These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
7. [Molecular genetics of inherited neuropathies]. Takashima H Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790 [TBL] [Abstract][Full Text] [Related]
8. Polytherapy with a combination of three repurposed drugs (PXT3003) down-regulates Pmp22 over-expression and improves myelination, axonal and functional parameters in models of CMT1A neuropathy. Chumakov I; Milet A; Cholet N; Primas G; Boucard A; Pereira Y; Graudens E; Mandel J; Laffaire J; Foucquier J; Glibert F; Bertrand V; Nave KA; Sereda MW; Vial E; Guedj M; Hajj R; Nabirotchkin S; Cohen D Orphanet J Rare Dis; 2014 Dec; 9():201. PubMed ID: 25491744 [TBL] [Abstract][Full Text] [Related]
9. Multiple functions of the paranodal junction of myelinated nerve fibers. Rosenbluth J J Neurosci Res; 2009 Nov; 87(15):3250-8. PubMed ID: 19224642 [TBL] [Abstract][Full Text] [Related]
10. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families]. Pou Serradell A; Monells J; Téllez MJ; Fossas P; Löfgren A; Meuleman J; Timmerman V; De Jonghe P; Ceuterick C; Martin JJ Rev Neurol (Paris); 2002 May; 158(5 Pt 1):579-88. PubMed ID: 12072826 [TBL] [Abstract][Full Text] [Related]
11. Cation binding at the node of Ranvier in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies. Yoshikawa H; Nishimura T; Kaido M; Toyooka K; Fujimura H; Sakoda S; Yanagihara T Acta Neuropathol; 1996; 91(6):587-94. PubMed ID: 8781657 [TBL] [Abstract][Full Text] [Related]
12. Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies. Li J; Ghandour K; Radovanovic D; Shy RR; Krajewski KM; Shy ME; Nicholson GA Arch Neurol; 2007 Jul; 64(7):974-8. PubMed ID: 17620487 [TBL] [Abstract][Full Text] [Related]
14. A transgenic mouse model for human hereditary neuropathy with liability to pressure palsies. Maycox PR; Ortuño D; Burrola P; Kuhn R; Bieri PL; Arrezo JC; Lemke G Mol Cell Neurosci; 1997; 8(6):405-16. PubMed ID: 9143558 [TBL] [Abstract][Full Text] [Related]
15. Myelin and axon pathology in a long-term study of PMP22-overexpressing mice. Verhamme C; King RH; ten Asbroek AL; Muddle JR; Nourallah M; Wolterman R; Baas F; van Schaik IN J Neuropathol Exp Neurol; 2011 May; 70(5):386-98. PubMed ID: 21487305 [TBL] [Abstract][Full Text] [Related]
16. Hereditary neuropathy with liability to pressure palsies: description of seven patients without known family history. Beydoun SR; Sykes SN; Ganguly G; Lee TS Acta Neurol Scand; 2008 Apr; 117(4):266-72. PubMed ID: 17922888 [TBL] [Abstract][Full Text] [Related]
17. Tuning PAK Activity to Rescue Abnormal Myelin Permeability in HNPP. Hu B; Arpag S; Zhang X; Möbius W; Werner H; Sosinsky G; Ellisman M; Zhang Y; Hamilton A; Chernoff J; Li J PLoS Genet; 2016 Sep; 12(9):e1006290. PubMed ID: 27583434 [TBL] [Abstract][Full Text] [Related]
18. Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease. Mathis S; Corcia P; Tazir M; Camu W; Magdelaine C; Latour P; Biberon J; Guennoc AM; Richard L; Magy L; Funalot B; Vallat JM Neuromuscul Disord; 2014 Jun; 24(6):524-8. PubMed ID: 24792522 [TBL] [Abstract][Full Text] [Related]
19. Many facets of the peripheral myelin protein PMP22 in myelination and disease. Naef R; Suter U Microsc Res Tech; 1998 Jun; 41(5):359-71. PubMed ID: 9672419 [TBL] [Abstract][Full Text] [Related]
20. Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice. Klein D; Patzkó Á; Schreiber D; van Hauwermeiren A; Baier M; Groh J; West BL; Martini R Brain; 2015 Nov; 138(Pt 11):3193-205. PubMed ID: 26297559 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]