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Revista De Neurologia|December 31, 2004
[A patient with bilateral lesion in the striatum and slowly progressive dystonia secondary to T14487C mutation in the ND6 gene of complex I of the mitochondrial respiratory chain]M Raspall-Chaure, A Solano, E Vázquez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Association study of the serotoninergic system in migraine in the Spanish populationR Corominas, M J Sobrido, M Ribasés, et al.
American Journal of Human Genetics|May 20, 1999
Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factorS Mardy, Y Miura, F Endo, et al.
Genome Research|November 15, 2000
Fusion of the human gene for the polyubiquitination coeffector UEV1 with Kua, a newly identified geneT M Thomson, J J Lozano, N Loukili, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|October 22, 2016
Proxy-reported quality of life in adolescents and adults with dyskinetic cerebral palsy is associated with executive functions and cortical thicknessO Laporta-Hoyos, J Ballester-Plané, P Póo, et al.
Orphanet Journal of Rare Diseases|February 1, 2018
Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous systemL Marti-Sanchez, J D Ortigoza-Escobar, A Darling, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 19, 2024
EPITRANS. Quality assessment of the epilepsy transition processZ Ortiz de Zarate, E Fonseca, L Abraira, et al.
Cephalalgia : an International Journal of Headache|August 30, 2014
Candidate-gene association study searching for genetic factors involved in migraine chronificationM A Louter, J Fernandez-Morales, B de Vries, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 5, 2019
A clinical diagnostic algorithm for early onset cerebellar ataxiaR Brandsma, C C Verschuuren-Bemelmans, D Amrom, et al.
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