Search Results - "Jiménez Legido, M"

Opsoclonus-myoclonus syndrome: clinical characteristics, therapeutic considerations, and prognostic factors in a Spanish paediatric cohort by Cantarín-Extremera, V, Jiménez-Legido, M, Aguilera-Albesa, S, Hedrera-Fernández, A, Arrabal-Fernández, L, Gorría-Redondo, N, Martí-Carrera, I, Yoldi-Pedtri, M E, Sagaseta-De Ilúrdoz, M, González-Gutiérrez-Solana, L

“…Opsoclonus-myoclonus-ataxia syndrome is a rare neuroinflammatory disorder with onset during childhood; aetiology may be paraneoplastic, para-infectious, or…”
Get full text

Implementation of a pediatric unit of acquired brain injury in subacute phase in the public health system. Epidemiological, clinical and initial evolution characteristics of the patients attended by Jiménez-Legido, M, Cantarín-Extremera, V, Vara-Arias, M T, Rodríguez-Palero, S, Cartas-Carrión, S C, Esteso-Orduña, B, Cámara Barrio, S, Méndez-Caba, J, Ruíz-Falcó Rojas, M L

“…Acquired brain injury (ABI) is defined as a neurological injury, acutely occurred, at some point in life causing impairment or loss of functional capacity. In…”
Get more information

Study of paediatric patients with the clinical and biochemical phenotype of glucose transporter type 1 deficiency syndrome by Jiménez Legido, M, Cortés Ledesma, C, Bernardino Cuesta, B, López Marín, L, Cantarín Extremera, V, Pérez-Cerdá, C, Pérez González, B, López Martín, E, González Gutiérrez-Solana, L

“…Glucose transporter type 1 (GLUT1) deficiency syndrome may present a range of phenotypes, including epilepsy, intellectual disability, and movement disorders…”
Get full text

Opsoclonus-myoclonus syndrome: Clinical characteristics, therapeutic considerations, and prognostic factors in a Spanish paediatric cohort by Cantarín-Extremera, V., Jiménez-Legido, M., Aguilera-Albesa, S., Hedrera-Fernández, A., Arrabal-Fernández, L., Gorría-Redondo, N., Martí-Carrera, I., Yoldi-Pedtri, M.E., Sagaseta-De Ilúrdoz, M., González-Gutiérrez-Solana, L.

“…Opsoclonus-myoclonus-ataxia syndrome is a rare neuroinflammatory disorder with onset during childhood; aetiology may be paraneoplastic, para-infectious, or…”
Get full text

Study of paediatric patients with the clinical and biochemical phenotype of glucose transporter type 1 deficiency syndrome by Jiménez Legido, M., Cortés Ledesma, C., Bernardino Cuesta, B., López Marín, L., Cantarín Extremera, V., Pérez-Cerdá, C., Pérez González, B., López Martín, E., González Gutiérrez-Solana, L.

“…Glucose transporter type 1 (GLUT1) deficiency syndrome may present a range of phenotypes, including epilepsy, intellectual disability, and movement disorders…”
Get full text

Síndrome opsoclono-mioclono: características clínicas, aspectos terapéuticos y factores pronósticos en una cohorte pediátrica española by Cantarín-Extremera, V., Jiménez-Legido, M., Aguilera-Albesa, S., Hedrera-Fernández, A., Arrabal-Fernández, L., Gorría-Redondo, N., Martí-Carrera, I., Yoldi-Pedtri, M.E., Sagaseta-De Ilúrdoz, M., González-Gutiérrez-Solana, L.

“…El síndrome opsoclono-mioclono-ataxia es un raro trastorno de inicio pediátrico; de base neuroinflamatoria y origen paraneoplásico, parainfeccioso o…”
Get full text

Estudio de pacientes pediátricos con fenotipo clínico y bioquímico de síndrome de déficit de transportador de glucosa cerebral (GLUT-1) by Jiménez Legido, M., Cortés Ledesma, C., Bernardino Cuesta, B., López Marín, L., Cantarín Extremera, V., Pérez-Cerdá, C., Pérez González, B., López Martín, E., González Gutiérrez-Solana, L.

“…El síndrome de déficit del transportador de glucosa cerebral (GLUT1DS) puede presentar fenotipos variados, incluyendo epilepsia, déficit intelectual y…”
Get full text

Immunoadsorption and plasmapheresis: possible treatments for Rasmussen's encephalitis? by Cantarín-Extremera, V, Jiménez-Legido, M, Sebastián-Pérez, E, Duat-Rodríguez, A, Ruiz-Falcó Rojas, M L

Get full text

Complicaciones neurológicas en casos de bronquiolitis por virus respiratorio sincitial: estado febril y otras manifestaciones neurológicas by Jiménez Legido, María, Cantarín Extremera, Verónica, Almodóvar Martín, José Luis, Bernardino Cuesta, Beatriz

Get full text

Inmunoadsorción y plasmaféresis: ¿posibilidades de tratamiento en la encefalitis de Rasmussen? by Cantarín Extremera, Verónica, Jiménez Legido, María, Sebastián Pérez, Elena, Duat Rodríguez, Anna, Ruiz-Falcó Rojas, María Luz

Get full text

Dos nuevos casos de síndrome de Leigh por mutación m.13513G>A en el gen MTND5 by Jiménez Legido, María, Bernardino Cuesta, Beatriz, López Marín, Laura, Cantarín Extremera, Verónica, Blázquez Encinar, Alberto, Martín Casanueva, Miguel Ángel, González Gutiérrez-Solana, Luis

Get full text

Encefalitis por anticuerpos contra el receptor de NMDA con afectación hemisférica unilateral by Jiménez Legido, María, Cantarín Extremera, Verónica, Bernardino Cuesta, Beatriz, García Fernández, Marta, López Marín, Laura, Duat Rodríguez, Anna, Ruiz-Falcó Rojas, María Luz, González Gutiérrez-Solana, Luis

Get full text

Infantile epileptic encephalopathies: what matters is genetics by Garcia-Penas, J J, Jimenez-Legido, M

“…Epileptic encephalopathies in infancy are defined as conditions where the sustained epileptic activity itself may contribute to the severe neurological and…”
Get full text

Neurological complications in cases of bronchiolitis due to respiratory syncytial virus: febrile status and other neurological manifestations by Jimenez-Legido, M, Cantarin-Extremera, V, Almodovar-Martin, J L, Bernardino-Cuesta, B

Get full text

West syndrome associated with 14q12 duplication by Jimenez-Legido, M, Garcia-Penas, J J

Get full text

Two new cases of Leigh syndrome caused by mutation m.13513G> A in the MTND5 gene by Jimenez-Legido, M, Bernardino-Cuesta, B, Lopez-Marin, L, Cantarin-Extremera, V, Blazquez-Encinar, A, Martin-Casanueva, M A, Gutierrez-Solana, L G

Get full text

Anti-NMDA receptor encephalitis with unilateral hemispheric affectation by Jimenez-Legido, M, Cantarin-Extremera, V, Bernardino-Cuesta, B, Garcia-Fernandez, M, Lopez-Marin, L, Duat-Rodriguez, A, Ruiz-Falco Rojas, M L, Gutierrez-Solana, L G

Get full text

Neurological complications in cases of bronchiolitis due to respiratory syncytial virus: febrile status and other neurological manifestations by Jimenez-Legido, M, Cantarin-Extremera, V, Almodovar-Martin, J L, Bernardino-Cuesta, B

Get full text

West syndrome associated with 14q12 duplication by Jimenez-Legido, M, Garcia-Penas, J J

Get full text

Anti-NMDA receptor encephalitis with unilateral hemispheric affectation by Jimenez-Legido, M, Cantarin-Extremera, V, Bernardino-Cuesta, B, Garcia-Fernandez, M, Lopez-Marin, L, Duat-Rodriguez, A, Ruiz-Falco Rojas, M L, Gutierrez-Solana, L G

Get full text