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	501.	Tomaculous neuropathy in an airline pilot. [electronic resource] by Salazar, Guillermo J Producer: 20070927 In: Aviation, space, and environmental medicine vol. 78 Availability: No items available. Save to lists Add to cart (remove)
	502.	PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variability. [electronic resource] by Kawarai, Toshitaka Yamazaki, Hiroki Miyamoto, Ryosuke Takamatsu, Naoko Mori, Atsuko Osaki, Yusuke Orlacchio, Antonio Nodera, Hiroyuki Hashiguchi, Akihiro Higuchi, Yujiro Yoshimura, Akiko Takashima, Hiroshi Kaji, Ryuji Producer: 20200703 In: Neuromuscular disorders : NMD vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	503.	Neurophysiology of fastest voluntary muscle contraction in hereditary neuropathy. [electronic resource] by Logigian, E L Hefter, H H Reiners, K Freund, H J Producer: 19900223 In: Annals of neurology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	504.	[Chronic hereditary ataxic polyneuropathy]. [electronic resource] by Nogués, M Leiguarda, R Sevlever, G García, H Producer: 20001107 In: Medicina vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	505.	Genetic evaluation of inherited motor/sensory neuropathy. [electronic resource] by Chance, Phillip F Producer: 20050930 In: Supplements to Clinical neurophysiology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	506.	Differential diagnosis of Charcot-Marie-Tooth disease and related neuropathies. [electronic resource] by Pareyson, D Producer: 20040820 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	507.	Characterisation of pain in people with hereditary neuropathy with liability to pressure palsy. [electronic resource] by Beales, Darren Fary, Robyn Little, Cameron Nambiar, Shruti Sveinall, Hakon Yee, Yen Leng Tampin, Brigitte Mitchell, Tim Producer: 20180625 In: Journal of neurology vol. 264 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	508.	Corticosteroid- responsive asymmetric neuropathy with a myelin protein zero gene mutation. [electronic resource] by Watanabe, M Yamamoto, N Ohkoshi, N Nagata, H Kohno, Y Hayashi, A Tamaoka, A Shoji, S Producer: 20021004 In: Neurology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	509.	Variation in the classification of polyneuropathies among European physicians. [electronic resource] by Tankisi, H Johnsen, B Fuglsang-Frederiksen, A de Carvalho, M Fawcett, P R W Labarre-Vila, A Liguori, R Nix, W Olsen, M Schofield, I Producer: 20030508 In: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	510.	Hereditary neuropathies. [electronic resource] by Parman, Yesim Producer: 20071120 In: Current opinion in neurology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	511.	Genetic axonal neuropathies and neuronopathies of pre-natal and infantile onset. [electronic resource] by Yiu, Eppie M Ryan, Monique M Producer: 20130709 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)
	512.	Striking phenotypic variability in familial TRPV4-axonal neuropathy spectrum disorder. [electronic resource] by Aharoni, Sharon Harlalka, Gaurav Offiah, Amaka Shuper, Avinoam Crosby, Andrew H McEntagart, Meriel Producer: 20120430 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	513.	Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update. [electronic resource] by Tazir, Meriem Hamadouche, Tarik Nouioua, Sonia Mathis, Stephane Vallat, Jean-Michel Producer: 20150806 In: Journal of the neurological sciences vol. 347 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	514.	BICD2 mutational analysis in hereditary spastic paraplegia and hereditary motor and sensory neuropathy. [electronic resource] by Kropatsch, Regina Schmidt, Helena M Buttkereit, Pia Epplen, Jörg T Hoffjan, Sabine Producer: 20190705 In: Muscle & nerve vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	515.	The heterogeneity of Leber's congenital amaurosis. [electronic resource] by Aikawa, J Noro, T Tada, K Narisawa, K Hashimoto, T Producer: 19900125 In: Journal of inherited metabolic disease vol. 12 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	516.	Sensory-motor chronic neuropathy in two siblings: atypical presentation of tomaculous neuropathy. [electronic resource] by Malandrini, A Guazzi, G C Federico, A Producer: 19930129 In: Clinical neuropathology vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	517.	Peripheral neuropathy in German shepherd dogs. [electronic resource] by Furuoka, H Amanai, H Taniyama, H Matsui, T Producer: 19930106 In: Journal of comparative pathology vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	518.	Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion. [electronic resource] by Mouton, P Tardieu, S Gouider, R Birouk, N Maisonobe, T Dubourg, O Brice, A LeGuern, E Bouche, P Producer: 19990517 In: Neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	519.	Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene. [electronic resource] by Stögbauer, F Young, P Kerschensteiner, M Ringelstein, E B Assmann, G Funke, H Producer: 19980904 In: Muscle & nerve vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	520.	Isolated vitamin E deficiency mimicking distal hereditary motor neuropathy in a 13-year-old boy. [electronic resource] by Fusco, Carlo Frattini, Daniele Pisani, Francesco Gellera, Cinzia Della Giustina, Elvio Producer: 20090408 In: Journal of child neurology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1188 results.