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pro vyhledávání: '"Nieto Barrera M"'
Autor:
Nieto-Barrera, M, Brozmanova, M, Capovilla, G, Christe, W, Pedersen, B, Kane, K, O'Neill, Fiona *
Publikováno v:
In Epilepsy Research 2001 46(2):145-155
Publikováno v:
In Seizure: European Journal of Epilepsy December 2000 9(8):590-594
Autor:
Nieto-Barrera M, Candau Fernández-Mensaque R, Campaña-Marchal C, Nieto-Jiménez M, Díaz-Fernandez F
Publikováno v:
Revista de Neurología. 36:1044
Introduccion. La encefalopatia progresiva con edema, hipsarritmia y atrofia optica (sindrome PEHO) es un proceso patologico que se inicia en los primeros meses de la vida y conduce rapidamente a una encefalopatia muy grave. Se aporta el caso de un ni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86f8c05b65fade04d516745567d9cd28
https://doi.org/10.33588/rn.3611.2003080
https://doi.org/10.33588/rn.3611.2003080
Publikováno v:
Revista de Neurología. 37:64
Objetivo. La epilepsia mioclonica grave de la infancia (EMGI) es un sindrome epileptico reconocido en las ICE de 1985 y 1989 y en la propuesta del Grupo de Trabajo de Clasificacion y Terminologia de la ILAE en 2001. Se describe su desarrollo historic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c7f551de9c606e6df0e8ebdcd02b17c
https://doi.org/10.33588/rn.3701.2003184
https://doi.org/10.33588/rn.3701.2003184
Autor:
Nieto-Barrera M
Publikováno v:
Revista de Neurología. 32:650
INTRODUCTION The idiopathic generalized epilepsies of children form a neurobiological continuum which starts during the first years of life, until adolescence. In this group, infantile absence epilepsy may be considered to be the maximum expression o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b405109e7ce3ef06e611dad5979e460d
https://doi.org/10.33588/rn.3207.2000516
https://doi.org/10.33588/rn.3207.2000516
Autor:
Nieto-Barrera M
Publikováno v:
Revista de Neurología. 28:73
Introduction Non epileptic paroxysmal events (NEPE) are clinical disorders of usually sudden appearance, brief and originated by a cerebral disfunction of diverse causes with a common character to be no epileptic. Development The non epileptic paroxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f63304437a0e098ffc29ed88026ae196
https://doi.org/10.33588/rn.2801.98353
https://doi.org/10.33588/rn.2801.98353
Autor:
Nieto-Barrera M
Publikováno v:
Revista de Neurología. 28:101
INTRODUCTION Females with Rett syndrome (RS) are actually known to present with a more heterogenous pattern of phenotypes than originally considered. DEVELOPMENT This means that a number of clinical variants exist. These clinical variants are those p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd6d2ddfe050f6831bdc4a97b0b76293
https://doi.org/10.33588/rn.2801.98358
https://doi.org/10.33588/rn.2801.98358
Autor:
Nieto-Barrera M
Publikováno v:
Revista de Neurología. 28:278
Myoclonic jerks occur in a number of different syndromes. There is many classifications of myoclonus. It is preferred the Fejerman classification, slightly modified that present the following five groups: 1. Myoclonus without encephalopathy and witho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec98a7ac6e4198dab26b76f192cc6176
https://doi.org/10.33588/rn.2803.98387
https://doi.org/10.33588/rn.2803.98387
Autor:
Nieto-Barrera M
Publikováno v:
Revista de Neurología. 26:298
The correct diagnosis of the epileptic patient must establish the type of seizures according to the 1981 ILAE ICES, and the epileptic syndrome according to the 1989 ILAE ICE. Some children, at the onset of epilepsy, are difficult to classify. These a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd900c41b603654229c949cd7a7c50da
https://doi.org/10.33588/rn.26150.981069
https://doi.org/10.33588/rn.26150.981069
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