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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 1
2004 2
2005 1
2008 2
2011 1
2012 2
2013 1
2020 0
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11 results
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Page 1
Inherited peripheral neuropathies.
Saporta MA, Shy ME. Saporta MA, et al. Neurol Clin. 2013 May;31(2):597-619. doi: 10.1016/j.ncl.2013.01.009. Epub 2013 Mar 5. Neurol Clin. 2013. PMID: 23642725 Free PMC article. Review.
Update on Charcot-Marie-Tooth disease.
Patzkó A, Shy ME. Patzkó A, et al. Curr Neurol Neurosci Rep. 2011 Feb;11(1):78-88. doi: 10.1007/s11910-010-0158-7. Curr Neurol Neurosci Rep. 2011. PMID: 21080241 Free PMC article. Review.
Charcot-Marie-Tooth neuropathies: diagnosis and management.
Jani-Acsadi A, Krajewski K, Shy ME. Jani-Acsadi A, et al. Semin Neurol. 2008 Apr;28(2):185-94. doi: 10.1055/s-2008-1062264. Semin Neurol. 2008. PMID: 18351520 Review.
Phenotypic presentation of the Ser63Del MPZ mutation.
Miller LJ, Patzko A, Lewis RA, Shy ME. Miller LJ, et al. J Peripher Nerv Syst. 2012 Jun;17(2):197-200. doi: 10.1111/j.1529-8027.2012.00398.x. J Peripher Nerv Syst. 2012. PMID: 22734905 Free PMC article.
Dysmyelinated lower motor neurons retract and regenerate dysfunctional synaptic terminals.
Yin X, Kidd GJ, Pioro EP, McDonough J, Dutta R, Feltri ML, Wrabetz L, Messing A, Wyatt RM, Balice-Gordon RJ, Trapp BD. Yin X, et al. J Neurosci. 2004 Apr 14;24(15):3890-8. doi: 10.1523/JNEUROSCI.4617-03.2004. J Neurosci. 2004. PMID: 15084670 Free PMC article.
Gain of glycosylation: a new pathomechanism of myelin protein zero mutations.
Prada V, Passalacqua M, Bono M, Luzzi P, Scazzola S, Nobbio LA, Capponi S, Bellone E, Mandich P, Mancardi G, Shy M, Schenone A, Grandis M. Prada V, et al. Ann Neurol. 2012 Mar;71(3):427-31. doi: 10.1002/ana.22695. Ann Neurol. 2012. PMID: 22451207 Free PMC article.
Expression of laminin receptors in schwann cell differentiation: evidence for distinct roles.
Previtali SC, Nodari A, Taveggia C, Pardini C, Dina G, Villa A, Wrabetz L, Quattrini A, Feltri ML. Previtali SC, et al. J Neurosci. 2003 Jul 2;23(13):5520-30. doi: 10.1523/JNEUROSCI.23-13-05520.2003. J Neurosci. 2003. PMID: 12843252 Free PMC article.
Different cellular and molecular mechanisms for early and late-onset myelin protein zero mutations.
Grandis M, Vigo T, Passalacqua M, Jain M, Scazzola S, La Padula V, Brucal M, Benvenuto F, Nobbio L, Cadoni A, Mancardi GL, Kamholz J, Shy ME, Schenone A. Grandis M, et al. Hum Mol Genet. 2008 Jul 1;17(13):1877-89. doi: 10.1093/hmg/ddn083. Epub 2008 Mar 12. Hum Mol Genet. 2008. PMID: 18337304
Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis.
Bolino A, Bolis A, Previtali SC, Dina G, Bussini S, Dati G, Amadio S, Del Carro U, Mruk DD, Feltri ML, Cheng CY, Quattrini A, Wrabetz L. Bolino A, et al. J Cell Biol. 2004 Nov 22;167(4):711-21. doi: 10.1083/jcb.200407010. J Cell Biol. 2004. PMID: 15557122 Free PMC article.
Conditional disruption of beta 1 integrin in Schwann cells impedes interactions with axons.
Feltri ML, Graus Porta D, Previtali SC, Nodari A, Migliavacca B, Cassetti A, Littlewood-Evans A, Reichardt LF, Messing A, Quattrini A, Mueller U, Wrabetz L. Feltri ML, et al. J Cell Biol. 2002 Jan 7;156(1):199-209. doi: 10.1083/jcb.200109021. Epub 2002 Jan 3. J Cell Biol. 2002. PMID: 11777940 Free PMC article.
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