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	981.	Familial spastic paraparesis syndrome associated with HTLV-I infection. [electronic resource] by Salazar-Grueso, E F Holzer, T J Gutierrez, R A Casey, J M Desai, S M Devare, S G Dawson, G Roos, R P Producer: 19900925 In: The New England journal of medicine vol. 323 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	982.	Hereditary motor and sensory neuropathies. [electronic resource] by Vance, J M Producer: 19910411 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	983.	De novo mutation of the myelin Po gene in Déjérine-Sottas disease (hereditary motor and sensory neuropathy type III): two amino acid insertion after Asp 118. [electronic resource] by Ikegami, T Nicholson, G Ikeda, H Ishida, A Johnston, H Wise, G Ouvrier, R Hayasaka, K Producer: 19990630 In: Human mutation vol. Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	984.	Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia. [electronic resource] by Bouhouche, A Benomar, A Bouslam, N Chkili, T Yahyaoui, M Producer: 20060717 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	985.	Mutation analysis of PMP22 in Slovak patients with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies. [electronic resource] by Resko, Peter Radvansky, Jan Odnogova, Zuzana Baldovic, Marian Minarik, Gabriel Polakova, Helena Palffy, Roland Kadasi, Ludevit Producer: 20120306 In: General physiology and biophysics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	986.	Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency. [electronic resource] by Bertini, E Dionisi-Vici, C Garavaglia, B Burlina, A B Sabatelli, M Rimoldi, M Bartuli, A Sabetta, G DiDonato, S Producer: 19920402 In: European journal of pediatrics vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	987.	Mitochondrial cytopathy presenting as hereditary sensory neuropathy with progressive external ophthalmoplegia, ataxia and fatal myoclonic epileptic status. [electronic resource] by van Domburg, P H Gabreëls-Festen, A A Gabreëls, F J de Coo, R Ruitenbeek, W Wesseling, P ter Laak, H Producer: 19960813 In: Brain : a journal of neurology vol. 119 ( Pt 3) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	988.	Vestibular neuropathy accompanying auditory and peripheral neuropathies. [electronic resource] by Fujikawa, S Starr, A Producer: 20010103 In: Archives of otolaryngology--head & neck surgery vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	989.	Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese. [electronic resource] by Chen, Shyue-Ru Lin, Kon-Ping Kuo, Hung-Chou Chen, Chiung-Mei Hsieh, Sung-Tsang Lee, Ming-Jen Yang, Chih-Chao Liu, Chin-San Huang, Chin-Chang Lyu, Rong-Kuo Ro, Long-Sun 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)
	990.	The LITAF/SIMPLE I92V sequence variant results in an earlier age of onset of CMT1A/HNPP diseases. [electronic resource] by Sinkiewicz-Darol, Elena Lacerda, Andressa Ferreira Kostera-Pruszczyk, Anna Potulska-Chromik, Anna Sokołowska, Beata Kabzińska, Dagmara Brunetti, Craig R Hausmanowa-Petrusewicz, Irena Kochański, Andrzej Producer: 20150827 In: Neurogenetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	991.	PMP22-Related neuropathies and other clinical manifestations in Chinese han patients with charcot-marie-tooth disease type 1. [electronic resource] by Zhan, Yajing Zi, Xiaohong Hu, Zhengmao Peng, Ying Wu, Lingqian Li, Xiaobo Jiang, Mingming Liu, Lei Xie, Yongzhi Xia, Kun Tang, Beisha Zhang, Ruxu Producer: 20150820 In: Muscle & nerve vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	992.	Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex. [electronic resource] by Umehara, F Takenaga, S Nakagawa, M Takahashi, K Izumo, S Matsumuro, K Sakota, S Nishimura, T Yoshikawa, H Osame, M Producer: 19940317 In: Acta neuropathologica vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	993.	Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group. [electronic resource] by Lopes, J LeGuern, E Gouider, R Tardieu, S Abbas, N Birouk, N Gugenheim, M Bouche, P Agid, Y Brice, A Producer: 19960725 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	994.	Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy. [electronic resource] by Khajavi, Mehrdad Shiga, Kensuke Wiszniewski, Wojciech He, Feng Shaw, Chad A Yan, Jiong Wensel, Theodore G Snipes, G Jackson Lupski, James R Producer: 20071004 In: American journal of human genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	995.	Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: a comparison. [electronic resource] by Hung, Chia-Cheng Lee, Chien-Nan Lin, Chia-Yun Cheng, Wen-Fang Chen, Chi-An Hsieh, Sung-Tsang Yang, Chih-Chao Jong, Yuh-Jyh Su, Yi-Ning Lin, Win-Li Producer: 20080417 In: Electrophoresis vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	996.	HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL. [electronic resource] by Šafka Brožková, D Haberlová, J Mazanec, R Laštůvková, J Seeman, P Producer: 20170522 In: Clinical genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	997.	Clinical and pathological observations in men lacking the gap junction protein connexin 32. [electronic resource] by Hahn, A F Ainsworth, P J Naus, C C Mao, J Bolton, C F Producer: 20010301 In: Muscle & nerve. Supplement vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	998.	Strachan's syndrome: variation on a theme. [electronic resource] by Cockerell, O C Ormerod, I E Producer: 19930811 In: Journal of neurology vol. 240 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	999.	Hereditary neuropathy with liability to pressure palsies in childhood. [electronic resource] by Gabreëls-Festen, A A Gabreëls, F J Joosten, E M Vingerhoets, H M Renier, W O Producer: 19920902 In: Neuropediatrics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1000.	Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I). [electronic resource] by Gabreëls-Festen, A A Joosten, E M Gabreëls, F J Jennekens, F G Janssen-van Kempen, T W Producer: 19920521 In: Journal of the neurological sciences vol. 107 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.