Raspall M - Search Results

1

EPITRANS. Quality assessment of the epilepsy transition process.

Ortiz de Zarate Z, Fonseca E, Abraira L, Santamarina E, Campos-Fernández D, Quintana M, Sánchez J, Goméz-Andrés D, Sala J, Raspall M, Felipe-Rucián A, Del Toro M, Macaya A, Toledo M. Ortiz de Zarate Z, et al. Among authors: raspall m. Eur J Paediatr Neurol. 2024 Jan;48:121-128. doi: 10.1016/j.ejpn.2024.01.004. Epub 2024 Jan 12. Eur J Paediatr Neurol. 2024. PMID: 38241904

2

Levetiracetam as first-line monotherapy for Idiopathic Generalized Epilepsy in women.

Ballvé A, Salas-Puig J, Quintana M, Campos D, Llauradó A, Raspall M, Fonseca E, Abraira L, Santamarina E, Toledo M. Ballvé A, et al. Among authors: raspall m. Acta Neurol Scand. 2021 Apr;143(4):407-412. doi: 10.1111/ane.13389. Epub 2021 Jan 15. Acta Neurol Scand. 2021. PMID: 33452703

3

Neonatal rigid-akinetic syndrome and dentato-olivary dysplasia.

Raspall M, Ortega-Aznar A, del Toro M, Roig M, Macaya A. Raspall M, et al. Pediatr Neurol. 2006 Feb;34(2):132-4. doi: 10.1016/j.pediatrneurol.2005.08.003. Pediatr Neurol. 2006. PMID: 16458826

4

Rufinamide in children and adults in routine clinical practice.

Jaraba S, Santamarina E, Miró J, Toledo M, Molins A, Burcet J, Becerra JL, Raspall M, Pico G, Miravet E, Cano A, Fossas P, Fernández S, Falip M. Jaraba S, et al. Among authors: raspall m. Acta Neurol Scand. 2017 Jan;135(1):122-128. doi: 10.1111/ane.12572. Epub 2016 Feb 29. Acta Neurol Scand. 2017. PMID: 26923380

5

Progressive vacuolating glycine leukoencephalopathy with pulmonary hypertension.

del Toro M, Arranz JA, Macaya A, Riudor E, Raspall M, Moreno A, Vazquez E, Ortega A, Matsubara Y, Kure S, Roig M. del Toro M, et al. Among authors: raspall m. Ann Neurol. 2006 Jul;60(1):148-52. doi: 10.1002/ana.20887. Ann Neurol. 2006. PMID: 16802295

6

Usefulness of intravenous lacosamide in status epilepticus.

Santamarina E, Toledo M, Sueiras M, Raspall M, Ailouti N, Lainez E, Porta I, De Gracia R, Quintana M, Alvarez-Sabín J, Xavier Salas Puig XS. Santamarina E, et al. Among authors: raspall m. J Neurol. 2013 Dec;260(12):3122-8. doi: 10.1007/s00415-013-7133-6. J Neurol. 2013. PMID: 24122063

7

Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome.

Vidal S, Brandi N, Pacheco P, Gerotina E, Blasco L, Trotta JR, Derdak S, Del Mar O'Callaghan M, Garcia-Cazorla À, Pineda M, Armstrong J; Rett Working Group. Vidal S, et al. Sci Rep. 2021 Sep 7;11(1):18146. doi: 10.1038/s41598-021-97262-y. Sci Rep. 2021. PMID: 34493777 Free PMC article. No abstract available.

8

The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome.

Vidal S, Brandi N, Pacheco P, Gerotina E, Blasco L, Trotta JR, Derdak S, Del Mar O'Callaghan M, Garcia-Cazorla À, Pineda M, Armstrong J; Rett Working Group. Vidal S, et al. Sci Rep. 2017 Sep 25;7(1):12288. doi: 10.1038/s41598-017-11620-3. Sci Rep. 2017. PMID: 28947817 Free PMC article.

9

Clinical tuberculosis in 2 of 3 siblings with interleukin-12 receptor beta1 deficiency.

Caragol I, Raspall M, Fieschi C, Feinberg J, Larrosa MN, Hernández M, Figueras C, Bertrán JM, Casanova JL, Español T. Caragol I, et al. Among authors: raspall m. Clin Infect Dis. 2003 Jul 15;37(2):302-6. doi: 10.1086/375587. Epub 2003 Jul 7. Clin Infect Dis. 2003. PMID: 12856223

10

X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients.

Xiol C, Vidal S, Pascual-Alonso A, Blasco L, Brandi N, Pacheco P, Gerotina E, O'Callaghan M, Pineda M, Armstrong J; Rett Working Group. Xiol C, et al. Sci Rep. 2019 Aug 19;9(1):11983. doi: 10.1038/s41598-019-48385-w. Sci Rep. 2019. PMID: 31427717 Free PMC article.

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