interpretation
|
Tanno, Luciana K. | Darlenski, Razvigor | Sanchez-Garcia, Silvia | Bonini, Matteo | Vereda, Andrea | Kolkhir, Pavel | Antolin-Amerigo, Dario | Dimov, Vesselin | Gallego-Corella, Claudia | Aldave Becerra, Juan Carlos | Diaz, Alexander | Bellido Linares, Virginia | Villa, Leonor | Rosenwasser, Lanny J. | Sanchez-Borges, Mario | Ansotegui, Ignacio | Pawankar, Ruby | Bieber, Thomas
|
2016
|
10.1186/S40413-016-0098-Z
|
|
|
2016: No disponible**, 2020: Q3
|
|
Journal-article
|
International survey on skin patch test procedures, attitudes and interpretation
|
|
2016
|
10.1186/S40413-016-0098-Z
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Artículo en revista científica
|
International survey on skin patch test procedures, attitudes and interpretation
|
Tanno L.K.
|
2016
|
10.1186/S40413-016-0098-Z
|
World Allergy Organization Journal
|
|
Q1
|
|
Journal-article
|
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia
|
|
2015
|
10.1016/J.JACI.2015.08.010
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Journal - Letter
|
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia
|
Crestani, Elena | Volpi, Stefano | Candotti, Fabio | Giliani, Silvia | Notarangelo, Lucia Dora | Chu, Julia | Becerra, Juan Carlos Aldave | Buchbinder, David | Chou, Janet | Geha, Raif S. | Kanariou, Maria | King, Alejandra | Mazza, Cinzia | Moratto, Daniele | Sokolic, Robert | Garabedian, Elizabeth | Porta, Fulvio | Putti, Maria Caterina | Wakim, Rima H. | Tsitsikov, Erdyni | Pai, Sung-Yun | Notarangelo, Luigi D.
|
2015
|
10.1016/J.JACI.2015.08.010
|
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
|
|
Q1
|
|
Artículo en revista científica
|
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia
|
Crestani E.
|
2015
|
10.1016/J.JACI.2015.08.010
|
Journal of Allergy and Clinical Immunology
|
|
Q1
|
|
Artículo en revista científica
|
First report of the hyper-IgM syndrome registry of the latin american society for immunodeficiencies: Novel mutations, unique infections, and outcomes
|
Cabral-Marques O.
|
2014
|
10.1007/S10875-013-9980-4
|
Journal of Clinical Immunology
|
|
Q1
|
|
Journal-article
|
First report of the hyper-IgM syndrome registry of the latin american society for immunodeficiencies: Novel mutations, unique infections, and outcomes
|
|
2014
|
10.1007/S10875-013-9980-4
|
|
Scopus - Elsevier a través de ORCID
|
|
|
Journal - Article
|
First Report of the Hyper-IgM Syndrome Registry of the Latin American Society for Immunodeficiencies: Novel Mutations, Unique Infections, and Outcomes
|
Cabral-Marques, Otavio | Klaver, Stefanie | Schimke, Lena F. | Ascendino, Evelyn H. | Ali Khan, Taj | Soeiro Pereira, Paulo Vitor | Falcai, Angela | Vargas-Hernandez, Alexander | Santos-Argumedo, Leopoldo | Bezrodnik, Liliana | Moreira, Ileana | Seminario, Gisela | Di Giovanni, Daniela | Gomez Raccio, Andrea | Porras, Oscar | Weber, Cristina Worm | Ferreira, Janaira Fernandes | Tavares, Fabiola Scancetti | de Carvalho, Elisa | Cavalcante Valente, Claudia Franca | Kuntze, Gisele | Galicchio, Miguel | King, Alejandra | Rosario-Filho, Nelson Augusto | BaptistellaGrota, Milena | dos Santos Vilela, Maria Marluce | Watanabe di Gesu, Regina Sumiko | Lima, Simone | de Souza Moura, Leiva | Talesnik, Eduardo | Mansour, Eli | Roxo-Junior, Persio | Carlos Aldave, Juan | Goudouris, Ekaterine | Pinto-Mariz, Fernanda | Berron-Ruiz, Laura | Staines-Boone, Tamara | Cordova Calderon, Wilmer O. | del Carmen Zarate-Hernandez, Maria | Grumach, Anete S. | Sorensen, Ricardo | Durandy, Anne | Torgerson, Troy R. | Costa Carvalho, Beatriz Tavares | Espinosa-Rosales, Francisco | Ochs, Hans D. | Condino-Neto, Antonio
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2014
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10.1007/S10875-013-9980-4
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JOURNAL OF CLINICAL IMMUNOLOGY
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Q2
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Journal-article
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A 1-year-old girl with a gain-of-function STAT1 mutation treated with hematopoietic stem cell transplantation
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2013
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10.1007/S10875-013-9947-5
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Scopus - Elsevier a través de ORCID
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Artículo en revista científica
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A 1-year-old girl with a gain-of-function STAT1 mutation treated with hematopoietic stem cell transplantation
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Aldave J.C.
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2013
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10.1007/S10875-013-9947-5
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Journal of Clinical Immunology
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Q1
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Journal - Letter
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A 1-Year-Old Girl with a Gain-of-Function STAT1 Mutation Treated with Hematopoietic Stem Cell Transplantation
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Carlos Aldave, Juan | Cachay, Enrique | Nunez, Luis | Chunga, Ausberto | Murillo, Sergio | Cypowyj, Sophie | Bustamante, Jacinta | Puel, Anne | Casanova, Jean-Laurent | Koo, Armando
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2013
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10.1007/S10875-013-9947-5
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JOURNAL OF CLINICAL IMMUNOLOGY
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Q3
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