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	961.	Hereditary neuropathy with liability to pressure palsies: assocation with central nervous system demyelination. [electronic resource] by Amato, A A Barohn, R J Producer: 19960529 In: Muscle & nerve vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	962.	Segmental duplications: an 'expanding' role in genomic instability and disease. [electronic resource] by Emanuel, B S Shaikh, T H Producer: 20011205 In: Nature reviews. Genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	963.	Neuromyotonia in mice with hereditary myelinopathies. [electronic resource] by Zielasek, J Martini, R Suter, U Toyka, K V Producer: 20000519 In: Muscle & nerve vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	964.	Differences between hereditary motor and sensory neuropathy type 2 and chronic idiopathic axonal neuropathy. A clinical and electrophysiological study. [electronic resource] by Teunissen, L L Notermans, N C Franssen, H van der Graaf, Y Oey, P L Linssen, W H van Engelen, B G Ippel, P F van Dijk, G W Gabreëls-Festen, A A Wokke, J H Producer: 19970801 In: Brain : a journal of neurology vol. 120 ( Pt 6) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	965.	Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. [electronic resource] by Wallace, D C Singh, G Lott, M T Hodge, J A Schurr, T G Lezza, A M Elsas, L J Nikoskelainen, E K Producer: 19890119 In: Science (New York, N.Y.) vol. 242 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	966.	Hereditary neuropathy with liability to pressure palsies: distinguishing clinical and electrophysiological features among patients with multiple entrapment neuropathy. [electronic resource] by Hirota, N Kaji, R Yoshikawa, H Nishimura, T Ikeda, T Yanagihara, T Kimura, J Producer: 19970110 In: Journal of the neurological sciences vol. 139 Availability: No items available. Save to lists Add to cart (remove)
	967.	Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristics. [electronic resource] by Elliott, J L Kwon, J M Goodfellow, P J Yee, W C Producer: 19970226 In: Neurology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	968.	Dysmyelinating sensory-motor neuropathy in merosin-deficient congenital muscular dystrophy. [electronic resource] by Di Muzio, A De Angelis, M V Di Fulvio, P Ratti, A Pizzuti, A Stuppia, L Gambi, D Uncini, A Producer: 20030501 In: Muscle & nerve vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	969.	Cellular characterization of MPZ mutations presenting with diverse clinical phenotypes. [electronic resource] by Lee, Yi-Chung Lin, Kon-Ping Chang, Ming-Hong Liao, Yi-Chu Tsai, Ching-Piao Liao, Kwong-Kum Soong, Bing-Wen Producer: 20110126 In: Journal of neurology vol. 257 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	970.	[Multifocal motor neuropathies with conduction block: long-term follow-up of ten patients treated with IVIg]. [electronic resource] by Cros, D Drake, K Producer: 20061130 In: Revue neurologique vol. 162 Spec No 1 Availability: No items available. Save to lists Add to cart (remove)
	971.	Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephaly. [electronic resource] by Gonzaga-Jauregui, Claudia Lotze, Timothy Jamal, Leila Penney, Samantha Campbell, Ian M Pehlivan, Davut Hunter, Jill V Woodbury, Suzanne L Raymond, Gerald Adesina, Adekunle M Jhangiani, Shalini N Reid, Jeffrey G Muzny, Donna M Boerwinkle, Eric Lupski, James R Gibbs, Richard A Wiszniewski, Wojciech Producer: 20140220 In: JAMA neurology vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	972.	Proteasome impairment in neural cells derived from HMSN-P patient iPSCs. [electronic resource] by Murakami, Nagahisa Imamura, Keiko Izumi, Yuishin Egawa, Naohiro Tsukita, Kayoko Enami, Takako Yamamoto, Takuya Kawarai, Toshitaka Kaji, Ryuji Inoue, Haruhisa Producer: 20171030 In: Molecular brain vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	973.	Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype. [electronic resource] by Rautenstrauss, B Nelis, E Grehl, H Pfeiffer, R A Van Broeckhoven, C Producer: 19950228 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	974.	Hereditary motor and sensory neuropathy type 2C is genetically distinct from types 2B and 2D. [electronic resource] by Nagamatsu, M Jenkins, R B Schaid, D J Klein, D M Dyck, P J Producer: 20000601 In: Archives of neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	975.	Distinctive patterns of sonographic nerve enlargement in Charcot-Marie-Tooth type 1A and hereditary neuropathy with pressure palsies. [electronic resource] by Goedee, Stephan H Brekelmans, Geert J F van den Berg, Leonard H Visser, Leo H Producer: 20150901 In: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	976.	A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies. [electronic resource] by Lorenzetti, D Pareyson, D Sghirlanzoni, A Roa, B B Abbas, N E Pandolfo, M Di Donato, S Lupski, J R Producer: 19950213 In: American journal of human genetics vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	977.	Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases. [electronic resource] by Schenone, A Abbruzzese, M Uccelli, A Mandich, P James, R Bellone, E Giunchedi, M Rolando, S Capello, E Mandich R [corrected to Mandich, P ] Producer: 19940624 In: Journal of the neurological sciences vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	978.	Glial fibrillary acidic protein as a marker of axonal damage in chronic neuropathies. [electronic resource] by Notturno, Francesca Capasso, Margherita DeLauretis, Angelo Carpo, Marinella Uncini, Antonino Producer: 20090825 In: Muscle & nerve vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	979.	N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome. [electronic resource] by Rakocević-Stojanović, V Milić-Rasić, V Perić, S Baets, J Timmerman, V Dierick, I Pavlović, S De Jonghe, P Producer: 20101122 In: Journal of the neurological sciences vol. 296 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	980.	Different nerve ultrasound patterns in charcot-marie-tooth types and hereditary neuropathy with liability to pressure palsies. [electronic resource] by Padua, Luca Coraci, Daniele Lucchetta, Marta Paolasso, Ilaria Pazzaglia, Costanza Granata, Giuseppe Cacciavillani, Mario Luigetti, Marco Manganelli, Fiore Pisciotta, Chiara Piscosquito, Giuseppe Pareyson, Davide Briani, Chiara Producer: 20171212 In: Muscle & nerve vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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