Zobrazeno 1 - 10
of 21
pro vyhledávání: '"J M, López Terradas"'
Autor:
J M, López-Terradas Covisa
Publikováno v:
Revista de neurologia. 37(3)
The question of when to begin and when to stop therapy with antiepileptic agents is one of the most widely discussed matters among specialists in epilepsy, due to the potential risks of such pharmacological therapy in the long term. In this paper we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8965a9241448070140d15148b475c7a9
https://pubmed.ncbi.nlm.nih.gov/12938062
https://pubmed.ncbi.nlm.nih.gov/12938062
Autor:
J M, López-Terradas
Publikováno v:
Revista de neurologia. 28
Epilepsy and seizures are often misinterpreted as identical phenomenon and treatment of seizures confused with treatment of epilepsy. In this paper the concept of both epilepsy and seizures are revised and also the more new etiopathogenics hypothesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::211ee9c11a580485690097a2783a8bff
https://pubmed.ncbi.nlm.nih.gov/10778479
https://pubmed.ncbi.nlm.nih.gov/10778479
Autor:
J M, López-Terradas
Publikováno v:
Revista de neurologia. 28
The peroxisome is an organelle found in all nucleated cells of mammalian. Its name is due to H2O2 formation as result of cell respiration catalyzed by oxidases and catalases and play and important role on myelination and neuronal migration. Peroxisom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c1532d930e3d6eef6b503e6d3a82267b
https://pubmed.ncbi.nlm.nih.gov/10778485
https://pubmed.ncbi.nlm.nih.gov/10778485
Publikováno v:
Clinical genetics. 57(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::38b74b114059e85a6f499b000bfaa1a8
https://pubmed.ncbi.nlm.nih.gov/10735639
https://pubmed.ncbi.nlm.nih.gov/10735639
Autor:
J M, López-Terradas Covisa
Publikováno v:
Revista de neurologia. 28(1)
In this paper we review and bring up to date non-epileptic paroxystic motor disorders, since knowledge of these is necessary to avoid confusion with epileptic crises.Particular attention has been paid to the etiopathogenesis, classification and treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::be7fb5cc7106e03fac054c742dec92b8
https://pubmed.ncbi.nlm.nih.gov/10101774
https://pubmed.ncbi.nlm.nih.gov/10101774
Autor:
M A, Martínez Granero, F, Argüelles, M C, Roche Herrero, F, Omeñaca, J M, López Terradas, A, Ortigado
Publikováno v:
Anales espanoles de pediatria. 48(1)
The objectives of this study were to determine in our newborn population the frequency of facial asymmetry during crying or congenital hypoplasia of the depressor anguli oris muscle (DAOM) without associated major malformations and to evaluate the co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89eaa5205a74d73ff94b80025dd6b99b
https://pubmed.ncbi.nlm.nih.gov/9859565
https://pubmed.ncbi.nlm.nih.gov/9859565
Autor:
L G, Gutiérrez-Solana, M L, Ruiz-Falcó, J J, García-Peñas, A, Chabás, S, Manzano-Blanco, G, Gómez-Mardones, J M, López-Terradas
Publikováno v:
Revista de neurologia. 24(134)
Sandhoff's disease is a severe form of gangliosidosis GM2 which presents in the first year of life, basically as progressive psychomotor retardation and/or a macular red cherry spot. Our patient presented the clinical picture characteristic of the di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7186734bc135e70e1d7e1b3e6a897c19
https://pubmed.ncbi.nlm.nih.gov/8983726
https://pubmed.ncbi.nlm.nih.gov/8983726
Autor:
Maria J. Ramos, A. Pérez-Jiménez, E. Alvarez, J. M. López-Terradas, Teresa Ferrer, C. Pérez-Conde
Publikováno v:
Neuropediatrics. 27(1)
We report on four children, from different families, who suffer from a congenital autonomic disorder, presumably inherited. Three of them have a sensory neuropathy but do not fit any described hereditary sensory and autonomic neuropathy. All four wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2624b22d27eab42b1f2bb841999e52
https://pubmed.ncbi.nlm.nih.gov/8677021
https://pubmed.ncbi.nlm.nih.gov/8677021
Autor:
C, Campos Tristán, L G, Gutiérrez Solana, F, Martín Casillas, M L, Ruiz-Falcó Rojas, J M, López-Terradas, J, Vázquez-Cano
Publikováno v:
Anales espanoles de pediatria. 39(1)
We report two patients who were less than two years old that were diagnosed as having Angelman syndrome. Cytogenetic confirmation of the disease was performed. We emphasize clinical and electroencephalographic features in infants that allow an early
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::20de90c5221b5bc1939dbb2fb5edbb5e
https://pubmed.ncbi.nlm.nih.gov/8363146
https://pubmed.ncbi.nlm.nih.gov/8363146
Autor:
M L, Ruiz-Falcó Rojas, L G, Gutiérrez-Solana, M A, Arias Alvarez, A, Barrio Nicolás, J M, López-Terradas Covisa
Publikováno v:
Anales espanoles de pediatria. 38(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4d992925d72da3fcfff6515196a11764
https://pubmed.ncbi.nlm.nih.gov/8384806
https://pubmed.ncbi.nlm.nih.gov/8384806