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Orbic acid in Charcot-Marie-Tooth illness type 1Avan Paassen et al. Or…

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Orbic acid in Charcot-Marie-Tooth Marimastat disorder type 1Avan Paassen et al. Orphanet Journal of Unusual Ailments 2014, 9:38 http://www.ojrd.com/content/9/1/Page fourteen of134.135.136.137.138.139.one hundred forty.141.142. 143.a hundred and forty four.one hundred forty five.146.147.148.149.a hundred and fifty.151.152.153.(CMT-TRIAAL and CMT-TRAUK): a double-blind randomised demo. Lancet Neurol 2011, 10:320?28. Burns J, Ouvrier RA, Yiu EM, Ryan MM: Prolonged cure of childhood Charcot-Marie-Tooth ailment with high-dose ascorbic acid. J Peripher Nerv Syst 2011, 16:272?74. Robertson JF, Willsher Computer, Winterbottom L, Blamey RW, Thorpe S: Onapristone, a progesterone receptor antagonist, as first-line remedy in most important breast most cancers. Eur J Most cancers 1999, 35:214?18. Sahenk Z, Nagaraja HN, McCracken BS, King WM, Freimer ML, Cedarbaum JM, Mendell JR: NT-3 promotes nerve regeneration and sensory enhancement in CMT1A mouse styles as well as in people. Neurology 2005, sixty five:681?89. Sahenk Z, Galloway G, Clark KR, Malik V, Rodino-Klapac LR, Kaspar BK, Chen L, Braganza C, Montgomery C, Mendell JR: AAV1.NT-3 Gene Remedy for Charcot-Marie-Tooth Neuropathy. Mol Ther 2014, 22:511?21. Orfali W, Nicholson RN, Guiot MC, Peterson AC, Snipes GJ: An eight.5-kb segment of your PMP22 promoter responds to lack of axon indicators in the course of Wallerian degeneration, but does not reply to specific axonal alerts in the course of nerve regeneration. J Neurosci Res 2005, PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/12711626 eighty:37?6. Jones EA, Lopez-Anido C, Srinivasan R, Krueger C, Chang LW, Nagarajan R, Svaren J: Regulation of the PMP22 gene by an intronic enhancer. J Neurosci 2011, 31:4242?250. Jang SW, Lopez-Anido C, MacArthur R, Svaren J, Inglese J: Identification of drug modulators concentrating on gene-dosage disorder CMT1A. ACS Chem Biol 2012, 7:1205?213. Sereda M, Griffiths I, Puhlhofer A, Stewart H, Rossner MJ, Zimmerman F, Magyar JP, Schneider A, Hund E, Meinck HM, Suter U, Nave KA: A transgenic rat model of Charcot-Marie-Tooth condition. Neuron 1996, 16:1049?060. De Visser M, Verhamme C: Ascorbic acid for treatment in CMT1A: what's subsequent? Lancet Neurol 2011, ten:291?ninety three. Prospect PF, Alderson MK, Leppig KA, Lensch MW, Matsunami N, Smith B, Swanson PD, Odelberg SJ, Disteche CM, Chicken TD: DNA deletion affiliated with hereditary neuropathy with legal responsibility to pressure palsies. Cell 1993, seventy two:143?fifty one. Mouton P, Tardieu S, Gouider R, Birouk N, Maisonobe T, Dubourg O, Brice A, LeGuern E, Bouche P: Spectrum of medical and electrophysiologic attributes in HNPP patients along with the 17p11.two deletion. Neurology 1999, fifty two:1440?446. Meretoja P, PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/9221828 Silander K, Kalimo H, Aula P, Meretoja A, Savontaus ML: Epidemiology of hereditary neuropathy with legal responsibility to pressure palsies (HNPP) in south western Finland. Neuromuscul Disord 1997, 7:529?32. Possibility PF: Inherited focal, episodic neuropathies: hereditary neuropathy with liability to tension palsies and hereditary neuralgic amyotrophy. Neuromolecular Med 2006, 8:159?74. Gouider R, LeGuern E, Gugenheim M, Tardieu S, Maisonobe T, Leger JM, Vallat JM, Agid Y, Bouche P, Brice A: Clinical, electrophysiologic, and molecular correlations in thirteen families with hereditary neuropathy with liability to pressure palsies and also a chromosome 17p11.2 deletion. Neurology 1995, forty five:2018?023. Lenssen PP, Gabreels-Festen AA, Valentijn LJ, Jongen PJ, Van Beersum SE, Van Engelen BG, Van Wensen PJ, Bolhuis PA, Gabreels FJ, Mariman EC: Hereditary neuropathy with liability to force palsies. Phenotypic variances among individuals with the frequent deletion and also a PMP22 frame shift mutation. Brain 1998, 121(8):1451?458. Gabreels-Festen AA,.

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