L. Prieto

发表

Phenylalanine Hydroxylase (PAH) Genotyping in PKU Argentine Patients

P. Lapunzina, F. Santos-Simarro, A. Chiesa, 2019, Journal of Inborn Errors of Metabolism and Screening.

Neonatal Screening Program for Congenital Adrenal Hyperplasia: Adjustments to the Recall Protocol

L. Gruñeiro-Papendieck, A. Chiesa, C. Bergadá, 2001, Hormone Research in Paediatrics.

Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection

I. Bergadá, L. Gruñeiro-Papendieck, A. Chiesa, 2017, Hormone Research in Paediatrics.

Neonatal TSH Levels as an Index of Iodine Sufficiency: Differences Related to Time of Screening Sampling and Methodology

L. Gruñeiro-Papendieck, A. Chiesa, S. Bengolea, 2004, Hormone Research in Paediatrics.

Thyroid Disorders of Neonates Born to Mothers with Graves' Disease

L. Gruñeiro-Papendieck, A. Chiesa, L. Prieto, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Flow cytometry in diagnosis of central nervous system leukemic involvement.

D. Subirá, L. Prieto, P. Palomino, 1996, The Journal of pediatrics.

Usefulness of thyroxine and free thyroxine filter paper measurements in neonatal screening for congenital hypothyroidism of preterm babies

L. Gruñeiro-Papendieck, A. Chiesa, C. Bergadá, 2000, Journal of medical screening.

Prevalence and Etiology of Congenital Hypothyroidism Detected through an Argentine Neonatal Screening Program (1997-2010)

L. Gruñeiro-Papendieck, A. Chiesa, M. Calcagno, 2013, Hormone Research in Paediatrics.

Congenital adrenal hyperplasia and early newborn screening: 17α-hydroxyprogesterone (17α-OHP) during the first days of life

A. Chiesa, C. Bergadá, S. Bengolea, 1998 .

Neonatal Screening for Congenital Adrenal Hyperplasia: Experience and Results in Argentina

A. Chiesa, L. Prieto, Virginia Méndez, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Congenital adrenal hyperplasia and early newborn screening: 17 alpha-hydroxyprogesterone (17 alpha-OHP) during the first days of life.

A. Chiesa, C. Bergadá, S. Bengolea, 1998, Journal of medical screening.

The C105fs114X Is the Prevalent Thyrotropin Beta-Subunit Gene Mutation in Argentinean Patients with Congenital Central Hypothyroidism

J. Heinrich, L. Gruñeiro-Papendieck, A. Chiesa, 2004, Hormone Research in Paediatrics.

Efficacy of Congenital Hypothyroidism Neonatal Screening in Preterms less than 32 Weeks of Gestational Age: More Evidence

L. Gruñeiro-Papendieck, A. Chiesa, L. Prieto, 2005, Journal of pediatric endocrinology & metabolism : JPEM.