Viviana Dalamon

Summary

Country: Argentina

Publications

  1. ncbi Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients
    Viviana Dalamon
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Consejo Nacional de Investigaciones Cientificas y Tecnicas, Universidad de Buenos Aires, Vuelta de Obligado 2490, 1428 Buenos Aires, Argentina
    Hear Res 207:43-9. 2005
  2. doi Performance of speech perception after cochlear implantation in DFNB1 patients
    Viviana Dalamon
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Consejo Nacional de Investigaciones Cientificas y Tecnicas, Universidad de Buenos Aires, Buenos Aires, Argentina
    Acta Otolaryngol 129:395-8. 2009
  3. doi GJB2 and GJB6 genes: molecular study and identification of novel GJB2 mutations in the hearing-impaired Argentinean population
    Viviana Dalamon
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Consejo Nacional de Investigaciones Cientificas y Tecnicas, Universidad de Buenos Aires, Buenos Aires, Argentina
    Audiol Neurootol 15:194-202. 2010
  4. doi Identification of four novel connexin 26 mutations in non-syndromic deaf patients: genotype-phenotype analysis in moderate cases
    Viviana Dalamon
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Dr Héctor N Torres INGEBI Consejo Nacional de Investigaciones Científicas y Técnicas CONICET, Ciudad Autonoma de Buenos Aires, Argentina
    Mol Biol Rep 40:6945-55. 2013
  5. ncbi Detection of germline mutations in argentine retinoblastoma patients: low and full penetrance retinoblastoma caused by the same germline truncating mutation
    Viviana Dalamon
    Catedra de Genetica y Biologia Molecular, Facultad de Farmacia y Bioquimica, Universidad de Buenos Aires, Argentina
    J Biochem Mol Biol 37:246-53. 2004
  6. ncbi RB1 germ-line deletions in Argentine retinoblastoma patients
    Cecilia Fernandez
    Genetics and Molecular Biology Department, Faculty of Pharmacy, Jose de San Martin Hospital, Buenos Aires University, Buenos Aires, Argentina
    Mol Diagn Ther 11:55-61. 2007
  7. ncbi Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy
    Florencia Giliberto
    Genetica y Biologia Molecular, Facultad de Farmacia y Bioquimica, Instituto de Neurociencias Aplicadas del Hospital de Clinicas, Universidad de Buenos Aires, Buenos Aires, Argentina
    Neurol Res 26:83-7. 2004
  8. ncbi Direct deletion analysis in two Duchenne muscular dystrophy symptomatic females using polymorphic dinucleotide (CA)n loci within the dystrophin gene
    Florencia Giliberto
    Catedra de Genetica y Biologia Molecular, Facultad de Famacia y Bioquimica, University of Buenos Aires, and Hospital de Clinicas Jose de San Martin, Buenos Aires, Argentina
    J Biochem Mol Biol 36:179-84. 2003
  9. pmc Electrical properties and functional expression of ionic channels in cochlear inner hair cells of mice lacking the alpha10 nicotinic cholinergic receptor subunit
    María Eugenia Gómez-Casati
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Consejo Nacional de Investigaciones Cientificas y Tecnicas, Vuelta de Obligado 2490, Buenos Aires 1428, Argentina
    J Assoc Res Otolaryngol 10:221-32. 2009

Collaborators

Detail Information

Publications9

  1. ncbi Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients
    Viviana Dalamon
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Consejo Nacional de Investigaciones Cientificas y Tecnicas, Universidad de Buenos Aires, Vuelta de Obligado 2490, 1428 Buenos Aires, Argentina
    Hear Res 207:43-9. 2005
    ..The present study demonstrates that mutations in the GJB2 gene and the delGJB6-D13S1830 are prevalent in the Argentinean population...
  2. doi Performance of speech perception after cochlear implantation in DFNB1 patients
    Viviana Dalamon
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Consejo Nacional de Investigaciones Cientificas y Tecnicas, Universidad de Buenos Aires, Buenos Aires, Argentina
    Acta Otolaryngol 129:395-8. 2009
    ..These data have important implications for the selection of prognostic indicators of the outcome of cochlear implantation...
  3. doi GJB2 and GJB6 genes: molecular study and identification of novel GJB2 mutations in the hearing-impaired Argentinean population
    Viviana Dalamon
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Consejo Nacional de Investigaciones Cientificas y Tecnicas, Universidad de Buenos Aires, Buenos Aires, Argentina
    Audiol Neurootol 15:194-202. 2010
    ..Most important, it adds two novel GJB2 mutations to be taken into consideration in the genetic diagnosis of non-syndromic sensorineural hearing loss...
  4. doi Identification of four novel connexin 26 mutations in non-syndromic deaf patients: genotype-phenotype analysis in moderate cases
    Viviana Dalamon
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Dr Héctor N Torres INGEBI Consejo Nacional de Investigaciones Científicas y Técnicas CONICET, Ciudad Autonoma de Buenos Aires, Argentina
    Mol Biol Rep 40:6945-55. 2013
    ..This work shows the high prevalence of GJB2 mutations in the Argentinean population and presents an analysis of moderate phenotypes in our cohort. ..
  5. ncbi Detection of germline mutations in argentine retinoblastoma patients: low and full penetrance retinoblastoma caused by the same germline truncating mutation
    Viviana Dalamon
    Catedra de Genetica y Biologia Molecular, Facultad de Farmacia y Bioquimica, Universidad de Buenos Aires, Argentina
    J Biochem Mol Biol 37:246-53. 2004
    ..This analysis proved to be a useful method for the detection of mutations in the RB1 gene, and contributed to the adequate genetic counseling to patients and relatives...
  6. ncbi RB1 germ-line deletions in Argentine retinoblastoma patients
    Cecilia Fernandez
    Genetics and Molecular Biology Department, Faculty of Pharmacy, Jose de San Martin Hospital, Buenos Aires University, Buenos Aires, Argentina
    Mol Diagn Ther 11:55-61. 2007
    ..Because early diagnosis is necessary for implementing effective treatment and preserving vision, it is important to identify the mutations in the affected family...
  7. ncbi Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy
    Florencia Giliberto
    Genetica y Biologia Molecular, Facultad de Farmacia y Bioquimica, Instituto de Neurociencias Aplicadas del Hospital de Clinicas, Universidad de Buenos Aires, Buenos Aires, Argentina
    Neurol Res 26:83-7. 2004
    ..Therefore, though mutations with variable locations may lead to cognitive impairment, our results show that deletions in the distal portion of the gene are basically related to mental retardation...
  8. ncbi Direct deletion analysis in two Duchenne muscular dystrophy symptomatic females using polymorphic dinucleotide (CA)n loci within the dystrophin gene
    Florencia Giliberto
    Catedra de Genetica y Biologia Molecular, Facultad de Famacia y Bioquimica, University of Buenos Aires, and Hospital de Clinicas Jose de San Martin, Buenos Aires, Argentina
    J Biochem Mol Biol 36:179-84. 2003
    ..The use of microsatellite genotyping within the DMD gene enables the detection of the mutant allele in female carriers. It is also a useful method to provide DMD families with more accurate genetic counseling...
  9. pmc Electrical properties and functional expression of ionic channels in cochlear inner hair cells of mice lacking the alpha10 nicotinic cholinergic receptor subunit
    María Eugenia Gómez-Casati
    Instituto de Investigaciones en Ingenieria Genetica y Biologia Molecular, Consejo Nacional de Investigaciones Cientificas y Tecnicas, Vuelta de Obligado 2490, Buenos Aires 1428, Argentina
    J Assoc Res Otolaryngol 10:221-32. 2009
    ..The present results show that the alpha10 nAChR subunit is not essential for the correct establishment of the intrinsic electrical properties of IHCs during development...