Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotoniaZIMON, Magdalena; BAETS, Jonathan; AUER-GRUMBACH, Michaela et al.Nature genetics. 2012, Vol 44, Num 10, pp 1080-1083, issn 1061-4036, 4 p.Article

Late-onset hereditary axonal neuropathiesBENNETT, C. L; LAWSON, V. H; BIRD, T. D et al.Neurology. 2008, Vol 71, Num 1, pp 14-20, issn 0028-3878, 7 p.Article

Acute motor axonal neuropathy-an atypical presentationLANDAU, Yuval E; DABBY, Ron; AMIR, Jacob et al.Pediatric neurology. 2007, Vol 36, Num 4, pp 271-273, issn 0887-8994, 3 p.Article

Acute motor-sensory axonal neuropathy after cervical spine surgeryMISCUSI, Massimo; CURRA, Antonio; DELLA ROCCA, Carlo et al.Journal of neurosurgery. Spine. 2012, Vol 17, Num 1, pp 82-85, issn 1547-5654, 4 p.Article

Monospecific high-affinity and complement activating anti-GM1 antibodies are determinants in experimental axonal neuropathyNOTTURNO, Francesca; DEL BOCCIO, Piero; LUCIANI, Mirella et al.Journal of the neurological sciences. 2010, Vol 293, Num 1-2, pp 76-81, issn 0022-510X, 6 p.Article

Various immunization protocols for an acute motor axonal neuropathy rabbit model comparedSUSUKI, Keiichiro; NISHIMOTO, Yukihiro; KOGA, Michiaki et al.Neuroscience letters. 2004, Vol 368, Num 1, pp 63-67, issn 0304-3940, 5 p.Article

A Novel Recessive NEFL Mutation Causes a Severe, Early-Onset Axonal NeuropathyYUM, Sabrina W; JUNXIAN ZHANG; MO, Katie et al.Annals of neurology. 2009, Vol 66, Num 6, pp 759-770, issn 0364-5134, 12 p.Article

Microtubules, Axonal Transport, and NeuropathyHOLZBAUR, Erika L. F; SCHERER, Steven S.The New England journal of medicine. 2011, Vol 365, Num 24, pp 2330-2332, issn 0028-4793, 3 p.Article

Short-chain acyl-CoA dehydrogenase deficiency associated with early onset severe axonal neuropathyKURIAN, M. A; HARTLEY, L; ZOLKIPLI, Z et al.Neuropediatrics. 2004, Vol 35, Num 5, pp 312-316, issn 0174-304X, 5 p.Article

POEMS syndrome with prominent acute axonal lesionsMATHIS, S; MAGY, L; KABORE, R et al.Journal of the neurological sciences. 2012, Vol 313, Num 1-2, pp 185-188, issn 0022-510X, 4 p.Article

Involvement of the Globus Pallidus in Giant Axonal NeuropathyEROL, Ilknur; ALEHAN, Fusun; ALKAN, Ozlem et al.Pediatric neurology. 2012, Vol 47, Num 5, pp 382-384, issn 0887-8994, 3 p.Article

Immunoglobulin improves a model of acute motor axonal neuropathy by preventing axonal degenerationNISHIMOTO, Y; KOGA, M; KAMIJO, M et al.Neurology. 2004, Vol 62, Num 11, pp 1939-1944, issn 0028-3878, 6 p.Article

Striking Phenotypic Variability in Familial TRPV4-Axonal Neuropathy Spectrum DisorderAHARONI, Sharon; HARLALKA, Gaurav; OFFIAH, Amaka et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 3153-3156, issn 1552-4825, 4 p.Article

Oxaliplatin-induced neurotoxicity: changes in axonal excitability precede development of neuropathyPARK, Susanna B; LIN, Cindy S.-Y; KRISHNAN, Arun V et al.Brain. 2009, Vol 132, pp 2712-2723, issn 0006-8950, 12 p., 10Article

Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutationsNICHOLSON, G. A; MAGDELAINE, C; ZHU, D et al.Neurology. 2008, Vol 70, Num 19, pp 1678-1681, issn 0028-3878, 4 p., 1Article

Chronic axonal neuropathy with triosephosphate isomerase deficiencyWILMSHURST, Jo M; WISE, Grahame A; POLLARD, John D et al.Pediatric neurology. 2004, Vol 30, Num 2, pp 146-148, issn 0887-8994, 3 p.Article

Progressive idiopathic axonal neuropathy: A comparative clinical and histopathological study with vasculitic neuropathyVRANCKEN, Alexander F. J. E; NOTERMANS, Nicolette C; JANSEN, Gerard H et al.Journal of neurology. 2004, Vol 251, Num 3, pp 269-278, issn 0340-5354, 10 p.Article

Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathyECHANIZ-LAGUNA, Andoni; DUBOURG, Odile; LATOUR, Philippe et al.Neurology. 2014, Vol 82, Num 21, pp 1919-1926, issn 0028-3878, 8 p.Article

Serologic Marker of Acute Motor Axonal Neuropathy in ChildhoodNISHIMOTO, Yukihiro; SUSUKI, Keiichiro; YUKI, Nobuhiro et al.Pediatric neurology. 2008, Vol 39, Num 1, pp 67-70, issn 0887-8994, 4 p.Article

Acute motor conduction block neuropathy followed by axonal degeneration and poor recoveryRAJABALLY, Yusuf A; STRENS, L. H. A; ABBOTT, R. J et al.Neurology. 2006, Vol 66, Num 2, pp 287-288, issn 0028-3878, 2 p.Article

Tubulin cofactor B plays a role in the neuronal growth coneLOPEZ-FANARRAGA, M; CARRANZA, G; BELLIDO, J et al.Journal of neurochemistry. 2007, Vol 100, Num 6, pp 1680-1687, issn 0022-3042, 8 p.Article

Giant Axonal Neuropathy Caused by Compound Heterozygosity for a Maternally Inherited Microdeletion and a Paternal Mutation Within the GAN GeneBUYSSE, Karen; VERGULT, Sarah; MUSSCHE, Silke et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 11, pp 2802-2804, issn 1552-4825, 3 p.Article

Structural requirements of anti-GDla antibodies determine their target specificityLOPEZ, Pablo H. H; GANG ZHANG; BIANCHET, Mario A et al.Brain. 2008, Vol 131, pp 1926-1939, issn 0006-8950, 14 p., 7Article

Dysfunction of nodes of Ranvier: A mechanism for anti-ganglioside antibody-mediated neuropathiesSUSUKI, Keiichiro; YUKI, Nobuhiro; SCHAFER, Dorothy P et al.Experimental neurology (Print). 2012, Vol 233, Num 1, pp 534-542, issn 0014-4886, 9 p.Article

Electrodiagnostic criteria for Guillain―Barrè syndrome: A critical revision and the need for an updateUNCINI, Antonino; KUWABARA, Satoshi.Clinical neurophysiology. 2012, Vol 123, Num 8, pp 1487-1495, issn 1388-2457, 9 p.Article