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Audiologic evaluation in Charcot-Marie-Tooth disease.
Pérez H, Vílchez J, Sevilla T, Martínez L. Pérez H, et al. Scand Audiol Suppl. 1988;30:211-3. Scand Audiol Suppl. 1988. PMID: 3227273
Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis.
Palau F, Löfgren A, De Jonghe P, Bort S, Nelis E, Sevilla T, Martin JJ, Vilchez J, Prieto F, Van Broeckhoven C. Palau F, et al. Hum Mol Genet. 1993 Dec;2(12):2031-5. doi: 10.1093/hmg/2.12.2031. Hum Mol Genet. 1993. PMID: 8111370
[Genetics of peripheral neuropathies and hereditary ataxias].
Palau F, Sevilla T. Palau F, et al. Neurologia. 1995 Dec;10 Suppl 1:32-43. Neurologia. 1995. PMID: 8838557 Review. Spanish.
[Distal spinal muscular atrophy].
Sevilla T. Sevilla T. Neurologia. 1996 Dec;11 Suppl 5:58-65. Neurologia. 1996. PMID: 9044574 Review. Spanish.
Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.
Bort S, Nelis E, Timmerman V, Sevilla T, Cruz-Martínez A, Martínez F, Millán JM, Arpa J, Vílchez JJ, Prieto F, Van Broeckhoven C, Palau F. Bort S, et al. Hum Genet. 1997 Jun;99(6):746-54. doi: 10.1007/s004390050442. Hum Genet. 1997. PMID: 9187667
The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease.
Cuesta A, Pedrola L, Sevilla T, García-Planells J, Chumillas MJ, Mayordomo F, LeGuern E, Marín I, Vílchez JJ, Palau F. Cuesta A, et al. Nat Genet. 2002 Jan;30(1):22-5. doi: 10.1038/ng798. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743580
Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.
Sevilla T, Cuesta A, Chumillas MJ, Mayordomo F, Pedrola L, Palau F, Vílchez JJ. Sevilla T, et al. Brain. 2003 Sep;126(Pt 9):2023-33. doi: 10.1093/brain/awg202. Epub 2003 Jun 23. Brain. 2003. PMID: 12821518
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