Hypoxic hepatitis as diabetic ketoacidosis complication

Autor: Javier Ampuero, Emilio Suárez-García, Marina Millán, Manuel Romero-Gómez

Publikováno v: Revista Espanola de Enfermedades Digestivas, Vol 106, Iss 4, Pp 294-295 (2014)

Externí odkaz: https://doaj.org/article/9c0845e285e94f798854bf3a9195a50a

Seguimiento bioquímico, serológico y virológico en pacientes con infección crónica por el virus de la hepatitis B no tratados: portador inactivo, hepatitis crónica HBeAg negativo e inmunotolerante

Autor: Emilio Suárez García

Publikováno v: Gastroenterología y Hepatología. 37:5-7

Biochemical, serological and virologic follow-up is necessary for patients with chronic untreated HBV infection while the infection persists. For patients who are inactive carriers, follow-up helps detect reactivation or loss of HBsAg. After the loss

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c72a9c450f7b2ffafe29cf8f62cf999b
https://doi.org/10.1016/s0210-5705(14)70062-7

Antiphospholipid Antibodies Are Related to Portal Vein Thrombosis in Patients with Liver Cirrhosis

Autor: Emilio Suárez García, Manuel Castro Fernández, L. Grande, Daniel Lopez Lacomba, Manuel Romero Gómez, Inmaculada Marchante

Publikováno v: Journal of Clinical Gastroenterology. 31:237-240

The pathogenesis of portal vein thrombosis (PVT) in cirrhotic liver patients is not known. PVT has been related to liver dysfunction, neoplasm, hemodynamic factors, and hypercoagulability states. PVT has been reported in patients with antiphospholipi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd50a6670c6ab0889bc08105f881b239
https://doi.org/10.1097/00004836-200010000-00011

Resistencias farmacológicas en la hepatitis B crónica

Autor: Blanca Figueruela López, Emilio Suárez García

Publikováno v: Gastroenterología y Hepatología Continuada. 8:162-164

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2d23a81d748b9476469cfd188908cfee
https://doi.org/10.1016/s1578-1550(09)71173-8

Novel (60%) and Recurrent (40%) Androgen Receptor Gene Mutations in a Series of 59 Patients with a 46,XY Disorder of Sex Development

Autor: Mónica Fernández-Cancio, J. Martínez-Mora, E. Vicens-Calvet, M. Carrera, M. Andrade, M. Gussinyé, Antonio Perez-Aytes, Emilio Suárez García, C. Piró, Teresa Vendrell, G. Lledó, M. Del Campo, Laura Audí, Pablo Lapunzina, L. Castaño, Diego Yeste, J. Sánchez del Pozo, José Luis Arroyo, Andrés Blanco Blanco, Maria Clemente, José I Labarta, A. Carrascosa, I. Hernández de la Calle, J. A. Bermúdez de la Vega, J. Forn, Joaquim Calaf, Pilar Andaluz, J. del Valle, E. Mayayo, Nuria Toran, E. Vilaró, Isabel Salinas, M. Beneyto, O. Angerri, Ángel Segura, María Caimari, Ricardo Gracia-Bouthelier, María Angeles Albisu, M. J. Martínez-Sopena, Elisabeth Gabau, V. Borrás, M. J. Martínez-Aedo, María Luisa Granada, Antonio M. Rodríguez

Publikováno v: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Universitat Politècnica de Catalunya (UPC)

Background: Androgen receptor (AR) gene mutations are the most frequent cause of 46, XY disorders of sex development (DSD) and are associated with a variety of phenotypes, ranging from phenotypic women [complete androgen insensitivity syndrome (CAIS)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee95fe3c9ea372221848db8eb441771e
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=12781