Sevilla T - Search Results

1

Asymptomatic HyperCKemia in the Pediatric Population: A Prospective Study Utilizing Next-Generation Sequencing and Ancillary Tests.

Marti P, Pitarch-Castellano I, Muelas N, Azorín I, Fores L, Vilchez R, Sevilla T, Vilchez JJ. Marti P, et al. Among authors: sevilla t. Neurology. 2025 Jan 14;104(1):e210116. doi: 10.1212/WNL.0000000000210116. Epub 2024 Dec 12. Neurology. 2025. PMID: 39666917

2

Audiologic evaluation in Charcot-Marie-Tooth disease.

Pérez H, Vílchez J, Sevilla T, Martínez L. Pérez H, et al. Among authors: sevilla t. Scand Audiol Suppl. 1988;30:211-3. Scand Audiol Suppl. 1988. PMID: 3227273

3

[The diagnosis and prevalence of locus CMT1A duplication in Charcot-Marie-Tooth disease type 1].

Bort S, Sevilla T, Vílchez JJ, Prieto F, Palau F. Bort S, et al. Among authors: sevilla t. Med Clin (Barc). 1995 May 6;104(17):648-52. Med Clin (Barc). 1995. PMID: 7623491 Spanish.

4

Friedreich's ataxia: an epidemiological study in Valencia, Spain, based on consanguinity analysis.

López-Arlandis JM, Vílchez JJ, Palau F, Sevilla T. López-Arlandis JM, et al. Among authors: sevilla t. Neuroepidemiology. 1995;14(1):14-9. doi: 10.1159/000109774. Neuroepidemiology. 1995. PMID: 7898602

5

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. Among authors: sevilla t. Hum Mol Genet. 1993 Dec;2(12):2031-5. doi: 10.1093/hmg/2.12.2031. Hum Mol Genet. 1993. PMID: 8111370

6

[Disseminated encephalomyelitis. A study of 5 cases].

Coret F, Sevilla T, Vílchez JJ, Poyatos C. Coret F, et al. Among authors: sevilla t. Neurologia. 1993 Jun-Jul;8(6):197-203. Neurologia. 1993. PMID: 8352977 Spanish.

7

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. Among authors: sevilla t. Hum Genet. 1997 Jun;99(6):746-54. doi: 10.1007/s004390050442. Hum Genet. 1997. PMID: 9187667

8

Déjérine-Sottas neuropathy associated with de novo S79P mutation of the peripheral myelin protein 22 (PMP22) gene.

Bort S, Sevilla T, García-Planells J, Blesa D, Paricio N, Vílchez JJ, Prieto F, Palau F. Bort S, et al. Among authors: sevilla t. Hum Mutat. 1998;Suppl 1:S95-8. doi: 10.1002/humu.1380110132. Hum Mutat. 1998. PMID: 9452053 No abstract available.

9

Early onset cerebellar ataxia and preservation of tendon reflexes: clinical phenotypes associated with GAA trinucleotide repeat expanded and non-expanded genotypes.

De Castro M, Cruz-Martínez A, Vílchez JJ, Sevilla T, Pineda M, Berciano J, Palau F. De Castro M, et al. Among authors: sevilla t. J Peripher Nerv Syst. 1999;4(1):58-62. J Peripher Nerv Syst. 1999. PMID: 10197066

10

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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