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	221.	A case report of hereditary neuropathy with liability to pressure palsies accompanied by type 2 diabetes mellitus and psoriasis. [electronic resource] by Li, Jing Niu, Bing Wang, Xiaoling Hu, Huaiqiang Cao, Bingzhen Producer: 20170612 In: Medicine vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	222.	Compound Heterozygote Mutation of [electronic resource] by Fang, Xiao-Jing Zhang, Wei Lyu, He Wang, Zhao-Xia Wang, Wei-Wei Yuan, Yun Producer: 20170313 In: Chinese medical journal vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	223.	[Nerve conduction abnormalities in chronic inflammatory demyelinating polyneuropathy (CIDP)]. [electronic resource] by Baba, M Producer: 19920710 In: Rinsho shinkeigaku = Clinical neurology vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	224.	Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy. [electronic resource] by Yoneda, M Tsuji, S Yamauchi, T Inuzuka, T Miyatake, T Horai, S Ozawa, T Producer: 19890613 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	225.	[A case with hereditary motor and sensory neuropathy with multiple cranial nerves involvement]. [electronic resource] by Nakamura, N Oka, N Nakamura, S Akiguchi, I Kashii, S Producer: 19951010 In: Rinsho shinkeigaku = Clinical neurology vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	226.	Alport's syndrome and hereditary motor and sensory neuropathy type I--an unfortunate coincidence. [electronic resource] by Deal, J E Hall, S M Hughes, R A Rigden, S P Producer: 19930521 In: Pediatric nephrology (Berlin, Germany) vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	227.	Giant axonal neuropathy and anaesthesia. [electronic resource] by Diagos, P Bos, J A G Verrips, A Booij, L H D J Producer: 20030908 In: Anaesthesia vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	228.	Complications of surgery of the foot and ankle in hereditary neurologic disorders. [electronic resource] by Roy, D R Al-Sayyad, M J Producer: 20011204 In: Clinical orthopaedics and related research no. 391 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	229.	Inherited polyneuropathies. [electronic resource] by Rinaldi, Robert Patel, Atul Producer: 20140220 In: PM & R : the journal of injury, function, and rehabilitation vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	230.	[Coincidence of hereditary motor and sensory neuropathy type 1A and limb girdle muscular dystrophy type 2A]. [electronic resource] by Rudenskaya, G E Bulakh, M V Milovidova, T B Shchagina, O A Producer: 20190605 In: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	231.	[A case of hereditary motor and sensory neuropathy of neuronal type with retardation of motor development]. [electronic resource] by Nakano, S Ohnishi, A Yamamoto, T Oishi, T Murai, Y Producer: 19900921 In: Rinsho shinkeigaku = Clinical neurology vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	232.	[Hereditary familial neuropathies: genetic counseling and early diagnosis in primary care]. [electronic resource] by Bordas Julve, J M Avila Rivera, F Peñas López, F Cots Yago, J M Espel Masferrer, C Guarga Rojas, A Producer: 19911023 In: Atencion primaria vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	233.	Motor neuropathy with activity of monoclonal IgM antibody to GD1a ganglioside. [electronic resource] by Bollensen, E Schipper, H I Steck, A J Producer: 19891114 In: Journal of neurology vol. 236 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	234.	Phrenic nerve involvement in Déjérine-Sottas disease: a clinicopathological case study. [electronic resource] by Felice, K J Fratkin, J D Feldman, E L Sima, A A Producer: 19950316 In: Pediatric pathology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	235.	Nerve and muscle biopsy in a case of hereditary motor and sensory neuropathy type III with basal lamina onion bulbs. [electronic resource] by Bornemann, A Hansen, F J Schmalbruch, H Producer: 19961203 In: Neuropathology and applied neurobiology vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	236.	A-waves in patients with novel hereditary motor and sensory neuropathy Lom. [electronic resource] by Alexandrov, A S Christova, L G Ishpekova, B A Producer: 20020305 In: Acta physiologica et pharmacologica Bulgarica vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	237.	Pronator syndrome: compression neuropathy of the median nerve at level of pronator teres muscle. [electronic resource] by SOLNITZKY, O Producer: 19981101 In: Georgetown medical bulletin vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	238.	Two cases of Dandy-Walker syndrome and chronic polyneuropathy. [electronic resource] by Riikonen, R Lang, H Kalimo, H Röyttä, M Donner, M Producer: 19901204 In: Pediatric neuroscience vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	239.	Autosomal recessive hypermyelinating neuropathy. [electronic resource] by Sabatelli, M Mignogna, T Lippi, G Servidei, S Manfredi, G Ricci, E Bertini, E Lo Monaco, M Tonali, P Producer: 19940727 In: Acta neuropathologica vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	240.	Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A. [electronic resource] by Chapon, F Diraison, P Lechevalier, B Chazot, G Viader, F Bonnebouche, C Vandenberghe, A Timmerman, V Van Broeckhoven, C Vandenberghe, A Producer: 19961220 In: Journal of neurology, neurosurgery, and psychiatry vol. 61 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.