about
Pilocytic astrocytoma presenting as primary diffuse leptomeningeal gliomatosis: report of a unique case and review of the literature.Rapid disease development in scrapie-infected mice deficient for CD40 ligandExtracranial glioblastoma with synchronous metastases in the lung, pulmonary lymph nodes, vertebrae, cervical muscles and epidural space in a young patient - case report and review of literatureTenascin-C is expressed by human glioma in vivo and shows a strong association with tumor blood vessels.Atypical cervical spondylotic myelopathy mimicking intramedullary tumor.In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathyBrain slice invasion model reveals genes differentially regulated in glioma invasion.Microglia express GABA(B) receptors to modulate interleukin release.[Hypogonadism despite of normal testosterone levels].Decreased expression of the active subunit of the cystine/glutamate antiporter xCT is associated with loss of heterozygosity of 1p in oligodendroglial tumours WHO grade II.Expression of glucose transporter 1 is associated with loss of heterozygosity of chromosome 1p in oligodendroglial tumors WHO grade II.Expression of PACAP and glutamate transporter proteins in satellite oligodendrocytes of the human CNS.Congenital glioblastoma multiforme with abnormal vascularity presenting as intracranial hemorrhage in prenatal ultrasound.Decreased hemispheric Aquaporin-4 is linked to evolving brain edema following controlled cortical impact injury in rats.Post-mortem studies in glioblastoma patients treated with thermotherapy using magnetic nanoparticles.Rapid Multifocal Neurologic Decline in an Immunocompromised Patient.Functional and morphological changes in the dentate gyrus after experimental status epilepticus.Isolated cardiomegaly in the second trimester as an early sign of fetal hydrops due to intracranial arteriovenous malformation.Occurrence of a spinal anaplastic pilocytic astrocytoma and a supratentorial PNET in an adolescent.Progressive muscle atrophy with hypokalemic periodic paralysis and calcium channel mutation.[Progressive muscle atrophy. A rarely diagnosed variant of amyotrophic lateral sclerosis].Muscle and nerve pathology in Dunnigan familial partial lipodystrophy.[Sporadic cerebral amyloid angiopathy with ischemic leukoencephalopathy and microbleeds. Cause for a rapidly progressive dementia syndrome].Increased mRNA expression of tissue inhibitors of metalloproteinase-1 and -2 in Duchenne muscular dystrophy.Intrauterine onset of acute neuropathic type 2 Gaucher disease: identification of a novel insertion sequence.Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis.Clinicopathological Spectrum of Bilirubin Encephalopathy/KernicterusBasement membrane thickness of the vocal cord in cases of sudden infant death[Neurotuberculosis: a continuing clinical challenge]Myopathy and neuropathy with pipestem capillaries and vascular activated complement depositionA rare case of osteochondroma of the coccyxHuman pegivirus-1 associated leukoencephalitis: Clinical and molecular featuresAbsent in melanoma 2 regulates tumor cell proliferation in glioblastoma multiforme
P50
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P50
description
researcher
@en
wetenschapper
@nl
name
F K van Landeghem
@en
F K van Landeghem
@nl
type
label
F K van Landeghem
@en
F K van Landeghem
@nl
prefLabel
F K van Landeghem
@en
F K van Landeghem
@nl
P106
P31
P496
0000-0002-9404-7031