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Results 1 to 25 of 185

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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

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

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

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

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

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

Intermediate filament aggregation in fibroblasts of giant axonal neuropathy patients is aggravated in non dividing cells and by microtubule destabilizationBOMONT, Pascale; KOENIG, Michel.Human molecular genetics (Print). 2003, Vol 12, Num 8, pp 813-822, issn 0964-6906, 10 p.Article

Giant axonal neuropathy: A clinicoradiopathologic diagnosisISRANI, Anil; CHAKRABARTY, Biswaroop; GULATI, Sheffali et al.Neurology. 2014, Vol 82, Num 9, pp 816-817, issn 0028-3878, 2 p.Article

Time course of axonal regeneration in acute motor axonal neuropathyTAMURA, Noriko; KUWABARA, Satoshi; MISAWA, Sonoko et al.Muscle & nerve. 2007, Vol 35, Num 6, pp 793-795, issn 0148-639X, 3 p.Article

Giant axonal neuropathy: a conditional mutation affecting cytoskeletal organizationKLYMKOWSKY, M. W; PLUMMER, D. J.The Journal of cell biology. 1985, Vol 100, Num 1, pp 245-250, issn 0021-9525Article

Conduction block and axonal degeneration co-occurring in a patient with axonal Guillain-Barré syndromeKOKUBUN, Norito; SHAHRIZAILA, Nortina; HIRATA, Koichi et al.Journal of the neurological sciences. 2012, Vol 319, Num 1-2, pp 164-167, issn 0022-510X, 4 p.Article

The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathySCARANO, Valentina; MANCINI, Pietro; FILLA, Alessandro et al.Journal of neurology. 2005, Vol 252, Num 8, pp 901-903, issn 0340-5354, 3 p.Article

PROTEOMIC ANALYSIS IN GIANT AXONAL NEUROPATHY: NEW INSIGHTS INTO DISEASE MECHANISMSMUSSCHE, Silke; DE PAEPE, Boel; SMET, Joél et al.Muscle & nerve. 2012, Vol 46, Num 2, pp 246-256, issn 0148-639X, 11 p.Article

Extended phenotypic spectrum of KIF5A mutations: From spastic paraplegia to axonal neuropathyLIU, Yo-Tsen; LAURA, Matilde; PROUKAKIS, Christos et al.Neurology. 2014, Vol 83, Num 7, pp 612-619, issn 0028-3878, 8 p.Article

Sensory nerve conduction in demyelinating and axonal Guillain-Barré syndromesKUWABARA, Satoshi; OGAWARA, Kazue; MISAWA, Sonoko et al.European neurology. 2004, Vol 51, Num 4, pp 196-198, issn 0014-3022, 3 p.Article

Cerebral proton magnetic resonance spectroscopy of a patient with giant axonal neuropathyBROCKMANN, Knut; POUWELS, Petra J. W; DECHENT, Peter et al.Brain & development (Tokyo. 1979). 2003, Vol 25, Num 1, pp 45-50, issn 0387-7604, 6 p.Article

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