Search for 'Provider:Neurology,'

Eculizumab-related progressive multifocal leukoencephalopathy.

By Gómez Cibeira, Emilio | Ivánovic Barbeito, Yerko-Pétar | Gutiérrez Martínez, Eduardo | Morales Ruiz, Enrique | Abradelo de Usera, Manuel | Hilario Barrio, Amaya | Ramos González, Ana | Ruiz Morales, Juan Manuel | Villarejo Galende, Alberto . Neurology, 2016 . 86(4):399-400. , Formato Vancouver: Gómez Cibeira E, Ivanovic Barbeito Y, Gutiérrez Martínez E, Morales E, Abradelo M, Hilario A et al. Eculizumab-related progressive multifocal leukoencephalopathy. Neurology. 2016 Jan 26;86(4):399-400.

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Clinical Reasoning: Left hemiparesis, ataxia, and optic neuritis in a child previously treated for pineoblastoma.

By Vila Bedmar, Sara. Neurology, 2016 . 86(15):e161-5. , Formato Vancouver: Vila Bedmar S, Nourbakhsh B, Anzalone S, Waubant E. Clinical Reasoning: Left hemiparesis, ataxia, and optic neuritis in a child previously treated for pineoblastoma. Neurology. 2016 Apr 12;86(15):e161-e165.

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Classification systems of communication for use in epidemiological surveillance of children with cerebral palsy.

By Cruz Bértolo, Javier de la. Developmental medicine and child neurology, 2016 . 58(3):285-91. , Formato Vancouver: Virella D, Pennington L, Andersen GL, Andrada Mda G, Greitane A, Himmelmann K et al; Surveillance of Cerebral Palsy in Europe Network. Classification systems of communication for use in epidemiological surveillance of children with cerebral palsy. Dev Med Child Neurol. 2016 Mar;58(3):285-91.

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Babinski's Lost Legacy: A Remarkable Case of a Not-So-New Clinical Construct.

By Benito León, Julián. Journal of clinical neurology (Seoul, Korea); 2016 . 12(3):368-70. , Formato Vancouver: León Ruiz M, García Soldevilla MÁ, Benito León J, Vidal Díaz MB, Tejeiro Martínez J, García-Albea Ristol E. Babinski's Lost Legacy: A Remarkable Case of a Not-So-New Clinical Construct. J Clin Neurol. 2016 Jul;12(3):368-70.

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Sudden asymmetric bilateral ptosis as stroke onset.

By López Blanco, Roberto | Ivánovic Barbeito, Yerko-Pétar | Villarejo Galende, Alberto | Sánchez Sánchez, Carmen | Díaz Guzmán, Jaime. Practical neurology, 2015 . 15(3):224-5. , Formato Vancouver: López Blanco R, Ivánovic Barbeito Y, Villarejo Galende A, Sánchez Sánchez C, Díaz Guzmán J. Sudden asymmetric bilateral ptosis as stroke onset. Pract Neurol. 2015 Jun;15(3):224-5.

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Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy.

By Martín, Miguel Ángel | Blázquez Encinar, Alberto | Delmiro Magdalena, Aitor | Hernández Laín, Aurelio. Neurology, 2015 . 84(22):2286-8. , Formato Vancouver: Cámara Y, Carreño Gago L, Martín MA, Melià MJ, Blázquez A, Delmiro A et al. Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy. Neurology. 2015 Jun 2;84(22):2286-8.

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PET-Florbetapir findings in primary cerebral amyloidoma.

By Villarejo Galende, Alberto | Sarandeses Fernández, Pilar | Hernández Laín, Aurelio | Ramos González, Ana | Carro Díaz, Eva | Ricoy Campo, José Ramón | Hernández Gallego, Jesús. Journal of neurology, 2015 . 262(4):1052-4. , Formato Vancouver: Villarejo Galende A, Sarandeses P, Penas Prado M, Hernández Laín A, Ramos A, Hernández Martínez AC et al. PET-Florbetapir findings in primary cerebral amyloidoma. J Neurol. 2015;262(4):1052-4.

Place Hold on PET-Florbetapir findings in primary cerebral amyloidoma.

LAMA2-related congenital muscular dystrophy complicated by West syndrome.

By Camacho Salas, Ana | Núñez Enamorado, Noemí | Martínez de Aragón Calvo, Ana | Simón de las Heras, Rogelio. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2015 . 19(2):243-7. , Formato Vancouver: Camacho A, Núñez N, Dekomien G, Hernández Laín A, de Aragón AM, Simón R. LAMA2-related congenital muscular dystrophy complicated by West syndrome. Eur J Paediatr Neurol. 2015 Mar;19(2):243-7.

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Expression of regulatory proteins in choroid plexus changes in early stages of Alzheimer disease.

By Krzyzanowska, Agnieszka | García-Consuegra Galiana, Inés | Pascual, Consuelo | Antequera, Desiree | Carro Díaz, Eva. Journal of neuropathology and experimental neurology, 2015 . 74(4):359-69. , Formato Vancouver: Krzyzanowska A, García Consuegra I, Pascual C, Antequera D, Ferrer I, Carro E. Expression of regulatory proteins in choroid plexus changes in early stages of Alzheimer disease. J Neuropathol Exp Neurol. 2015 Apr;74(4):359-69.

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Association between Incident Cancer and Subsequent Stroke.

By González de la Aleja Tejera, Jesús | Martínez Salio, Antonio | Benito León, Julián. Annals of neurology, 2015 . 78(4):660. , Formato Vancouver: De la Aleja JG, Martínez Salio A, Benito León J. Association between Incident Cancer and Subsequent Stroke. Ann Neurol. 2015 Oct;78(4):660.

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NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

By Benito León, Julián | Calleja Castaño, Patricia | Díaz Sánchez, María. BMC neurology, 2014 . 14:87. , Formato Vancouver: Agúndez JA, García-Martín E, Martínez C, Benito-León J, Millán-Pascual J, Calleja P et al. NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis. BMC Neurol. 2014 Apr 23;14:87.

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Neurocutaneous melanosis: an illustrative patient.

By Guerra García, Pilar | Martínez de Aragón Calvo, Ana | Camacho Salas, Ana. Pediatric neurology, 2014 . 51(3):468-9. , Formato Vancouver: Guerra-García P, Martínez-de-Aragón A, Camacho A. Neurocutaneous melanosis: an illustrative patient. Pediatr Neurol. 2014 Sep;51(3):468-9.

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Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion.

By Arenas Barbero, Joaquín | Martín, Miguel A. | Martinez Azorin, Francisco | Delmiro Magdalena, Aitor. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2014 . 18(6):796-800. , Formato Vancouver: Castro-Gago M, Dacruz-Alvárez D, Pintos-Martínez E, Beiras-Iglesias A, Delmiro A, Arenas J et al. Exome sequencing identifies a CHKB mutation in Spanish patient with megaconial congenital muscular dystrophy and mtDNA depletion. Eur J Paediatr Neurol. 2014 Nov;18(6):796-800.

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Clinical features and molecular characterization of a patient with muscle-eye-brain disease: a novel mutation in the POMGNT1 gene.

By Simón de las Heras, Rogelio | Camacho Salas, Ana | Hernández Laín, Aurelio. Journal of child neurology, 2014 . 29(2):289-94. , Formato Vancouver: Raducu M, Cotarelo RP, Simón R, Camacho A, Rubio-Fernández M, Hernández-Laín A et al. Clinical features and molecular characterization of a patient with muscle-eye-brain disease: a novel mutation in the POMGNT1 gene. J Child Neurol. 2014 Feb;29(2):289-94.

Place Hold on Clinical features and molecular characterization of a patient with muscle-eye-brain disease: a novel mutation in the POMGNT1 gene.

Cause of death in mild cognitive impairment: a prospective study (NEDICES).

By Contador, Israel | Bermejo Pareja, Félix | Trincado Soriano, Rocío | Villarejo Galende, Alberto | Sánchez Ferro, Álvaro | Benito León, Julián. European journal of neurology, 2014 . 21(2):253-e9. , Formato Vancouver: Contador I, Bermejo-Pareja F, Mitchell AJ, Trincado R, Villarejo A, Sánchez-Ferro Á et al. Cause of death in mild cognitive impairment: a prospective study (NEDICES). Eur J Neurol. 2014 Feb;21(2):253-e9.

Place Hold on Cause of death in mild cognitive impairment: a prospective study (NEDICES).

Subcutaneous Route for Refractory Epilepsy.

By González Granados, Luis Ignacio | Camacho Salas, Ana | Simón de las Heras, Rogelio. Pediatric neurology, 2013 . 48(1):79. , Formato Vancouver: González-Granado LI, Simón R, Camacho-Salas A. Subcutaneous route for refractory epilepsy. Pediatr Neurol. 2013 Jan;48(1):79.

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Paraplegia after epidural anaesthesia.

By Benito León, Julián | Gonzalo Martínez, Juan Francisco | Labiano Fontcuberta, Andrés. Practical neurology, 2013 . 13(3):188-91. , Formato Vancouver: Labiano-Fontcuberta A, Benito-León J, Gonzalo-Martínez JF. Paraplegia after epidural anaesthesia. Pract Neurol. 2013 Jun;13(3):188-91.

Place Hold on Paraplegia after epidural anaesthesia.

Adverse events during the titration phase of interferon-beta in remitting-relapsing multiple sclerosis are not predicted by body mass index nor by pharmacodynamic biomarkers.

By Guijarro Castro, Cristina. BMC neurology, 2013 . 13:82. , Formato Vancouver: Muñoz D, Escartín A, Dapena D, Coret F, Fernández-Uría D, Pérez D et al. Adverse events during the titration phase of interferon-beta in remitting-relapsing multiple sclerosis are not predicted by body mass index nor by pharmacodynamic biomarkers. BMC Neurol. 2013 Jul 11;13:82.

Place Hold on Adverse events during the titration phase of interferon-beta in remitting-relapsing multiple sclerosis are not predicted by body mass index nor by pharmacodynamic biomarkers.

Late Infantile Neuronal Ceroid Lipofuscinosis: Mutations in the CLN2 Gene and Clinical Course in Spanish Patients.

By Martín Hernández, Elena. Journal of Child Neurology, 2013 . 28(4):470-8. , Formato Vancouver: Pérez-Poyato MS, Marfa MP, Abizanda IF, Rodríguez-Revenga L, Sánchez VC, González MJ et al. Late infantile neuronal ceroid lipofuscinosis: mutations in the CLN2 gene and clinical course in Spanish patients. J Child Neurol. 2013 Apr;28(4):470-8.

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Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.

By Núñez Enamorado, Noemí | Simón de las Heras, Rogelio. Lancet Neurology, 2013 . 12(12):1159-69. , Formato Vancouver: Rice GI, Forte GM, Szynkiewicz M, Chase DS, Aeby A, Abdel-Hamid MS et al. Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study. Lancet Neurol. 2013 Dec;12(12):1159-69.

Place Hold on Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.

The management of orthostatic hypotension in Parkinson's disease.

By Benito León, Julián | Sánchez Ferro, Álvaro. Frontiers in neurology, 2013 . 4:64. , Formato Vancouver: Sánchez-Ferro A, Benito-León J, Gómez-Esteban JC. The management of orthostatic hypotension in Parkinson's disease. Front Neurol. 2013 Jun 10;4:64.

Place Hold on The management of orthostatic hypotension in Parkinson's disease.

LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis.

By Benito León, Julián | Calleja Castaño, Patricia | Díaz Sánchez, María. BMC Neurology, 2013 . 13:34. , Formato Vancouver: García-Martín E, Lorenzo-Betancor O, Martínez C, Pastor P, Benito-León J, Millán-Pascual J et al. LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis. BMC Neurol. 2013 Apr 10;13:34.

Place Hold on LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis.

Resistance (Weight Lifting) Training in an Adolescent With McArdle Disease.

By Martín Casanueva, Miguel Ángel . Journal of Child Neurology, 2013 . 28(6):805-8. , Formato Vancouver: García-Benítez S, Fleck SJ, Naclerio F, Martín MA, Lucia A. Resistance (weight lifting) training in an adolescent with McArdle disease. J Child Neurol. 2013 Jun;28(6):805-8.

Place Hold on Resistance (Weight Lifting) Training in an Adolescent With McArdle Disease.

Cause of death in mild cognitive impairment: a prospective study (NEDICES).

By Benito León, Julián | Bermejo Pareja, Félix | Contador, Israel | Sánchez Ferro, Álvaro | Trincado Soriano, Rocío | Villarejo Galende, Alberto . European Journal of Neurology, 2014 . 21(2):253-e9. , Formato Vancouver: Contador I, Bermejo-Pareja F, Mitchell AJ, Trincado R, Villarejo A, Sánchez-Ferro Á et al. Cause of death in mild cognitive impairment: a prospective study (NEDICES). Eur J Neurol. 2014 Feb;21(2):253-e9.

Place Hold on Cause of death in mild cognitive impairment: a prospective study (NEDICES).

Rate of cognitive decline during the premotor phase of essential tremor: A prospective study.

By Benito León, Julián | Bermejo Pareja, Félix | Sánchez Ferro, Álvaro. Neurology, 2013 . 81(1):60-6. , Formato Vancouver: Benito-León J, Louis ED, Sánchez-Ferro Á, Bermejo-Pareja F. Rate of cognitive decline during the premotor phase of essential tremor: a prospective study. Neurology. 2013 Jul 2;81(1):60-6.

Place Hold on Rate of cognitive decline during the premotor phase of essential tremor: A prospective study.

Obesity and impaired cognitive functioning in the elderly: a population-based cross-sectional study (NEDICES).

By Benito León, Julián | Bermejo Pareja, Félix | Hernández Gallego, Jesús. European Journal of Neurology, 2013 . 20(6):899-906, e76-7. , Formato Vancouver: Benito-León J, Mitchell AJ, Hernández-Gallego J, Bermejo-Pareja F. Obesity and impaired cognitive functioning in the elderly: a population-based cross-sectional study (NEDICES). Eur J Neurol. 2013 Jun;20(6):899-906, e76-7.

Place Hold on Obesity and impaired cognitive functioning in the elderly: a population-based cross-sectional study (NEDICES).

Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry.

By Arenas Barbero, Joaquín | Cabello, A. | García-Consuegra Galiana, Inés | Martín Casanueva, Miguel Ángel . Journal of Neurology, Neurosurgery & Psychiatry, 2012 . 83(3):322-8. , Formato Vancouver: Lucía A, Ruiz JR, Santalla A, Nogales-Gadea G, Rubio JC, García-Consuegra I et al. Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry. J Neurol Neurosurg Psychiatry. 2012 Mar;83(3):322-8.

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Interrater reliability study of cerebral palsy diagnosis, neurological subtype, and gross motor function.

By Cruz Bértolo, Javier de la. Developmental medicine and child neurology, 2012 . 54(9):815-21. , Formato Vancouver: Sellier E, Horber V, Krägeloh-Mann I, De La Cruz J, Cans C. SCPE COLLABORATION. Interrater reliability study of cerebral palsy diagnosis, neurological subtype, and gross motor function. Dev Med Child Neurol. 2012 Sep;54(9):815-21.

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A short Scale for Evaluation of Neuropsychiatric Disorders in Parkinson’s Disease: first psychometric approach.

By Agüera Ortiz, Luis Fernando. Journal of Neurology, 2012 . 259(11):2299-308. , Formato Vancouver: Martínez-Martín P, Frades-Payo B, Agüera-Ortiz L, Ayuga-Martínez A. A short scale for evaluation of neuropsychiatric disorders in Parkinson's disease: first psychometric approach. J Neurol. 2012 Nov;259(11):2299-308.

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Levetiracetam-Induced Reversible Autistic Regression.

By Camacho Salas, Ana | Espín Jaime, José Carlos | Núñez Enamorado, Noemí | Simón de las Heras, Rogelio. Pediatric Neurology, 2012 . 47(1):65-7. , Formato Vancouver: Camacho A, Espín JC, Nuñez N, Simón R. Levetiracetam-induced reversible autistic regression. Pediatr Neurol. 2012 Jul;47(1):65-7.

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Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia.

By Esteban Pérez, Jesús | Gonzalo Martínez, Juan Francisco. Journal of Neurology, 2012 . 259(2):246-50. , Formato Vancouver: Sánchez-Ferrero E, Coto E, Corao AI, Díaz M, Gámez J, Esteban J, et al. Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia. J Neurol. 2012 Feb;259(2):246-50.

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Genotype and phenotype study of 34 Spanish patients diagnosed with oculopharyngeal muscular dystrophy.

By Gutiérrez Rivas, Eduardo. Journal of Neurology, 2012 . 259(8):1546-52. , Formato Vancouver: Tondo M, Gámez J, Gutiérrez-Rivas E, Médel-Jiménez R, Martorell L. Genotype and phenotype study of 34 Spanish patients diagnosed with oculopharyngeal muscular dystrophy. J Neurol. 2012 Aug;259(8):1546-52.

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Clinical and imaging features of the room tilt illusion.

By Herrero San Martín, Alejandro | Herreros Rodríguez, Jaime | Romero Muñoz, Juan Pablo | Sierra Hidalgo, Fernando. Journal of Neurology, 2012 . 259(12):2555-64. , Formato Vancouver: Sierra-Hidalgo F, de Pablo-Fernández E, Herrero-San Martín A, Correas-Callero E, Herreros-Rodríguez J, Romero-Muñoz JP, et al. Clinical and imaging features of the room tilt illusion. J Neurol. 2012 Dec;259(12):2555-64.

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Acute neurological deterioration as a result of two synchronous hemorrhagic spinal ependymomas

By Castaño León, Ana María | Hernández Laín, Aurelio | Lagares Gómez-Abascal, Alfonso | Martinez Perez, Rafael | Martín Munárriz, Pablo | Paredes Sansinenea, Ígor. Surgical Neurology International, 2012 . 3:33. , Formato Vancouver: Martínez-Pérez R, Hernández-Laín A, Paredes I, Munárriz PM, Castaño-León AM,Lagares A. Acute neurological deterioration as a result of two synchronous hemorrhagic spinal ependymomas. Surg Neurol Int. 2012;3:33.

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Gastrostomy tube feeding of children with cerebral palsy: variation across six European countries

By Cruz Bértolo, Javier de la. Developmental Medicine and Child Neurology, 2012 . 54(10):938-944. , Formato Vancouver: Dahlseng MO, Andersen GL, DA Graca Andrada M, Arnaud C, Balu R, De la Cruz J, et al. Gastrostomy tube feeding of children with cerebral palsy: variation across six European countries. Dev Med Child Neurol. 2012;54(10):938-44.

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Intraparenchymal schwannomas: report of two new cases studied with MRI and review of the literature.

By Jiménez Roldán, Luis | Díez Lobato, Ramiro | Paredes Sansinenea, Ígor | Ramos González, Ana | Ricoy Campo, José Ramón. Clinical neurology and neurosurgery, 2012 . 114(1):42-6. , Formato Vancouver: Paredes I, Jiménez Roldán L, Ramos A, Lobato RD, Ricoy JR. Intraparenchymal schwannomas: report of two new cases studied with MRI and review of the literature. Clin Neurol Neurosurg. 2012 Jan;114(1):42-6.

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Primary adenosine monophosphate (AMP) deaminase deficiency in a hypotonic infant

By García-Consuegra Galiana, Inés | Martín Casanueva, Miguel Ángel . Journal of Child Neurology, 2011 . 26(6):734-737. , Formato Vancouver: Castro-Gago M, Gómez-Lado C, Pérez-Gay L, Eirís-Puñal J, Martínez EP, García-Consuegra I, et al. Primary adenosine monophosphate (AMP) deaminase deficiency in a hypotonic infant. J Child Neurol. 2011;26(6):734-7.

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Uveitis and pediatric sarcoidosis: does IgG really matter?

By González Granados, Luis Ignacio. Archives of Neurology, 2011 . 68(1):136. , Formato Vancouver: González-Granado LI. Uveitis and pediatric sarcoidosis: does IgG really matter? Arch Neurol. 2011;68(1):136.

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Frailty in elderly persons with essential tremor: a population-based study (NEDICES)

By Benito León, Julián | Bermejo Pareja, Félix. European Journal of Neurology, 2011 . 18(10):1251-1257. , Formato Vancouver: Louis ED, Benito-León J, Vega S, Bermejo-Pareja F; Neurological Disorders in Central Spain (NEDICES) Study Group. Frailty in elderly persons with essential tremor: a population-based study (NEDICES). Eur J Neurol. 2011 Oct;18(10):1251-7.

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Prevalence of tics in schoolchildren in central Spain: A population-based study

By Benito León, Julián. Pediatric Neurology, 2011 . 45(2):100-108. , Formato Vancouver: Cubo E, Gabriel y Galán JM, Villaverde VA, Velasco SS, Benito VD, Macarrón JV, et al. Prevalence of tics in schoolchildren in central Spain: a population-based study. Pediatr Neurol. 2011; 45(2):100-8.

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Essential tremor--a neurodegenerative disorder associated with cognitive defects?

By Bermejo Pareja, Félix. Nature Reviews. Neurology, 2011 . 7(5):273-282. , Formato Vancouver: Bermejo-Pareja F. Essential tremor--a neurodegenerative disorder associated with cognitive defects? Nat Rev Neurol. 2011 May;7(5):273-82.

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Management of essential tremor, including medical and surgical approaches

By Benito León, Julián. Handbook of Clinical Neurology, 2011 . 100:449-456. , Formato Vancouver: Benito-León J, Louis ED. Management of essential tremor, including medical and surgical approaches. Handb Clin Neurol. 2011;100:449-56.

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Normal pressure subdural hygroma with mass effect as a complication of decompressive craniectomy

By Cicuéndez Lopez-Ocaña, Marta | Delgado, Manuel A. | Lagares Gómez-Abascal, Alfonso | Martinez Perez, Rafael | Martín Munárriz, Pablo | Paredes Sansinenea, Ígor. Surgical Neurology International, 2011 . 2:88. , Formato Vancouver: Paredes I, Cicuendez M, Delgado MA, Martinez-Pérez R, Munarriz PM, Lagares A. Normal pressure subdural hygroma with mass effect as a complication of decompressive craniectomy. Surg Neurol Int. 2011;2:88.

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Impaired health-related quality of life predicts progression of disability in multiple sclerosis

By Benito León, Julián. European Journal of Neurology, 2013 . 20(1):79-86. , Formato Vancouver: Benito León J, Mitchell AJ, Rivera Navarro J, Morales González JM. Impaired health-related quality of life predicts progression of disability in multiple sclerosis. Eur J Neurol. 2013;20(1):79-86.

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Clinical heterogeneity and underlying pathophysiological mechanisms of lateral flexion of the trunk in Parkinson’s disease.

By Pablo Fernández, Eduardo de | Villarejo Galende, Alberto . Journal of Neurology, 2012 . 259(4):771-2. , Formato Vancouver: de Pablo-Fernández E, Villarejo-Galende A. Clinical heterogeneity and underlying pathophysiological mechanisms of lateral flexion of the trunk in Parkinson's disease. J Neurol. 2012 Apr;259(4):771-2.

Place Hold on Clinical heterogeneity and underlying pathophysiological mechanisms of lateral flexion of the trunk in Parkinson’s disease.