The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism. |
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Acute cerebellitis following Epstein-Barr virus infection in two young women |
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Alteraciones neurológicas inducidas por fármacos |
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Antibodies to Borrelia burgdorferi in Guillain-Barré syndrome |
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Anticipation in myotonic dystrophy: a parental-sex-related phenomenon |
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Antiganglioside antibodies in acute self-limiting ataxic neuropathy: incidence and significance |
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Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson's disease |
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Association between synapsin III gene promoter SNPs and multiple sclerosis in Basque patients. |
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[Autoimmune hepatitis in a patient with multiple sclerosis under treatment with glatiramer acetate] |
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Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. |
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Clinical signs of brain death simulated by Guillain-Barré syndrome |
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Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease |
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Cognitive function in facioscapulohumeral dystrophy correlates with the molecular defect. |
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Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1. |
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Conduction velocity through the somesthetic pathway in chronic renal failure |
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Correction: Pathogenic LRRK2 Mutations Do Not Alter Gene Expression in Cell Model Systems or Human Brain Tissue. |
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Creation of an open-access, mutation-defined fibroblast resource for neurological disease research |
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Distinctive age-related temporal cortical thinning in asymptomatic granulin gene mutation carriers. |
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Drug-induced parkinsonism: a growing list |
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Early treatment of Parkinson's disease with cabergoline delays the onset of motor complications. Results of a double-blind levodopa controlled trial. The PKDS009 Study Group. |
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The effect of visual cues on the number and duration of freezing episodes in Parkinson's patients. |
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Enfermedad de Parkinson : conocimientos y actitudes prácticas |
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Frequency of myotonic dystrophy gene carriers in cataract patients. |
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"Frontotemporoparietal" dementia: clinical phenotype associated with the c.709-1G>A PGRN mutation. |
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Generalized chorea induced by nonketotic hyperglycemia |
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Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy |
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Genetic variation in α-synuclein kinases (CK-2β and GRK-5) and risk of Parkinson's disease. |
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Genética y avances en el diagnóstico molecular de las enfermedades neurológicas XI cursos de verano de la Universidad del País Vasco = Herriko Unibertsitateko XI. udako Ikastaroak |
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Hepatotoxicity due to ticlopidine |
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Higher frequency of certain cancers in LRRK2 G2019S mutation carriers with Parkinson disease: a pooled analysis |
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Hypoxic ischaemic encephalopathy: lesions on magnetic resonance |
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Late onset familial periodic cerebellar ataxia |
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LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene. |
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Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain). |
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Lithium therapy in torsion dystonia |
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LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicity. |
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Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants |
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Mitochondrial polymporphisms in Parkinson's Disease |
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Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings. |
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Neurogenetic disorders in the Basque population |
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Neurología : información para pacientes y familiares |
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Neurología para médicos de atención primaria |
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Neurología práctica general |
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Neurophysiological assessment of alpha pattern coma. |
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Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers. |
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A new type of epidemiological study: questionnaire administered by medical personnel |
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Nocturnal akathisia in Parkinson's disease: treatment with clozapine. |
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Pacientes con problemas neurológicos de interés, c2010: |
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[Parkinsonism induced by sulpiride and veralipride: two different stories] |
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Pathogenic Parkinson's disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation |
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Phenotypic variability in familial prion diseases due to the D178N mutation. |
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Prevalence of essential tremor: a door-to-door survey in bidasoa, spain |
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Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis. A report of 50 cases. |
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Somatosensory evoked potentials: abnormalities with focal brain lesions remote from the primary sensorimotor area |
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Treatment with hemiballism with reserpine |
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The validity of Hodkinson's Abbreviated Mental Test for dementia screening in Guipuzcoa, Spain |
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Y por fin-- ¡el diagnóstico! : casos clínicos neurológicos de diagnóstico difícil |
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