Your search returned 1188 results.

Results
	761.	Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation. [electronic resource] by Lenssen, P P Gabreëls-Festen, A A Valentijn, L J Jongen, P J van Beersum, S E van Engelen, B G van Wensen, P J Bolhuis, P A Gabreëls, F J Mariman, E C Producer: 19980911 In: Brain : a journal of neurology vol. 121 ( Pt 8) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	762.	Clinical characterisation of sensory neuropathy with anti-FGFR3 autoantibodies. [electronic resource] by Tholance, Yannick Moritz, Christian Peter Rosier, Carole Ferraud, Karine Lassablière, François Reynaud-Federspiel, Evelyne França, Marcondes C Martinez, Alberto R M Camdessanché, Jean-Philippe Antoine, Jean-Christophe Producer: 20200706 In: Journal of neurology, neurosurgery, and psychiatry vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	763.	BAEP changes in Leber's hereditary optic atrophy: further confirmation of multisystem involvement. [electronic resource] by Mondelli, M Rossi, A Scarpini, C Dotti, M T Federico, A Producer: 19900731 In: Acta neurologica Scandinavica vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	764.	Hereditary spastic diplegia with mental retardation in two young siblings. [electronic resource] by Gustavson, K H Modrzewska, K Erikson, A Producer: 19900119 In: Clinical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	765.	Hereditary motor and sensory neuropathy with optic atrophy. Ultrastructural and morphometric observations on nerve fibers, mitochondria, and dense-cored vesicles. [electronic resource] by Sommer, C Schröder, J M Producer: 19890926 In: Archives of neurology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	766.	Detection of hereditary motor sensory neuropathy type I in childhood. [electronic resource] by Feasby, T E Hahn, A F Bolton, C F Brown, W F Koopman, W J Producer: 19921204 In: Journal of neurology, neurosurgery, and psychiatry vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	767.	Progressive infantile axonal polyneuropathy. [electronic resource] by Geller, T J Connolly, A M Kotagal, S Prensky, A L Producer: 20001220 In: Journal of child neurology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	768.	Hereditary motor and sensory neuropathy with minifascicle formation in a patient with 46XY pure gonadal dysgenesis: a new clinical entity. [electronic resource] by Sugie, Kazuma Futamura, Naonobu Suzumura, Akio Tate, Genshu Umehara, Fujio Producer: 20020328 In: Annals of neurology vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	769.	Small heat shock protein 27 mutation in a Japanese patient with distal hereditary motor neuropathy. [electronic resource] by Kijima, Kazuki Numakura, Chikahiko Goto, Tomohide Takahashi, Takao Otagiri, Tesshu Umetsu, Kazuo Hayasaka, Kiyoshi Producer: 20060502 In: Journal of human genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	770.	Phenotype variant of the common duplication at 17p11.2. [electronic resource] by Finsterer, Josef Producer: 20070329 In: European neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	771.	Hereditary motor and sensory neuropathy type VI with optic atrophy. [electronic resource] by Voo, Irene Allf, Bryan E Udar, Nitin Silva-Garcia, Rosamaria Vance, Jeffrey Small, Kent W Producer: 20031009 In: American journal of ophthalmology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	772.	Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability. [electronic resource] by Zhang, Feng Seeman, Pavel Liu, Pengfei Weterman, Marian A J Gonzaga-Jauregui, Claudia Towne, Charles F Batish, Sat Dev De Vriendt, Els De Jonghe, Peter Rautenstrauss, Bernd Krause, Klaus-Henning Khajavi, Mehrdad Posadka, Jan Vandenberghe, Antoon Palau, Francesc Van Maldergem, Lionel Baas, Frank Timmerman, Vincent Lupski, James R Producer: 20100629 In: American journal of human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	773.	Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease. [electronic resource] by Pitceathly, Robert D S Murphy, Sinéad M Cottenie, Ellen Chalasani, Annapurna Sweeney, Mary G Woodward, Cathy Mudanohwo, Ese E Hargreaves, Iain Heales, Simon Land, John Holton, Janice L Houlden, Henry Blake, Julian Champion, Michael Flinter, Frances Robb, Stephanie A Page, Rupert Rose, Michael Palace, Jacqueline Crowe, Carol Longman, Cheryl Lunn, Michael P Rahman, Shamima Reilly, Mary M Hanna, Michael G Producer: 20121204 In: Neurology vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	774.	Lipomas of the Brachial Plexus: A Case Series and Review of the Literature. [electronic resource] by Graf, Alexander Yang, Kai King, David Dzwierzynski, William Sanger, James Hettinger, Patrick Producer: 20200602 In: Hand (New York, N.Y.) vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	775.	Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene. [electronic resource] by Fusco, Carlo Spagnoli, Carlotta Salerno, Grazia Gabriella Pavlidis, Elena Frattini, Daniele Pisani, Francesco Producer: 20180723 In: Italian journal of pediatrics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	776.	Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle. [electronic resource] by Sabatelli, M Bertini, E Ricci, E Salviati, G Magi, S Papacci, M Tonali, P 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)
	777.	X-linked dominant hereditary motor and sensory neuropathy. [electronic resource] by Hahn, A F Brown, W F Koopman, W J Feasby, T E Producer: 19910110 In: Brain : a journal of neurology vol. 113 ( Pt 5) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	778.	A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2? [electronic resource] by LeGuern, E Gouider, R Ravisé, N Lopes, J Tardieu, S Gugenheim, M Abbas, N Bouche, P Agid, Y Brice, A Producer: 19961022 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	779.	[Polyneuropathy: diagnosis and management]. [electronic resource] by Notermans, N C van Doorn, P A Producer: 19980615 In: Nederlands tijdschrift voor geneeskunde vol. 141 Availability: No items available. Save to lists Add to cart (remove)
	780.	Peripheral neuropathy in systemic lupus erythematosus. [electronic resource] by Huynh, C Ho, S L Fong, K Y Cheung, R T Mok, C C Lau, C S Producer: 19990721 In: Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1188 results.