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Browsing by Author Faber, C.G.

Full Text	Issue Date	Title	Author(s)
	2012	Functional profiles of SCN9A variants in dorsal root ganglion neurons and superior cervical ganglion neurons correlate with autonomic symptoms in small fibre neuropathy	Han, C.; Hoeijmakers, J.G.; Liu, S.; Gerrits, M.M.; te Morsche, R.H., et al
	2012	[Small fibre neuropathy: knowledge is power].	Hoeijmakers, J.G.; Bakkers, M.; Blom, E.W.; Drenth, J.P.H.; Merkies, I.S., et al
	2012	Nav1.7-related small fiber neuropathy: impaired slow-inactivation and DRG neuron hyperexcitability.	Han, C.; Hoeijmakers, J.G.; Ahn, H.S.; Zhao, P.; Shah, P., et al
	2012	Gain of function Nanu1.7 mutations in idiopathic small fiber neuropathy.	Faber, C.G.; Hoeijmakers, J.G.; Ahn, H.S.; Cheng, X.; Han, C., et al
	2012	Effect of enzyme therapy and prognostic factors in 69 adults with Pompe disease: an open-label single-center study	de Vries, J.M.; van der Beek, N.A.; Hop, W.C.J.; Karstens, F.P.; Wokke, J.H.J., et al
	2012	Long-term remission of CIDP after pulsed dexamethasone or short-term prednisolone treatment	Eftimov, F.; Vermeulen, M; Doorn, P.A. van; Brusse, E.; Schaik, I.N. van, et al
	2012	Pain relief and quality-of-life improvement after spinal cord stimulation in painful diabetic polyneuropathy: a pilot study	Pluijms, W.A.; Slangen, R.; Bakkers, M.; Faber, C.G.; Merkies, I.S., et al
	2011	Intra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7.	Estacion, M.; Han, C.; Choi, J.S.; Hoeijmakers, J.G.; Lauria, G., et al
	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, et al
	2010	Pulsed high-dose dexamethasone versus standard prednisolone treatment for chronic inflammatory demyelinating polyradiculoneuropathy (PREDICT study): a double-blind, randomised, controlled trial.	Schaik, I.N. van; Eftimov, F.; Doorn, P.A. van; Brusse, E.; Berg, L.H. van den, et al
	2009	Muscle ultrasound measurements and functional muscle parameters in non-dystrophic myotonias suggest structural muscle changes.	Trip, J.; Pillen, S.; Faber, C.G.; Engelen, B.G.M. van; Zwarts, M.J., 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	Health status in non-dystrophic myotonias: close relation with pain and fatigue.	Trip, J.; Vries, J. de; Drost, G.; Ginjaar, H.B.; Engelen, B.G.M. van, 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
	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
	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	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
	2007	Warm-up phenomenon in myotonia associated with the V445M sodium channel mutation.	Trip, J.; Faber, C.G.; Ginjaar, H.B.; Engelen, B.G.M. van; Drost, G.
	2007	The Dutch neuromuscular database CRAMP (Computer Registry of All Myopathies and Polyneuropathies): development and preliminary data.	Engelen, B.G.M. van; Veenendaal, H. van; Doorn, P.A. van; Faber, C.G.; Hoeven, J.H. van, et al
	2006	Drug treatment for myotonia.	Trip, J.; Drost, G.; Engelen, B.G.M. van; Faber, C.G.
	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	Het spectrum van de erfelijke skeletspierkanalopathieën	Trip, J.; Drost, G.; Ginjaar, H.B.; Engelen, B.G.M. van; Faber, C.G.
	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