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Scopus Author ID: 57194944605
SciProfiles: 630454

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Employment (1)

Instituto de Investigaciones en Ingeniería Genética y Biología Molecular: Buenos Aires, Buenos Aires, AR

2005-03 to present | associate researcher (Laboratory of Genetics and Physiology of Hearing)
Employment
Source: Self-asserted source
Viviana Dalamon

Education and qualifications (1)

Universidad de Buenos Aires: Buenos Aires, AR

1991-03 to 1997-03
Education
Source: Self-asserted source
Viviana Dalamon

Professional activities (2)

Genetics Society: Buenos Aires, AR

2019 to present
Membership
Source: Self-asserted source
Viviana Dalamon

Argentinean Society of Clinical Research: Buenos Aires, AR

2003 to present
Service
Source: Self-asserted source
Viviana Dalamon

Works (26)

Key role of the TM2-TM3 loop in calcium potentiation of the α9α10 nicotinic acetylcholine receptor

Cellular and Molecular Life Sciences
2024-12 | Journal article
DOI: 10.1007/s00018-024-05381-2
Contributors: Sofia L. Gallino; Lucía Agüero; Juan C. Boffi; Gustavo Schottlender; Paula Buonfiglio; Viviana Dalamon; Irina Marcovich; Agustín Carpaneto; Patricio O. Craig; Paola V. Plazas et al.
Source: check_circle
Crossref

Comment on De Rosa et al. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America. <i>Genes</i> 2024, <i>15</i>, 178

Genes
2024-10 | Journal article | Author
DOI: 10.3390/genes15111401
Contributors: Ana Belén Elgoyhen; Paula Buonfiglio; Viviana Dalamon
Source: check_circle
Multidisciplinary Digital Publishing Institute

From Past to Present: Pompe Disease, Pseudodeficiency Alleles, and Diagnostic Challenges

2024-10-04 | Preprint
DOI: 10.1101/2024.10.03.24314698
Contributors: Florencia Giliberto; Paula Inés Buonfiglio; Gabriel Capellino; Carmen Llames Massini; Viviana Dalamón; Leonela Luce; Micaela Carcione
Source: check_circle
Crossref

In silico and in vivo analyses of a novel variant in MYO6 identified in a family with postlingual non-syndromic hearing loss from Argentina

NAR Genomics and Bioinformatics
2024-09-28 | Journal article
DOI: 10.1093/nargab/lqae162
Contributors: Paula I Buonfiglio; Carlos D Bruque; Lucía Salatino; Vanesa Lotersztein; Mariela Pace; Sofia Grinberg; Ana B Elgoyhen; Paola V Plazas; Viviana Dalamón
Source: check_circle
Crossref

Comprehensive Approach for the Genetic Diagnosis of Patients with Waardenburg Syndrome

Journal of Personalized Medicine
2024-08-27 | Journal article
DOI: 10.3390/jpm14090906
Contributors: Paula Inés Buonfiglio; Agustín Izquierdo; Mariela Vanina Pace; Sofia Grinberg; Vanesa Lotersztein; Paloma Brun; Carlos David Bruque; Ana Belén Elgoyhen; Viviana Dalamón
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Co-release of GABA and ACh from medial olivocochlear neurons fine tunes cochlear efferent inhibition

2024-08-16 | Preprint
DOI: 10.1101/2024.08.12.607644
Contributors: Tais Castagnola; Valeria C Castagna; Siân R. Kitcher; Lester Torres Cadenas; Mariano N Di Guilmi; Maria Eugenia Gomez Casati; Paula I Buonfiglio; Viviana Dalamón; Eleonora Katz; Ana Belén Elgoyhen et al.
Source: check_circle
Crossref

Novel Pathogenic Variants in the Gene Encoding Stereocilin (<i>STRC</i>) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean Subjects

Biomedicines
2023-10 | Journal article | Author
DOI: 10.3390/biomedicines11112943
Contributors: María Domínguez Ruiz; Laura Ruiz-Palmero; Paula Buonfiglio; Irene García-Vaquero; Elena Gómez-Rosas; Marina Goñi; Manuela Villamar; Matías Morín; MIGUEL ANGEL MORENO-PELAYO; Ana Belén Elgoyhen et al.
Source: check_circle
Multidisciplinary Digital Publishing Institute

Mitochondrial DNA variants in a cohort from Argentina with suspected Leber’s hereditary optic neuropathy (LHON)

PLOS ONE
2023-02-24 | Journal article
DOI: 10.1371/journal.pone.0275703
Contributors: Paula I. Buonfiglio; Enrico Baruffini; Sebastián Menazzi; Liliana Francipane; Vanesa Lotersztein; Verónica Ferreiro; Ana Belén Elgoyhen; Viviana Dalamón
Source: check_circle
Crossref

Theragnosis for Duchenne muscular dystrophy

Frontiers in pharmacology
2021-06-03 | Journal article
Source: Self-asserted source
Viviana Dalamon

GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort

Genes
2020-10-21 | Journal article
DOI: 10.3390/genes11101233
Part of ISSN: 2073-4425
Source: Self-asserted source
Viviana Dalamon
grade
Preferred source (of 3)‎

Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: A case report

BMC Medical Genetics
2016 | Journal article
DOI: 10.1186/s12881-016-0298-y
EID:

2-s2.0-84977664394

Part of ISBN:

14712350
Contributors: Dalamón, V.K.; Buonfiglio, P.; Larralde, M.; Craig, P.; Lotersztein, V.; Choate, K.; Pallares, N.; Diamante, V.; Elgoyhen, A.B.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Gap-junctional channel and hemichannel activity of two recently identified connexin 26 mutants associated with deafness

Pflugers Archiv European Journal of Physiology
2016 | Journal article
DOI: 10.1007/s00424-016-1788-7
EID:

2-s2.0-84954308082

Part of ISBN:

14322013 00316768
Contributors: Dalamon, V.; Fiori, M.C.; Figueroa, V.A.; Oliva, C.A.; del Rio, R.; Gonzalez, W.; Canan, J.; Elgoyhen, A.B.; Altenberg, G.A.; Retamal, M.A.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

MLPA analysis of an Argentine cohort of patients with dystrophinopathy: Association of intron breakpoints hot spots with STR abundance in DMD gene

Journal of the Neurological Sciences
2016 | Journal article
DOI: 10.1016/j.jns.2016.03.047
EID:

2-s2.0-84962807480

Part of ISBN:

18785883 0022510X
Contributors: Luce, L.N.; Dalamon, V.; Ferrer, M.; Parma, D.; Szijan, I.; Giliberto, F.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Identification of four novel connexin 26 mutations in non-syndromic deaf patients: Genotype-phenotype analysis in moderate cases

Molecular Biology Reports
2013 | Journal article
DOI: 10.1007/s11033-013-2814-x
EID:

2-s2.0-84890433979

Part of ISBN:

03014851 15734978
Contributors: Dalamón, V.; Florencia Wernert, M.; Lotersztein, V.; Craig, P.O.; Diamante, R.R.; Barteik, M.E.; Curet, C.; Paoli, B.; Mansilla, E.; Elgoyhen, A.B.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

GJB2 and GJB6 genes: Molecular study and identification of novel GJB2 mutations in the hearing-impaired argentinean population

Audiology and Neurotology
2010 | Journal article
DOI: 10.1159/000254487
EID:

2-s2.0-77950095765

Part of ISBN:

14203030 14219700
Contributors: Dalamón, V.; Lotersztein, V.; Béhèran, A.; Lipovsek, M.; Diamante, F.; Pallares, N.; Francipane, L.; Frechtel, G.; Paoli, B.; Mansilla, E. et al.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Electrical properties and functional expression of ionic channels in cochlear inner hair cells of mice lacking the α10 nicotinic cholinergic receptor subunit

JARO - Journal of the Association for Research in Otolaryngology
2009 | Journal article
DOI: 10.1007/s10162-009-0164-0
EID:

2-s2.0-67349269089

Part of ISBN:

15253961
Contributors: Gómez-Casati, M.E.; Wedemeyer, C.; Taranda, J.; Lipovsek, M.; Dalamon, V.; Elgoyhen, A.B.; Katz, E.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Performance of speech perception after cochlear implantation in DFNB1 patients

Acta Oto-Laryngologica
2009 | Journal article
DOI: 10.1080/00016480802566295
EID:

2-s2.0-66349128627

Part of ISBN:

00016489 16512553
Contributors: Dalamón, V.; Lotersztein, V.; Lipovsek, M.; Béhern, A.; Mondino, M.E.; Diamante, F.; Pallares, N.; Diamante, V.; Elgoyhen, A.B.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

The relevance of molecular biology studies in the genetic counselling of argentine retinoblastoma families,Importancia de los estudios de biología molecular en el asesoramiento genético de familias argentinas con retinoblastoma

Archivos de la Sociedad Espanola de Oftalmologia
2009 | Journal article
EID:

2-s2.0-77953692093

Part of ISBN:

03656691
Contributors: Parma, D.L.; Dalamon, V.K.; Fernández, C.; Szijan, I.; Damel, A.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

RB1 germ-line deletions in argentine retinoblastoma patients

Molecular Diagnosis and Therapy
2007 | Journal article
DOI: 10.1007/BF03256222
EID:

2-s2.0-33846963140

Part of ISBN:

11771062
Contributors: Fernández, C.; Repetto, K.; Dalamon, V.; Bergonzi, F.; Ferreiro, V.; Szijan, I.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients

Hearing Research
2005 | Journal article
DOI: 10.1016/j.heares.2005.04.012
EID:

2-s2.0-24944556454

Part of ISBN:

03785955
Contributors: Dalamón, V.; Béhèran, A.; Diamante, F.; Pallares, N.; Diamante, V.; Elgoyhen, A.B.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Detection of germline mutations in Argentine retinoblastoma patients: Low and full penetrance retinoblastoma caused by the same germline truncating mutation

Journal of Biochemistry and Molecular Biology
2004 | Journal article
DOI: 10.5483/bmbrep.2004.37.2.246
EID:

2-s2.0-2342458365

Part of ISBN:

12258687
Contributors: Dalamón, V.; Surace, E.; Giliberto, F.; Ferreiro, V.; Fernandez, C.; Szijan, I.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy

Neurological Research
2004 | Journal article
DOI: 10.1179/016164104773026589
EID:

2-s2.0-0842310824

Part of ISBN:

01616412
Contributors: Giliberto, F.; Ferreiro, V.; Dalamon, V.; Szijan, I.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Direct deletion analysis in two duchenne muscular dystrophy symptomatic females using polymorphic dinucleotide (CA)<inf>n</inf> loci within the dystrophin gene

Journal of Biochemistry and Molecular Biology
2003 | Journal article
DOI: 10.5483/bmbrep.2003.36.2.179
EID:

2-s2.0-0842326250

Part of ISBN:

12258687
Contributors: Giliberto, F.; Ferreiro, V.; Dalamón, V.; Surace, E.; Cotignola, J.; Esperante, S.; Borelina, D.; Baranzini, S.; Szijan, I.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

NF2 tumor suppressor gene: A comprehensive and efficient detection of somatic mutations by denaturing HPLC and microarray-CGH

NeuroMolecular Medicine
2003 | Journal article
DOI: 10.1385/NMM:3:1:41
EID:

2-s2.0-0042326348

Part of ISBN:

15351084
Contributors: Szijan, I.; Rochefort, D.; Bruder, C.; Surace, E.; Machiavelli, G.; Dalamon, V.; Cotignola, J.; Ferreiro, V.; Campero, A.; Basso, A. et al.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Detection of mutations in argentine retinoblastoma patients by segregation of polymorphisms, exon analysis and cytogenetic test

Ophthalmic Research
2001 | Journal article
DOI: 10.1159/000055690
EID:

2-s2.0-0035679258

Part of ISBN:

00303747
Contributors: Dalamon, V.; Surace, E.; Borelina, D.; Ziembar, M.; Esperante, S.; Francipane, L.; Davila, M.; Parma, D.; Szijan, I.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier

Carrier detection in Duchenne and Becker muscular dystrophy Argentine families

Clinical Genetics
1998 | Journal article
DOI: 10.1111/j.1399-0004.1998.tb03771.x
EID:

2-s2.0-0032421067

Part of ISBN:

00099163
Contributors: Baranzini, S.E.; Giliberto, F.; Dalamon, V.; Barreiro, C.; García-Erro, M.; Grippo, J.; Szijan, I.
Source: Self-asserted source
Viviana Dalamon via Scopus - Elsevier
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