Your search returned 1188 results.

Results
	621.	Rodent models with expression of PMP22: Relevance to dysmyelinating CMT and HNPP. [electronic resource] by Jouaud, Maxime Mathis, Stéphane Richard, Laurence Lia, Anne-Sophie Magy, Laurent Vallat, Jean-Michel Producer: 20200528 In: Journal of the neurological sciences vol. 398 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	622.	[The nosological situation of hereditary motor and sensory neuropathies (HMSN, Charcot-Marie-Tooth disease, neural muscular atrophy)]. [electronic resource] by Warzok, R Wattig, B Schwesinger, G Schneeweiss, H Heydenreich, F Producer: 19910312 In: Zentralblatt fur allgemeine Pathologie u. pathologische Anatomie vol. 136 Availability: No items available. Save to lists Add to cart (remove)
	623.	Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous system. [electronic resource] by Magy, L Birouk, N Vallat, J M Gouider, R Maisonobe, T Bouche, P Lyon-Caen, O Fontaine, B Producer: 19970710 In: Neurology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	624.	A Dejerine-Sottas neuropathy family with a gene mapped on chromosome 8. [electronic resource] by Ionasescu, V V Kimura, J Searby, C C Smith, W L Ross, M A Ionasescu, R Producer: 19960522 In: Muscle & nerve vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	625.	Glimpsing myelin's protein glue. [electronic resource] by Barinaga, M Producer: 19961011 In: Science (New York, N.Y.) vol. 273 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	626.	Hereditary neuropathies in children: the contribution of the new genetics. [electronic resource] by Ouvrier, R A Producer: 19961030 In: Seminars in pediatric neurology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	627.	Rare forms of autosomal recessive neurodegenerative ataxia. [electronic resource] by Koenig, Michel Producer: 20040308 In: Seminars in pediatric neurology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	628.	The phenotype of the Gly94fsX222 PMP22 insertion. [electronic resource] by de Vries, Sara D J Verhamme, Camiel van Ruissen, Fred van Paassen, Barbara W Arts, Willem F Kerkhoff, Henk van Engelen, Baziel G M Lammens, Martin de Visser, Marianne Baas, Frank van der Kooi, Anneke J Producer: 20111026 In: Journal of the peripheral nervous system : JPNS vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	629.	Compression neuropathy caused by cancer metastasis to the optic nerve canal. [electronic resource] by Tamai, Hiroshi Ishida, Kazuyuki Murakami, Kensuke Narita, Norio Tominaga, Teiji Fuse, Nobuo Producer: 20140714 In: BMC research notes vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	630.	Compression of Root Level in a Patient with Hereditary Neuropathy with Liability to Pressure Palsy Diagnosed by Magnetic Resonance Imaging. [electronic resource] by Park, Donghwi Ryu, Ju Seok Kim, Ki-Jeong Producer: 20170731 In: American journal of physical medicine & rehabilitation vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	631.	Effect of Intrathecal Baclofen on Delayed-Onset Paroxysmal Dystonia due to Compression Injury Resulting From Congenital and Progressive Spinal Bone Deformities in Chondrodysplasia Punctata. [electronic resource] by Okazaki, Tetsuya Saito, Yoshiaki Ueda, Riyo Sugihara, Susumu Tamasaki, Akiko Nishimura, Yoko Ohno, Koyo Togawa, Masami Ohno, Takako Horie, Akiyoshi Honda, Masashi Takenaka, Atsushi Nagashima, Hideki Maegaki, Yoshihiro Producer: 20161213 In: Pediatric neurology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	632.	Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism. [electronic resource] by Vilkki, J Savontaus, M L Nikoskelainen, E K Producer: 19890906 In: American journal of human genetics vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	633.	Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies. [electronic resource] by Nelis, E Haites, N Van Broeckhoven, C Producer: 19990311 In: Human mutation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	634.	MR imaging of the cauda equina in hereditary motor sensory neuropathies: correlations with sural nerve biopsy. [electronic resource] by Cellerini, M Salti, S Desideri, V Marconi, G Producer: 20010531 In: AJNR. American journal of neuroradiology vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	635.	Inherited neuropathy can cause postpartum foot drop. [electronic resource] by Peters, Gary Hinds, Nigel P Producer: 20050222 In: Anesthesia and analgesia vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	636.	Ambulatory disabilities and the use of walking aids in patients with hereditary motor and sensory neuropathy type I (HMSN I). [electronic resource] by van der Linden, Marleen H Kalkman, Joke S Hendricks, Henk T Schillings, Maartje L Zwarts, Machiel J Bleijenberg, Gijs van Engelen, Baziel G M Producer: 20090324 In: Disability and rehabilitation. Assistive technology vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	637.	[Clinical report of hereditary motor and sensory neuropathy with proximal dominance in Shiga prefecture]. [electronic resource] by Takahashi, Mitsuo Mitsui, Yoshiyuki Yorifuji, Shiro Nakamura, Yuusaku Tsukamoto, Yoshihumi Nishimoto, Kazuhiro Producer: 20080123 In: Rinsho shinkeigaku = Clinical neurology vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	638.	A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier? [electronic resource] by Brusse, Esther Majoor-Krakauer, Danielle de Graaf, Bianca M Visser, Gerhard H Swagemakers, Sigrid Boon, Agnita J W Oostra, Ben A Bertoli-Avella, Aida M Producer: 20091207 In: Neurogenetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	639.	Four novel point mutations in the PMP22 gene with phenotypes of HNPP and Dejerine-Sottas neuropathy. [electronic resource] by Brožková, Dana Mazanec, Radim Rychlý, Zdeněk Haberlová, Jana Böhm, Jiří Staněk, Jan Plevová, Pavlína Lisoňová, Jana Sabová, Jana Sakmaryová, Iva Seeman, Pavel Producer: 20111205 In: Muscle & nerve vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	640.	[Clinical and epidemiological characteristics of hereditary motor-sensory neuropathy 1X caused by the mutation c. 259C> G (p. P87A) in the GJB1 gene of patients from the Republic of Bashkortostan]. [electronic resource] by Saifullina, E V Magzhanov, R V Khidiyatova, I M Khusnutdinova, E K Producer: 20170814 In: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1188 results.