Your search returned 1188 results.

Results
	141.	[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy]. [electronic resource] by Korn-Lubetzki, I Steiner, I Producer: 20051213 In: Revue neurologique vol. 161 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	142.	Absence of HINT1 mutations in a UK and Spanish cohort of patients with inherited neuropathies. [electronic resource] by Horga, Alejandro Cottenie, Ellen Tomaselli, Pedro J Rojas-García, Ricard Salvado, Maria Villarreal-Pérez, Liliana Gamez, Josep Márquez-Infante, Celedonio Houlden, Henry Reilly, Mary M Producer: 20160622 In: Journal of neurology vol. 262 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	143.	[Incidence of hereditary diseases of the nervous system among different populations (review of the literature)]. [electronic resource] by Markova, E D Magzhanov, R V Producer: 19910207 In: Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952) vol. 90 Availability: No items available. Save to lists Add to cart (remove)
	144.	Classification of the hereditary motor and sensory neuropathies. [electronic resource] by Reilly, M M Producer: 20010222 In: Current opinion in neurology vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	145.	Giant axonal neuropathy in two siblings: clinical histopathological findings. [electronic resource] by Hergüner, M O Zorludemir, S Altunbasak, S Producer: 20050222 In: Clinical neuropathology vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	146.	Muscular dystrophies, dilated cardiomyopathy, lipodystrophy and neuropathy: the nuclear connection. [electronic resource] by Maidment, Stephen L Ellis, Juliet A Producer: 20040223 In: Expert reviews in molecular medicine vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	147.	Canine inherited motor and sensory neuropathies: an updated classification in 22 breeds and comparison to Charcot-Marie-Tooth disease. [electronic resource] by Granger, Nicolas Producer: 20110809 In: Veterinary journal (London, England : 1997) vol. 188 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	148.	Hereditary neuropathy with liability to pressure palsy in childhood. [electronic resource] by György, Ilona Bíró, Anna Mechler, Ferenc Molnár, Mária Judit Producer: 20081231 In: Ideggyogyaszati szemle vol. 61 Availability: No items available. Save to lists Add to cart (remove)
	149.	Recessive hereditary motor and sensory neuropathy caused by IGHMBP2 gene mutation. [electronic resource] by Shi, Chang-He Song, Bo Luo, Hai-Yang Mao, Cheng-Yuan Shang, Dan-Dan Cao, Yuan Sun, Shi-Lei Wu, Jun Zhuang, Zheng-Ping Xu, Yu-Ming Producer: 20151102 In: Neurology vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	150.	Leber's optic neuropathy and mitral valve prolapse. [electronic resource] by Banerjee, A K MacSweeney, J E Hykin, P G Sanders, M D Producer: 19900316 In: Journal of the Royal Society of Medicine vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	151.	[A case of sensory ataxic neuropathy, dysarthria, and ophthalmoparesis with multiple mitochondrial DNA deletions]. [electronic resource] by Tanaka, Koji Tateishi, Takahisa Kawamura, Nobutoshi Ohyagi, Yasumasa Urata, Michiyo Kira, Jun-ichi Producer: 20140228 In: Rinsho shinkeigaku = Clinical neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	152.	Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurologic phenotype. [electronic resource] by Scarpini, Gaia Spagnoli, Carlotta Salerno, Grazia Gabriella Rizzi, Susanna Frattini, Daniele Fusco, Carlo Producer: 20200205 In: Neuromuscular disorders : NMD vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	153.	Familial spastic paraplegia. [electronic resource] by Phanthumchinda, K Somrealvongkul, B Producer: 19890728 In: Journal of the Medical Association of Thailand = Chotmaihet thangphaet vol. 72 Availability: No items available. Save to lists Add to cart (remove)
	154.	[Sensori-motor neuropathy associated with congenital bilateral club feet: histological and ultrastructural study of the sural nerve]. [electronic resource] by Yoshimura, N Fukuhara, N Noguchi, T Producer: 19890106 In: No to shinkei = Brain and nerve vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	155.	A case of progressive hypertrophic neuropathy in childhood with facial diplegia (Dejerine-Sottas disease). [electronic resource] by Sunwoo, I N Kim, J S Chi, J G Suh, Y L Producer: 19890111 In: Yonsei medical journal vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	156.	Orthotic management of the lower limb in children with hereditary motor sensory neuropathy (HMSN). [electronic resource] by Uygur, F Bek, N Kürklü, B Yilmaz, O Producer: 20020206 In: Prosthetics and orthotics international vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	157.	[CLINICAL AND CYTOGENETIC FINDINGS ON A FAMILIAL STRAIN OF NEURAL PROGRESSIVE MUSCULAR ATROPHY OF THE CHARCOT-MARIE TYPE]. [electronic resource] by IMBERCIADORI, E Producer: 19961201 In: Rivista di neurobiologia : organo ufficiale della Societa dei neurologi, neuroradiologi e neurochirurghi ospedalieri vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	158.	Hereditary neuropathy with liability to pressure palsies: a clinical and genetic study of a Taiwanese family. [electronic resource] by Tsai, Yu-Tai Kuo, Hung-Chou Chu, Chun-Che Lin, Kon-Ping Huang, Chin-Chang Producer: 20050428 In: Chang Gung medical journal vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	159.	Rapid quantitative PCR diagnostic strategy for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies. [electronic resource] by Chen, Shun-Sheng Producer: 20060413 In: Journal of the Chinese Medical Association : JCMA vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	160.	Allele-specific all-or-none PCR product diagnostic strategy for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies. [electronic resource] by Lin, Kon-Ping Chou, Chi-Hsiang Lee, Hsiang-Ying Soong, Bing-Wen Producer: 20060413 In: Journal of the Chinese Medical Association : JCMA vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
1
2
3
4
5
6
7
8
9
10
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1188 results.