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	1001.	Congenital fumarase deficiency presenting with hypotonia and areflexia. [electronic resource] by Narayanan, V Diven, W Ahdab-Barmada, M Producer: 19961031 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)
	1002.	Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPP. [electronic resource] by Nelis, E De Jonghe, P De Vriendt, E Patel, P I Martin, J J Van Broeckhoven, C Producer: 19981001 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1003.	Central motor conduction in a family with hereditary motor and sensory neuropathy with pyramidal signs (HMSN V). [electronic resource] by Schnider, A Hess, C W Koppi, S Producer: 19911001 In: Journal of neurology, neurosurgery, and psychiatry vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1004.	Germline mosaicism of MPZ gene in Dejerine-Sottas syndrome (HMSN III) associated with hereditary stomatocytosis. [electronic resource] by Takashima, H Nakagawa, M Kanzaki, A Yawata, Y Horikiri, T Matsuzaki, T Suehara, M Izumo, S Osame, M Producer: 19990901 In: Neuromuscular disorders : NMD vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1005.	Peripheral neuropathy associated with monoclonal IgG of undetermined significance: clinical, electrophysiologic, pathologic and therapeutic study of 14 cases. [electronic resource] by Hermosilla, E Lagueny, A Vital, C Vital, A Ferrer, X Steck, A Julien, J Producer: 20000926 In: Journal of the peripheral nervous system : JPNS vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	1006.	Dejerine-Sottas' neuropathy caused by the missense mutation PMP22 Ser72Leu. [electronic resource] by Marques, W Neto, J M Pina Barreira, A A Producer: 20041102 In: Acta neurologica Scandinavica vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1007.	Improved testing for CMT1A and HNPP using multiplex ligation-dependent probe amplification (MLPA) with rapid DNA preparations: comparison with the interphase FISH method. [electronic resource] by Slater, Howard Bruno, Damien Ren, Hua La, Phung Burgess, Trent Hills, Louise Nouri, Sara Schouten, Jan Choo, K H Andy Producer: 20041025 In: Human mutation vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1008.	Mendelian disorders of PI metabolizing enzymes. [electronic resource] by Staiano, Leopoldo De Leo, Maria Giovanna Persico, Maria De Matteis, Maria Antonietta Producer: 20150825 In: Biochimica et biophysica acta vol. 1851 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1009.	Progressive arm weakness and tonic hand spasm from multifocal motor neuropathy in the brachial plexus. [electronic resource] by Veltkamp, R Krause, M Schranz, C Meinck, H-M Producer: 20030822 In: Muscle & nerve vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1010.	Isolated paralysis of the serratus anterior muscle: surgical release of the distal segment of the long thoracic nerve in 52 patients. [electronic resource] by Le Nail, L R Bacle, G Marteau, E Corcia, P Favard, L Laulan, J Producer: 20150720 In: Orthopaedics & traumatology, surgery & research : OTSR vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1011.	Wearable Haptics and Immersive Virtual Reality Rehabilitation Training in Children With Neuromotor Impairments. [electronic resource] by Bortone, Ilaria Leonardis, Daniele Mastronicola, Nicola Crecchi, Alessandra Bonfiglio, Luca Procopio, Caterina Solazzi, Massimiliano Frisoli, Antonio Producer: 20190617 In: IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1012.	[Two siblings of Leber's congenital amaurosis with an increase in very long chain fatty acid in blood: relationship between peroxisomal disorders and Leber's congenital amaurosis]. [electronic resource] by Haginoya, K Aikawa, J Noro, T Watanabe, M Iinuma, K Narisawa, K Tada, K Producer: 19891107 In: No to hattatsu = Brain and development vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	1013.	Clinicopathologic analysis of 124 biopsy-proven peripheral nerve diseases. [electronic resource] by Hong, S M Ha, H Suh, J H Kim, K K Khang, S K Ro, J Y Park, S H Producer: 20000717 In: Journal of Korean medical science vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1014.	Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies. [electronic resource] by Thomas, P K Kalaydjieva, L Youl, B Rogers, T Angelicheva, D King, R H Guergueltcheva, V Colomer, J Lupu, C Corches, A Popa, G Merlini, L Shmarov, A Muddle, J R Nourallah, M Tournev, I Producer: 20011101 In: Annals of neurology vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1015.	Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation. [electronic resource] by Ibdah, J A Tein, I Dionisi-Vici, C Bennett, M J IJlst, L Gibson, B Wanders, R J Strauss, A W Producer: 19981013 In: The Journal of clinical investigation vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1016.	[Clinical-genetic correlations in the hereditary motor-sensor neuropathy caused by mutations in the MPZ (P0) gene]. [electronic resource] by Milovidova, T B Dadali, E L Fedotov, V P Shchagina, O A Poliakov, A V Producer: 20120524 In: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova vol. 111 Availability: No items available. Save to lists Add to cart (remove)
	1017.	Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. [electronic resource] by Taioli, Federica Cabrini, Ilaria Cavallaro, Tiziana Acler, Michele Fabrizi, Gian Maria Producer: 20110411 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)
	1018.	Mouse models of PI(3,5)P2 deficiency with impaired lysosome function. [electronic resource] by Lenk, Guy M Meisler, Miriam H Producer: 20140731 In: Methods in enzymology vol. 534 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1019.	Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree. [electronic resource] by Timmerman, V Raeymaekers, P Nelis, E De Jonghe, P Muylle, L Ceuterick, C Martin, J J Van Broeckhoven, C Producer: 19921006 In: Journal of the neurological sciences vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1020.	Rigid spine syndrome associated with sensory-motor axonal neuropathy resembling Charcot-Marie-Tooth disease is characteristic of Bcl-2-associated athanogene-3 gene mutations even without cardiac involvement. [electronic resource] by Noury, Jean-Baptiste Maisonobe, Thierry Richard, Pascale Delague, Valérie Malfatti, Edoardo Stojkovic, Tanya Producer: 20190128 In: Muscle & nerve vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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