Zobrazeno 1 - 10
of 41
pro vyhledávání: '"F. Benito González"'
Autor:
F. Benito González, P. Blanco Pérez, A. Cañizo álvarez, J.L. Gómez González, T. Flores Corral, E Coscarón Blanco
Publikováno v:
Acta Otorrinolaringológica Española. 55:148-151
Angiomyolipoma is an uncommon hamartomatous renal tumor very prone to spontaneous bleeding. However it is possible to find it in extrarenal sites, being the liver the most frequent one. The rest of sites recorded in literature are exceptional. In fac
Autor:
D. Moreno Jiménez, A. Muñoz Herrera, F. Benito González, J.M. Serradilla López, S. Santa Cruz Ruiz, M. González Sánchez, P. Blanco Pérez, A. Batuecas Caletrio
Publikováno v:
Acta Otorrinolaringológica Española. 57:193-195
The third branquial arch anomalies represent less than 1% of this deformites. The clinical manifestation can be varied althouth the formation of cysts is the commonest one and may appear at any time in life. We report the clinical case of a 7 year ol
Publikováno v:
Acta otorrinolaringologica espanola. 60
The development of knowledge of paragangliomas has been inextricably linked to the development of all fields of medicine. Throughout history, both knowledge of diseases and technical improvements in diagnosis have served to understand these tumors, a
Autor:
A, Batuecas Caletrío, P, Blanco Pérez, S, Santa Cruz Ruiz, S Santa, Cruz Ruiz, J M, Serradilla López, M, González Sánchez, D, Moreno Jiménez, F, Benito González, A, Muñoz Herrera
Publikováno v:
Acta otorrinolaringologica espanola. 57(4)
The third branquial arch anomalies represent less than 1% of this deformites. The clinical manifestation can be varied althouth the formation of cysts is the commonest one and may appear at any time in life. We report the clinical case of a 7 year ol
Autor:
E, Coscarón Blanco, P, Blanco Pérez, S, Santa Cruz Ruiz, A, Muñoz Herrera, F, Benito González, J L, Paniagua Escudero
Publikováno v:
Anales otorrinolaringologicos ibero-americanos. 32(2)
The parapharyngeal space-occupying lessions may develop from any of the structures located inside it. Uncommon although possible ethiologies for them are anatomic variations of the course of the internal carotid artery. These anatomic variants mainly
Autor:
E, Coscarón Blanco, J L, Gómez González, P, Blanco Pérez, A, Cañizo Alvarez, F, Benito González, T, Flores Corral
Publikováno v:
Acta otorrinolaringologica espanola. 55(3)
Angiomyolipoma is an uncommon hamartomatous renal tumor very prone to spontaneous bleeding. However it is possible to find it in extrarenal sites, being the liver the most frequent one. The rest of sites recorded in literature are exceptional. In fac
Autor:
J Benito, González, F Benito, González, A, Muñoz Herrera, A, Nieto García, P, Antúñez Plaza, D, Pérez Plasencia, A, del Cañizo Alvarez
Publikováno v:
Anales otorrinolaringologicos ibero-americanos. 30(5)
Plasmocytomas are neoplasic disorders arising from plasma cells that include Multiple Myeloma (MM) Solitary Plasmocytoma of the bone and Extramedullary Plasmacytoma (EMP). EMP are solitary tumours consisting of plasma cell proliferation that occurs i
Autor:
J J, Benito González, F, Benito González, S, Santa Cruz Ruiz, J L, Gómez González, E, Coscarón Blanco, M, Cordero Sánchez, A, del Cañizo Alvarez
Publikováno v:
Anales otorrinolaringologicos ibero-americanos. 30(1)
Tuberculous otitis media (TOM) is a rare cause of chronic suppurative infection of the middle ear. Due to that the symptoms and signs are often indistinguishable from those of nontuberculosis chronic otitis media and the fact that the index of suspic
Autor:
J, Benito González, L, Beltrán Mateos, F, Benito González, D, Pérez Plasencia, S, Santa Cruz Ruiz, T, Figueroa García
Publikováno v:
Anales otorrinolaringologicos ibero-americanos. 27(5)
Down beat nystagmus is a central nystagmus. In the literature reviewed the two most common causes that can produce it are cerebellar degenerations and Chiari malformation. The site of lesion causing this nystagmus appears to be the brainstem or the c
Autor:
J, Benito González, D, Pérez Plasencia, F, Benito González, P, Blanco Pérez, F, Aguirre García, T, Mories, A, Cañizo Alvarez
Publikováno v:
Acta otorrinolaringologica espanola. 50(6)
Pendred syndrome is an autosomal recessive disorder characterized by congenital deafness and goiter. The gene responsible for this syndrome is located on chromosome 7q31. The disorder is related to a defect in iodine organification, but the molecular