Search Results - "Hauw, J.‐J."
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Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases
Published in Neuropathology and applied neurobiology (01-04-2020)“…Aims In the search for blood‐based biomarkers of neurodegenerative diseases, we characterized the concentration of total prion protein (t‐PrP) in the plasma of…”
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Dyslipidemia is a protective factor in amyotrophic lateral sclerosis
Published in Neurology (25-03-2008)“…Amyotrophic lateral sclerosis (ALS) is the most serious form of degenerative motor neuron disease in adults, characterized by upper and lower motor neuron…”
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Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease
Published in Molecular psychiatry (01-11-2009)“…The only recognized genetic determinant of the common forms of Alzheimer's disease (AD) is the ɛ4 allele of the apolipoprotein E gene (APOE). To identify new…”
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Synapse and primary cilia dysfunctions in Autism Spectrum Disorders. Avenues to normalize these functions
Published in Revue neurologique (25-06-2024)“…An update on the plasticity of the brain networks involved in autism (autism spectrum disorders [ASD]), and the increasing role of their synapses and primary…”
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Measles Sclerosing Subacute PanEncephalitis (SSPE), an intriguing and ever-present disease: Data, assumptions and new perspectives
Published in Revue neurologique (01-11-2021)“…Subacute sclerosing panencephalitis (SSPE) is a rare, non-treatable and fatal neurological complication of measles, still present due to the return of the…”
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Predictors for malignant middle cerebral artery infarctions : A postmortem analysis
Published in Neurology (28-03-2006)“…Early detection of malignant infarction of the middle cerebral artery (MI-MCA) is important because of possible treatment by hemicraniectomy. To investigate…”
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The significance of cortical pathology in progressive supranuclear palsy : Clinico-pathological data in 10 cases
Published in Brain (London, England : 1878) (01-08-1996)“…Several observations suggest that the cortical lesions of progressive supranuclear palsy (PSP) play a role in the clinical symptoms and signs of the disease,…”
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Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)
Published in Neurology (01-11-1994)“…We present the preliminary neuropathologic criteria for progressive supranuclear palsy (PSP) as proposed at a workshop held at the National Institutes of…”
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Olig2 expression, GFAP, p53 and 1p loss analysis contribute to glioma subclassification
Published in Neuropathology and applied neurobiology (01-02-2005)“…The expression of Olig2, a basic helix–loop–helix (bHLH) transcription factor involved in oligodendroglial specification, was investigated by…”
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BSE transmission to macaques
Published in Nature (London) (27-06-1996)“…The recent description in the United Kingdom of a new variant of Creutzfeldt-Jacob disease (vCJD) with a unique clinicopathological presentation has raised…”
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Validity and Reliability of the Preliminary NINDS Neuropathologic Criteria for Progressive Supranuclear Palsy and Related Disorders
Published in Journal of neuropathology and experimental neurology (01-01-1996)“…We investigated the validity and reliability of diagnoses made by eight neuropathologists who used the preliminary NINDS neuropathologic diagnostic criteria…”
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Doctor Francoise Cathala and history of prions diseases
Published in Revue neurologique (01-12-2015)“…Doctor Françoise Cathala Pagesy, MD, MS, born on July 7, 1921 in Paris, passed away peacefully at home on November 5, 2012. Unconventional, passionate and…”
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Spreading of protein misfolding: A new paradigm in neurology
Published in Revue neurologique (01-12-2015)“…Protein misfolding and spreading ("transconformation") are being better understood. Described in Prions diseases, this new paradigm in the field of…”
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Accumulation of flotillin-1 in tangle-bearing neurones of Alzheimer's disease
Published in Neuropathology and applied neurobiology (01-10-2003)“…The protein flotillin‐1 is associated with the ‘lipid rafts’, that is, membrane microdomains that are enriched in cholesterol and sphingolipids. We compared…”
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Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticus
Published in Neurology (15-06-2010)“…Nonconvulsive status epilepticus (NCSE) in patients with confusion may be difficult to distinguish from nonepileptic (metabolic/toxic, postanoxic, and…”
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Preservation of midbrain catecholaminergic neurons in very old human subjects
Published in Brain (London, England : 1878) (01-02-2000)“…Parkinson's disease is characterized by a progressive degeneration of dopaminergic neurons in the midbrain, yet the cause of this neuronal loss is still…”
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The relationship between Bunina bodies, skein-like inclusions and neuronal loss in amyotrophic lateral sclerosis
Published in Acta neuropathologica (01-06-2002)“…Specific pathological hallmarks have been described in amyotrophic lateral sclerosis (ALS), which include motor neuronal loss, Bunina bodies (BBs) and skein…”
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Prevalence of nephroangiosclerosis in patients with fatal stroke
Published in Neurology (10-03-2009)“…Glomerular filtration rate and decline in renal function can be improved by global cardiovascular prevention. However, the prevalence of nephroangiosclerosis…”
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Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein
Published in Science (American Association for the Advancement of Science) (17-01-1997)“…The agent responsible for transmissible spongiform encephalopathies (TSEs) is thought to be a malfolded, protease-resistant version (PrPres) of the normal…”
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