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	901.	The phenotype of motor neuropathies associated with BSCL2 mutations is broader than Silver syndrome and distal HMN type V. [electronic resource] by Irobi, Joy Van den Bergh, Peter Merlini, Luciano Verellen, Christine Van Maldergem, Lionel Dierick, Ines Verpoorten, Nathalie Jordanova, Albena Windpassinger, Christian De Vriendt, Els Van Gerwen, Veerle Auer-Grumbach, Michaela Wagner, Klaus Timmerman, Vincent De Jonghe, Peter Producer: 20041015 In: Brain : a journal of neurology vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	902.	Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations. [electronic resource] by Vallat, Jean-Michel Ouvrier, Robert A Pollard, John D Magdelaine, Corinne Zhu, Danqing Nicholson, Garth A Grew, Simon Ryan, Monique M Funalot, Benoît Producer: 20081223 In: Journal of neuropathology and experimental neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	903.	HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry. [electronic resource] by Alavi, Afagh Shamshiri, Hosein Nafissi, Shahriar Khani, Marzieh Klotzle, Brandy Fan, Jian-Bing Steemers, Frank Elahi, Elahe Producer: 20151124 In: Neurobiology of aging vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	904.	Increased accumulation of transferrin by motor neurons of the mouse mutant progressive motor neuronopathy (pmn/pmn). [electronic resource] by Moos, T Producer: 19950927 In: Journal of neurocytology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	905.	Changes in concanavalin A-reactive proteins in neurological disorders. [electronic resource] by Saso, L Valentini, G Leone, M G Grippa, E Guglielmi, R Paris, L Cantore, G Silvestrini, B Producer: 19991119 In: Journal of clinical laboratory analysis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	906.	EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy. [electronic resource] by Boerkoel, C F Takashima, H Bacino, C A Daentl, D Lupski, J R Producer: 20020116 In: Neurogenetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	907.	Proximal arm weakness is the most common presentation in young Korean soldiers diagnosed as having hereditary neuropathy with liability to pressure palsy (HNPP). [electronic resource] by Kim, Kyoung-Eun Yeom, J Producer: 20170106 In: Journal of the Royal Army Medical Corps vol. 162 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	908.	Hereditary motor and sensory neuropathy with calf hypertrophy is associated with 17p11.2 duplication. [electronic resource] by Uncini, A Di Muzio, A Chiavaroli, F Gambi, D Sabatelli, M Archidiacono, N Antonacci, R Marzella, R Rocchi, M Producer: 19940609 In: Annals of neurology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	909.	Intermediate CAG repeat lengths (53,54) for MJD/SCA3 are associated with an abnormal phenotype. [electronic resource] by van Alfen, N Sinke, R J Zwarts, M J Gabreëls-Festen, A Praamstra, P Kremer, B P Horstink, M W Producer: 20010628 In: Annals of neurology vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	910.	Electrodiagnostic features of hereditary neuropathy with liability to pressure palsies. [electronic resource] by Andersson, P B Yuen, E Parko, K So, Y T Producer: 20000127 In: Neurology vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	911.	Co-segregation of LMNA and PMP22 gene mutations in the same family. [electronic resource] by Pegoraro, Elena Gavassini, Bruno F Benedetti, Sara Menditto, Immacolata Zara, Gabriella Padoan, Roberta Mostacciuolo, Maria Luisa Ferrari, Maurizio Angelini, Corrado Producer: 20060302 In: Neuromuscular disorders : NMD vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	912.	Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom. [electronic resource] by Berger, Philipp Sirkowski, Erich E Scherer, Steven S Suter, Ueli Producer: 20041221 In: Neurobiology of disease vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	913.	Treatment of chronic immune-mediated neuropathies: impact of the rare diseases centers network in Italy. [electronic resource] by Nobile-Orazio, E Producer: 20130816 In: Revue neurologique vol. 169 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	914.	Prospective comparison of acute motor axonal neuropathy and acute inflammatory demyelinating polyradiculoneuropathy in 140 children with Guillain-Barré syndrome in India. [electronic resource] by Kalita, Jayantee Kumar, Mritunjai Misra, Usha K Producer: 20190327 In: Muscle & nerve vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	915.	Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood. [electronic resource] by Ouvrier, R Producer: 19961217 In: Journal of child neurology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	916.	[Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary]. [electronic resource] by Herczegfalvi, Agnes Pikó, Henriett Karcagi, Veronika Producer: 20081231 In: Ideggyogyaszati szemle vol. 61 Availability: No items available. Save to lists Add to cart (remove)
	917.	Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication. [electronic resource] by Uncini, A Di Guglielmo, G Di Muzio, A Gambi, D Sabatelli, M Mignogna, T Tonali, P Marzella, R Finelli, P Archidiacono, N Producer: 19950619 In: Muscle & nerve vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	918.	Sensory nerve pathology in multifocal motor neuropathy. [electronic resource] by Corse, A M Chaudhry, V Crawford, T O Cornblath, D R Kuncl, R W Griffin, J W Producer: 19960509 In: Annals of neurology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	919.	BSCL2 mutations in two Dutch families with overlapping Silver syndrome-distal hereditary motor neuropathy. [electronic resource] by van de Warrenburg, Bart P C Scheffer, Hans van Eijk, Jeroen J J Versteeg, Martina H A Kremer, Hannie Zwarts, Machiel J Schelhaas, H Jurgen van Engelen, Baziel G M Producer: 20060413 In: Neuromuscular disorders : NMD vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	920.	Late-onset HMSN 2: further evidence of genetic heterogeneity. [electronic resource] by Dyck, Peter J Producer: 20080731 In: Neurology vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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