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	481.	Hereditary motor and sensory neuropathy with proximal dominant involvement: clinical, pathological, and genetic features. [electronic resource] by Nakagawa, M Takashima, H Suehara, M Saito, M Saito, A Kanzato, N Matsuzaki, T Hirata, K Izumo, S Terwilliger, J D Osame, M Producer: 19991221 In: Annals of the New York Academy of Sciences vol. 883 Availability: No items available. Save to lists Add to cart (remove)
	482.	Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 gene. [electronic resource] by Ionasescu, V V Ionasescu, R Searby, C Neahring, R Producer: 19951017 In: Neurology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	483.	Retinal changes in familial peripheral sensory and motor neuropathy associated with anterior cervical hypertrichosis. [electronic resource] by Garty, B Z Snir, M Kremer, I Yassur, Y Trattner, A Producer: 19971027 In: Journal of pediatric ophthalmology and strabismus vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	484.	[A patient with Kennedy-Alter-Sung syndrome showing cardiomyopathy]. [electronic resource] by Hattori, T Ikeda, S Yoshida, K Yanagisawa, N Furihata, K Yoshida, K Producer: 19961001 In: Rinsho shinkeigaku = Clinical neurology vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	485.	Type I spinal muscular atrophy can mimic sensory-motor axonal neuropathy. [electronic resource] by Anagnostou, Evdokia Miller, Steven P Guiot, Marie-Christine Karpati, Greoge Simard, Louise Dilenge, Marie-Emmanuelle Shevell, Michael I Producer: 20050503 In: Journal of child neurology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	486.	Perrault syndrome: evidence for progressive nervous system involvement. [electronic resource] by Fiumara, Agata Sorge, Giovanni Toscano, Antonio Parano, Enrico Pavone, Lorenzo Opitz, John M Producer: 20050124 In: American journal of medical genetics. Part A vol. 128A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	487.	Severe hypotension and hepatic dysfunction in a patient undergoing scoliosis surgery in the prone position. [electronic resource] by Yuen, V M Y Chow, B F M Irwin, M G Producer: 20050908 In: Anaesthesia and intensive care vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	488.	A case of rare recessive oculopharyngeal muscular dystrophy (OPMD) coexisting with hereditary neuropathy with liability to pressure palsies (HNPP). [electronic resource] by Marsh, Eleanor A Robinson, David O Producer: 20080814 In: Clinical neurology and neurosurgery vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	489.	Hereditary motor sensory neuropathy (type 1) presenting with transient and persistent central nervous system manifestations: a novel genetic mutation. [electronic resource] by Absoud, Michael Brueton, Louise Gupta, Rajat Quinlivan, Ros Wassmer, Evangeline Producer: 20110506 In: Developmental medicine and child neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	490.	[Charcot-Marie-Tooth (CMT) disease: an update]. [electronic resource] by Vallat, Jean-Michel Funalot, Benoît Producer: 20101222 In: Medecine sciences : M/S vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	491.	Severe Dejerine-Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion. [electronic resource] by Voermans, Nicol C Kleefstra, Tjitske Gabreëls-Festen, Anneke A Faas, Brigitte H W Kamsteeg, Erik-Jan Houlden, Henry Laurá, Matilde Polke, James M Pandraud, Amelie van Ruissen, Fred van Engelen, Baziel G Reilly, Mary M Producer: 20121029 In: Journal of the peripheral nervous system : JPNS vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	492.	A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy. [electronic resource] by Parker, W D Oley, C A Parks, J K Producer: 19890615 In: The New England journal of medicine vol. 320 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	493.	Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy. [electronic resource] by Vilkki, J Savontaus, M L Kalimo, H Nikoskelainen, E K Producer: 19890720 In: Human genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	494.	Mutation analysis of the human pancreatic phospholipase A2 gene in a family with distal hereditary motor neuropathy type II linked to 12q24. [electronic resource] by Beuten, J De Vriendt, E De Jonghe, P Martin, J J Van Broeckhoven, C Timmerman, V Producer: 19970612 In: Neuroscience letters vol. 223 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	495.	A clinicophysiologic study of central and peripheral motor conduction in hereditary demyelinating motor and sensory neuropathy. [electronic resource] by Mano, Y Nakamuro, T Ikoma, K Takayanagi, T Mayer, R F Producer: 19930415 In: Electromyography and clinical neurophysiology vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	496.	Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models. [electronic resource] by Snipes, G J Suter, U Producer: 19960119 In: Brain pathology (Zurich, Switzerland) vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	497.	Facial nerve dysfunction in hereditary motor and sensory neuropathy type I and III. [electronic resource] by Glocker, F X Rösler, K M Linden, D Heinen, F Hess, C W Lücking, C H Producer: 19990923 In: Muscle & nerve vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	498.	[Sensorimotor polyneuropathy in Hajdu-Cheney syndrome. Apropos of a case]. [electronic resource] by Paz-Sendín, L Hernández-González, G González-Torres, R Gámez-Morales, L Suárez-Conejero, A M Producer: 20011231 In: Revista de neurologia vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	499.	Hereditary neuropathy with liability to pressure palsies: electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation. [electronic resource] by Del Colle, R Fabrizi, G M Turazzini, M Cavallaro, T Silvestri, M Rizzuto, N Producer: 20030731 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	500.	CNS involvement in hereditary neuropathy with pressure palsies (HNPP). [electronic resource] by Tackenberg, B Möller, J C Rindock, H Bien, S Sommer, N Oertel, W H Rosenow, F Schepelmann, K Hamer, H M Bandmann, O Producer: 20070116 In: Neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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