Miras MB - Search Results

1

Silent but Not Harmless: A Synonymous SLC5A5 Gene Variant Leading to Dyshormonogenic Congenital Hypothyroidism.

Geysels RC, Bernal Barquero CE, Martín M, Peyret V, Nocent M, Sobrero G, Muñoz L, Signorino M, Testa G, Castro RB, Masini-Repiso AM, Miras MB, Nicola JP. Geysels RC, et al. Among authors: miras mb. Front Endocrinol (Lausanne). 2022 May 4;13:868891. doi: 10.3389/fendo.2022.868891. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35600585 Free PMC article.

2

Growth hormone (GH) treatment reduces peripheral thyroid hormone action in girls with Turner syndrome.

Susperreguy S, Miras MB, Montesinos MM, Mascanfroni ID, Muñoz L, Sobrero G, Silvano L, Masini-Repiso AM, Coleoni AH, Targovnik HM, Pellizas CG. Susperreguy S, et al. Among authors: miras mb. Clin Endocrinol (Oxf). 2007 Oct;67(4):629-36. doi: 10.1111/j.1365-2265.2007.02936.x. Epub 2007 Jul 30. Clin Endocrinol (Oxf). 2007. PMID: 17666093

3

Thyroglobulin reference values in a pediatric infant population.

Sobrero G, Muñoz L, Bazzara L, Martin S, Silvano L, Iorkansky S, Bergoglio L, Spencer C, Miras M. Sobrero G, et al. Thyroid. 2007 Nov;17(11):1049-54. doi: 10.1089/thy.2007.0059. Thyroid. 2007. PMID: 17949265

4

Serum levels of adiponectin and leptin in children born small for gestational age: relation to insulin sensitivity parameters.

Miras M, Ochetti M, Martín S, Silvano L, Sobrero G, Castro L, Onassis M, Tolosa de Talamoni N, Pérez A, Picotto G, Díaz de Barboza G, Muñoz L. Miras M, et al. J Pediatr Endocrinol Metab. 2010 May;23(5):463-71. doi: 10.1515/jpem.2010.077. J Pediatr Endocrinol Metab. 2010. PMID: 20662345

5

Growth hormone treatment in children with idiopathic short stature: correlation of growth response with peripheral thyroid hormone action.

Susperreguy S, Muñoz L, Tkalenko NY, Mascanfroni ID, Alamino VA, Montesinos MM, Masini-Repiso AM, Miras MB, Pellizas CG. Susperreguy S, et al. Among authors: miras mb. Clin Endocrinol (Oxf). 2011 Mar;74(3):346-53. doi: 10.1111/j.1365-2265.2010.03924.x. Clin Endocrinol (Oxf). 2011. PMID: 21091751 Clinical Trial.

6

Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5'-untranslated region in a patient with congenital hypothyroidism.

Nicola JP, Nazar M, Serrano-Nascimento C, Goulart-Silva F, Sobrero G, Testa G, Nunes MT, Muñoz L, Miras M, Masini-Repiso AM. Nicola JP, et al. J Clin Endocrinol Metab. 2011 Jul;96(7):E1100-7. doi: 10.1210/jc.2011-0349. Epub 2011 May 11. J Clin Endocrinol Metab. 2011. PMID: 21565787

7

Vitamin D receptor genotypes are associated with bone mass in patients with Turner syndrome.

Peralta López M, Miras M, Silvano L, Pérez A, Muñoz L, Centeno V, Sobrero G, Ulla M, Tolosa de Talamoni N. Peralta López M, et al. J Pediatr Endocrinol Metab. 2011;24(5-6):307-12. doi: 10.1515/jpem.2011.047. J Pediatr Endocrinol Metab. 2011. PMID: 21823528

8

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. J Pediatr Endocrinol Metab. 2011;24(7-8):511-7. doi: 10.1515/jpem.2011.196. J Pediatr Endocrinol Metab. 2011. PMID: 21932590

9

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

10

Association of vitamin D receptor gene Cdx2 polymorphism with bone markers in Turner syndrome patients.

Peralta López M, Centeno V, Miras M, Silvano L, Pérez A, Muñoz L, Sobrero G, Ulla M, Tolosa de Talamoni N. Peralta López M, et al. J Pediatr Endocrinol Metab. 2012;25(7-8):669-71. doi: 10.1515/jpem-2012-0098. J Pediatr Endocrinol Metab. 2012. PMID: 23155691

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