A Novel Adrenocorticotropin Receptor Mutation Alters Its Structure and Function, Causing Familial Glucocorticoid Deficiency
Artigas, Rocío A, Gonzalez, Angel, Riquelme, Erick, Carvajal, Cristian A, Cattani, Andreína, Martínez-Aguayo, Alejandro, Kalergis, Alexis M, Pérez-Acle, Tomas, Fardella, Carlos E
Published in The journal of clinical endocrinology and metabolism (01.08.2008)
Published in The journal of clinical endocrinology and metabolism (01.08.2008)
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Subclinical endothelial inflammation markers in a family with type I familial hyperaldosteronism caused by a de novo mutation
Stehr, Carlos B, Carvajal, Cristian A, Lacourt, Patricia, Alcaíno, Hernán, Mellado, Rosemarie, Cattani, Andreína, Mosso, Lorena M, Lavandera, Sergio, Fardella, Carlos E
Published in Revista medíca de Chile (01.09.2008)
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Published in Revista medíca de Chile (01.09.2008)
Journal Article
Salt-wasting congenital adrenal hyperplasia : Detection of mutations in CYP21B gene in a Chilean population
FARDELLA, C. E, POGGI, H, PINEDA, P, SOTO, J, TORREALBA, I, CATTANI, A, OESTREICHER, E, FORADORI, A
Published in The journal of clinical endocrinology and metabolism (01.09.1998)
Published in The journal of clinical endocrinology and metabolism (01.09.1998)
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Journal Article
A novel insertion in the FOXL2 gene in a Chilean patient with blepharophimosis ptosis epicanthus inversus syndrome type I
Martinez-Aguayo, Alejandro, Poggi, Helena, Cattani, Andreina, Molina, Marcela, Romeo, Eliana, Lagos, Marcela
Published in Journal of Pediatric Endocrinology and Metabolism (01.01.2014)
Published in Journal of Pediatric Endocrinology and Metabolism (01.01.2014)
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A Deletion of More than 800 kb Is the Most Recurrent Mutation in Chilean Patients with SHOX Gene Defects
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
Published in Hormone research in paediatrics (01.01.2015)
Published in Hormone research in paediatrics (01.01.2015)
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A126: Clusters of Autoimmune Diseases in Children and the Role of PTPN22 C1858T Gene Polymorphism in Pediatric Polyautoimmunity
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
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.03.2014)
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.03.2014)
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Salt-Wasting Congenital Adrenal Hyperplasia: Detection of Mutations in CYP21B Gene in a Chilean Population1
Fardella, Carlos E, Poggi, Helena, Pineda, Pedro, Soto, Julia, Torrealba, Isabel, Cattani, AndreÍna, Oestreicher, Eveline, Foradori, Arnaldo
Published in The journal of clinical endocrinology and metabolism (01.09.1998)
Published in The journal of clinical endocrinology and metabolism (01.09.1998)
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Journal Article
Marcadores de inflamación endotelial subclínica en una familia con hiperaldosteronismo familiar tipo I por mutación de novo
Stehr, Carlos B, Carvajal, Cristian A, Lacourt, Patricia, Alcaíno, Hernán, Mellado, Rosemarie, Cattani, Andreína, Mosso, Lorena M, Lavandera, Sergio, Fardella, Carlos E
Published in Revista medíca de Chile (01.09.2008)
Published in Revista medíca de Chile (01.09.2008)
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Journal Article
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
Malloy, Peter J, Xu, Rong, Cattani, Andreina, Reyes, M Loreto, Feldman, David
Published in Journal of bone and mineral research (01.06.2004)
Published in Journal of bone and mineral research (01.06.2004)
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Journal Article
Breast US in children and adolescents
García, C J, Espinoza, A, Dinamarca, V, Navarro, O, Daneman, A, García, H, Cattani, A
Published in Radiographics (01.11.2000)
Published in Radiographics (01.11.2000)
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Journal Article
Bone metabolism in children with epidermolysis bullosa
Reyes, M.Loreto, Cattani, Andreina, Gajardo, Hector, García, Cristián, McGrath, John A., Palisson, Francis
Published in The Journal of pediatrics (01.04.2002)
Published in The Journal of pediatrics (01.04.2002)
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Journal Article
Y Chromosome Sequences in Turner's Syndrome: Association with Virilization and Gonadoblastoma
Mancilla, E.E., Poggi, H., Repetto, G., Rumie, H., Garcia, H., Ugarte, F., Hidalgo, S., Jara, A., Muzzo, S., Panteon, E., Torrealba, I., Foradori, A., Cattani, A.
Published in Journal of Pediatric Endocrinology and Metabolism (01.10.2003)
Published in Journal of Pediatric Endocrinology and Metabolism (01.10.2003)
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Journal Article
Persistent neonatal hyperinsulinism. Analysis of the differential diagnosis. Report of two cases
Hernández, M Isabel, Hodgson, M Isabel, Cattani, Andreina
Published in Revista medíca de Chile (01.08.2004)
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Published in Revista medíca de Chile (01.08.2004)
Journal Article
Peripheral precocious puberty caused by a juvenile granulosa cell ovarian tumor, with iso and heterosexual manifestations in a six years old girl
Schulin-Zeuthen, Carolina, Yamamoto, Masami, Pires, Yumay, Mayerson, David, Cattani, Andreina
Published in Revista medíca de Chile (01.01.2003)
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Published in Revista medíca de Chile (01.01.2003)
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