Resultados da busca - Yeste, Diego

Hyperinsulinaemic hypoglycaemia, renal Fanconi syndrome and liver disease due to a mutation in the HNF4A gene por Clemente, María, Vargas, Alejandro, Ariceta, Gema, Martínez, Rosa, Campos, Ariadna, Yeste, Diego

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Hypophosphatasia: A Novel Mutation Associated with an Atypical Newborn Presentation por Esmel-Vilomara, Roger, Hernández, Susana, Campos-Martorel, Ariadna, González-Roca, Eva, Yeste, Diego, Castillo, Félix

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A New MAMLD1 Variant in an Infant With Microphallus and Hypospadias With Hormonal Pattern Suggesting Partial Hypogonadotropic Hypogonadism—Case Report por Yeste, Diego, Aguilar-Riera, Cristina, Canestrino, Gennaro, Fernández-Alvarez, Paula, Clemente, María, Camats-Tarruella, Núria

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Growth Hormone Treatment and Papilledema: A Prospective Pilot Study por Martín-Begué, Nieves, Mogas, Eduard, Dod, Charlotte Wolley, Alarcón, Silvia, Clemente, María, Campos-Martorell, Ariadna, Fábregas, Ana, Yeste, Diego

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Human growth hormone (GH1) gene polymorphism map in a normal-statured adult population por Esteban, Cristina, Audí, Laura, Carrascosa, Antonio, Fernández-Cancio, Mónica, Pérez-Arroyo, Annalisa, Ulied, Angels, Andaluz, Pilar, Arjona, Rosa, Albisu, Marian, Clemente, María, Gussinyé, Miquel, Yeste, Diego

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Safety Outcomes During Pediatric GH Therapy: Final Results From the Prospective GeNeSIS Observational Program por Child, Christopher J, Zimmermann, Alan G, Chrousos, George P, Cummings, Elisabeth, Deal, Cheri L, Hasegawa, Tomonobu, Jia, Nan, Lawrence, Sarah, Linglart, Agnès, Loche, Sandro, Maghnie, Mohamad, Pérez Sánchez, Jacobo, Polak, Michel, Predieri, Barbara, Richter-Unruh, Annette, Rosenfeld, Ron G, Yeste, Diego, Yorifuji, Tohru, Blum, Werner F

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Gene expression signatures predict response to therapy with growth hormone por Stevens, Adam, Murray, Philip, De Leonibus, Chiara, Garner, Terence, Koledova, Ekaterina, Ambler, Geoffrey, Kapelari, Klaus, Binder, Gerhard, Maghnie, Mohamad, Zucchini, Stefano, Bashnina, Elena, Skorodok, Julia, Yeste, Diego, Belgorosky, Alicia, Siguero, Juan-Pedro Lopez, Coutant, Regis, Vangsøy-Hansen, Eirik, Hagenäs, Lars, Dahlgren, Jovanna, Deal, Cheri, Chatelain, Pierre, Clayton, Peter

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Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe por Nowotny, Hanna, Neumann, Uta, Tardy-Guidollet, Véronique, Ahmed, S Faisal, Baronio, Federico, Battelino, Tadej, Bertherat, Jérôme, Blankenstein, Oliver, Bonomi, Marco, Bouvattier, Claire, Brac de la Perrière, Aude, Brucker, Sara, Cappa, Marco, Chanson, Philippe, Claahsen-van der Grinten, Hedi L, Colao, Annamaria, Cools, Martine, Davies, Justin H, Dörr, Helmut-Günther, Fenske, Wiebke K, Ghigo, Ezio, Giordano, Roberta, Gravholt, Claus H, Huebner, Angela, Husebye, Eystein Sverre, Igbokwe, Rebecca, Juul, Anders, Kiefer, Florian W, Léger, Juliane, Menassa, Rita, Meyer, Gesine, Neocleous, Vassos, Phylactou, Leonidas A, Rohayem, Julia, Russo, Gianni, Scaroni, Carla, Touraine, Philippe, Unger, Nicole, Vojtková, Jarmila, Yeste, Diego, Lajic, Svetlana, Reisch, Nicole

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