Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Alejandra Consuelo-Sanchez"'
Autor:
Estefanía Vásquez-Echeverri, Marco Antonio Yamazaki-Nakashimada, Edna Venegas Montoya, Selma Cecilia Scheffler Mendoza, Lina Maria Castano-Jaramillo, Edgar Alejandro Medina-Torres, Maria Edith González-Serrano, Melissa Espinosa-Navarro, Juan Carlos Bustamante Ogando, María Guadalupe González-Villarreal, Margarita Ortega Cisneros, Pedro Francisco Valencia Mayoral, Alejandra Consuelo Sanchez, Gustavo Varela-Fascinetto, Rosa María Nideshda Ramírez-Uribe, Yuridia Salazar Gálvez, Laura Cecilia Bonifaz Alonzo, Ezequiel Moisés Fuentes-Pananá, Noemí Gómez Hernández, César Mauricio Rojas Maruri, Jean-Laurent Casanova, Sara Elva Espinosa-Padilla, Aidé Tamara Staines Boone, Gabriel López-Velázquez, Bertrand Boisson, Saul Oswaldo Lugo Reyes
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice. 11:1261-1280.e8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc720358d851ea8d90161bb58533f987
https://doi.org/10.1016/j.jaip.2022.12.045
https://doi.org/10.1016/j.jaip.2022.12.045
Autor:
Barbara K. Burton, Alejandra Consuelo Sanchez, Maria Kostyleva, Ana Maria Martins, Sachin Marulkar, Florian Abel, Ivo Barić
Publikováno v:
J Pediatr Gastroenterol Nutr
bjectives: Sebelipase alfa is approved for treatment of lysosomal acid lipase deficiency (LAL-D). This single-arm, open-label study (NCT02112994) evaluated sebelipase alfa efficacy and safety in patients with LAL-D. Methods: Patients >8 months of age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aea838e9b78a072616c63677e52bcd38
https://pubmed.ncbi.nlm.nih.gov/35576532
https://pubmed.ncbi.nlm.nih.gov/35576532
Autor:
Barbara K. Burton, Ivo Barić, Alejandra Consuelo Sanchez, Ana Maria Martins, Sachin Marulkar, Maria Kostyleva, Florian Abel
Publikováno v:
Journal of Hepatology. 70:e121-e122
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eddbe577543c1261dd3be246066ad02
https://doi.org/10.1016/s0618-8278(19)30214-2
https://doi.org/10.1016/s0618-8278(19)30214-2
Publikováno v:
Journal of Hepatology. 68:S81
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd36ebf5ae689151aae77559f29ca3dd
https://doi.org/10.1016/s0168-8278(18)30380-5
https://doi.org/10.1016/s0168-8278(18)30380-5
Autor:
Manisha Balwani, Eugen Mengel, Yijun Yang, Heidi Peters, Vratislav Smolka, Vassili Valayannopoulos, Barbara K. Burton, Gregory M. Enns, Anthony G. Quinn, Christina M. Laukaitis, Maurizio Scarpa, Ivo Barić, Fatih Süheyl Ezgü, Sandra Rojas-Caro, Katryn N. Furuya, Stephen Eckert, Zachary Goodman, François Feillet, John P. Kane, Richard W. Erbe, T. Andrew Burrow, K Otfried Schwab, Alejandra Consuelo-Sanchez, Can Ficicioglu, Scott Nightingale, Edward G. Neilan, Patrick Deegan, Carmen Camarena Grande, Marnie Wood, Maja Di Rocco, Mahmut Çoker
Publikováno v:
New England Journal of Medicine
New England Journal of Medicine, Massachusetts Medical Society, 2015, 373 (11), pp.1010-1020. ⟨10.1056/NEJMoa1501365⟩
New England Journal of Medicine, Massachusetts Medical Society, 2015, 373 (11), pp.1010-1020. ⟨10.1056/NEJMoa1501365⟩
BackgroundLysosomal acid lipase is an essential lipid-metabolizing enzyme that breaks down endocytosed lipid particles and regulates lipid metabolism. We conducted a phase 3 trial of enzyme-replacement therapy in children and adults with lysosomal ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4382231b354e63ae1046f299b6bc977c
https://hal.univ-lorraine.fr/hal-01667323
https://hal.univ-lorraine.fr/hal-01667323
Autor:
Tayde López-Santaella, Teresa Álvarez y Muñoz, Mara Medeiros-Domingo, Sarbelio Moreno-Espinosa, Alejandra Consuelo-Sánchez, Onofre Muñoz-Hernández, Rosa Elena Sarmiento-Silva, Alicia Sotomayor-González, María Elena Trujillo-Ortega, Montserrat Elemi García-Hernández, Blanca Itzel Taboada-Ramírez, Francisco Arenas-Huertero
Publikováno v:
Annals of Hepatology, Vol 19, Iss 3, Pp 295-301 (2020)
Introduction and objectives: Cases of viral hepatitis reported in Mexico are typically identified as hepatitis A, B and C. However, unspecified cases are reported annually. Hepatitis E virus (HEV) is an emergent agent that causes a self-limiting infe
Externí odkaz:
https://doaj.org/article/3d2ac2737ed4412281a022b882c59d19
Autor:
Rodrigo Ortegón-Gallareta, Rodrigo Vázquez-Frías, Gerardo Blanco-Rodriguez, Alejandra Consuelo-Sánchez, Claudia Jimena Ortiz-Rivera, Juan Rafael Murillo-Eliosa, Alan I. Vicenteño-León, Pedro Valencia-Mayoral
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 6 (2022)
Background: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disease characterized by the development of polyps in the gastrointestinal tract, mucocutaneous pigmentation, and the risk of developing malignant neoplasms. This study a
Externí odkaz:
https://doaj.org/article/c09a29521b7540c5969fa47b04e6e39f
Autor:
Alejandra Consuelo-Sánchez, Rodrigo Vázquez-Frias, Alejandra Reyes-De La Rosa, Carlos P. Acosta-Rodríguez-Bueno, María P. Ortal-Vite, Jorge J. Cebolla
Publikováno v:
Annals of Hepatology, Vol 18, Iss 4, Pp 646-650 (2019)
Introduction and Objectives: Lysosomal acid lipase deficiency (LAL-D) is an autosomal recessive disease caused by mutations in the LIPA gene, located on the long arm of chromosome 10 (10q23.31). Up until now, more than 59 mutations have been describe
Externí odkaz:
https://doaj.org/article/3972cae7db2e42e3a066bb254f90f627
Autor:
Ana Caren Cortés-Márquez, Sandra Mendoza-Elizalde, Francisco Arenas-Huertero, Jimena Trillo-Tinoco, Pedro Valencia-Mayoral, Alejandra Consuelo-Sánchez, Jonathan Zarate-Franco, Ada Ruth Dionicio-Avendaño, José de Jesús Herrera-Esquivel, Elio Germán Recinos-Carrera, Christian Colín-Valverde, Sandra Rivera-Gutiérrez, Alfonso Reyes-López, Juan Carlos Vigueras-Galindo, Norma Velázquez-Guadarrama
Publikováno v:
BMC Infectious Diseases, Vol 18, Iss 1, Pp 1-9 (2018)
Abstract Background Helicobacter pylori is a major aetiologic agent associated with gastritis. H. pylori infections increase the expression of the Toll-like receptor (TLR), which in turn modulates the expression of microRNA (miRNA)-146a and miRNA-155
Externí odkaz:
https://doaj.org/article/9cfccec695424c8794d4a24c73ed5585
Autor:
María de Jesús Galaviz-Ballesteros, Carlos Patricio Acosta-Rodríguez-Bueno, Alejandra Consuelo-Sánchez, Isidro Franco-Álvarez, Odilo Iván Olalla-Mora, Rodrigo Vázquez-Frias
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 73, Iss 5, Pp 331-334 (2016)
Introducción: El síndrome de pseudo-Bartter (SPB) se define como una alcalosis metabólica hipoclorémica con hipocaliemia en ausencia de tubulopatía. Los pacientes con fibrosis quística (FQ), al presentar alteraciones hidrolectrolíticas, pueden
Externí odkaz:
https://doaj.org/article/674f7b63122a450ba4dfa9a56d449682