Reporte de un probable caso de Hemoglobina S / Talasemia Beta

Autor: John Ramírez Cuentas, Olga Lizama Olaya, Josilú Martínez La Rosa, Mercy Jhong Olivera, Eduardo Salazar Lindo

Publikováno v: Revista Médica Herediana, Vol 15, Iss 3, Pp 173-178 (2004)

We report the case of a patient with Hemoglobin S / Thalassemia. It is feasible to recognize this infrequent disease by its clinical presentation and the aid of clinical laboratory . On this patient, the diagnosis was established based on the clinica

Externí odkaz: https://doaj.org/article/0d9b32095253449996b71a321c6931bd

Meningitis neonatal: estudio multicéntrico en Lima, Perú

Autor: María Luz Rospigliosi-López, Daniel Guillén-Pinto, Luis Florián, Oscar Eguiluz-Loaiza, Alfredo Tori, Bárbara Málaga-Espinoza, Lizet Cuba, Leidi Vilchez-Fernández, Joselyn Ye-Tay, Sonia Villasante-Valera, María Rivas, Pilar Medina-Alva, Olga Lizama-Olaya, María Luisa Stiglich, Andrea Montenegro-Rivera, Carmen Dávila-Aliaga

Publikováno v: Revista Peruana de Medicina Experimental y Salud Pública. 37:210-9

Objective: To determine the incidence and the clinical, bacteriological and cerebrospinal fluid characteristics of neonatal meningitis in Lima hospitals. Materials and methods: An observational, multicenter study was conducted in six hospitals in the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caeca0e5a8db2508bd6467295a9618f8
https://doi.org/10.17843/rpmesp.2020.372.4772

Hemoglobin S / Beta Thalassemia. Report of a probable case

Autor: Olga Lizama Olaya, Eduardo Salazar Lindo, Mercy Jhong Olivera, John Helmut Ramirez Cuentas, Josilú Martínez La Rosa

Publikováno v: Revista Medica Herediana, Volume: 15, Issue: 3, Pages: 173-178, Published: JUL 2004
Revista Médica Herediana, Vol 15, Iss 3, Pp 173-178 (2004)
Revista Medica Herediana; Vol 15 No 3 (2004): julio-setiembre; 173
Revista Medica Herediana; Vol. 15 Núm. 3 (2004): julio-setiembre; 173
Revistas-Universidad Peruana Cayetano Heredia
Universidad Peruana Cayetano Heredia
instacron:UPCH

We report the case of a patient with Hemoglobin S / Thalassemia. It is feasible to recognize this infrequent disease by its clinical presentation and the aid of clinical laboratory . On this patient, the diagnosis was established based on the clinica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ce9d381fb3485acd10a54ba05889a82
http://www.scielo.org.pe/scielo.php?script=sci_arttext&pid=S1018-130X2004000300010&lng=en&tlng=en