Parenting Styles and Coping Strategies in PKU Early Detected Children von Campos, María L. Pardo, Enacan, Rosa, Valle, Maria G., Chiesa, Ana

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Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases von Enacán, Rosa E, Masnata, María E, Belforte, Fiorella, Papendieck, Patricia, Olcese, María C, Siffo, Sofía, Gruñeiro-Papendieck, Laura, Targovnik, Héctor, Rivolta, Carina M, Chiesa, Ana E

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Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection von Braslavsky, Débora, Méndez, Maria Virginia, Prieto, Laura, Keselman, Ana, Enacan, Rosa, Gruñeiro-Papendieck, Laura, Jullien, Nicolas, Savenau, Alexandru, Reynaud, Rachel, Brue, Thierry, Bergadá, Ignacio, Chiesa, Ana

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Phenylalanine Hydroxylase (PAH) Genotyping in PKU Argentine Patients von Enacán, Rosa E., Miñana, Mariana Nuñez, Fernandez, Luis, Valle, Maria Gabriela, Salerno, Mercedes, Fraga, Claudia I., Santos-Simarro, Fernando, Prieto, Laura, Lapunzina, Pablo, Specola, Norma, Chiesa, Ana Elena

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Hipotiroidismo congénito transitorio por defectos bialélicos del genDUOX2. Dos casos clínicos von Enacán, Rosa E, Masnata, María E, Belforte, Fiorella, Papendieck, Patricia, Olcese, María C, Siffo, Sofía, Gruñeiro-Papendieck, Laura, Targovnik, Héctor, Rivolta, Carina M, Chiesa, Ana E.

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