A Novel Adrenocorticotropin Receptor Mutation Alters Its Structure and Function, Causing Familial Glucocorticoid Deficiency von Artigas, Rocío A., Gonzalez, Angel, Riquelme, Erick, Carvajal, Cristian A., Cattani, Andreína, Martínez-Aguayo, Alejandro, Kalergis, Alexis M., Pérez-Acle, Tomas, Fardella, Carlos E.

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Factores endocrinos reguladores del crecimiento von Cattani Ortega, Andreina

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Enfoque del paciente con talla baja o con trastornos del crecimiento von Cattani Ortega, Andreina

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Características del crecimiento y desarrollo físico von Cattani Ortega, Andreina

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Principales características de la pubertad normal y patológica von Cattani Ortega, Andreina

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Subclinical endothelial inflammation markers in a family with type I familial hyperaldosteronism caused by a de novo mutation von Stehr, Carlos B, Carvajal, Cristian A, Lacourt, Patricia, Alcaíno, Hernán, Mellado, Rosemarie, Cattani, Andreína, Mosso, Lorena M, Lavandera, Sergio, Fardella, Carlos E

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What is the best method for estimating final height in patients with precocious puberty? von Quiroga, Daniela, Bruera, María José, Vidaurre, Josefa, Cerda, Jaime, Cattani, Andreina, García, Hernán

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A Deletion of More than 800 kb Is the Most Recurrent Mutation in Chilean Patients with SHOX Gene Defects von Poggi, Helena, Vera, Alejandra, Avalos, Carolina, Lagos, Marcela, Mellado, Cecilia, Aracena, Mariana, Aravena, Teresa, Garcia, Hernan, Godoy, Claudia, Cattani, Andreina, Reyes, Loreto, Lacourt, Patricia, Rumie, Hana, Mericq, Veronica, Arriaza, Marta, Martinez-Aguayo, Alejandro

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A126: Clusters of Autoimmune Diseases in Children and the Role of PTPN22 C1858T Gene Polymorphism in Pediatric Polyautoimmunity von Borzutzky, Arturo, Seiltgens, Cristián, Iruretagoyena, Mirentxu, Cristi, Francisca, Ponce, María Jesús, Melendez, Patricia, Martinez‐Aguayo, Alejandro, Hodgson, María Isabel, Talesnik, Eduardo, Riera, Francisca, Méndez, Cecilia, Harris, Paul R., García, Hernán, Gana, Juan Cristobal, Godoy, Claudia, Cattani, Andreina

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Cuál es el mejor método de estimación de talla final en pacientes con pubertad precoz? von Quiroga, Daniela, Bruera, María José, Vidaurre, Josefa, Cerda, Jaime, Cattani, Andreina, García, Hernán

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Salt-wasting congenital adrenal hyperplasia : Detection of mutations in CYP21B gene in a Chilean population von FARDELLA, C. E, POGGI, H, PINEDA, P, SOTO, J, TORREALBA, I, CATTANI, A, OESTREICHER, E, FORADORI, A

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A Unique Insertion/Substitution in Helix H1 of the Vitamin D Receptor Ligand Binding Domain in a Patient With Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets von Malloy, Peter J, Xu, Rong, Cattani, Andreina, Reyes, M Loreto, Feldman, David

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Breast US in children and adolescents von García, C J, Espinoza, A, Dinamarca, V, Navarro, O, Daneman, A, García, H, Cattani, A

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Salt-Wasting Congenital Adrenal Hyperplasia: Detection of Mutations in CYP21B Gene in a Chilean Population1 von Fardella, Carlos E, Poggi, Helena, Pineda, Pedro, Soto, Julia, Torrealba, Isabel, Cattani, AndreÍna, Oestreicher, Eveline, Foradori, Arnaldo

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Marcadores de inflamación endotelial subclínica en una familia con hiperaldosteronismo familiar tipo I por mutación de novo von Stehr, Carlos B, Carvajal, Cristian A, Lacourt, Patricia, Alcaíno, Hernán, Mellado, Rosemarie, Cattani, Andreína, Mosso, Lorena M, Lavandera, Sergio, Fardella, Carlos E

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Bone metabolism in children with epidermolysis bullosa von Reyes, M.Loreto, Cattani, Andreina, Gajardo, Hector, García, Cristián, McGrath, John A., Palisson, Francis

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Persistent neonatal hyperinsulinism. Analysis of the differential diagnosis. Report of two cases von Hernández, M Isabel, Hodgson, M Isabel, Cattani, Andreina

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Breast US in Children and Adolescents1 von Cristián J. García, Aníbal Espinoza, Víctor Dinamarca, Oscar Navarro, Alan Daneman, Hernán García, Andreina Cattani

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Peripheral precocious puberty caused by a juvenile granulosa cell ovarian tumor, with iso and heterosexual manifestations in a six years old girl von Schulin-Zeuthen, Carolina, Yamamoto, Masami, Pires, Yumay, Mayerson, David, Cattani, Andreina

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Mutations in the Fibroblast Growth Factor Receptor 3 gene (FGFR3) in Chilean patients with idiopathic short stature, hypochondroplasia and achondroplasia von Mancilla, Edna E, Poggi, Helena, Repetto, Gabriela, García, Cristian, Foradori, Arnaldo, Cattani, Andreina

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