Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Julio, Orellana"'
Publikováno v:
Proceedings of the 8th International Conference on Geographical Information Systems Theory, Applications and Management.
Publikováno v:
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
instname
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[EN] Borondo’s Inn is a Manchego inn from the 16th century located in Daimiel (Ciudad Real), which is in a serious state of deterioration. This inn was built in an important region beside Real Road that connected Almagro with the Levante and southe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::210be8f80b8e47a85bcc466a5ad8e7ff
http://hdl.handle.net/10251/160472
http://hdl.handle.net/10251/160472
Autor:
Leopoldo Santos-Argumedo, Ricardo U. Sorensen, Edgar Borges de Oliveira-Júnior, Antonio Condino-Neto, Francisco J. Espinosa-Rosales, Stefanie Klaver, Wilma Carvalho Neves Forte, Julio Orellana, Otavio Cabral-Marques, Silvia Danielian, Carolina Prando, Liliana Bezrodnik, Miguel Galicchio, Lena Friederick Schimke, Dino Pietropaolo-Cienfuegos, Alejandra King, Lizbeth Blancas-Galicia, Beatriz Tavares Costa-Carvalho, Jacinta Bustamante, Anete Sevciovic Grumach, Nuria Bengala Zurro, Matías Oleastro, Marcia Buzolin, Oscar Porras, Alejandro Lozano, Paulo Vitor Soeiro Pereira, Lorena Regairaz, Pérsio Roxo-Junior
Publikováno v:
Pediatric Blood & Cancer. 62:2101-2107
(59.4%), granulomata (49.3%), skin infections (42%), chronic diarrhea (41.9%), otitis (29%), sepsis (23.2%), abscesses (21.7%), recurrent urinary tract infection (20.3%), and osteomyelitis (15.9%). Adverse reactions to bacillus Calmette-Gu� (BCG) v
Autor:
Julio Orellana, Marcela Rodriguez M, Ramón E. Pogonza, María I. Pereira, Telma Varela, J.C. Muiño, María J. Lauria, Marcela O. Miño
Publikováno v:
Journal of Allergy and Clinical Immunology. 143:AB12
Autor:
Olga Akiko Takano, Pérsio Roxo Júnior, Carmen L. Navarrete Suarez, Carolina Cm. Prando, Célia Martínez Cuellar, Cecilia Montenegro, Gesmar Rodrigues Silva Segundo, Nelson Rosario, Ekaterine S. Goudouris, Cristina M. Kokron, Flavia Amendola Anisio de Carvalho, Julio Orellana, Lorena Regairaz, Natalia Alozano, Vera M. Dantas, Carmen C. Fernandez, Antonio Condino-Neto, Valéria Soraya de Farias Sales, María Edith González Serrano, Myrthes Toledo Barros, E.O. Dantas, Jessica Pino, Ileana Moreira, Diana Cabanillas, José Luis Franco, Maria Claudia Ortega López, Beatriz Tavares Costa-Carvalho, Maria Dolores Mogica Martinez, Maryanna Peres, Arnaldo Carlos Porto Neto, Alejandro Alozano, Danielli Christinni Bichuetti-Silva, Marina Fernandes Almeida Cheik, Anete Sevciovic Grumach, Gustavo Vijoditz, Leticia Hernandez, Liliana Bezrodnik, Jairo A. Rodríguez, Maria Marluce dos Santos Vilela, Victor Nudelman, Jessica Loekmanwidjaja, Francisco Javier Rodriguez Quiroz, Janaíra Fernandes Ferreira, Daniel Enrique Mendonza Quispe, Virginia Patiño, Wilmer Cordova Calderon, Nelma Maria Neves Antunes, Camila Teles Machado Pereira, Juliana Themudo Lessa Mazzucchelli, Annie Mafra Oliveira, Aristoteles Alvarez Cardona, Aniela Bonorino Xexeo Castelo Branco, Maria Enriqueta Nunez, Daniele Comin Costa, Carolina Sanchez Aranda, Herberto José Chong Neto, Flaviane Rabello, Monica Souza, Líllian S.L. Moraes, Wilma Carvalho Neves Forte, Fabiola Scancetti Tavares, Maria Isabel Santos Valdomir Nadaf, Isabella Prado Mota
Publikováno v:
Journal of Allergy and Clinical Immunology. 143:AB113
Autor:
Ernesto Juaneda, Julio Orellana, Alejandra Cháves, Norma Teresa Rossi, Blanca L. Pereyra, Alicia Sturich, Luis Alday, Cecilia del Carmen Montes, Roberto De Rossi
Publikováno v:
Archivos Argentinos de Pediatria. 111:423-427
The 22q11.2 microdeletion is the most common deletion syndrome, with a prevalence of 1/4000-1/6000 among newborn infants and a wide phenotypic variability. The diagnosis of the 22q11.2 microdeletion is made through cytogenetics or fluorescence in sit
Autor:
Renata Formankova, Nermeen Galal, Funda Erol Cipe, Tomohiro Morio, Francisco J. Espinosa-Rosales, Diana Liberatore, Nima Rezaei, Viviana Listello, Masafumi Yamada, Graham Davies, Gyan Joshi, Anna Shcherbina, Reem Elfeky, María I. Pereira, Vojtech Thon, Ryuta Nishikomori, Fabiola Scancetti Tavares, Oscar Porras, Jose Gonçalo Marques, Anete Sevciovic Grumach, I. Esteves, Liliana Bezrodnik, Shereen M. Reda, Yoshitoshi Ohtsuka, Danuta Kowalczyk, Luciana Cristina Matos Cunha, Jorge Pinto, Bénédicte Neven, José Luis Franco, Maria Marluce dos Santos Vilela, Beatriz Tavares Costa Carvalho, Salem Al-Tamemi, Zohreh Nademi, Tadashi Ariga, Pérsio Roxo, Leticia Hernandez-Nieto, Anna Szaflarska, M. Enriqueta Nuñez-Nuñez, Beatriz E. Marciano, Thomas A. Fleisher, Waleed Al-Herz, Alisan Yildiran, Sergio D. Rosenzweig, Yu-Lung Lau, Heike Toshio, Juliana Themudo Lessa Mazzucchelli, S. Kiliç, Chiung Yu Huang, Aydan Ikinciogullari, Carlos Torres-Lozano, Z. Allwood, Andrea C. Gómez Raccio, Mary Slatter, Sara Elva Espinosa-Padilla, Figen Dogu, Andrew R. Gennery, Julio Orellana
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Journal of Allergy and Clinical Immunology; Vol 133
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Universidade de São Paulo (USP)
instacron:USP
Journal of Allergy and Clinical Immunology; Vol 133
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Ikinciogullari, Aydan/0000-0003-1145-0843; Pinto, Jorge A/0000-0003-2987-3238; Dogu, Figen/0000-0002-7869-4941; FRANCO, JOSE/0000-0001-5664-6415; Nishikomori, Ryuta/0000-0002-9407-6158; Al-Tamemi, Salem/0000-0002-7232-2629; Nishikomori, Ryuta/0000-00
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6614aefa90aa8a5100bc57546453b852
Autor:
Cecilia, Del Carmen Montes, Alicia, Sturich, Alejandra, Chaves, Ernesto, Juaneda, Julio, Orellana, Roberto, De Rossi, Blanca, Pereyra, Luis, Alday, Norma Teresa, Rossi
Publikováno v:
Archivos argentinos de pediatria. 111(5)
The 22q11.2 microdeletion is the most common deletion syndrome, with a prevalence of 1/4000-1/6000 among newborn infants and a wide phenotypic variability. The diagnosis of the 22q11.2 microdeletion is made through cytogenetics or fuorescence in situ
Autor:
Pablo Romero, María I. Pereira, Estela Pautasso, Horacio M. Serra, Ana Romero Boni, Telma Varela, Maria ofelia Miño, Julio Orellana, Stefanía Santo, Adriana Cassinerio, Omar Romero
Publikováno v:
Journal of Allergy and Clinical Immunology. 137:AB174