Zobrazeno 1 - 4
of 4
pro vyhledávání: '"William Campano"'
Autor:
Jesús Domínguez-Rojas, William Campano, Jaime Tasayco, Andrea Siu-Lam, Cesia Ortega-Ocas, Noé Atamari-Anahui
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 2 (2022)
Background: Acquired thrombotic thrombocytopenic purpura (TTP) is a rare disease. In middle and low-income countries, specific resources are required for its diagnosis due to the lack of diagnostic tests and the variable response to plasma exchange,
Externí odkaz:
https://doaj.org/article/ce39b98fb3d749578b21df4020873ad1
Autor:
Noé Atamari-Anahui, Jesús Domínguez-Rojas, Luis Ruiz-Solsol, Maryori López-Turpo, Amarilis Castillo-Delgadillo, David Quiñonez Saif, William Campano
Publikováno v:
Revista de Gastroenterología del Perú. 42:131-135
El síndrome de Budd-Chiari es causado por una obstrucción del flujo sanguíneo del hígado. Los casos publicados del síndrome antifosfolípido asociado a SBC son limitados en la población pediátrica. Reportamos el caso de una adolescente de 15 a
Autor:
Noé, Atamari-Anahui, Jesús, Domínguez-Rojas, Luis, Ruiz-Solsol, Maryori, López-Turpo, Amarilis, Castillo-Delgadillo, David, Quiñonez Saif, J William, Campano Cornejo
Publikováno v:
Revista de gastroenterologia del Peru : organo oficial de la Sociedad de Gastroenterologia del Peru. 42(2)
Budd-Chiari syndrome is caused by an obstruction of blood flow to the liver. Published cases of the antiphospholipid syndrome associated with BCS are limited in the pediatric population. We report a 15-year-old adolescent who presented with fever, as
Autor:
Jesus Dominguez-Rojas, William Campano, Andrea Siu-Lam, Jaime Tasayco, Cesia Ortega-Ocas, Noé Atamari-Anahui
Acquired thrombotic thrombocytopenic purpura (TTP) is a rare disease. In middle and low-income countries, specific resources are required for its diagnosis due to the lack of diagnostic tests and the variable response to plasma exchange, especially i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f0e12478df8762275f72439c68c4bb8
https://doi.org/10.21203/rs.3.rs-726252/v1
https://doi.org/10.21203/rs.3.rs-726252/v1