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	1061.	Mutations in demyelinating peripheral neuropathies support molecular model of myelin P0-glycoprotein extracellular domain. [electronic resource] by Kirschner, D A Saavedra, R A Producer: 19950130 In: Journal of neuroscience research vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1062.	Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging. [electronic resource] by Pallotti, F Chen, X Bonilla, E Schon, E A Producer: 19960925 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	1063.	Assessment of pain and health-related quality of life in slowly progressive neuromuscular disease. [electronic resource] by Abresch, Richard T Carter, Gregory T Jensen, Mark P Kilmer, David D Producer: 20020927 In: The American journal of hospice & palliative care vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1064.	Congenital hypomyelinating neuropathy: two patients with long-term follow-up. [electronic resource] by Phillips, J P Warner, L E Lupski, J R Garg, B P Producer: 19990607 In: Pediatric neurology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1065.	Autonomic function in patients with hereditary motor and sensory neuropathy type I and Lambert-Eaton myasthenic syndrome. [electronic resource] by Kalmijn, S Oey, P L Wokke, J H Wieneke, G H Producer: 19991110 In: Electromyography and clinical neurophysiology vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	1066.	The inherited neuropathies. [electronic resource] by Klein, Christopher J Producer: 20070508 In: Neurologic clinics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1067.	CNS involvement in hereditary neuropathy with pressure palsies (HNPP). [electronic resource] by Iwasaki, Yasuo Iguchi, Hiroaki Ikeda, Ken Kano, Osamu Producer: 20070705 In: Neurology vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1068.	Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies. [electronic resource] by Ginanneschi, Federica Filippou, Georgios Giannini, Fabio Carluccio, Maria A Adinolfi, Antonella Frediani, Bruno Dotti, Maria T Rossi, Alessandro Producer: 20130611 In: Journal of the peripheral nervous system : JPNS vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1069.	Clinical, electrophysiological, and molecular findings in early onset hereditary neuropathy with liability to pressure palsy. [electronic resource] by Potulska-Chromik, Anna Sinkiewicz-Darol, Elena Ryniewicz, Barbara Lipowska, Marta Kabzińska, Dagmara Kochański, Andrzej Kostera-Pruszczyk, Anna Producer: 20150218 In: Muscle & nerve vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1070.	A novel WARS mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family. [electronic resource] by Wang, Binghao Li, Xiaobo Huang, Shunxiang Zhao, Huadong Liu, Jun Hu, Zhengmao Lin, Zhiqiang Liu, Lei Xie, Yongzhi Jin, Qingwen Zhao, Huihui Tang, Beisha Niu, Qi Zhang, Ruxu Producer: 20200812 In: Clinical genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1071.	Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies. [electronic resource] by Mariman, E C Gabreëls-Festen, A A van Beersum, S E Jongen, P J van de Looij, E Baas, F Bolhuis, P A Ropers, H H Gabreëls, F J Producer: 19940329 In: Human genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1072.	P0 (protein zero) mutation S34C underlies instability of internodal myelin in S63C mice. [electronic resource] by Avila, Robin L D'Antonio, Maurizio Bachi, Angela Inouye, Hideyo Feltri, M Laura Wrabetz, Lawrence Kirschner, Daniel A Producer: 20110209 In: The Journal of biological chemistry vol. 285 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1073.	The prevention of neurogenetic disease. [electronic resource] by Rosenberg, R N Iannaccone, S T Producer: 19950508 In: Archives of neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1074.	Coenzyme Q10 therapy in hereditary motor sensory neuropathy type VI with novel mitofusin 2 mutation. [electronic resource] by Takahashi, Ryoichi Ikeda, Tokuhei Hamaguchi, Ayumi Iwasa, Kazuo Yamada, Masahito Producer: 20120823 In: Internal medicine (Tokyo, Japan) vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1075.	Atrophic changes in the trigeminal nerves of patients with trigeminal neuralgia due to neurovascular compression and their association with the severity of compression and clinical outcomes. [electronic resource] by Leal, Paulo Roberto Lacerda Barbier, Charlotte Hermier, Marc Souza, Miguel Angelo Cristino-Filho, Gerardo Sindou, Marc Producer: 20140929 In: Journal of neurosurgery vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1076.	A new approach to ELISA-based anti-glycolipid antibody evaluation of highly adhesive serum samples. [electronic resource] by Usuki, Seigo O'Brien, Dawn Rivner, Michael H Yu, Robert K Producer: 20140902 In: Journal of immunological methods vol. 408 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1077.	Clinical, electrophysiological, genetic, and imaging features of six Chinese Han patients with hereditary neuropathy with liability to pressure palsies (HNPP). [electronic resource] by Chen, Bin Niu, Songtao Wang, Xingao Li, Wei Chen, Na Zhang, Zaiqiang Producer: 20180627 In: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1078.	Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli). [electronic resource] by Weiller, C Ferbert, A Producer: 19910801 In: European archives of psychiatry and clinical neuroscience vol. 240 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1079.	Familial progressive sensorimotor neuropathy with agenesis of the corpus callosum (Andermann syndrome): a clinical, neuroradiological and histopathological study. [electronic resource] by Deleu, D Bamanikar, S A Muirhead, D Louon, A Producer: 19970602 In: European neurology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1080.	Genetic basis of inherited peripheral neuropathies. [electronic resource] by Suter, U Patel, P I Producer: 19940706 In: Human mutation vol. 3 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.