MIRAS, MIRTA BEATRIZ

Etiologia y Evolucion de Recien Nacidos con Hipotiroidismo Congenito y Glandula Eutopica / Etiology and Evolution of Newborns with Congenital Hypothyroidism and Eutopic Thyroid Gland.

RAEM; Año: 2017

MIRAS, MIRTA BEATRIZ

Sindrome de interrupcion del tallo pituitario. Relaciones clinicas, bioquimicas y neurorradiologicas

REVISTA ARGENTINA DE ENDOCRINOLOGIA Y METABOLISMO; Año: 2017

FRANCHIONI, L.

Effects of carbamazepine on cortisol levels and behavioral responses to stress in the fish Jenynsia Multidentata

PHYSIOLOGY AND BEHAVIOR; Lugar: Amsterdam; Año: 2016 vol. 158 p. 68 - 75

MUÑOZ, L.; OCHETTI, M.; PEREZ, G.; SORBERA, G.; SILVANO, L.; MARTIN, S.; TESTA, G.; MIRAS, M.

Measurement of Serum 17 a-Hydrixyprogesterone in Infants by Radioimnunoassay

Pediatric Endocrinology Reviews; Año: 2015 vol. 12 p. 366 - 372

MAHLER GA; LUSSANA MS; LEIVA SE; MUÑOZ NL; BERGOGLIO, LM

Optimización de una Estrategia Bioquímica para el Diagnóstico de Hipotiroidismo Primario

Bioquinforma; Lugar: Córdoba; Año: 2014

MUÑOZ, LILIANA

Clinical and molecular studies related to bone metabolism in patients with congenital adrenal hyperplasia

JOURNAL OF PEDIATRIC ENDOCRINOLOGY; Año: 2014 vol. 0 p. 1161 - 1166

C. E. CITTERIO, G. A. MACHIAVELLI, M. B. MIRAS, L. GRUÑEIRO-PAPENDIECK, K. LACHLAN, G. SOBRERO, ANA CHIESAD, J. WALKER, LILIANA MUÑOZ, G. TESTA, F. S. BELFORTE, R. GONZÁLEZ-SARMIENTO, C. M. RIVOLTA, H. M. TARGOVNIK

New insights into thyroglobulin gene: Molecular analysis of seven novel mutations associated with goiter and hypothyroidism

Lugar: Amsterdam; Año: 2013 vol. 365 p. 277 - 291

E. M. COTELLA, I. MESTRES LASCANO, L. FRANCHIONI, G. M. LEVIN, AND M. M. SUÁREZ

Long-term effects of maternal separation on chronic stress response suppressed by amitriptyline treatment

Lugar: Londres; Año: 2013 p. 1 - 5

FRANCISCO ALVAREZ-NAVA; ROBERTO LANES; JOSE MIGUEL QUINTERO; MIRTA MIRAS; HUGO FIDELEFF; VERONICA MERICQ; HENRY MARCANO; WILLIAM ZABALA; MARISOL SOTO; TATIANA PARDO; LISBETH BORJAS; JOALICE VILLALOBOS; PETER GUNCZLER; NANCY UNANUE; NATALIA TKALENKO; ADRIANA BOYANOFSKY; LILIANA SILVANO; LILIANA FRANCHIONI; MIRIAM LLANO; GABRIEL FIDELEFF; MIRIAM AZARETZKY; MARTHA SUAREZ

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

International Journal of Pediatric Endocrinology; Lugar: Heidelberg; Año: 2013 vol. 10 p. 1 - 7

TESTA, GRACIELA

New insights into thyroglobulin gene: Molecular analysis of seven novel mutations associated with goiter and hypothyroidism

MOLECULAR AND CELLULAR ENDOCRINOLOGY.; Año: 2013 vol. 365 p. 277 - 291

FIORELLA S. BELFORTE, MIRTA B. MIRAS, MARÍA C. OLCESE, GABRIELA SOBRERO, GRACIELA TESTA, LILIANA MUÑOZ, LAURA GRUÑEIRO-PAPENDIECK, ANA CHIESA, ROGELIO GONZÁLEZ-SARMIENTO, HÉCTOR M. TARGOVNIK AND CARINA M. RIVOLTA

Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene

Lugar: Londres; Año: 2012 vol. 76 p. 568 - 576

MARÍA PERALTA LÓPEZ, VIVIANA CENTENO, MIRTA MIRAS, LILIANA SILVANO, ADRIANA PÉREZ, LILIANA MUÑOZ, GABRIELA SOBRERO, MARÍ A ULLA AND NORI TOLOSA DE TALAMONI

Association of vitamin D receptor gene Cdx 2 polymorphism with bone markers in Turner syndrome patients

JOURNAL OF PEDIATRIC ENDOCRINOLOGY AND METABOLISM; Año: 2012 vol. 25 p. 669 - 671

LILIANA SILVANO, MIRTA MIRAS, ADRIANA PÉREZ,GABRIELA PICOTTO, GABRIELA DÍAZ DE BARBOZA, LILIANA MUÑOZ, SILVIA MARTIN, GABRIELA SOBRERO, PEDRO ARMELINI, VERÓNICA MERICQ, NORI TOLOSA DE TALAMONI, AND COLLABORATING GROUP

Comparative analysis of clinical, biochemical and genetic aspects associated with bone mineral density in small for gestational age children

Lugar: Berlin; Año: 2011 vol. 24 p. 511 - 517

JUAN PABLO NICOLA, MAGALÍ NAZAR, CAROLINE SERRANO-NASCIMENTO, FRANCEMILSON GOULART-SILVA, GABRIELA SOBRERO, GRACIELA TESTA, MARIA TEREZA NUNES, LILIANA MUÑOZ, MIRTA MIRAS, AND ANA MARÍA MASINI-REPISO

Iodide Transport Defect: Functional Characterization of a Novel Mutation in the Na
/I Symporter 5
-Untranslated Region in a Patient with Congenital Hypothyroidism

Lugar: New York; Año: 2011 vol. 96 p. 100 - 107

MARÍA PERALTA LÓPEZ, MIRTA MIRAS, LILIANA SILVANO, ADRIANA PÉREZ, LILIANA MUÑOZ, VIVIANA CENTENO, GABRIELA SOBRERO, MARÍA ULLA AND NORI TOLOSA DE TALAMONI

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

Lugar: Berlin; Año: 2011 vol. 24 p. 307 - 312

SEBASTIÁN SUSPERREGUY, LILIANA MUÑOZ, NATALIA Y. TKALENKO, IVAN D. MASCANFRONI, VANINA A. ALAMINO, MARÍA M. MONTESINOS, ANA M. MASINI-REPISO, MIRTA B. MIRAS AND CLAUDIA G. PELLIZAS

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

Lugar: Londres; Año: 2011 vol. 74 p. 346 - 353

MIRTA MIRAS, MARIANA OCHETTI, SILVIA MARTÍN, LILIANA SILVANO, GABRIELA SOBRERO, LAURA CASTRO, MARIANA ONASSIS, NORI TOLOSA DE TALAMONI, ADRIANA PÉREZ, GABRIELA PICOTTO, GABRIELA DÍAZ DE BARBOZA, LILIANA MUÑOZ

Serum Levels of Adiponectin and Leptin in Children Born Small for Gestational Age: Relation to Insulin Sensitivity Parameters

Lugar: Jerusalen; Año: 2010 vol. 23 p. 463 - 471

GABRIELA SOBRERO,LILIANA MUÑOZ, LEONARDO BAZZARA,SILVIA MARTIN, LILIANA SILVANO, SONIA IORKANSKY, LILIANA BERGOGLIO, CAROLE SPENCER, MIRTA MIRAS

Thyroglobulin Reference Values in a Pediatric Infant Population

Lugar: New York; Año: 2007 vol. 17 p. 1049 - 1054

S. SUSPERREGUY, M. B. MIRAS, M. M. MONTESINOS, I. D. MASCANFRONI, L. MUÑOZ, G. SOBRERO, L. SILVANO, A. M. MASINI-REPISO, A. H. COLEONI, H. M. TARGOVNIK AND C. G. PELLIZAS

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

Lugar: Londres; Año: 2007 vol. 67 p. 629 - 636