Zobrazeno 1 - 10
of 36
pro vyhledávání: '"E, Bauzano Poley"'
Publikováno v:
Anales de Pediatría, Vol 69, Iss 3, Pp 232-238 (2008)
Introducción: El síndrome de Angelman se caracteriza por retraso mental, epilepsia, déficit del lenguaje, dismorfia facial y un fenotipo conductual característico. Los criterios clínicos diagnósticos están definidos por consenso desde 1995. Es
Publikováno v:
Anales de Pediatría, Vol 68, Iss 4, Pp 401-403 (2008)
Publikováno v:
Revista de neurologia. 51(10)
The term 'epileptic spasm' must be used to refer to a type of seizure that is typically found in childhood. Clinically, it is expressed as brief axial contractions, in flexion, extension or mixed, which can be symmetrical or asymmetrical and usually
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 69(3)
Angelman syndrome is characterised by mental retardation, epilepsy, speech impairment, facial dysmorphism and a characteristic behavioural phenotype. Diagnostic clinical criteria have been defined by consensus since 1995. It is caused by deficiency o
Publikováno v:
Revista de neurologia. 36(7)
Among the differents techniques for motor unit number estimation (MUNE) there is the statistical one (Poisson), in which the activation of motor units is carried out by electrical stimulation and the estimation performed by means of a statistical ana
Autor:
E, Bauzano Poley
Publikováno v:
Revista de neurologia. 36(4)
This work reviews the causes of insomnia in children and attempts to show the difficulties involved in performing a diagnosis to differentiate it from other sleep disorders.Insomnia is a disorder in which the sufferer has difficulty in falling or sta
Publikováno v:
Revista de neurologia. 32(8)
Reflex epileptic seizures are caused by a specific sensorial stimulus which determines their classification. Photosensitive epilepsies are the commonest forms and are included with the idiopathic generalized epilepsies.We analyze the different respon
Publikováno v:
Revista de neurologia. 32(4)
The idiopathic generalized epilepsies of childhood form a heterogeneous group of epileptic syndromes, with certain clinical and electroencephalographic characteristics in common. From the onset, the seizures affect both cerebral hemispheres with gene
Publikováno v:
Revista de neurologia. 27(160)
We present a male patient which presented distal muscular stiffness, from the first hours of the life. At this time, he also presented episodes of generalized muscular hypertonia with cyanosis and apnoea, started by somato-sensorial stimuli. Those ep
Publikováno v:
Revista de neurologia. 26(150)
Symptomatic epilepsy secondary to hereditary metabolic or degenerative disorders, is usually associated to neurological deterioration. Though epilepsy by itself does not induce neurological deterioration, we should remind that some epileptics encepha