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Browsing by Author Visser, M. de

Full Text	Issue Date	Title	Author(s)
	2011	Population based epidemiology of amyotrophic lateral sclerosis using capture-recapture methodology	Huisman, M.H.; Jong, S.W. de; Doormaal, P.T. van; Weinreich, S.S.; Schelhaas, H.J., et al
	2011	Renal uptake of different radiolabelled peptides is mediated by megalin: SPECT and biodistribution studies in megalin-deficient mice	Vegt, E.; Melis, M.; Eek, A.; Visser, M. de; Brom, M., et al
	2011	Family history of neurodegenerative and vascular diseases in ALS: a population-based study	Huisman, M.H.; Jong, S.W. de; Verwijs, M.C.; Schelhaas, H.J.; Kooi, A.J. van der, et al
	2011	The phenotype of the Gly94fsX222 PMP22 insertion	Vries, S.D. de; Verhamme, C.; Ruissen, F. van; Paassen, B.W. van; Arts, W.F.M., et al
	2010	FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.	Groen, E.J.; Es, M.A. van; Vught, P.W. van; Spliet, W.G.; Engelen-Lee, J. van, et al
	2010	Dynamic and static small-animal SPECT in rats for monitoring renal function after 177Lu-labeled Tyr3-octreotate radionuclide therapy.	Melis, M.; Swart, J.; Visser, M. de; Berndsen, S.C.; Koelewijn, S., et al
	2010	Exercise therapy and cognitive behavioural therapy to improve fatigue, daily activity performance and quality of life in postpoliomyelitis syndrome: the protocol of the FACTS-2-PPS trial.	Koopman, F.S.; Beelen, A.; Gerrits, K.H.; Bleijenberg, G.; Abma, T.A., et al
	2010	The SNAQ(RC), an easy traffic light system as a first step in the recognition of undernutrition in residential care.	Kruizenga, H.M.; Vet, H.C. de; Marissing, C.M. Van; Stassen, E.E.; Strijk, J.E., et al
	2010	The effect of the weak androgen oxandrolone on psychological and behavioral characteristics in growth hormone-treated girls with Turner syndrome.	Menke, L.A.; Sas, T.C.J.; Visser, M. de; Kreukels, B.P.; Stijnen, T., et al
	2010	Lower atovaquone/proguanil concentrations in patients taking efavirenz, lopinavir/ritonavir or atazanavir/ritonavir.	Luin, M. van; Ende, M.E. van der; Richter, C.; Visser, M. de; Faraj, D., et al
	2010	Nephrotoxicity in mice after repeated imaging using 111In-labeled peptides.	Melis, M.; Vegt, E.; Konijnenberg, M.W.; Visser, M. de; Bijster, M., et al
	2009	Redefining the clinical phenotypes of non-dystrophic myotonic syndromes.	Trip, J.; Drost, G.; Ginjaar, H.B.; Nieman, F.H.; Kooi, A.J. van der, et al
	2009	International study on the psychometric attributes of the non-motor symptoms scale in Parkinson disease.	Martinez-Martin, P.; Rodriguez-Blazquez, C.; Abe, K.; Bhattacharyya, K.B.; Bloem, B.R., et al
	2009	Versatile conjugation of octreotide to dendrimers by cycloaddition ("click") chemistry to yield high-affinity multivalent cyclic Peptide dendrimers.	Yim, C.B.; Boerman, O.C.; Visser, M. de; Jong, M. de; Dechesne, A.C., et al
	2009	The Phenotype of the Gly94Fsx222 Pmp22 Insertion	Vries, S.C. de; Kooi, A.J. van der; Verhamme, C.; Ruissen, F. van; Arts, W.F.M., et al
	2009	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Es, M.A. van; Veldink, J.H.; Saris, C.G.; Blauw, H.M.; Vught, P.W. van, et al
	2009	Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes.	Brugman, F.; Veldink, J.H.; Franssen, H.; Visser, M. de; Jong, J.M. de, et al
	2009	Clinical identification of dysarthria types among neurologists, residents in neurology and speech therapists.	Graaff, M. Van der; Kuiper, T.; Zwinderman, A.; Warrenburg, B.P.C. van de; Poels, P.J.E., et al
	2009	Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis.	Piepers, S.; Veldink, J.H.; Jong, S.W. de; Tweel, I. van de; Pol, W.L. van der, et al
	2009	Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis.	Es, M.A. van; Vught, P.W. van; Veldink, J.H.; Andersen, P.M.; Birve, A., et al
	2009	Complete remission of severe idiopathic cold urticaria on interleukin-1 receptor antagonist (anakinra).	Bodar, E.J.; Simon, A.; Visser, M. de; Meer, J.W.M. van der
	2008	The Lambert-Eaton myasthenic syndrome 1988-2008 : a clinical picture in 97 patients	Titulaer, M.J.; Wirtz, P.W.; Kuks, J.B.; Schelhaas, H.J.; Kooi, A.J. van der, et al
	2008	Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes.	Brugman, F.; Scheffer, H.; Wokke, J.H.; Nillesen, W.M.; Visser, M. de, et al
	2008	Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.	Monnier, N.; Marty, I.; Faure, J.; Castiglioni, C.; Desnuelle, C., et al
	2008	A natural history study of late onset spinal muscular atrophy types 3b and 4.	Piepers, S.; Berg, L.H. van den; Brugman, F.; Scheffer, H.; Ruiterkamp-Versteeg, M., et al
	2008	Motor axon loss is associated with hand dysfunction in Charcot-Marie-Tooth disease 1a.	Videler, A.J.; Dijk, J.P. van; Beelen, A.; Visser, M. de; Nollet, F., et al
	2008	In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia.	Trip, J.; Drost, G.; Verbove, D.J.; Kooi, A.J. van der; Kuks, J.B., et al
	2007	Phenotype of Charcot-Marie-Tooth disease Type 2.	Bienfait, H.M.; Baas, F.; Koelman, J.H.; Haan, R.J. de; Engelen, B.G.M. van, et al
	2006	Long-term outcome in polymyositis and dermatomyositis	Bronner, I.M.; Meulen, M.F. van der; Visser, M. de; Kalmijn, S.; Venrooij, W.J.W. van, et al
	2006	Comparison of CMT1A and CMT2: similarities and differences.	Bienfait, H.M.; Verhamme, C.; Schaik, I.N. van; Koelman, J.H.; Visser, B.W. de, et al
	2005	Report on the Dutch consensus development meeting for implementation and further development of population screening for colorectal cancer based on FOBT.	Visser, M. de; Ballegooijen, M. van; Bloemers, S.M.; Deventer, S.J.H. van; Jansen, J.B.M.J., et al
	2005	Vier vernieuwingen in de CBO richtlijn myositis.	Jennekens, F.G.I.; Hoogendijk, J.E.; Engelen, B.G.M. van; Coo, I.F.M. de; Hoogen, F.H.J. van den, et al
	2005	[The practice guideline 'Dermatomyositis, polymyositis and sporadic inclusion body myositis']	Hoogendijk, J.E.; Bijlsma, J.W.J.; Engelen, B.G.M. van; Lindeman, E.J.M.; Royen-Kerkhof, A. van, et al
	2005	Inclusion body myositis Clinical features and clinical course of the disease in 64 patients.	Badrising, U.A.; Maat-Schieman, M.L.; Houwelingen, J.C. van; Doorn, P.A. van; Duinen, S.G. van, et al
	2005	Change in serum albumin and subsequent decline in functional status in older persons.	Schalk, B.W.; Visser, M. de; Penninx, B.W.; Baadenhuijsen, H.; Bouter, L.M., et al
	2004	Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis.	Badrising, U.A.; Schreuder, G.M.; Giphart, M.J.; Geleijns, K.; Verschuuren, J.J., et al
	2004	The epidemiology of the Lambert-Eaton myasthenic syndrome in the Netherlands.	Wirtz, P.W.; Dijk, J.G. van; Doorn, P.A. van; Engelen, B.G.M. van; Kooi, A.J. van der, et al
	2004	Molecular analysis of myophosphorylase deficiency in Dutch patients with McArdle's disease.	Martin, M.A.; Rubio, J.C.; Wevers, R.A.; Engelen, B.G.M. van; Steenbergen-Spanjers, G.C.H., et al
	1997	Vocational perspectives and neuromuscular disorders	Andries, F.; Wevers, C.W.J.; Wintzen, A.R.; Busch, H.F.M.; Höweler, C.J., et al
	1996	Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease	Gabreëls-Festen, A.A.W.M.; Hoogendijk, J.E.; Meijerink, P.H.S.; Gabreëls, F.J.M.; Bolhuis, P.A., et al
	1996	The clinical spectrum of limb girdle muscular dystrophy : a survey in the Netherlands	Kooi, A.J. van der; Barth, P.G.; Busch, H.F.M.; Haan, R.J. de; Ginjaar, H.B., et al
	1996	Two divergent types of nerve pathology in patients with different Po mutations in Charcot-Marie-Tooth disease	Gabreëls-Festen, A.A.W.M.; Hoogendijk, J.E.; Meijerink, P.H.S.; Gabreëls, F.J.M.; Bolhuis, P.A., et al
	1996	Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies	Meijerink, P.H.S.; Hoogendijk, J.E.; Gabreëls-Festen, A.A.W.M.; Zorn, I.; Veldman, H., et al
	1995	Ziekte van Wilson; ontmaskering met behulp van kernspinresonantie-tomografie	Berg, J.S.P. van den; Hoogenraad, T.U.; Duyn, J.A.; Verbeeten, B.; Aalfs, C.M., et al