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	821.	Déjérine-Sottas neuropathy associated with de novo S79P mutation of the peripheral myelin protein 22 (PMP22) gene. [electronic resource] by Bort, S Sevilla, T García-Planells, J Blesa, D Paricio, N Vílchez, J J Prieto, F Palau, F 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)
	822.	Inherited neuropathies: from gene to disease. [electronic resource] by Keller, M P Chance, P F Producer: 19990609 In: Brain pathology (Zurich, Switzerland) vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	823.	Correlation between muscle atrophy on MRI and manual strength testing in hereditary neuropathies. [electronic resource] by del Porto, Lana A Nicholson, Garth A Ketheswaren, Pon Producer: 20101124 In: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	824.	Genetic spectrum of hereditary neuropathies with onset in the first year of life. [electronic resource] by Baets, Jonathan Deconinck, Tine De Vriendt, Els Zimoń, Magdalena Yperzeele, Laetitia Van Hoorenbeeck, Kim Peeters, Kristien Spiegel, Ronen Parman, Yesim Ceulemans, Berten Van Bogaert, Patrick Pou-Serradell, Adolf Bernert, Günther Dinopoulos, Argirios Auer-Grumbach, Michaela Sallinen, Satu-Leena Fabrizi, Gian Maria Pauly, Fernand Van den Bergh, Peter Bilir, Birdal Battaloglu, Esra Madrid, Ricardo E Kabzińska, Dagmara Kochanski, Andrzej Topaloglu, Haluk Miller, Geoffrey Jordanova, Albena Timmerman, Vincent De Jonghe, Peter Producer: 20111108 In: Brain : a journal of neurology vol. 134 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	825.	Diagnosis of Leber's optic neuropathy by means of polymerase chain reaction amplification. [electronic resource] by Hotta, Y Hayakawa, M Saito, K Kanai, A Nakajima, A Fujiki, K Producer: 19891208 In: American journal of ophthalmology vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	826.	Expression of P0 protein in sural nerve of a patient with hereditary motor and sensory neuropathy type III. [electronic resource] by Tachi, N Kasai, K Chiba, S Naganuma, M Uyemura, K Hayasaka, K Producer: 19941110 In: Journal of the neurological sciences vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	827.	Peripheral nerve extracellular matrix remodeling in Charcot-Marie-Tooth type I disease. [electronic resource] by Palumbo, Camilla Massa, Roberto Panico, Maria Beatrice Di Muzio, Antonio Sinibaldi, Paola Bernardi, Giorgio Modesti, Andrea Producer: 20021017 In: Acta neuropathologica vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	828.	Hereditary neuropathy with liability to pressure palsies in infancy. [electronic resource] by Goikhman, Igor Meer, Jacob Zelnik, Nathanel Producer: 20031209 In: Pediatric neurology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	829.	Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience. [electronic resource] by Luigetti, Marco Del Grande, Alessandra Conte, Amelia Lo Monaco, Mauro Bisogni, Giulia Romano, Angela Zollino, Marcella Rossini, Paolo Maria Sabatelli, Mario Producer: 20141230 In: Journal of the neurological sciences vol. 341 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	830.	Variable phenotypic expression and onset in MYH14 distal hereditary motor neuropathy phenotype in a large, multigenerational North American family. [electronic resource] by Iyadurai, Stanley Arnold, W David Kissel, John T Ruhno, Corey Mcgovern, Vicki L Snyder, Pamela J Prior, Thomas W Roggenbuck, Jennifer Burghes, Arthur H Kolb, Stephen J Producer: 20170818 In: Muscle & nerve vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	831.	[Autoantibodies in nervous system diseases]. [electronic resource] by Humbel, R L Schmit, P Gilson, G Producer: 19961216 In: Bulletin de la Societe des sciences medicales du Grand-Duche de Luxembourg vol. 133 Availability: No items available. Save to lists Add to cart (remove)
	832.	Abnormalities of visual function in hereditary motor and sensory neuropathy. [electronic resource] by Honan, W P Heron, J R Foster, D H Edgar, G K Scase, M O Producer: 19930402 In: Journal of the neurological sciences vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	833.	Many facets of the peripheral myelin protein PMP22 in myelination and disease. [electronic resource] by Naef, R Suter, U Producer: 19980917 In: Microscopy research and technique vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	834.	Childhood multifocal acquired demyelinating sensory and motor neuropathy. [electronic resource] by Wakamoto, Hiroyuki Chisaka, Aya Inoue, Naozou Nakano, Naoko Producer: 20080709 In: Muscle & nerve vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	835.	Rapidly progressive amyotrophic lateral sclerosis in a young patient with hereditary neuropathy with liability to pressure palsies. [electronic resource] by Canali, Elena Chiari, Annalisa Sola, Patrizia Fioravanti, Valentina Valzania, Franco Pentore, Roberta Nichelli, Paolo Mandrioli, Jessica Producer: 20100810 In: Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	836.	The relationship of nerve fibre pathology to sensory function in entrapment neuropathy. [electronic resource] by Schmid, Annina B Bland, Jeremy D P Bhat, Manzoor A Bennett, David L H Producer: 20150318 In: Brain : a journal of neurology vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	837.	[Current issues in hereditary neuropathies]. [electronic resource] by Lacour, A Producer: 20150219 In: Revue neurologique vol. 169 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	838.	Predicting the pathogenicity of aminoacyl-tRNA synthetase mutations. [electronic resource] by Oprescu, Stephanie N Griffin, Laurie B Beg, Asim A Antonellis, Anthony Producer: 20180208 In: Methods (San Diego, Calif.) vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	839.	Hereditary motor and sensory neuropathy type 1 (HMSN1) associated with cranial neuropathy: an autopsy case report. [electronic resource] by Takase, Y Takahashi, K Takada, K Tatsumi, H Tabuchi, Y Producer: 19910404 In: Acta neurologica Scandinavica vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	840.	Giant axonal neuropathy and leukodystrophy. [electronic resource] by Stollhoff, K Albani, M Goebel, H H Producer: 19910614 In: Pediatric neurology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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