Search Results - "Hemelsoet, D."

Neurological manifestations and neuro‐invasive mechanisms of the severe acute respiratory syndrome coronavirus type 2 by Vonck, K., Garrez, I., De Herdt, V., Hemelsoet, D., Laureys, G., Raedt, R., Boon, P.

“…Background and purpose Infections with coronaviruses are not always confined to the respiratory tract and various neurological manifestations have been…”
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Dysphagia, dysarthria and aphasia following a first acute ischaemic stroke: incidence and associated factors by De Cock, E., Batens, K., Hemelsoet, D., Boon, P., Oostra, K., De Herdt, V.

“…Background and purpose Dysphagia, dysarthria and aphasia are common symptoms following acute stroke; however, limited data are available from recent…”
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A long-term neuropsychological evaluation in Fabry disease by Loret, G., Miatton, M., Vingerhoets, G., Poppe, B., Hemelsoet, D.

“…Fabry disease (FD) is a X-linked multi-systemic metabolic disorder with mainly renal, cardiac and neurological dysfunction. The neuropsychological impact is…”
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Cerebral vasospasm in acute porphyria by Olivier, P., Van Melkebeke, D., Honoré, P.‐J., Defreyne, L., Hemelsoet, D.

“…Background and purpose Porphyrias are a group of inherited metabolic disorders resulting from a specific deficiency along the pathway of haem biosynthesis. A…”
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The genetic causes of basal ganglia calcification, dementia, and bone cysts DAP12 and TREM2 by KLÜNEMANN, H. H, RIDHA, B. H, PELTONEN, L, PALONEVA, J, MAGY, L, WHERRETT, J. R, HEMELSOET, D. M, KEEN, R. W, DE BLEECKER, J. L, ROSSOR, M. N, MARIENHAGEN, J, KLEIN, H. E

“…Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), or Nasu-Hakola disease, is a presenile dementia associated with loss of…”
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Tapia’s syndrome in the intensive care unit: a rare cause of combined cranial nerve palsy following intubation by Coninckx, M., Cardoen, S., Hemelsoet, D.

“…Tapia’s syndrome is characterized by unilateral paralysis of the tongue and vocal cord, and is caused by a concurrent lesion of both the recurrent laryngeal…”
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Accelerating patient access to oncology medicines with multiple indications in Europe by Lawlor, R., Wilsdon, T., Darquennes, E., Hemelsoet, D., Huismans, J., Normand, R., Roediger, A.

“…Background: In recent years, innovation in oncology has created new challenges for pricing and reimbursement systems. Oncology medicines with multiple…”
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Early-onset dementia, leukoencephalopathy and brain calcifications: a clinical, imaging and pathological comparison of ALSP and PLOSL/Nasu Hakola disease by Coomans, C., Sieben, A., Lammens, M., Ceuterick-de Groote, C., Vandenbroecke, C., Goethals, I., Van Melkebeke, D., Hemelsoet, D.

“…Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia, and Nasu Hakola disease or polycystic lipomembranous osteodysplasia with sclerosing…”
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Plasmapheresis in Susac syndrome by El Tahry, R, Dhondt, A, Hemelsoet, D

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Imaging Features of Hypertrophic Olivary Degeneration by Van Eetvelde, Ruth, Lemmerling, M, Backaert, T, Favoreel, N, Geerts, B, Sommeling, C, Hemelsoet, D, Dekeyzer, S

“…Hypertrophic olivary degeneration (HOD) is a unique form of transneuronal degeneration caused by a disruption of the dentato-rubro-olivary pathway, also known…”
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Right hand knob infarction by Dekeyzer, Sven, Acou, M., Hemelsoet, D.

“…A 69-year-old man presented at the ER with paresis of the left arm since one week. Except for hypertension and lumbosciatic pain, there was no past medical…”
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Biotinidase deficiency: A treatable cause of opticospinal syndrome in young adults by Van Iseghem, V., Sprengers, M., De Zaeytijd, J., Sindic, C.J.M., Willekens, B., Dermaut, B., Hemelsoet, D., Laureys, G.

“…•Biotinidase deficiency is a rare autosomal metabolic disorder.•It is easily tested by measuring biotinidase activity in serum or through whole blood spotted…”
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A novel Csf1r mutation in hereditary diffuse leuko/INS;encephalopathy with spheroids by Rademakers, R, Baker, M, Lammens, M, Maes, J, Hemelsoet, D

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Stroke Versus Seizure - Perfusion Computerized Tomography in a Patient with Aphasia by Dekeyzer, S, Vanden Bossche, S, Keereman, V, Hemelsoet, D, Van Driessche, V

“…Both stroke and seizures have varied clinical presentations and their differentiation in the acute setting is not always straightforward. We present the case…”
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Post-traumatic spontaneous recurrent hypothermia: a variant of Shapiro's syndrome by Hemelsoet, D. M., De Bleecker, J. L.

“…A 49‐year‐old man presented with episodic hypothermia many years after sustaining a contusional brain injury. Brain magnetic resonance imaging demonstrated the…”
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The neurological illness of Friedrich Nietzsche by Hemelsoet, D, Hemelsoet, K, Devreese, D

“…Friedrich Nietzsche (1844-1900), one of the most profound and influential modern philosophers, suffered since his very childhood from severe migraine. At 44 he…”
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Ischemic stroke and hyperhomocysteinemia: truth or myth? by Terwecoren, A, Steen, E, Benoit, D, Boon, P, Hemelsoet, D

“…Hyperhomocysteinemia is generally acknowledged as a treatable risk factor for atherotrombotic diseases, but a causal relationship between both is not yet…”
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Questioning the Pathogenic Role of the GLA p.Ala143Thr “Mutation” in Fabry Disease: Implications for Screening Studies and ERT by Terryn, W., Vanholder, R., Hemelsoet, D., Leroy, B. P., Van Biesen, W., De Schoenmakere, G., Wuyts, B., Claes, K., De Backer, J., De Paepe, G., Fogo, A., Praet, M., Poppe, B.

“…Fabry disease is an X-linked inborn error of glycosphingolipid metabolism caused by quantitative or qualitative defects in the lysosomal enzyme…”
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Organisation of inhospital acute stroke care and minimum criteria for stroke care units. Recommendations of the Belgian Stroke Council by Thijs, V, Peeters, A, Dewindt, A, Hemelsoet, D, De Klippel, N, Laloux, P, Redondo, P, Cras, P, De Deyn, P P, Desfontaines, Ph, Brouns, R, De Raedt, S, Van Landegem, W, Vandermeeren, Y, Vanhooren, G

“…There is ample evidence from randomized trials that for patients with stroke, stroke unit care is superior to care in general medical or neurological wards…”
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Do corticosubcortical lacunes exist? A clinicopathological case report by De Reuck, J, Nieuwenhuis, L, Hemelsoet, D

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