Search Results - "Pals, P"
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Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
Published in Neurology (15-04-2008)“…Leucine-rich repeat kinase 2 (LRRK2) mutations are the most common cause of Parkinson disease (PD). Several dominantly inherited pathogenic substitutions have…”
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2
Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C
Published in Journal of neurology, neurosurgery and psychiatry (2010)“…Background:m.14487T>C, a missense mutation (p.M63V) affecting the ND6 subunit of complex I of the mitochondrial respiratory chain, has been reported in…”
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3
Progranulin variability has no major role in Parkinson disease genetic etiology
Published in Neurology (07-10-2008)“…Different loss-of-function mutations were identified underlying PGRN haploinsufficiency in patients with frontotemporal lobar degeneration. PGRN mutations were…”
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4
Lyme neuroborreliosis
Published in JBR-BTR : organe de la Societe royale belge de radiologie (SRBR) = orgaan van de Koninklijke Belgische Vereniging voor Radiologie (KBVR) (01-07-2013)“…Background: A 24-year-old woman presented to the emergency department with headache, apathy, aphasia and mild paresis of the right leg. Routine laboratory…”
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A comparison of permutation and mixed-model regression methods for the analysis of simulated data in the context of a group-randomized trial
Published in Statistics in medicine (15-02-2006)“…Our first purpose was to determine whether, in the context of a group‐randomized trial (GRT) with Gaussian errors, permutation or mixed‐model regression…”
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Phosphorylated tau in cerebrospinal fluid as a marker for Creutzfeldt–Jakob disease
Published in Journal of neurology, neurosurgery and psychiatry (01-07-2002)“…Objective: To determine the concentrations of microtubule associated protein tau and multiple phosphorylated tau epitopes in the cerebrospinal fluid of…”
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7
Opsoclonus-myoclonus syndrome: a clinicopathological confrontation
Published in Acta neurologica Belgica (01-09-2006)“…Opsoclonus-myoclonus syndrome (OMS), a movement disorder characterised by chaotic eye movements and myoclonus, is a rare clinical entity. We present two cases…”
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A Retrospective Study of Creutzfeldt-Jakob Disease in Belgium
Published in European journal of epidemiology (01-07-1999)“…Using data from Belgian neuropathological archives, completed with the results of a comprehensive study of available medical records, we found 100 patients who…”
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Retrospective study of Creutzfeldt-Jakob disease in Belgium : neuropathological findings
Published in Acta neuropathologica (01-04-2000)“…Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that affects about 1 in 10(6) inhabitants in most countries. Recently, a new variant of CJD has…”
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α-Synuclein promoter confers susceptibility to Parkinson's disease
Published in Annals of neurology (01-10-2004)“…Familial Parkinson's disease (PD) has been linked to missense and genomic multiplication mutations of the α‐synuclein gene (SNCA). Genetic variability within…”
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11
Delayed diagnosis in a patient with Creutzfeldt-Jakob disease in a psychiatric hospital
Published in Tijdschrift voor psychiatrie (2016)“…A 51-year-old female teacher of dance was referred to the diagnostic unit of our psychiatric hospital with symptoms of anxiety and depression. The clinical…”
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12
Creutzfeldt-Jakob disease and blood transfusion
Published in Acta neurologica Belgica (01-09-1998)“…Experimental data suggest that blood components from patients with CJD may carry infectivity. However, most of the studies have been made on the classic form…”
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13
The role of cytokines, astrocytes, microglia and apoptosis in Creutzfeldt-Jakob disease
Published in Neurobiology of aging (2002)“…In order to investigate inflammation and apoptosis in Creutzfeldt-Jakob disease (CJD) patients, we analyzed astrocytes, microglia and apoptotic neurons in…”
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14
Calculation of transmission loss factors in the presence of constraints
Published in DRPT2000. International Conference on Electric Utility Deregulation and Restructuring and Power Technologies. Proceedings (Cat. No.00EX382) (2000)“…This paper presents a new method of calculating transmission loss factors. The method is distinctive by virtue of the fact that it takes account of the effect…”
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Conference Proceeding -
15
Case-Control Study of Environmental Risk Factors for Parkinson's Disease in Belgium
Published in European journal of epidemiology (2003)“…The aetiology of Parkinson's disease (PD) is unknown and said to be multifactorial. We report on a retrospective epidemiological case control study, performed…”
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16
Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt–Jakob Disease phenotype
Published in Neuroscience letters (02-11-2001)“…We investigated the risk associated with the codon 129 polymorphism in the prion protein gene (PRNP) and apolipoprotein E gene (APOE) isoforms for development…”
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Antigen Retrieval in Prion Protein Immunohistochemistry
Published in The journal of histochemistry and cytochemistry (01-11-1999)“…Transmissible spongiform encephalopathies are a group of neurodegenerative diseases occurring in both humans and animals and are most likely caused by prions…”
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Transmissible spongiform encephalopathies: the story of a pathogenic protein
Published in Peptides (New York, N.Y. : 1980) (01-07-2002)“…An overview is provided from the first description of the transmissible spongiform encephalopathies (TSE) to recent major discoveries in this research field…”
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Safety measures for handling laboratory specimen and patients with Creutzfeldt-Jakob disease
Published in Nederlands tijdschrift voor geneeskunde (17-07-1999)“…Creutzfeldt-Jakob disease (CJD) is a transmissible subacute spongiform encephalopathy that invariably leads to death. The presumed causative agent, the prion…”
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Two-dimensional quantum spin Hamiltonians: Spectral properties
Published in Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics (01-01-1994)Get full text
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