Výsledky vyhledávání

[Clinical and electroencephalographic aspects of late infantile neuronal ceroid lipofuscinosis]

Autor: R, Caraballo, A, Sologuestua, V L, Ruggieri, S, Monges, R, Cersósimo, A L, Taratuto, C, Medina, N, Fejerman

Publikováno v: Revista de neurologia. 40(3)

In this paper we describe the clinical characteristics, and particularly the epileptic seizures and electroencephalographic findings, in 15 patients with a pathology diagnosis of late infantile neuronal ceroid lipofuscinosis (NCL).Nine female and six

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3c79539e3caa44ba1b184e3fa660a853
https://pubmed.ncbi.nlm.nih.gov/15750896

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[Hemiparetic cerebral palsy and startle epilepsy]

Autor: R, Caraballo, M, Semprino, R, Cersósimo, A, Sologuestua, H A, Arroyo, N, Fejerman

Publikováno v: Revista de neurologia. 38(2)

We analyzed electroclinical features and evolution in nine patients with hemiparetic cerebral palsy associated with SE.Nine patients with mean age 12.3 years and a follow up from 1 to 11 years were studied, analyzing etiology, neurological examinatio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5e4e2521e0df0c68bfeb6759050b6f6f
https://pubmed.ncbi.nlm.nih.gov/14752709

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[Pyridoxine dependence: the importance of the clinical diagnosis and early treatment]

Autor: R, Caraballo, F, Garro, R, Cersósimo, C, Buompadre, L A, Gañez, N, Fejerman

Publikováno v: Revista de neurologia. 38(1)

We described the electroclinical features, evolution and family history of two patients with definitive diagnosis of pyridoxine dependency.The first patient is a 15-month-old girl who at 1 month of age started with seizures and irritability. At two m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3c80c6dcf3022ac27a264c785e9e96ae
https://pubmed.ncbi.nlm.nih.gov/14730491

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Validación de la prueba nacional de pesquisa de trastornos de desarrollo psicomotor en niños menores de 6 años

Publikováno v: Revista chilena de pediatría, Volume: 75, Issue: 1, Pages: 75-76, Published: JAN 2004
Revista chilena de pediatría v.75 n.1 2004
SciELO Chile
CONICYT Chile
instacron:CONICYT

Introducción:El uso de una prueba de pesquisa en los primeros años de vida permite la detección temprana de retrasos en el desarrollo psicomotor y su tratamiento oportuno. En la Argentina contamos con una Prueba Nacional de Pesquisa preparada en b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d22c2a1640852bc17b84037471f20a88
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062004000100012&lng=en&tlng=en

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[Posterior reversible encephalopathy in infancy]

Autor: H A, Arroyo, L A, Gañez, N, Fejerman

Publikováno v: Revista de neurologia. 37(6)

Posterior reversible encephalopathy (PRE) is a radiological clinical syndrome that was initially reported in adults and which is characterised by seizures, headache, visual disorders, decreased awareness and anomalous neuroimages. It is an acute tran

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e2af6a6cc929e1f6167e8a9867e2b78d
https://pubmed.ncbi.nlm.nih.gov/14533065

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[Delayed-type subacute measles encephalitis]

Autor: R, Caraballo, S, Monges, R, Cersósimo, L, Cassar, I, Yepez, N, Fejerman

Publikováno v: Revista de neurologia. 37(4)

We analyze the clinical, neurological, EEG, neuroradiological features and evolution of two patients with subacute measles encephalitis.The patients, aged five years and eleven months respectively showed an acute, progressive neurological compromise

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::78521a146835698bea567d66c91f1f62
https://pubmed.ncbi.nlm.nih.gov/14533106

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[Angelman syndrome: the electroclinical characteristics in 35 patients]

Autor: R, Cersósimo, R, Caraballo, A, Espeche, L, Cassar, M V, Torrado, L, Chertkoff, E, Baialardo, H A, Arroyo, N, Fejerman

Publikováno v: Revista de neurologia. 37(1)

The purpose of this study is to report on 35 patients with Angelman syndrome (AS) in whom we evaluated the electroclinical characteristics and the progression of their epilepsy.The following factors were evaluated: sex, family background, neurologica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::281a068d912f97cb83231c006919c1d3
https://pubmed.ncbi.nlm.nih.gov/12861501

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[Reflex myoclonic epilepsy in infancy: a new reflex epilepsy syndrome or a variant of benign myoclonic epilepsy in infancy]

Autor: R, Caraballo, L, Cassar, S, Monges, I, Yepez, S, Galicchio, R, Cersósimo, N, Fejerman

Publikováno v: Revista de neurologia. 36(5)

We report a clinical and EEG study of 8 children with reflex myoclonic epilepsy of infancy to further confirm the existence of this syndrome first described by Ricci et al in 1995.Between February 1990 to July 2002, we identified 64 epileptic patient

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::482959235442f2f10ad0f48367864c53
https://pubmed.ncbi.nlm.nih.gov/12640595

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[Benign focal epilepsies in infancy, childhood and adolescence]

Autor: N, Fejerman

Publikováno v: Revista de neurologia. 34(1)

INTRODUCTION. The last proposal for a classification of epileptic seizures and syndromes of the International League Against Epilepsy (ILAE) includes recognition of several groups of epileptic syndromes and among them one of idiopathic focal epilepsi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b8a0c0f94cad4d354114ef4fc25c1fd5
https://pubmed.ncbi.nlm.nih.gov/11988887

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