Your search returned 1188 results.

Results
	581.	Genetic dosage compensation via co-occurrence of PMP22 duplication and PMP22 deletion. [electronic resource] by Hirt, Nina Eggermann, Katja Hyrenbach, Sonja Lambeck, Johann Busche, Andreas Fischer, Judith Rudnik-Schöneborn, Sabine Gaspar, Harald Producer: 20150615 In: Neurology vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	582.	[Peroneal muscle atrophy with talipes cavus. Pyramidal symptoms and sensory disorders in one family. On the problem of the nosological classification of hereditary spinal diseases and polyneuropathies]. [electronic resource] by Schnider, A Hess, C W Meier, C Producer: 19910124 In: Schweizerische medizinische Wochenschrift vol. 120 Availability: No items available. Save to lists Add to cart (remove)
	583.	HMSN III phenotype due to homozygous expression of a dominant HMSN II gene. [electronic resource] by Sghirlanzoni, A Pareyson, D Balestrini, M R Bellone, E Berta, E Ciano, C Mandich, P Marazzi, R Producer: 19921218 In: Neurology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	584.	The status of HMSN type III. [electronic resource] by Gabreëls-Festen, A A Gabreëls, F J Jennekens, F G Janssen-van Kempen, T W Producer: 19940608 In: Neuromuscular disorders : NMD vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	585.	New form of autosomal-recessive axonal hereditary sensory motor neuropathy. [electronic resource] by Eckhardt, S M Hicks, E M Herron, B Morrison, P J Aicardi, J Producer: 19990112 In: Pediatric neurology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	586.	Involvement of the visual pathway in hereditary neuropathy with liability to pressure palsies. [electronic resource] by Schneider, C Reiners, K Friedl, W Ebner, R Toyka, K V Producer: 20000706 In: Journal of neurology vol. 247 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	587.	Varying occurrence of vocal cord paralysis in a family with autosomal dominant hereditary motor and sensory neuropathy. [electronic resource] by Donaghy, M Kennett, R Producer: 19991026 In: Journal of neurology vol. 246 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	588.	COMPRESSION NEUROPATHY OF THE ULNAR NERVE AT THE ELBOW. [electronic resource] by COPP, E P Producer: 19961201 In: Annals of physical medicine vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	589.	Hereditary motor and sensory neuropathy associated with juvenile glaucoma. [electronic resource] by Unoki, K Sakamoto, Y Ohba, N Kiwaki, T Umehara, F Isashiki, Y Nakagawa, M Osame, M Producer: 20011025 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 119 Availability: No items available. Save to lists Add to cart (remove)
	590.	Laryngeal and phrenic nerve involvement in a patient with hereditary neuropathy with liability to pressure palsies (HNPP). [electronic resource] by Cortese, A Piccolo, G Lozza, A Schreiber, A Callegari, I Moglia, A Alfonsi, E Pareyson, D Producer: 20180124 In: Neuromuscular disorders : NMD vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	591.	Charcot‑Marie‑Tooth type 1A drug therapies: role of adenylyl cyclase activity and G‑protein coupled receptors in disease pathomechanism. [electronic resource] by Kiepura, Artur Jan Kochański, Andrzej Producer: 20190130 In: Acta neurobiologiae experimentalis vol. 78 Availability: No items available. Save to lists Add to cart (remove)
	592.	Reducing the risk of misdiagnosis of indirect ELISA by normalizing serum-specific background noise: The example of detecting anti-FGFR3 autoantibodies. [electronic resource] by Moritz, Christian P Tholance, Yannick Lassablière, François Camdessanché, Jean-Philippe Antoine, Jean-Christophe Producer: 20200313 In: Journal of immunological methods vol. 466 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	593.	[The natural history of cardiac involvement in Portuguese-type familial amyloid polyneuropathy]. [electronic resource] by Fonseca, C Ceia, F Carvalho, A Nogueira, J S Morais, H Conceição, I Luís, M L Luís, A S Producer: 19970423 In: Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	594.	[Referral of patients with polyneuropathy by the family physician: influence of type of symptoms but not of age]. [electronic resource] by van Dijk, G W Notermans, N C van der Graaf, Y Donders, R C Hol, M Wokke, J H Producer: 19980615 In: Nederlands tijdschrift voor geneeskunde vol. 141 Availability: No items available. Save to lists Add to cart (remove)
	595.	Atypical hereditary neuropathy with liability to pressure palsies (HNPP): the value of direct DNA diagnosis. [electronic resource] by Sessa, M Nemni, R Quattrini, A Del Carro, U Wrabetz, L Canal, N Producer: 19980130 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	596.	A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths. [electronic resource] by Nakagawa, M Suehara, M Saito, A Takashima, H Umehara, F Saito, M Kanzato, N Matsuzaki, T Takenaga, S Sakoda, S Izumo, S Osame, M Producer: 19990512 In: Neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	597.	Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12). [electronic resource] by Moog, U Engelen, J J Weber, B W Van Gelderen, M Steyaert, J Baas, F Sijstermans, H M Fryns, J P Producer: 20040720 In: Genetic counseling (Geneva, Switzerland) vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	598.	Intraneural perineurioma affecting multiple nerves: a case report and literature review. [electronic resource] by Wang, Lei-Ming Zhong, Yan-Feng Zheng, Dan-Feng Sun, A-Ping Zhang, Ying-Shuang Dong, Rong-Fang Pan, Yi Producer: 20150526 In: International journal of clinical and experimental pathology vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	599.	The use of whole-exome sequencing to disentangle complex phenotypes. [electronic resource] by Williams, Hywel J Hurst, John R Ocaka, Louise James, Chela Pao, Caroline Chanudet, Estelle Lescai, Francesco Stanescu, Horia C Kleta, Robert Rosser, Elisabeth Bacchelli, Chiara Beales, Philip Producer: 20161007 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	600.	A CMT2 family carrying the P7R mutation in the N- terminal region of the HSPB1 gene. [electronic resource] by Fortunato, Fernanda Neri, Marcella Geroldi, Alessandro Bellone, Emilia De Grandis, Domenico Ferlini, Alessandra Gualandi, Francesca Producer: 20190104 In: Clinical neurology and neurosurgery vol. 163 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1188 results.