M. Miras

发表

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

Adriana Pérez, M. Miras, Mariana Ochetti, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR

A. Lerário, A. Jorge, B. Mendonca, 2019, Endocrine connections.

Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism

R. González-Sarmiento, Cintia E. Citterio, J. Weill, 2017, Molecular and Cellular Endocrinology.

Thyroglobulin reference values in a pediatric infant population.

C. Spencer, M. Miras, S. Martin, 2007, Thyroid : official journal of the American Thyroid Association.

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

A. M. Masini-Repiso, M. Miras, L. Muñoz, 2011, Clinical endocrinology.

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

J. Nicola, A. M. Masini-Repiso, M. Miras, 2022, Frontiers in Endocrinology.

Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis

R. González-Sarmiento, H. Targovnik, A. Chiesa, 2022, Endocrine.

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

H. Targovnik, A. M. Masini-Repiso, M. Miras, 2007, Clinical endocrinology.

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

V. Mericq, L. Borjas, N. Unanue, 2013, International Journal of Pediatric Endocrinology.

Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene

R. González-Sarmiento, H. Targovnik, L. Gruñeiro-Papendieck, 2012, Clinical endocrinology.

Compound heterozygous DUOX2 gene mutations (c.2335-1G>C/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysis

Cintia E. Citterio, H. Targovnik, M. Miras, 2016, Molecular and Cellular Endocrinology.

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

Adriana Pérez, M. Miras, L. Silvano, 2012, Journal of pediatric endocrinology & metabolism : JPEM.

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

K. Lachlan, R. González-Sarmiento, Cintia E. Citterio, 2013, Molecular and Cellular Endocrinology.

Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations

A. Jorge, B. Mendonca, M. Nishi, 2017, Clinical endocrinology.

Evaluation of diagnostic accuracy of insulin-like growth factor (IGF)-I and IGF-binding protein-3 in growth hormone-deficient children and adults using ROC plot analysis.

M. Miras, H. Fideleff, H. Boquete, 2003, The Journal of clinical endocrinology and metabolism.

Comparison Between GH assay: serum GH Cut-off Levels by ECLIA Performed in Pharmacological Estimulation Tests in Children With Short Stature

M. Miras, Mariana Ochetti, L. Silvano, 2014 .

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

C. Serrano-Nascimento, J. Nicola, A. M. Masini-Repiso, 2011, The Journal of clinical endocrinology and metabolism.

A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis.

Carlos P. Modenutti, N. Calcaterra, Marcelo Martí, 2021, The Journal of clinical endocrinology and metabolism.

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

V. Mericq, Adriana Pérez, M. Miras, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Treatment of Hypopituitary Children with Synthetic Met-Growth Hormone (Somatrem): Two Years Experience

J. Heinrich, Alicia S. Martínez, C. Bergadá, 1991 .

Five new cases of 46,XX aromatase deficiency: clinical follow-up from birth to puberty, a novel mutation, and a founder effect.

A. Belgorosky, M. Rivarola, N. Saraco, 2015, The Journal of clinical endocrinology and metabolism.

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

Adriana Pérez, M. Miras, L. Silvano, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

The p.Cys1281Tyr variant in the hinge module/flap region of thyroglobulin causes intracellular transport disorder and congenital hypothyroidism

H. Targovnik, K. Scheps, M. Miras, 2023, Molecular and Cellular Endocrinology.

EFFECTS OF PROLONGED IGF-I TREATMENT IN CHILDREN WITH GROWTH HORMONE INSENSITIVITY SYNDROME (GHIS)

L. Ghizzoni, P. Backeljauw, D. Donaldson, 1993, Pediatric Research.

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

Adriana Pérez, M. Miras, Mariana Ochetti, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

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

M. Miras, L. Muñoz, I. Mascanfroni, 2011, Clinical endocrinology.