Zobrazeno 1 - 10 of 187 pro vyhledávání: '"C Garaizar"'
1
Benign Paroxysmal Tonic Upgaze of Childhood With Ataxia, A Neuroophthalmological Syndrome of Familial Origin?
Autor: J M Prats, Jaume Campistol, C Garaizar
Publikováno v: DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
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r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
A new neuro-ophthalmological syndrome has been described recently, consisting of paroxysmal tonic upward deviation of the eyes with ataxia. Episodes occur daily and are always relieved by sleep. Onset is usually under one year of age and the symptoms
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af319169c55f07a3c2e2e23b8fc8dbd5
https://doi.org/10.1111/j.1469-8749.1993.tb11666.x
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2
INFANTILE SPASMS TREATED WITH HIGH DOSES OF SODIUM VALPROATE: INITIAL RESPONSE AND FOLLOW-UP
Autor: M. L. Garcia-Nieto, J. M. Prats, P. Madoz, M. J. Rua, C. Garaizar
Publikováno v: Developmental Medicine & Child Neurology. 33:617-625
SUMMARY A long-term follow-up study of 42 patients with West syndrome treated with high doses of sodium valproate is presented. Control of the hypsarrhythmic EEG pattern was achieved after two weeks for over three-quarters of the patients with sodium
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7103e3ddec51cdeacba751c17582b77
https://doi.org/10.1111/j.1469-8749.1991.tb14932.x
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3
Operculum Syndrome in Childhood: a Rare Cause of Persistent Speech Disturbance
Autor: M. J. Urroz, J. M. Uterga, C. Garaizar, J. M. Prats
Publikováno v: Developmental Medicine & Child Neurology. 34:359-364
An infant is described who developed operculum syndrome during an acute encephalitic illness. Presenting symptoms were cortical pseudobulbar palsy and focal seizures of facial origin. Persistent mutism--with normal language comprehension and orofacia
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::67f506d2b8e72dd30d4c8371dfffff0f
https://doi.org/10.1111/j.1469-8749.1992.tb11440.x
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4
Fármacos antiepilépticos utilizados en la infancia. Nuevos productos y nuevos conceptos
Autor: A. Villaverde Bello, C. Garaizar Axpe, M. Â Herrera Isasi, T. Pérez Concha, A. Álvarez Ruiz de Larrinaga
Publikováno v: Anales de Pediatría, Vol 58, Iss 2, Pp 136-145 (2003)
Introducción: Desde 1990 se han comercializado en nuestro país ocho nuevos fármacos antiepilépticos (FAE), y otros más lo seránen un futuro próximo Objetivo: Revisar los conceptos que guían el desarrollo de los nuevos fármacos, indicaciones,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0226a4e53618fde91c83d1781ff4e17
http://www.sciencedirect.com/science/article/pii/S1695403303780175
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5
Síndromes miasténicos congénitos. Valoración clínica y electromiográfica
Autor: M.A. Martin Santidrian, J.M.a Prats Viñas, C. Garaizar Axpe, C. Ruiz Espinosa
Publikováno v: Anales de Pediatría, Vol 56, Iss 1, Pp 10-16 (2002)
Antecedentes: Los síndromes miasténicos congénitos son los defectos de la transmisión neuromuscular más frecuentes en la infancia. Causan hipotonía, debilidad e insuficiencia respiratoria que puede conllevar graves consecuencias. Su filiación
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd3053e54bd4a2450c1b74d207d219d5
https://doi.org/10.1016/s1695-4033(02)77758-8
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6
[Factors related to the short term remission of tics in children with Tourette syndrome]
Autor: A, García-Ribes, I, Martí-Carrera, M J, Martínez-González, C, Garaizar, J M, Prats-Viñas
Publikováno v: Revista de neurologia. 37(10)
Tourette syndrome shows a fluctuating evolution, often masked by its comorbidity.To study the clinical factors predicting the initial remission of tics in children with Tourette syndrome. Patients and methods. All patients attended during the last 5
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a97ab6b050e95769273259f9d3765045
https://pubmed.ncbi.nlm.nih.gov/14634915
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8
[Mitochondrial leukoencephalopathy of infancy: is it an early expression of Leigh syndrome?]
Autor: I, Rouco Axpe, C, Garaizar Axpe, M, Labairu Echevarría, P, Sanjurjo Crespo, L, Aldamiz Echevarría, J M, Prats Viñas
Publikováno v: Neurologia (Barcelona, Spain). 18(5)
Leigh syndrome is probably the most frequent metabolic disorder in infancy and childhood. The classic form of the disease is characterized by bilateral lesions of basal ganglia and brainstem. The extensive involvement of white matter, without radiolo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::68e05691f90d1961e6822726b24e3516
https://pubmed.ncbi.nlm.nih.gov/12768509
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10
[Disturbances of neuroblast migration and amniocentesis. An under diagnosed problem?]
Autor: J M, Prats Viñas, C, Garaizar, M J, Martínez González, A, García Ribes
Publikováno v: Revista de neurologia. 36(1)
Performing amniocentesis between the fourth and sixth months of gestation is a widespread practice. However, it can entail serious consequences, apart from the loss of the foetus, such as injuries to the developing central nervous system.Over the pas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5cacd485f6f658dba1ba8d881eadbee7
https://pubmed.ncbi.nlm.nih.gov/12577210
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