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Items: 1 to 20 of 38

1.

[Use of benzodiazepines in prolonged seizures and status epilepticus in the community].

Sánchez-Carpintero R, Camino R, Smeyers P, Raspall-Chaure M, Martínez-Bermejo A, Ruiz-Falcó ML, Verdú A, Sanmarti FX, Blanco O, Santos Borbujo J, Picó G, Cebollero MA.

An Pediatr (Barc). 2014 Dec;81(6):400.e1-6. doi: 10.1016/j.anpedi.2014.03.023. Epub 2014 Nov 4. Spanish.

2.

Recommendations for the radiological diagnosis and follow-up of neuropathological abnormalities associated with tuberous sclerosis complex.

Rovira À, Ruiz-Falcó ML, García-Esparza E, López-Laso E, Macaya A, Málaga I, Vázquez E, Vicente J.

J Neurooncol. 2014 Jun;118(2):205-23. doi: 10.1007/s11060-014-1429-y. Epub 2014 Apr 27.

PMID:
24771286
3.

Encephalopathy with electrical status epilepticus during sleep: cognitive and executive improvement after epilepsy surgery.

Fournier-Del Castillo C, García-Fernández M, Pérez-Jiménez MÁ, Ugalde-Canitrot A, Alvarez-Linera J, Ruiz-Falcó ML, Villarejo-Ortega F.

Seizure. 2014 Mar;23(3):240-3. doi: 10.1016/j.seizure.2013.09.002. Epub 2013 Sep 8. No abstract available.

4.

[Role of iron in the treatment of attention deficit-hyperactivity disorder].

Soto-Insuga V, Calleja ML, Prados M, Castaño C, Losada R, Ruiz-Falcó ML.

An Pediatr (Barc). 2013 Oct;79(4):230-5. doi: 10.1016/j.anpedi.2013.02.008. Epub 2013 Apr 11. Spanish.

5.

PLP1 gene analysis in 88 patients with leukodystrophy.

Martínez-Montero P, Muñoz-Calero M, Vallespín E, Campistol J, Martorell L, Ruiz-Falcó MJ, Santana A, Pons R, Dinopoulos A, Sierra C, Nevado J, Molano J.

Clin Genet. 2013 Dec;84(6):566-71. doi: 10.1111/cge.12103. Epub 2013 Mar 11.

PMID:
23347225
6.

Seizure and developmental outcomes after hemispherectomy in children and adolescents with intractable epilepsy.

Villarejo-Ortega F, García-Fernández M, Fournier-Del Castillo C, Fabregate-Fuente M, Álvarez-Linera J, De Prada-Vicente I, Budke M, Ruiz-Falcó ML, Pérez-Jiménez MÁ.

Childs Nerv Syst. 2013 Mar;29(3):475-88. doi: 10.1007/s00381-012-1949-8. Epub 2012 Nov 1.

PMID:
23114926
7.

GM2 gangliosidoses in Spain: analysis of the HEXA and HEXB genes in 34 Tay-Sachs and 14 Sandhoff patients.

Gort L, de Olano N, Macías-Vidal J, Coll MA; Spanish GM2 Working Group..

Gene. 2012 Sep 10;506(1):25-30. Epub 2012 Jul 10.

PMID:
22789865
8.

[Characteristics and evolution of patients with Alice in Wonderland syndrome].

Losada-Del Pozo R, Cantarín-Extremera V, García-Peñas JJ, Duat-Rodríguez A, López-Marín L, Gutiérrez-Solana LG, Ruiz-Falcó ML.

Rev Neurol. 2011 Dec 1;53(11):641-8. Spanish.

9.

[Paroxysmal tonic upward gaze deviation triggered by valproic acid within the context of focal epilepsy].

Cantarin-Extremera V, Gutierrez-Solana LG, Duat-Rodriguez A, Lopez-Marin L, Ruiz-Falco ML, Leon-Gonzalez M, Perez-Villena A.

Rev Neurol. 2011 Sep 1;53(5):318-9. Spanish. No abstract available.

10.

[Panayiotopoulos syndrome: academic difficulties and behavioural disorders].

Pérez-Villena A, López-Marín L, Cantarín-Extremera V, Leon-Gonzalez M, Fournier-Del Castillo C, Ruiz-Falcó ML.

Rev Neurol. 2011 Jun 16;52(12):705-12. Spanish.

11.

[Clinical, electroencephalographic and genomic characteristics of patients with epilepsy with febrile seizures plus].

Cantarín-Extremera V, García-Peñas JJ, Gutiérrez-Solana LG, García-Fernández M, Ruiz-Falcó ML, Duat-Rodríguez A, López-Marín L.

Rev Neurol. 2011 Apr 1;52(7):404-11. Spanish.

12.

Clinical, polysomnographic and laboratory characteristics of narcolepsy-cataplexy in a sample of children and adolescents.

Peraita-Adrados R, García-Peñas JJ, Ruiz-Falcó L, Gutiérrez-Solana L, López-Esteban P, Vicario JL, Miano S, Aparicio-Meix M, Martinez-Sopena MJ.

Sleep Med. 2011 Jan;12(1):24-7. doi: 10.1016/j.sleep.2010.02.017. Epub 2010 Nov 2.

PMID:
21050810
13.

Phenytoin-induced visual disturbances mimicking Delirium Tremens in a child.

Marín LL, García-Peñas JJ, Herguedas JL, Gutiérrez-Solana LG, Ruiz-Falcó M, Rodriguez AD, Extremera VC.

Eur J Paediatr Neurol. 2010 Sep;14(5):460-3. doi: 10.1016/j.ejpn.2010.05.008. Epub 2010 Jun 17.

PMID:
20728059
14.

[Contiguous gene deletion syndrome in Xp21].

Duat-Rodríguez A, Gutiérrez-Solana LG, García-Peñas JJ, Ruiz-Falcó ML.

Rev Neurol. 2010 Feb 1-15;50(3):192. Spanish. No abstract available.

15.

An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study.

Steenweg ME, Jakobs C, Errami A, van Dooren SJ, Adeva Bartolomé MT, Aerssens P, Augoustides-Savvapoulou P, Baric I, Baumann M, Bonafé L, Chabrol B, Clarke JT, Clayton P, Coker M, Cooper S, Falik-Zaccai T, Gorman M, Hahn A, Hasanoglu A, King MD, de Klerk HB, Korman SH, Lee C, Meldgaard Lund A, Mejaski-Bosnjak V, Pascual-Castroviejo I, Raadhyaksha A, Rootwelt T, Roubertie A, Ruiz-Falco ML, Scalais E, Schimmel U, Seijo-Martinez M, Suri M, Sykut-Cegielska J, Trefz FK, Uziel G, Valayannopoulos V, Vianey-Saban C, Vlaho S, Vodopiutz J, Wajner M, Walter J, Walter-Derbort C, Yapici Z, Zafeiriou DI, Spreeuwenberg MD, Celli J, den Dunnen JT, van der Knaap MS, Salomons GS.

Hum Mutat. 2010 Apr;31(4):380-90. doi: 10.1002/humu.21197. Review.

PMID:
20052767
16.

L-2-Hydroxyglutaric aciduria: pattern of MR imaging abnormalities in 56 patients.

Steenweg ME, Salomons GS, Yapici Z, Uziel G, Scalais E, Zafeiriou DI, Ruiz-Falco ML, Mejaski-Bosnjak V, Augoustides-Savvopoulou P, Wajner M, Walter J, Verhoeven-Duif NM, Struys EA, Jakobs C, van der Knaap MS.

Radiology. 2009 Jun;251(3):856-65. doi: 10.1148/radiol.2513080647.

PMID:
19474378
17.

[Para-infectious seizures in children: a retrospective study of 34 cases].

Lara-Herguedas J, García-Peñas JJ, Ruiz-Falcó ML, Gutiérrez-Solana LG, Duat-Rodríguez A, Arrabal-Fernández ML, López-Marín L.

Rev Neurol. 2008 Mar 16-31;46(6):321-5. Spanish.

18.

X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy.

Fernandez-Moreira D, Ugalde C, Smeets R, Rodenburg RJ, Lopez-Laso E, Ruiz-Falco ML, Briones P, Martin MA, Smeitink JA, Arenas J.

Ann Neurol. 2007 Jan;61(1):73-83.

PMID:
17262856
19.

[Hemiconvulsion-hemiplegia syndrome: two case reports with findings from magnetic resonance imaging of the brain in diffusion-weighted sequences].

Arrese-Gispert L, Gutiérrez-Solana LG, García-Peñas JJ, Ruiz-Falcó ML.

Rev Neurol. 2005 Sep 16-30;41(6):344-8. Spanish.

20.

[Benign intracranial hypertension and heterozygosity for factor V Leiden mutation].

Pérez Martínez A, Cerezo Bueno MJ, García Peñas JJ, Gutiérrez-Solana L, Ruiz-Falcó ML.

An Pediatr (Barc). 2005 Aug;63(2):172-4. Spanish. Erratum in: An Pediatr (Barc). 2005 Sep;63(3):291.

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