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Nationwide genetic analysis of more than 600 families with inherited eye diseases in Argentina.
Schlottmann PG, Luna JD, Labat N, Yadarola MB, Bainttein S, Esposito E, Ibañez A, Barbaro EI, Álvarez Mendiara A, Picotti CP, Chirino Misisian A, Andreussi L, Gras J, Capalbo L, Visotto M, Dipierri JE, Alcoba E, Fernández Gabrielli L, Ávila S, Aucar ME, Martin DM, Ormaechea GJ, Inga ME, Francone AA, Charles M, Zompa T, Pérez PJ, Lotersztein V, Nuova PJ, Canonero IB, Mahroo OA, Michaelides M, Arno G, Daich Varela M. Schlottmann PG, et al. Among authors: lotersztein v. NPJ Genom Med. 2023 May 22;8(1):8. doi: 10.1038/s41525-023-00352-1. NPJ Genom Med. 2023. PMID: 37217489 Free PMC article.
Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.
Espeche LD, Solari AP, Mori MÁ, Arenas RM, Palomares M, Pérez M, Martínez C, Lotersztein V, Segovia M, Armando R, Dain LB, Nevado J, Lapunzina P, Rozental S. Espeche LD, et al. Among authors: lotersztein v. Mol Biol Rep. 2020 Sep;47(9):6863-6878. doi: 10.1007/s11033-020-05743-6. Epub 2020 Sep 13. Mol Biol Rep. 2020. PMID: 32920771
Inflammatory cutaneous lesions and pulmonary manifestations in a new patient with autosomal recessive ISG15 deficiency case report.
Buda G, Valdez RM, Biagioli G, Olivieri FA, Affranchino N, Bouso C, Lotersztein V, Bogunovic D, Bustamante J, Martí MA. Buda G, et al. Among authors: lotersztein v. Allergy Asthma Clin Immunol. 2020 Sep 3;16:77. doi: 10.1186/s13223-020-00473-7. eCollection 2020. Allergy Asthma Clin Immunol. 2020. PMID: 32944031 Free PMC article.
Acitretin embryopathy: a case report.
Barbero P, Lotersztein V, Bronberg R, Perez M, Alba L. Barbero P, et al. Among authors: lotersztein v. Birth Defects Res A Clin Mol Teratol. 2004 Oct;70(10):831-3. doi: 10.1002/bdra.20078. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15470719
14 results