Heterozygous IGFALS Gene Variants in Idiopathic Short Stature and Normal Children: Impact on Height and the IGF System von Domené, Horacio M., Scaglia, Paula A., Martínez, Alicia S., Keselman, Ana C., Karabatas, Liliana M., Pipman, Viviana R., Bengolea, Sonia V., Guida, María C., Ropelato, María G., Ballerini, María G., Lescano, Eva M., Blanco, Miguel A., Heinrich, Juan J., Rey, Rodolfo A., Jasper, Héctor G.

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Growth Hormone Insensitivity Associated with a STAT5b Mutation von Kofoed, Eric M, Hwa, Vivian, Little, Brian, Woods, Katie A, Buckway, Caroline K, Tsubaki, Junko, Pratt, Katherine L, Bezrodnik, Liliana, Jasper, Hector, Tepper, Alejandro, Heinrich, Juan J, Rosenfeld, Ron G

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Deficiency of the Circulating Insulin-like Growth Factor System Associated with Inactivation of the Acid-Labile Subunit Gene von Domené, Horacio M, Bengolea, Sonia V, Martínez, Alicia S, Ropelato, M. Gabriela, Pennisi, Patricia, Scaglia, Paula, Heinrich, Juan J, Jasper, Héctor G

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A Novel Missense Mutation in the SH2 Domain of the STAT5B Gene Results in a Transcriptionally Inactive STAT5b Associated with Severe IGF-I Deficiency, Immune Dysfunction, and Lack... von Scaglia, Paula A, Martínez, Alicia S, Feigerlová, Eva, Bezrodnik, Liliana, Gaillard, María Isabel, Di Giovanni, Daniela, Ballerini, María Gabriela, Jasper, Héctor G, Heinrich, Juan J, Fang, Peng, Domené, Horacio M, Rosenfeld, Ron G, Hwa, Vivian

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Estrogen priming effect on growth hormone (GH) provocative test : A useful tool for the diagnosis of GH deficiency von MARTINEZ, Alicia S, DOMENE, Horacio M, ROPELATO, M. Gabriela, JASPER, Héctor G, PENNISI, Patricia A, ESCOBAR, Maria E, HEINRICH, Juan J

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Normal Growth Spurt and Final Height despite Low Levels of All Forms of Circulating Insulin-Like Growth Factor-I in a Patient with Acid-Labile Subunit Deficiency von Domené, Horacio M., Martínez, Alicia S., Frystyk, Jan, Bengolea, Sonia V., Ropelato, María G., Scaglia, Paula A., Chen, Jian-Wen, Heuck, Carsten, Wolthers, Ole D., Heinrich, Juan J., Jasper, Héctor G.

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Peripheral Venous Thrombosis in Children and Adolescents with Adipsic Hypernatremia Secondary to Hypothalamic Tumors von Bergadá, Ignacio, Aversa, Luis, Heinrich, Juan J.

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Congenital Secondary Hypothyroidism Due to a Mutation C105Vfs114X Thyrotropin-β Mutation: Genetic Study of Five Unrelated Families from Switzerland and Argentina von Deladoëy, Johnny, Vuissoz, Jean-Marc, Domené, Horacio M., Malik, Naseem, Gruneiro-Papendieck, Laura, Chiesa, Ana, Heinrich, Juan J., Mullis, Primus E.

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The C105fs114X Is the Prevalent Thyrotropin Beta-Subunit Gene Mutation in Argentinean Patients with Congenital Central Hypothyroidism von Domené, Horacio M., Gruñeiro-Papendieck, Laura, Chiesa, Ana, Iorcansky, Sonia, Herzovich, Viviana C., Papazian, Regina, Forclaz, Verónica, Prieto, Laura, Sansó, Gabriela, Scaglia, Paula, Bre, Mónica, Chamoux, Alfredo, Heinrich, Juan J.

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Identification of the first patient with a confirmed mutation of the JAK-STAT system von Rosenfeld, Ron G, Kofoed, Eric, Buckway, Caroline, Little, Brian, Woods, Katie A, Tsubaki, Junko, Pratt, Katherine A, Bezrodnik, Liliana, Jasper, Hector, Tepper, Alejandro, Heinrich, Juan J, Hwa, Vivian

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Decreased Generation and Function of CD4+CD25hi T Regulatory Cells in Human STAT5b Deficiency von Cleary, Aileen, Nadeau, Kari, Tu, Wenwei, Hwa, Vivian, Dionis, Kira Y., Bezrodnik, Liliana, Teper, Alejandro, Gaillard, Maria, Heinrich, Juan J., Krensky, Alan M., Rosenfeld, Ron G., Lewis, David B.

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Immunodeficiency Associated with a STAT-5b Mutation and Growth Hormone Insensitivity von Cleary, Aileen M., Hwa, Vivian, Tu, Wenwei, Dionis, Kira, Bezrodnik, Liliana, Teper, Alejandro, Gaillard, Maria, Heinrich, Juan J., Rosenfeld, Ron G., Lewis, David B.

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Estrogen Priming Effect on Growth Hormone (GH) Provocative Test: A Useful Tool for the Diagnosis of GH Deficiency1 von MartÍnez, Alicia S., Domené, Horacio M., Ropelato, M. Gabriela, Jasper, Héctor G., Pennisi, Patricia A., Escobar, MarÍa E., Heinrich, Juan J.

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Evaluación de los niveles séricos de la proteína de unión de alta afinidad de la hormona de crecimiento humana (GHBP) y del polimorfismo del exón 3 del gen del receptor de GH en ni... von Ballerini, María G, Scaglia, Paula, Domené, Horacio M, Martinez, Alicia, Keselman, Ana, Pipman, Viviana, Bengolea, Sonio V, Cassinelli, Hamilton, Karabatas, Liliana, Calcagno, María L, Heinrich, Juan J, Jasper, Héctor G, Ropelato, María G

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A novel E153X point mutation in the androgen receptor gene in a patient with complete androgen insensitivity syndrome von COPELLI, S. B, LUMBROSO, S, AUDRAN, F, PELLIZZARI, E. H, HEINRICH, J. J, CIGORRAGA, S. B, SULTAN, C, CHEMES, H. E

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Long‐term endocrine sequelae after surgery, radiotherapy, and chemotherapy in children with medulloblastoma von Pasqualini, Titania, Diez, Blanca, Domene, Horacio, Escobar, Maria Eugenia, Grueiro, Laura, Heinrich, Juan J., Martinez, Alicia, Iorcansky, Sonia, Sackmann‐Muriel, Federico, Rivarola, Marco

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Patterns of TSH response to TRH in children with hypopituitarism von de Papendieck, Laura Gruñeiro, Iorcansky, Sonia, Rivarola, Marco A., Heinrich, Juan J., Bergadá, César

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Growth in congenital adrenal hyperplasia von de Papendieck, Laura Gruneiro, Heinrich, Juan J., Bergada, Cesar

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Detection of Autoantibodies Against hGH in Sera of Idiopathic Hypopituitary Children von Llera, Andrea S., Cardoso, Alicia I., Stumpo, Rita Del Rosario, Martinez, Alicia S., Heinrich, Juan J., Poskus, Edgardo

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Development of leydig cells in the normal human testis A cytological, cytochemical and quantitative study von Mancini, Roberto E., Vilar, Oscar, Lavieri, Juan Carlos, Andrada, Juan A., Heinrich, Juan J.

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