Zobrazeno 1 - 10
of 150
pro vyhledávání: '"J.R. Ricoy"'
Publikováno v:
Clinical Neurology and Neurosurgery. 114:42-46
Intraparenchymal schwannomas are very rare tumours. We present two young adult patients operated for this type of lesion who show no signs of recurrence 2 years after surgery. These tumours have a bimodal peak of presentation: most occur in young pat
Autor:
Julio-Cesar Palomino, Juan-Carlos Martinez, Ana Cabello, J.R. Ricoy, Rafael Samaniego, Juan Manuel Sepúlveda
Publikováno v:
Cancer. 113:166-174
BACKGROUND. The authors analyzed the retinoblastoma (Rb) tumor-suppressor pathway in meningeal hemangiopericytomas (MHPCs). METHODS. Immunohistochemical detection of the Rb pathway proteins (Rb; E2F transcription factor 1 [E2F1]; cyclins D1, D3, and
Autor:
A. Barois, Norma B. Romero, Waney Squier, Caroline Sewry, J. Angus Dobbie, Carmen Navarro, Anne-Marie Childs, J.R. Ricoy, Cristina Reina, Francesco Muntoni, Sandeep Jayawant, Richard Appleton, Kristen J. Nowak, Nigel G. Laing, K.R. Walker, Sophie Clément, Roger C. Mountford
Publikováno v:
Annals of Neurology. 61:175-184
Objective To investigate seven congenital myopathy patients from six families: one French Gypsy, one Spanish Gypsy, four British Pakistanis, and one British Indian. Three patients required mechanical ventilation from birth, five died before 22 months
Autor:
Mercedes Gómez-Arnáiz, Elena Martín, María Vázquez, Fernando Mateos, Maria T. Garcia-Silva, Ana Cabello, Juan José García-Peñas, Rogelio Simón, Ana Ferreiro, J.R. Ricoy, Eloy Rivas
Publikováno v:
Pediatric Neurology. 33:350-356
Macrophagic myofasciitis is an unusual inflammatory myopathy, which has been almost exclusively reported in French adults with diffuse arthromyalgias and asthenia. It is characterized by an infiltrate of densely packed macrophages, with granular peri
Autor:
Enrique Mencía-Gutiérrez, J.R. Ricoy, Juan P. García-Torre, Esperanza Gutiérrez-Díaz, Irene Redondo-Marcos
Publikováno v:
Journal of Cutaneous Pathology. 31:539-543
Background: Cutaneous horn (cornu cutaneum) is a morphological designation for a protuberant mass of keratin that resembles the horn of an animal. It results from unusual cohesiveness of keratinized material from the superficial layers of the skin or
Autor:
Alfonso Lagares, Pedro Gonzalez, J.R. Ricoy, A. Cabrera, P. Miranda, Ana Ramos, Ramiro D. Lobato
Publikováno v:
Neurocirugía. 15:159-164
Among the group of pituitary adenomas surgically treated, about 25-30% are not associated with clinical or analytical findings of hormonal hypersecretion. The development of immunohistochemical techniques has allowed the demonstration of a subgroup o
Autor:
J.R. Ricoy, J.F. Alén, Alfonso Lagares, A. de la Lama, Pedro A. Gómez, Ramiro D. Lobato, G.R. Boto
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Summary Background The concurrence of multiple sclerosis (MS) and glioma is uncommon. Approximately 30 cases have been reported, but in only six of them the tumour was pure or mixed oligodendroglioma. The appearance of new neurological symptoms and s
Publikováno v:
European Journal of Ophthalmology. 13:482-485
Purpose To report a case of congenital phakomatous choristoma (PC) of the eyelid, a rare tumor of lenticular anlage in the subcutaneous tissue and dermis. Case A boy had a mass in the right lower eyelid near the inner canthus at birth. At age 10 mont
Publikováno v:
Acta Neurochirurgica. 144:735-740
We describe a patient with an intracranial extra skeletal myxoid chondrosarcoma (EMC), an unusual neoplasm of the deep soft tissues of the extremities. Very rarely are they localised as an intracranial lesion, and we believe it is very important to a
Autor:
Joaquín Arenas, Yolanda Campos, P. del Hoyo, Ana Cabello, A. López, A. García, J.R. Ricoy, S. Jiménez, Juan C. Rubio, M. A. Martín, Fernando de Bustos
Publikováno v:
Muscle & Nerve. 25:185-188
We report a patient with progressive external ophthalmoplegia (PEO), exercise intolerance, and deafness after aminoglycoside exposure, harboring two pathogenic mutations in her mtDNA: an A1555G in the 12S rRNA gene and a G4309A in the tRNA(Ile) gene.