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Effect of the parental origin of the X-chromosome on the clinical features, associated complications, the two-year-response to growth hormone (rhGH) and the biochemical profile in patients with turner syndrome.
Alvarez-Nava F, Lanes R, Quintero JM, Miras M, Fideleff H, Mericq V, Marcano H, Zabala W, Soto M, Pardo T, Borjas L, Villalobos J, Gunczler P, Unanue N, Tkalenko N, Boyanofsky A, Silvano L, Franchioni L, Llano M, Fideleff G, Azaretzky M, Suarez M. Alvarez-Nava F, et al. Among authors: miras m. Int J Pediatr Endocrinol. 2013 Jun 4;2013(1):10. doi: 10.1186/1687-9856-2013-10. Int J Pediatr Endocrinol. 2013. PMID: 23731950 Free PMC article.
Comparative analysis of clinical, biochemical and genetic aspects associated with bone mineral density in small for gestational age children.
Silvano L, Miras M, Pérez A, Picotto G, Díaz de Barboza G, Muñoz L, Martin S, Sobrero G, Armelini P, Mericq V, Tolosa de Talamoni N; Collaborating Group of Hospital de Niños de la Santísima Trinidad. Silvano L, et al. Among authors: miras m. J Pediatr Endocrinol Metab. 2011;24(7-8):511-7. doi: 10.1515/jpem.2011.196. J Pediatr Endocrinol Metab. 2011. PMID: 21932590
Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene.
Belforte FS, Miras MB, Olcese MC, Sobrero G, Testa G, Muñoz L, Gruñeiro-Papendieck L, Chiesa A, González-Sarmiento R, Targovnik HM, Rivolta CM. Belforte FS, et al. Among authors: miras mb. Clin Endocrinol (Oxf). 2012 Apr;76(4):568-76. doi: 10.1111/j.1365-2265.2011.04249.x. Clin Endocrinol (Oxf). 2012. PMID: 21981063
Five new cases of 46,XX aromatase deficiency: clinical follow-up from birth to puberty, a novel mutation, and a founder effect.
Marino R, Perez Garrido N, Costanzo M, Guercio G, Juanes M, Rocco C, Ramirez P, Warman DM, Ciaccio M, Pena G, Feyling JG, Miras M, Rivarola MA, Belgorosky A, Saraco N. Marino R, et al. Among authors: miras m. J Clin Endocrinol Metab. 2015 Feb;100(2):E301-7. doi: 10.1210/jc.2014-2967. Epub 2014 Nov 21. J Clin Endocrinol Metab. 2015. PMID: 25415177
Exome Sequencing Has a High Diagnostic Rate in Sporadic Congenital Hypopituitarism and Reveals Novel Candidate Genes.
Martinez-Mayer J, Vishnopolska S, Perticarari C, Iglesias Garcia L, Hackbartt M, Martinez M, Zaiat J, Jacome-Alvarado A, Braslavsky D, Keselman A, Bergadá I, Marino R, Ramírez P, Pérez Garrido N, Ciaccio M, Di Palma MI, Belgorosky A, Forclaz MV, Benzrihen G, D'Amato S, Cirigliano ML, Miras M, Paez Nuñez A, Castro L, Mallea-Gil MS, Ballarino C, Latorre-Villacorta L, Casiello AC, Hernandez C, Figueroa V, Alonso G, Morin A, Guntsche Z, Lee H, Lee E, Song Y, Marti MA, Perez-Millan MI. Martinez-Mayer J, et al. Among authors: miras m. J Clin Endocrinol Metab. 2024 Nov 18;109(12):3196-3210. doi: 10.1210/clinem/dgae320. J Clin Endocrinol Metab. 2024. PMID: 38717911
A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis.
Martín M, Modenutti CP, Gil Rosas ML, Peyret V, Geysels RC, Bernal Barquero CE, Sobrero G, Muñoz L, Signorino M, Testa G, Miras MB, Masini-Repiso AM, Calcaterra NB, Coux G, Carrasco N, Martí MA, Nicola JP. Martín M, et al. Among authors: miras mb. J Clin Endocrinol Metab. 2021 Jun 16;106(7):1867-1881. doi: 10.1210/clinem/dgab283. J Clin Endocrinol Metab. 2021. PMID: 33912899 Free PMC article.
143 results