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Full Text	Issue Date	Title	Author(s)
	2011	Coffee and muscle cramps.	Voermans, N.C.; Engelen, B.G.M. van
	2011	Neurological picture. The astrologist's posture: a useful clinical observation	Smits, B.W.; Sluijs, B.M. van der; van Engelen, B.G.
	2011	Accelerated skeletal muscle ageing is a molecular signature in OPMD.	Venema, A.; Anvar, S.A.; Hoen, P.A.C. 't; Sluijs, B.M. van der; Engelen, B.G. van; Maarel, S.M. van der; Raz, V.
	2011	High frequency of neuropathic pain in Ehlers-Danlos syndrome: an association with axonal polyneuropathy and compression neuropathy?	Voermans, N.C.; Knoop, H.; Engelen, B.G.M. van
	2011	Screening for antecedent Campylobacter jejuni infections and anti-ganglioside antibodies in idiopathic neuralgic amyotrophy	Eijk, J.J.J. van; Alfen, N. van; Tio-Gillen, A.P.; Maas, Marijke; Herbrink, P.; Portier, R.P.; Doorn, P.A. van; Engelen, B.G. van; Jacobs, B.C.
	2011	Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores.	Sambuughin, N.; Yau, K.S.; Duff, R.M.; Bayarsaikhan, M.; Lu, S.J.; Gonzalez-Mera, L.; Sivadorai, P.; Nowak, K.J.; Ravenscroft, G.; Mastaglia, F.L.; North, K.N.; Ilkovski, B.; Kremer, H.; Lammens, M.M.; Engelen, B.G.M. van; Fabian, V.; Lamont, P.; Davis, M.R.; Laing, N.G.; Goldfarb, L.G.
	2011	Diagnostic yield of muscle fibre conduction velocity in myopathies	Blijham, P.J.; Engelen, B.G. van; Drost, G.; Stegeman, D.F.; Schelhaas, H.J.; Zwarts, M.J.
	2011	Nature and frequency of respiratory involvement in chronic progressive external ophthalmoplegia	Smits, B.W.; Heijdra, Y.F.; Cuppen, F.; Engelen, B.G. van
	2011	Speech pathology interventions in patients with neuromuscular diseases: a systematic review	Knuijt, S.; Cup, E.H.C.; Pieterse, A.J.; Swart, B.J.M. de; Wilt, G.J. van der; Engelen, B.G.M. van; Oostendorp, R.A.B.; Hendricks, H.T.
	2011	Disease impact in chronic progressive external ophthalmoplegia: more than meets the eye	Smits, B.W.; Fermont, J.; Delnooz, C.C.S.; Kalkman, J.S.; Bleijenberg, G.; Engelen, B.G.M. van
	2011	Mitochondrial enzymes discriminate between mitochondrial disorders and chronic fatigue syndrome	Smits, B.; Heuvel, L.P.W.J. van den; Knoop, H.; Kusters, B.; Janssen, A.; Borm, G.F.; Bleijenberg, G.; Rodenburg, R.J.T.; Engelen, B.G.M. van
	2011	Fatigue is associated with muscle weakness in Ehlers-Danlos syndrome: an explorative study	Voermans, N.C.; Knoop, H.; Bleijenberg, G.; Engelen, B.G.M. van
	2011	Rituximab treatment in patients with refractory inflammatory myopathies	Mahler, E.A.; Blom, M.; Voermans, N.C.; Engelen, B.G. van; Riel, P.L. van; Vonk, M.C.
	2011	High disease impact of myotonic dystrophy type 2 on physical and mental functioning	Tieleman, A.A.; Jenks, K.M.; Kalkman, J.S.; Borm, G.F.; Engelen, B.G.M. van
	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.; Kerkhoff, H.; Engelen, B.G. van; Lammens, M.M.Y.; Visser, M. de; Baas, F.; Kooi, A.J. van der
	2011	High disease impact of myotonic dystrophy type 2 on physical and mental functioning	Tieleman, A.A.; Jenks, K.M.; Kalkman, J.S.; Borm, G.F.; Engelen, B.G.M. van
	2011	Mild muscular features in tenascin-x knockout mice, a model of ehlers-danlos syndrome	Voermans, N.C.; Verrijp, K.; Eshuis, L.; Balemans, M.C.M.; Egging, D.F.; Sterrenburg, E.; Rooij, I.A. van; Laak, J.A.W.M. van der; Schalkwijk, J.; Maarel, S. van der; Lammens, M.M.Y.; Engelen, B.G. van
	2011	Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype	Coenen, M.J.H.; Tieleman, A.A.; Schijvenaars, M.M.V.A.P.; Leferink, M.; Ranum, L.P.; Scheffer, H.; Engelen, B.G. van
	2011	Living with myotonic dystrophy; what can be learned from couples? A qualitative study	Cup, E.H.C.; Kinebanian, A.; Satink, T.J.; Pieterse, A.J.; Hendricks, H.T.; Oostendorp, R.A.B.; Wilt, G.J. van der; Engelen, B.G.M. van
	2011	Implementation of multidisciplinary advice to allied health care professionals regarding the management of their patients with neuromuscular diseases	Cup, E.H.C.; Pieterse, A.J.; Hendricks, H.T.; Engelen, B.G.M. van; Oostendorp, R.A.B.; Wilt, G.J. van der
	2011	Causes and consequences of cerebral small vessel disease. The RUN DMC study: a prospective cohort study. Study rationale and protocol	Norden, A.G.W. van; Laat, K.F. de; Gons, R.A.R.; Uden, I.W.M. van; Dijk, E.J. van; Oudheusden, L.J. van; Esselink, R.A.J.; Bloem, B.R.; Engelen, B.G. van; Zwarts, M.J.; Tendolkar, I.; Olde-Rikkert, M.G.M.; Vlugt, M.J. van der; Zwiers, M.P.; Norris, D.G.; Leeuw, F.E. de
	2011	Effects of shared medical appointments on quality of life and cost-effectiveness for patients with a chronic neuromuscular disease. Study protocol of a randomized controlled trial	Seesing, F.M.; Drost, G.; Wilt, G.J. van der; Engelen, B.G.M. van
	2010	The neglected brain in myotonic dystrophy types 1 and 2.	Engelen, B.G.M. van; Leeuw, F.E. de
	2010	TDP-43 plasma levels do not differentiate sporadic inclusion body myositis from other inflammatory myopathies.	Kuiperij, H.B.; Abdo, W.; Engelen, B.G.M. van; Schelhaas, H.J.; Verbeek, M.M.
	2010	Quality of life in the classic and hypermobility types of Elhers-Danlos syndrome : reply	Voermans, N.C.; Engelen, Baziel van
	2010	171st ENMC international workshop: Standards of care and management of facioscapulohumeral muscular dystrophy.	Tawil, R.; Maarel, S. van der; Padberg, G.W.A.M.; Engelen, B.G.M. van
	2010	The prevalence of dysphagia in neuromuscular disorders	Knuijt, S.; Kalf, J.G.; Swart, B.J.M. de; Drost, G.; Hendricks, H.T.; Geurts, A.C.H.; Engelen, B.G.M. van
	2010	Speech Pathology Interventions in Patients with Neuromuscular Diseases: A Systematic Review.	Knuijt, S.; Cup, E.H.C.; Pieterse, A.J.; Swart, B.J.M. de; Wilt, G.J. van der; Engelen, B.G.M. van; Oostendorp, R.A.B.; Hendricks, H.T.
	2010	Facioscapulohumerale spierdystrofie	Wilbers, J.; Frants, R.R.; Engelen, B.G.M. van; Padberg, G.W.A.M.; Maarel, S.M. van der
	2010	Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathy.	Voermans, N.C.; Guillard, M.; Doedee, R.; Lammens, M.M.Y.; Huizing, M.; Padberg, G.W.A.M.; Wevers, R.A.; Engelen, B.G.M. van; Lefeber, D.J.
	2010	Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores.	Sambuughin, N.; Yau, K.S.; Olive, M.; Duff, R.M.; Bayarsaikhan, M.; Lu, S.; Gonzalez-Mera, L.; Sivadorai, P.; Nowak, K.J.; Ravenscroft, G.; Mastaglia, F.L.; North, K.N.; Ilkovski, B.; Kremer, J.M.J.; Lammens, M.M.Y.; Engelen, B.G.M. van; Fabian, V.; Lamont, P.; Davis, M.R.; Laing, N.G.; Goldfarb, L.G.
	2010	Isolated eyelid closure myotonia in two families with sodium channel myotonia.	Stunnenberg, B.C.; Ginjaar, H.B.; Trip, J.; Faber, C.G.; Engelen, B.G.M. van; Drost, G.
	2010	Pain in Ehlers-Danlos syndrome is common, severe, and associated with functional impairment	Voermans, N.C.; Knoop, H.; Bleijenberg, G.; Engelen, B.G.M. van
	2010	Molecular therapy in myotonic dystrophy: focus on RNA gain-of-function.	Mulders, S.A.M.; Engelen, B.G.M. van; Wieringa, B.; Wansink, D.G.
	2010	Radicular dysfunction due to spinal deformities in Marfan syndrome at older age: three case reports.	Voermans, N.C.; Hosman, A.J.F.; Alfen, N. van; Bartels, R.H.M.A.; Kleuver, M. de; Akker, J.W. op den; Engelen, B.G.M. van
	2010	Postural instability in Charcot-Marie-Tooth type 1A patients is strongly associated with reduced somatosensation.	Linden, M.H. van der; Linden, S.C. van der; Hendricks, H.T.; Engelen, B.G.M. van; Geurts, A.C.H.
	2010	Muscle characteristics and altered myofascial force transmission in tenascin-X-deficient mice, a mouse model of Ehlers-Danlos syndrome.	Huijing, P.A.; Voermans, N.C.; Baan, G.C.; Buse, T.E.; Engelen, B.G.M. van; Haan, A. de
	2010	Increased plasticity of the nuclear envelope and hypermobility of telomeres due to the loss of A-type lamins.	Vos, W.H. De; Houben, F.; Hoebe, R.A.; Hennekam, R.; Engelen, B.G.M. van; Manders, E.M.; Ramaekers, F.C.S.; Broers, J.L.; Oostveldt, P. Van
	2010	New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype.	Delnooz, C.C.S.; Lefeber, D.J.; Langemeijer, S.M.C.; Hoffjan, S.; Dekomien, G.; Zwarts, M.J.; Engelen, B.G.M. van; Wevers, R.A.; Schelhaas, H.J.; Warrenburg, B.P.C. van de
	2010	Fatigue is a frequent and clinically relevant problem in Ehlers-Danlos Syndrome.	Voermans, N.C.; Knoop, H.; Kamp, N. van de; Hamel, B.C.J.; Bleijenberg, G.; Engelen, B.G.M. van
	2010	Only fat infiltrated muscles in resting lower leg of FSHD patients show disturbed energy metabolism.	Kan, H.E.; Klomp, D.W.J.; Wohlgemuth, M.; Loosbroek-Wagemans, I.C.W.; Engelen, B.G.M. van; Padberg, G.W.A.M.; Heerschap, A.
	2010	Poor sleep quality and fatigue but no excessive daytime sleepiness in myotonic dystrophy type 2.	Tieleman, A.A.; Knoop, H.; Logt, A.E. van de; Bleijenberg, G.; Engelen, B.G.M. van; Overeem, S.
	2010	Employment status of patients with neuromuscular diseases in relation to personal factors, fatigue and health status: a secondary analysis.	Minis, M.A.; Kalkman, J.S.; Akkermans, R.P.; Engels, J.A.; Huijbregts, P.A.; Bleijenberg, G.; Oostendorp, R.A.B.; Engelen, B.G.M. van
	2010	Clinical features of facioscapulohumeral muscular dystrophy 2.	Greef, J.C. de; Lemmers, R.J.; Camano, P.; Day, J.W.; Sacconi, S.; Dunand, M.; Engelen, B.G.M. van; Kiuru-Enari, S.; Padberg, G.W.A.M.; Rosa, A.L.; Desnuelle, C.; Spuler, S.; Tarnopolsky, M.; Venance, S.L.; Frants, R.R.; Maarel, S.M. van der; Tawil, R.
	2010	Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy	Cats, E.A.; Pol, W.L. van der; Piepers, S.; Franssen, H.; Jacobs, B.C.; Berg-Vos, R.M. van den; Kuks, J.B.M.; Doorn, P.A. van; Engelen, B.G.M. van; Verschuuren, J.J.; Wokke, J.H.J.; Veldink, J.H.; Berg, L.H. van den
	2010	Effect of aerobic exercise training and cognitive behavioural therapy on reduction of chronic fatigue in patients with facioscapulohumeral dystrophy: protocol of the FACTS-2-FSHD trial.	Voet, N.B.M.; Bleijenberg, G.; Padberg, G.W.A.M.; Engelen, B.G.M. van; Geurts, A.C.H.
	2010	Strength training and aerobic exercise training for muscle disease	Voet, N.B.M.; Kooi, E.L. van der; Riphagen, I.I.; Lindeman, E.; Engelen, B.G.M. van; Geurts, A.C.H.
	2010	Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.	Leen, W.G.; Klepper, J.; Verbeek, M.M.; Leferink, M.; Hofste, T.; Engelen, B.G.M. van; Wevers, R.A.; Arthur, T.; Bahi-Buisson, N.; Ballhausen, D.; Bekhof, J.; Bogaert, P. van; Carrilho, I.; Chabrol, B.; Champion, M.P.; Coldwell, J.; Clayton, P.; Donner, E.; Evangeliou, A.; Ebinger, F.; Farrell, K.; Forsyth, R.J.; Goede, C.G. de; Gross, S.; Grunewald, S.; Holthausen, H.; Jayawant, S.; Lachlan, K.; Laugel, V.; Leppig, K.; Lim, M.J.; Mancini, G.; Marina, A.D.; Martorell, L.; McMenamin, J.; Meuwissen, M.E.; Mundy, H.; Nilsson, N.O.; Panzer, A.; Poll-The, B.T.; Rauscher, C.; Rouselle, C.M.; Sandvig, I.; Scheffner, T.; Sheridan, E.; Simpson, N.; Sykora, P.; Tomlinson, R.; Trounce, J.; Webb, D.; Weschke, B.; Scheffer, H.; Willemsen, M.A.A.P.
	2009	TDP-43 accumulation is common in myopathies with rimmed vacuoles.	Kusters, B.; Hoeve, B.J.A. van; Schelhaas, H.J.; Laak, H.J. ter; Engelen, B.G.M. van; Lammens, M.M.Y.
	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.; Mauser, H.; Kerkhoff, H.; Engelen, B.G.M. van; Visser, M. de; Baas, F.

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