about
Effects of intravenous administration of human umbilical cord blood stem cells in 3-acetylpyridine-lesioned ratsNeuroprotective role of liver growth factor "LGF" in an experimental model of cerebellar ataxiaQuerying phenotype-genotype relationships on patient datasets using semantic web technology: the example of Cerebrotendinous xanthomatosis.Neuroprotective activity of peripherally administered liver growth factor in a rat model of Parkinson's diseaseA multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes.Translating genetic findings into therapy in Parkinson disease.Cerebrotendinous xanthomatosis in Spain: clinical, prognostic, and genetic survey.Liver Growth Factor (LGF) Upregulates Frataxin Protein Expression and Reduces Oxidative Stress in Friedreich's Ataxia Transgenic Mice.Optimal excitation and emission wavelengths to analyze amino acids and optimize neurotransmitters quantification using precolumn OPA-derivatization by HPLC.New V272A presenilin 1 mutation with very early onset subcortical dementia and parkinsonism.Autosomal recessive Emery-Dreifuss muscular dystrophy caused by a novel mutation (R225Q) in the lamin A/C gene identified by exome sequencing.Amusia as an early manifestation of frontotemporal dementia caused by a novel progranulin mutation.A short neuropsychologic and cognitive evaluation of frontotemporal dementia.A novel ATTR L32V mutation causes familial amyloid polyneuropathy in a Bolivian family.Variability of age at onset in siblings with familial Alzheimer disease.Clinical-genetic correlations in familial Alzheimer's disease caused by presenilin 1 mutations.PLA2G6-associated neurodegeneration: New insights into brain abnormalities and disease progressionRNA-Seq blood transcriptome profiling in familial attention deficit and hyperactivity disorder (ADHD)Isolated continuous rhythmic lingual myoclonusThe clinical correlates of IgG antiganglioside antibodiesClinical-molecular study of a family with essential tremor, late onset seizures and periodic paralysisOculo-auricular phenomenon secondary to vestibular dysfunctionHistocompatibility class I and II antigens in extensive kindred with Sneddon's syndrome and related hypercoagulation disorders[Clinical variability and diagnostic controversies in CADASIL]Liver growth factor promotes the survival of grafted neural stem cells in a rat model of Parkinson's diseaseA novel myelin protein zero (V136G) homozygous mutation causing late onset demyelinating polyneuropathy with brain white matter lesionsAIDS dementia complex: incidence, clinical profile and impact of zidovudine treatment*[Usefulness of cholestanol levels in the diagnosis and follow-up of patients with cerebrotendinous xanthomatosis]Neurophysiological study in cerebrotendinous xanthomatosisIsolated palsy of the third nerve nuclear complex caused by cerebral toxoplasmosisLoss of taste and carbamazepineMolecular biology and genetics of Alzheimer's diseaseThe Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic InsightReduced cerebrospinal fluid monoamines in Alexander's disease: a clue to a symptomatic therapyClinical and genetical study of a familial form of REM sleep behavior disorder
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description
researcher ORCID ID = 0000-0002-4927-1886
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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Adriano Jiménez-Escrig
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P1153
55950496000
P21
P31
P496
0000-0002-4927-1886