Search Results - "HOOGERWAARD, E. M"

Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study by Hoogerwaard, EM, Bakker, E, Ippel, PF, Oosterwijk, JC, Majoor-Krakauer, DF, Leschot, NJ, Van Essen, AJ, Brunner, HG, van der Wouw, PA, Wilde, AAM, de Visser, M

“…Carriers of Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) may show muscle weakness or dilated cardiomyopathy. Studies focusing on…”
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Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period by HOOGERWAARD, E. M, DE VOOGT, W. G, WILDE, A. A. M, VAN DER WOUW, P. A, BAKKER, E, VAN OMMEN, G.-J. B, DE VISSER, M

“…We evaluated the course of cardiac involvement in 27 previously reported patients with Becker muscular dystrophy (BMD) originating from nine kindreds. Since…”
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Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy by Hoogerwaard, E.M., van der Wouw, P.A., Wilde, A.A.M., Bakker, E., Ippel, P.F., Oosterwijk, J.C., Majoor-Krakauer, D.F., van Essen, A.J., Leschot, N.J., de Visser, M.

“…A cross-sectional study in a cohort of DNA proven carriers of Duchenne (DMD) and Becker (BMD) muscular dystrophy was undertaken with the following objectives:…”
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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy by SCHADE VAN WESTRUM, S. M, HOOGERWAARD, E. M, WILDE, A. A. M, DE HAAN, R. J, DE VISSER, M, VAN DER KOOI, A. J, DEKKER, L, STANDAAR, T. S, BAKKER, E, IPPEL, P. F, OOSTERWIJK, J. C, MAJOOR-KRAKAUER, D. F, VAN ESSEN, A. J, LESCHOT, N. J

“…Cardiac involvement has been reported in carriers of dystrophin mutations giving rise to Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD)…”
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Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene by van Gool, W A, Hensels, G W, Hoogerwaard, E M, Wiezer, J H, Wesseling, P, Bolhuis, P A

“…The clinical features and disease course of six patients from a family with autosomal dominant inheritance of presenile dementia and a hypokinetic syndrome are…”
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Troponin T and troponin I in carriers of Duchenne and Becker muscular dystrophy with cardiac involvement by HOOGERWAARD, Edo M, SCHOUTEN, Yvonne, VAN DER KOOI, Anneke J, GORGELS, Jozef P. M. C, DE VISSER, Marianne, SANDERS, Gerard T. B

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Randomized Delayed-Start Trial of Levodopa in Parkinson’s Disease by Verschuur, Constant V.M, Suwijn, Sven R, Boel, Judith A, Post, Bart, Bloem, Bas R, van Hilten, Johannes J, van Laar, Teus, Tissingh, Gerrit, Munts, Alexander G, Deuschl, Guenther, Lang, Anthony E, Dijkgraaf, Marcel G.W, de Haan, Rob J, de Bie, Rob M.A

“…In a randomized, delayed-start trial of levodopa in Parkinson’s disease, with one group receiving the drug for 80 weeks and the other starting at 40 weeks, the…”
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Adjunctive dexamethasone in adults with meningococcal meningitis by HECKENBERG, Sebastiaan G. B, BROUWER, Matthijs C, DER ENDE, Arie Van, DE BEEK, Diederik Van

“…We evaluated the implementation and effectiveness of adjunctive dexamethasone in adults with meningococcal meningitis. We compared 2 Dutch prospective…”
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Levodopa Response in Patients With Early Parkinson Disease: Further Observations of the LEAP Study by Frequin, Henrieke L., Schouten, Jason, Verschuur, Constant V.M., Suwijn, Sven R., Boel, Judith A., Post, Bart, Bloem, Bastiaan R., van Hilten, Johannes J., van Laar, Teus, Tissingh, Gerrit, Munts, Alexander G., Dijk, Joke M., Deuschl, Günther, Lang, Anthony, Dijkgraaf, Marcel G.W., de Haan, Rob J., de Bie, Rob M.A.

“…The Levodopa in EArly Parkinson's Disease (LEAP) study enabled us to conduct post hoc analyses concerning the effects of levodopa in patients with early…”
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Integrated multidisciplinary care in Parkinson's disease: a non-randomised, controlled trial (IMPACT) by van der Marck, Marjolein A, MSc, Munneke, Marten, PhD, Mulleners, Wim, MD, Hoogerwaard, Edo M, MD, Borm, George F, Prof, Overeem, Sebastiaan, MD, Bloem, Bastiaan R, Prof

“…Summary Background A multidisciplinary approach is thought to be the best way to manage the motor and non-motor symptoms of Parkinson's disease, but how such…”
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Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophy by HOOGERWAARD, Edo M, GINJAAR, Ieke B, BAKKER, Egbert, DE VISSER, Marianne

“…Associations between clinical phenotype (muscle weakness, dilated cardiomyopathy) and dystrophin abnormalities in muscle tissue among definite carriers of…”
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Hypocalcemic delirium due to magnesium sulphate therapy in a pregnant woman with pre-eclampsia by Ganzevoort, J W, Hoogerwaard, E M, van der Post, J A M

“…A 34-year-old pregnant patient, admitted with severe pre-eclampsia and the 'haemolysis, elevated liver enzymes, low platelets' (HELLP) syndrome at 31 weeks…”
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The heartache of muscular dystrophy by Hoogerwaard, E M, Ginjaar, H B, Wilde, A A, Leschot, N J, de Voogt, W G, de Visser, M

“…Duchenne and Becker muscular dystrophy are caused by a mutation in the dystrophin gene, located on the short arm of the X chromosome. Three so called…”
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Prion disease: a new class of neurodegenerative disorders by van Gool, W A, Hoogerwaard, E M, Kuiper, M A, Portegies, P, Bolhuis, P A

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