Search Results - "Weber, Jacobiene W."

clinical spectrum of Blake's pouch cyst: report of six illustrative cases by Cornips, Erwin M. J, Overvliet, Geke M, Weber, Jacobiene W, Postma, Alida A, Hoeberigs, Christianne M, Baldewijns, Marcella M. L. L, Vles, Johannes S. H

“…Introduction Although Blake's pouch cyst (BPC) is frequently mentioned in the spectrum of posterior fossa cysts and cystlike malformations since its first…”
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Clinical characteristics and surgical outcome in 25 cases of childhood tight filum syndrome by Cornips, Erwin M.J, Vereijken, Ilse M.P, Beuls, Emile A.M, Weber, Jacobiene W, Soudant, Dan L.H.M, van Rhijn, Lodewijk W, Callewaert, Piet R.H, Vles, Johan S.H

“…Abstract Objective Tight filum syndrome (TFS) is caused by a thick (abnormal T1 MRI), shortened (low-lying conus), or non-elastic filum (strictly normal MRI)…”
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Pediatric Idiopathic Intracranial Hypertension Presenting With Sensorineural Hearing Loss by Reitsma, Sietze, Stokroos, Robert, Weber, Jacobiene W., van Tongeren, Joost

“…Objective: To present the rare case of a young boy with idiopathic intracranial hypertension presenting with bilateral sensorineural hearing loss developing…”
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Cognitive and behavioral effects of nocturnal epileptiform discharges in children with benign childhood epilepsy with centrotemporal spikes by Nicolai, Joost, Aldenkamp, Albert P., Arends, Johan, Weber, Jacobiene W., Vles, Johan S.H.

“…This review addresses the effects of subclinical localized epileptiform discharges during sleep in children with benign childhood epilepsy with centrotemporal…”
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EEG Characteristics Related to Educational Impairments in Children with Benign Childhood Epilepsy with Centrotemporal Spikes by Nicolai, Joost, Van Der Linden, Inge, Arends, Johan B. A. M., Van Mil, Saskia G. M., Weber, Jacobiene W., Vles, Johan S. H., Aldenkamp, Albert P.

“…Summary Purpose: Learning and behavioral difficulties often occur in benign childhood epilepsy with centrotemporal spikes (BCECTS). In recent years, several…”
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Diagnostic radiation exposure in children with spinal dysraphism: an estimation of the cumulative effective dose in a cohort of 135 children from The Netherlands by van Aalst, Jasper, Jeukens, Cécile R L P N, Vles, Johan S H, van Maren, Emiel A, Kessels, Alfons G H, Soudant, Dan L H M, Weber, Jacobiene W, Postma, Alida A, Cornips, Erwin M J

“…Objective Based on the assumption that children with spinal dysraphism are exposed to a large amount of ionising radiation for diagnostic purposes, our…”
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Posterior reversible encephalopathy syndrome in paediatric leukaemia by Panis, Bianca, Vlaar, Annemarie M.M, van Well, Gijs Th.J, Granzen, Bernd, Weber, Jacobiene W, Postma, Alida A, Klinkenberg, Sylvia

“…Abstract This report describes four patients with acute lymphoblastic leukaemia, suffering from posterior reversible encephalopathy syndrome during the…”
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lumbosacral angle does not reflect progressive tethered cord syndrome in children with spinal dysraphism by Cornips, Erwin M. J, Razenberg, Femke G. E. M, van Rhijn, Lodewijk W, Soudant, Dan L. H. M, van Raak, Elisabeth P. M, Weber, Jacobiene W, Robben, Simon G, Fock, Johanna M, Catsman-Berrevoets, Coriene E, Vles, Johannes S. H

“…Purpose Our goal was to validate the hypothesis that the lumbosacral angle (LSA) increases in children with spinal dysraphism who present with progressive…”
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Motor function in children with cryptogenic localization related epilepsy by Reijs, Rianne P, de la Parra, Nora M, van Mil, Saskia G.M, van Hall, Mariette H.J.A, Arends, Johan B.A.M, Weber, Jacobiene W, Renier, Willy O, Aldenkamp, Albert P

“…Abstract Introduction In CLRE specific learning difficulties and motor problems may occur. The aim of this study is to examine whether CLRE or the accompanying…”
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Solitary juvenile xanthogranuloma of the temporal muscle and bone penetrating the dura mater in a 2-month-old boy: Case report by CORNIPS, Erwin M. J, COX, Kimberly E. M, CREYTENS, David H. K. V, GRANZEN, Bernd, WEBER, Jacobiene W, TER LAAK-POORT, Mariel P

“…Juvenile xanthogranuloma (JXG) is a rare histiocytic disorder primarily observed during the first 2 years of life. Most patients present with a solitary…”
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Cryptogenic localization-related epilepsy with childhood onset: The problem of definition and prognosis by Reijs, Rianne P., van Mil, Saskia G.M., van Hall, Mariette H.J.A., Arends, Johan B.A.M., Weber, Jacobiene W., Renier, Wil O., Aldenkamp, Albert P.

“…Up to one-third of children with epilepsy are diagnosed with cryptogenic localization-related epilepsy (CLRE). CLRE is a large nonspecific category within the…”
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Cryptogenic localization related epilepsy in children from a tertiary outpatient clinic: Is neurological and neuropsychological outcome predictable? by Reijs, Rianne P, van Mil, Saskia G.M, Arends, Johan B.A.M, van Hall, Mariette H.J.A, Weber, Jacobiene W, Renier, Willy O, Aldenkamp, Albert P

“…Abstract Objectives Up to one-third of the children with epilepsy are diagnosed with cryptogenic localization related epilepsy (CLRE). As yet, there is a lack…”
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The validity of a separate classification of cryptogenic localization related epilepsy amongst childhood epilepsies by Reijs, Rianne P, van Mil, Saskia G.M, van Hall, Mariette H.J.A, Arends, Johan B.A.M, Weber, Jacobiene W, Renier, Willy O, Aldenkamp, Albert P

“…Summary Introduction One-third of children with epilepsy are classified as having a cryptogenic localization related epilepsy (CLRE). In cohort studies CLRE is…”
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Diagnostic radiation exposure in children with spinal dysraphism: an estimation of the cumulative effective dose in a cohort of 135 children from The Netherlands by Cornips, Erwin M. J, Postma, Alida A, Weber, Jacobiene W, Soudant, Dan L. H. M, Kessels, Alfons G. H, van Maren, Emiel A, Vles, Johan S. H, Jeukens, Cecile R. L. P. N, van Aalst, Jasper

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Solitary juvenile xanthogranuloma of the temporal muscle and bone penetrating the dura mater in a 2-month-old boy by Cornips, Erwin M J, Cox, Kimberly E M, Creytens, David H K V, Granzen, Bernd, Weber, Jacobiene W, Ter Laak-Poort, Mariel P

“…Juvenile xanthogranuloma (JXG) is a rare histiocytic disorder primarily observed during the first 2 years of life. Most patients present with a solitary…”
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