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Journal Abstract Search
163 related items for PubMed ID: 8608515
1. Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A. Graf WD, Chance PF, Lensch MW, Eng LJ, Lipe HP, Bird TD. Cancer; 1996 Apr 01; 77(7):1356-62. PubMed ID: 8608515 [Abstract] [Full Text] [Related]
3. Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease. LeGuern E, Gouider R, Mabin D, Tardieu S, Birouk N, Parent P, Bouche P, Brice A. Ann Neurol; 1997 Jan 01; 41(1):104-8. PubMed ID: 9005872 [Abstract] [Full Text] [Related]
8. A large family with Charcot-Marie-Tooth Type 1a and Type 2 diabetes mellitus. Koç F, Sarica Y, Yerdelen D, Baris I, Battaloglu E, Sert M. Int J Neurosci; 2006 Feb 01; 116(2):103-14. PubMed ID: 16393877 [Abstract] [Full Text] [Related]
10. The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication. Timmerman V, Nelis E, Van Hul W, Nieuwenhuijsen BW, Chen KL, Wang S, Ben Othman K, Cullen B, Leach RJ, Hanemann CO. Nat Genet; 1992 Jun 01; 1(3):171-5. PubMed ID: 1303230 [Abstract] [Full Text] [Related]
11. Molecular basis of hereditary neuropathies. Chance PF. Phys Med Rehabil Clin N Am; 2001 May 01; 12(2):277-91. PubMed ID: 11345007 [Abstract] [Full Text] [Related]