about
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin familyRecurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardationFetal exposure to teratogens: evidence of genes involved in autismAssociation between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis1H-NMR-based metabolomic profiling of CSF in early amyotrophic lateral sclerosisBlood Cell Palmitoleate-Palmitate Ratio Is an Independent Prognostic Factor for Amyotrophic Lateral SclerosisNovel SOD1 mutation p.V31A identified with a slowly progressive form of amyotrophic lateral sclerosis.A deletion causing NF2 exon 9 skipping is associated with familial autosomal dominant intramedullary ependymoma.Study of the serotonin transporter (SLC6A4) and BDNF genes in French patients with non syndromic mental deficiencyGastrointestinal symptoms resembling ulcerative proctitis caused by larvae of the drone fly Eristalis tenax.Inhibition of β-Glucocerebrosidase Activity Preserves Motor Unit Integrity in a Mouse Model of Amyotrophic Lateral Sclerosis.Iron metabolism disturbance in a French cohort of ALS patientsMutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder.Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation.NSC-34 Motor Neuron-Like Cells Are Unsuitable as Experimental Model for Glutamate-Mediated Excitotoxicity.Preanalytical conditions of point-of-care testing in the intensive care unit are decisive for analysis reliabilitySpecific Metabolome Profile of Exhaled Breath Condensate in Patients with Shock and Respiratory Failure: A Pilot Study.Advances in cellular models to explore the pathophysiology of amyotrophic lateral sclerosis.Roles of LIM kinases in central nervous system function and dysfunction.Metabolomics in amyotrophic lateral sclerosis: how far can it take us?Disruption of TCA Cycle and Glutamate Metabolism Identified by Metabolomics in an In Vitro Model of Amyotrophic Lateral Sclerosis.Inhibition of Pathogenic Mutant SOD1 Aggregation in Cultured Motor Neuronal Cells by Prevention of Its SUMOylation on Lysine 75.Analytical methodology for metabolomics study of adherent mammalian cells using NMR, GC-MS and LC-HRMS.A decrease in blood cholesterol after gastrostomy could impact survival in ALS.Amyotrophic Lateral Sclerosis, 2016: existing therapies and the ongoing search for neuroprotection.Further development of biomarkers in amyotrophic lateral sclerosis.Untargeted 1H-NMR metabolomics in CSF: toward a diagnostic biomarker for motor neuron disease.Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation.Metabolomics Study of Urine in Autism Spectrum Disorders Using a Multiplatform Analytical Methodology.Biomarkers in amyotrophic lateral sclerosis: combining metabolomic and clinical parameters to define disease progression.Biological follow-up in amyotrophic lateral sclerosis: decrease in creatinine levels and increase in ferritin levels predict poor prognosis.Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.Combined Metabolomics and Transcriptomics Approaches to Assess the IL-6 Blockade as a Therapeutic of ALS: Deleterious Alteration of Lipid Metabolism.Vitamin D is Not a Protective Factor in ALS.Comparative analysis of targeted metabolomics: dominance-based rough set approach versus orthogonal partial least square-discriminant analysis.Malnutrition at the time of diagnosis is associated with a shorter disease duration in ALS.[Chronic demyelinating polyneuropathy and B6 hypervitaminosis].Behavior and serotonergic disorders in rats exposed prenatally to valproate: a model for autism.1H-13C NMR-based urine metabolic profiling in autism spectrum disorders.Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband.
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P50
description
onderzoeker
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researcher ORCID ID = 0000-0002-5062-3156
@en
name
Christian Andres
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Christian Andres
@en
Christian Andres
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Christian Andres
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type
label
Christian Andres
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Christian Andres
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Christian Andres
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Christian Andres
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Christian R Andres
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Christian Andres
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Christian Andres
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Christian Andres
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Christian Andres
@nl
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