Search Results - "Aarsen, F.K"

P219 Paediatric arterial ischemic stroke: functional outcome and risk factors by Atsman-Berrevoets, C.E, Cnossen, M.H, Aarsen, F.K, Van den Akker, S.L.S, Danen, M.A, Appel, I.M

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P254 Persistent improvement of neurological status and quality of life in children with opsoclonus myoclonus syndrome at long term by Catsman-Berrevoets, C.E, Aarsen, F.K, Van Hemsbergen, M.L.C, van Noesel, M.M, Hakvoort-Cammel, F.G.A.J, Van den Heuvel-Eibrink, M.M

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P329 Cognitive deficits and predictors three years after diagnosis of a pilocytic astrocytoma in childhood by Aarsen, F.K, Paquier, P.F, Arts, W.F.M, Van Veelen-Vincent, M.L, Michiels, E, Lequin, M, Catsman-Berrevoets, C.E

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P252 Fatigue and depression in children with multiple sclerosis and monophasic variants by Ketelslegers, I.A, Catsman-Berrevoets, C.E, Boon, M, Eikelenboom, M.J, Stroink, H, Neuteboom, R.F, Aarsen, F.K, van de Putte, E.M, Hintzen, R.Q

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Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapy by EBBINK, B. J, AARSEN, F. K, GELDER, C. M. Van, DEN HOUT, J. M. P. Van, WEISGLAS-KUPERUS, N, JAEKEN, J, LEQUIN, M. H, ARTS, W. F. M, DER PLOEG, A. T. Van

“…Classic infantile Pompe disease affects many tissues, including the brain. Untreated infants die within their first year. Although enzyme-replacement therapy…”
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Does dexamethasone induce more neuropsychological side effects than prednisone in pediatric acute lymphoblastic leukemia? A systematic review by Warris, L.T., van den Heuvel-Eibrink, M.M., den Hoed, M.A.H., Aarsen, F.K., Pieters, R., van den Akker, E.L.T.

“…Steroid‐induced neuropsychological side effects impact quality of life in children with acute lymphoblastic leukemia. Dexamethasone induces more metabolic side…”
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P09.7 The neuropsychological and behavioural profile of children with tectum glioma and hydrocephalus compared to children who were treated for a cerebellar pilocytic astrocytoma by Aarsen, F.K., Arts, W.F.M., van Veelen-Vincent, M.L.C., Lequin, M.K., Catsman-Berrevoets, C.E.

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Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families by Mancini, G.M.S., Catsman-Berrevoets, C.E., de Coo, I.F.M., Aarsen, F.K., Kamphoven, J.H.J., Huijmans, J.G., Duran, M., van der Knaap, M.S., Jakobs, C., Salomons, G.S.

“…Four Dutch male patients, two brothers from unrelated families were referred for investigation of psychomotor and severe language/speech delay. All four…”
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