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pro vyhledávání: '"J P, García Iñiguez"'
Autor:
J P, García-Iñiguez, F J, López-Pisón, P, Madurga Revilla, I, Montejo Gañán, M, Domínguez Cajal, L, Monge Galindo, S B, Sánchez Marco, M C, García Jiménez
Publikováno v:
Neurologia (Barcelona, Spain). 34(5)
Acute cerebellitis is a rare inflammatory disease with a highly variable clinical course that ranges from benign self-limiting symptoms to a fulminant presentation associated with a high risk of death due to compression of the posterior fossa, acute
Autor:
V, Caballero Pérez, F J, López Pisón, M D, Miramar Gallart, A, González Álvarez, M C, García Jiménez, J P, García Iñiguez, C, Orden Rueda, I, Gil Hernández, C, Fuertes Rodrigo, R, Fernando Martínez, A, Rodríguez Valle, M J, Alcaine Villarroya
Publikováno v:
Neurologia (Barcelona, Spain). 32(9)
Global developmental delay (GDD) and intellectual disability (ID) are frequent reasons for consultation in paediatric neurology departments. Nowadays, array comparative genomic hybridisation (array-CGH) is one of the most widely used techniques for d
Autor:
E, Janer Subías, A, de Arriba Muñoz, J P, García Iñiguez, M, Ferrer Lozano, J, Sanchez Del Pozo, J I, Labarta Aizpun
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 82(1)
Osteopetrosis (OP) is a congenital bone disease which is caused by a functional disorder in osteoclasts with inability for normal bone resorption, leading to increased bone mineral density and bone sclerosis. It can be classified into different group
Autor:
L, Monge Galindo, R, Pérez Delgado, J, López-Pisón, A, Olloqui-Escalona, J P, García Iñiguez, I, Ruiz del Olmo Izuzquiza, J L, Peña-Segura
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 71(5)
There are transient intracranial hypertension cases, recognizable by bulging fontanelle in infants and by papilloedema in children. We present our experience in benign intracranial hypertension (BIH) cases, excluding traumatic brain injuries, encepha
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