Sevilla T - Search Results

1

Identification of a novel founder mutation in the DYSF gene causing clinical variability in the Spanish population.

Vilchez JJ, Gallano P, Gallardo E, Lasa A, Rojas-García R, Freixas A, De Luna N, Calafell F, Sevilla T, Mayordomo F, Baiget M, Illa I. Vilchez JJ, et al. Among authors: sevilla t. Arch Neurol. 2005 Aug;62(8):1256-9. doi: 10.1001/archneur.62.8.1256. Arch Neurol. 2005. PMID: 16087766

2

Staging Cardiac Damage and Prognosis in Asymptomatic Aortic Stenosis: Early Surgery Might Not Benefit All.

Sevilla T, Gil-Fernández JF, Candela-Ferre J, Rojas-Lavado G, González-Bartol E, Revilla-Orodea A, Gómez-Salvador I, San Román JA. Sevilla T, et al. J Am Soc Echocardiogr. 2023 Jan;36(1):121-123. doi: 10.1016/j.echo.2022.10.018. Epub 2022 Nov 1. J Am Soc Echocardiogr. 2023. PMID: 36332802 No abstract available.

3

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

4

[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.

5

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

6

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

7

[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.

8

[Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure].

Pou Serradell A, Espadaler JM, Aragonés JM, Bufill E, Alameda F, Vílchez JJ, Sevilla T, Piqueras A, Palau F, Bort S. Pou Serradell A, et al. Among authors: sevilla t. Neurologia. 1995 Nov;10(9):367-74. Neurologia. 1995. PMID: 8554792 Spanish.

9

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

10

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.

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