Vílchez JJ - Search Results

1

[Genetic analysis of Friedreich's ataxia using polymorphic DNA markers].

Palau F, Vílchez JJ, Beneyto M, López Arlandis JM, Castellano FM, Badía L, Prieto F. Palau F, et al. Among authors: vilchez jj. Med Clin (Barc). 1990 May 5;94(17):651-4. Med Clin (Barc). 1990. PMID: 1974690 Spanish.

2

Genetic diagnosis of Friedreich's ataxia.

Palau F, Monros E, Prieto F, Vilchez JJ, Lopez-Arlandis JM. Palau F, et al. Among authors: vilchez jj. Lancet. 1991 Oct 26;338(8774):1087. doi: 10.1016/0140-6736(91)91950-y. Lancet. 1991. PMID: 1681394 No abstract available.

3

[The presence of oligoclonal bands in the cerebrospinal fluid in various neurologic diseases].

Coret F, Vílchez JJ, Enguídanos MJ, López-Arlandis J, Fernández-Izquierdo S. Coret F, et al. Among authors: vilchez jj. Rev Clin Esp. 1989 Oct;185(5):231-4. Rev Clin Esp. 1989. PMID: 2608980 Spanish.

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: vilchez jj. Med Clin (Barc). 1995 May 6;104(17):648-52. Med Clin (Barc). 1995. PMID: 7623491 Spanish.

5

Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q.

Palau F, De Michele G, Vilchez JJ, Pandolfo M, Monrós E, Cocozza S, Smeyers P, Lopez-Arlandis J, Campanella G, Di Donato S, et al. Palau F, et al. Among authors: vilchez jj. Ann Neurol. 1995 Mar;37(3):359-62. doi: 10.1002/ana.410370312. Ann Neurol. 1995. PMID: 7695235

6

Mapping of Friedreich's ataxia locus by identification of recombination events in patients homozygous by descent.

Monrós E, Smeyers P, Rodius F, Cañizares J, Moltó MD, Vilchez JJ, Pandolfo M, Lopez-Arlandis J, de Frutos R, Prieto F, et al. Monrós E, et al. Among authors: vilchez jj. Eur J Hum Genet. 1994;2(4):291-9. doi: 10.1159/000472373. Eur J Hum Genet. 1994. PMID: 7704559

7

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: vilchez jj. Neuroepidemiology. 1995;14(1):14-9. doi: 10.1159/000109774. Neuroepidemiology. 1995. PMID: 7898602

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: vilchez jj. 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: vilchez jj. Hum Genet. 1997 Jun;99(6):746-54. doi: 10.1007/s004390050442. Hum Genet. 1997. PMID: 9187667

10

Phenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeat.

Monrós E, Moltó MD, Martínez F, Cañizares J, Blanca J, Vílchez JJ, Prieto F, de Frutos R, Palau F. Monrós E, et al. Among authors: vilchez jj. Am J Hum Genet. 1997 Jul;61(1):101-10. doi: 10.1086/513887. Am J Hum Genet. 1997. PMID: 9245990 Free PMC article.

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