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	1021.	Tract-Specific Diffusion Tensor Imaging Reveals Laterality of Neurological Symptoms in Patients with Cervical Compression Myelopathy. [electronic resource] by Maki, Satoshi Koda, Masao Saito, Junya Takahashi, Sho Inada, Taigo Kamiya, Koshiro Ota, Mitsutoshi Iijima, Yasushi Masuda, Yoshitada Matsumoto, Koji Kojima, Masatoshi Takahashi, Kazuhisa Obata, Takayuki Yamazaki, Masashi Furuya, Takeo Producer: 20170907 In: World neurosurgery vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1022.	Axonal dysfunction, dysmyelination, and conduction failure in hereditary neuropathy with liability to pressure palsies. [electronic resource] by Farrar, Michelle A Park, Susanna B Krishnan, Arun V Kiernan, Matthew C Lin, Cindy S-Y Producer: 20140708 In: Muscle & nerve vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1023.	Reduction of knee torques and leg-related functional abilities in hereditary motor and sensory neuropathy. [electronic resource] by Lindeman, E Leffers, P Reulen, J Spaans, F Drukker, J Producer: 19941208 In: Archives of physical medicine and rehabilitation vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1024.	Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study. [electronic resource] by Nelis, E Van Broeckhoven, C De Jonghe, P Löfgren, A Vandenberghe, A Latour, P Le Guern, E Brice, A Mostacciuolo, M L Schiavon, F Palau, F Bort, S Upadhyaya, M Rocchi, M Archidiacono, N Mandich, P Bellone, E Silander, K Savontaus, M L Navon, R Goldberg-Stern, H Estivill, X Volpini, V Friedl, W Gal, A Producer: 19961002 In: European journal of human genetics : EJHG vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1025.	Lethal neonatal autosomal recessive axonal sensorimotor polyneuropathy. [electronic resource] by Vedanarayanan, V V Smith, S Subramony, S H Bock, G O Evans, O B Producer: 19981027 In: Muscle & nerve vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1026.	Polyneuropathies in teenagers: a clinicopathological study of 45 cases. [electronic resource] by Kararizou, E Karandreas, N Davaki, P Davou, R Vassilopoulos, D Producer: 20060809 In: Neuromuscular disorders : NMD vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1027.	Comprehensive analysis of the TRPV4 gene in a large series of inherited neuropathies and controls. [electronic resource] by Fawcett, Katherine A Murphy, Sinead M Polke, James M Wray, Selina Burchell, Victoria S Manji, Hadi Quinlivan, Ros M Zdebik, Anselm A Reilly, Mary M Houlden, Henry Producer: 20130116 In: Journal of neurology, neurosurgery, and psychiatry vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1028.	Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria. [electronic resource] by Robert-Varvat, Florence Jousserand, Guillemette Bouhour, Françoise Vial, Christophe Cintas, Pascal Echaniz-Laguna, Andoni Delmont, Emilien Clavelou, Pierre Chauplannaz, Guy Jomir, Laurent Pereon, Yann Leonard-Louis, Sarah Manel, Veronique Antoine, Jean-Christophe Lacour, Arnaud Camdessanche, Jean-Philippe Producer: 20190128 In: Muscle & nerve vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1029.	Duffy locus linkage and HLA antigens in hereditary motor-sensory neuropathy. [electronic resource] by Nevsímalová, S Prazák, J Herzog, P Seemanová, E Producer: 19910610 In: Schweizer Archiv fur Neurologie und Psychiatrie (Zurich, Switzerland : 1985) vol. 142 Availability: No items available. Save to lists Add to cart (remove)
	1030.	Chronic cough due to Thr124Met mutation in the peripheral myelin protein zero (MPZ gene). [electronic resource] by Baloh, Robert H Jen, Joanna C Kim, Gilbert Baloh, Robert W Producer: 20041026 In: Neurology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1031.	MR imaging of demyelinating hypertrophic polyneuropathy. [electronic resource] by Rowin, Julie Producer: 20100607 In: Neurology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1032.	Neurofilament light mutation causes hereditary motor and sensory neuropathy with pyramidal signs. [electronic resource] by Hashiguchi, Akihiro Higuchi, Yujiro Nomura, Miwa Nakamura, Tomonori Arata, Hitoshi Yuan, Junhui Yoshimura, Akiko Okamoto, Yuji Matsuura, Eiji Takashima, Hiroshi Producer: 20151016 In: Journal of the peripheral nervous system : JPNS vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1033.	Dopamine-agonist responsive Parkinsonism in a patient with the SANDO syndrome caused by POLG mutation. [electronic resource] by Bandettini di Poggio, Monica Nesti, Claudia Bruno, Claudio Meschini, Maria Chiara Schenone, Angelo Santorelli, Filippo M Producer: 20140106 In: BMC medical genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1034.	Application of whole-exome sequencing for detecting copy number variants in CMT1A/HNPP. [electronic resource] by Jo, H-Y Park, M-H Woo, H-M Han, M H Kim, B-Y Choi, B-O Chung, K W Koo, S K 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)
	1035.	Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling. [electronic resource] by Gregianin, Elisa Pallafacchina, Giorgia Zanin, Sofia Crippa, Valeria Rusmini, Paola Poletti, Angelo Fang, Mingyan Li, Zhouxuan Diano, Laura Petrucci, Antonio Lispi, Ludovico Cavallaro, Tiziana Fabrizi, Gian M Muglia, Maria Boaretto, Francesca Vettori, Andrea Rizzuto, Rosario Mostacciuolo, Maria L Vazza, Giovanni Producer: 20170823 In: Human molecular genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1036.	17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1. [electronic resource] by Mancardi, G L Uccelli, A Bellone, E Sghirlanzoni, A Mandich, P Pareyson, D Schenone, A Abbruzzese, M Ajmar, F Producer: 19940812 In: European neurology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1037.	Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype. [electronic resource] by Timmerman, V De Jonghe, P Ceuterick, C De Vriendt, E Löfgren, A Nelis, E Warner, L E Lupski, J R Martin, J J Van Broeckhoven, C Producer: 19990715 In: Neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1038.	Autosomal recessive type II hereditary motor and sensory neuropathy with acrodystrophy. [electronic resource] by Thomas, P K Claus, D King, R H Producer: 19990706 In: Journal of neurology vol. 246 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1039.	Transthyretin familial amyloid polyneuropathy (TTR-FAP): Parameters for early diagnosis. [electronic resource] by Escolano-Lozano, Fabiola Barreiros, Ana Paula Birklein, Frank Geber, Christian Producer: 20190211 In: Brain and behavior vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1040.	Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C. [electronic resource] by Auer-Grumbach, Michaela Olschewski, Andrea Papić, Lea Kremer, Hannie McEntagart, Meriel E Uhrig, Sabine Fischer, Carina Fröhlich, Eleonore Bálint, Zoltán Tang, Bi Strohmaier, Heimo Lochmüller, Hanns Schlotter-Weigel, Beate Senderek, Jan Krebs, Angelika Dick, Katherine J Petty, Richard Longman, Cheryl Anderson, Neil E Padberg, George W Schelhaas, Helenius J van Ravenswaaij-Arts, Conny M A Pieber, Thomas R Crosby, Andrew H Guelly, Christian Producer: 20100217 In: Nature genetics vol. 42 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.