Mostrando 10 resultados de: 17
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Journal of Clinical Endocrinology and Metabolism(4)
Acta Paediatrica, International Journal of Paediatrics, Supplement(2)
Clinical Endocrinology(2)
Hormone Research(2)
Acta Pædiatrica(1)
Challenges and future for the delivery of growth hormone therapy
ArticleAbstract: Growth hormone (GH) has multiple roles in sustaining human development and homeostasis. Its pulsatilPalabras claves:eHealth, Growth hormone, Micro Electromechanical Systems (MEMS), Organs-on-chips, therapyAutores:Andrés Caicedo, Rosenfeld R.G.Fuentes:googlescopusBody changes in adolescent patients with growth hormone receptor deficiency receiving recombinant human insulin‐like growth factor I and luteinizing hormone‐releasing hormone analogue: preliminary results
ArticleAbstract: Auxological and body composition changes were studied in three adolescent patients (2 female, 1 malePalabras claves:Body Composition, bone age, Growth hormone receptor deficiency, height velocity, insulin‐like growth factor I, luteinizing hormone‐releasing hormone analogueAutores:Bachrach L.K., Davila N., Diamond F.B., Jaime Guevara-Aguirre, Martinez A., Martinez V., Moreno Z., Rosenbloom A.L., Rosenfeld R.G., Vasconez O.Fuentes:scopusA novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes
ArticleAbstract: Design, Setting, and Participants: Genomic DNA samples (15 affected and 26 unaffected from a six-genPalabras claves:Autores:Andres Zurita, Andrew S., Carolina Guevara, Dauber A., Geng J., Guo M., Hwa V., Jaime Guevara-Aguirre, Kerns S.L., Marco Guevara-Aguirre, Oddoux C., Ostrer H., Rosenfeld R.G., Shen Y.Fuentes:scopusA randomized, double blind, placebo-controlled trial on safety and efficacy of recombinant human insulin-like growth factor-I in children with growth hormone receptor deficiency
ArticleAbstract: GH insensitivity due to GH receptor deficiency is a rare autosomal recessive condition, characterizePalabras claves:Autores:Diamond F.B., Gargosky S.E., Jaime Guevara-Aguirre, Martinez L., Martinez V., Nonoshita L., Rosenbloom A.L., Rosenfeld R.G., Vasconez O.Fuentes:scopusNatural history of growth hormone receptor deficiency
Conference ObjectAbstract: This review discusses the natural history of growth hormone receptor deficiency (GHRD) in relation tPalabras claves:Body Composition, growth, Growth hormone receptor deficiency, Insulin-like growth factor I deficiency, INTELLECTUAL DEVELOPMENT, Laron syndrome, Natural HistoryAutores:Bachrach L.K., Jaime Guevara-Aguirre, Kranzier J.H., Martinez V., Rosenbloom A.L., Rosenfeld R.G.Fuentes:scopusGrowth hormone insensitivity
ArticleAbstract: Growth hormone insensitivity (GHI) may be primary, caused by defects in the GH receptor, or furtherPalabras claves:Autores:Jaime Guevara-Aguirre, Rosenbloom A.L., Rosenfeld R.G.Fuentes:scopusIGF generation in short stature
ArticleAbstract:Palabras claves:Growth hormone deficiency, Growth hormone insensitivity, Igf generation, IGF-I, IGFBP-3, Short statureAutores:Buckway C.K., Burren C.P., Jaime Guevara-Aguirre, Pratt K.L., Rosenfeld R.G., Selva K.A., Tjoeng E.Fuentes:scopusInsulin-like growth factor (IGF) parameters and tools for efficacy: The IGF-I generation test in children
Conference ObjectAbstract: Serum levels of growth hormone (GH)-dependent peptides could provide important and valuable measuresPalabras claves:CHILDREN, Growth hormone, Growth hormone deficiency, Igf generation, Insulin-like growth factor binding protein, Insulin-like growth factor IAutores:Buckway C.K., Jaime Guevara-Aguirre, Pratt K.L., Rosenfeld R.G., Selva K.A.Fuentes:scopusIntrauterine and postnatal growth failure with normal GH/IGF1 axis and insulin-resistant diabetes in a consanguineous kinship
ArticleAbstract: Objective: To describe the clinical and biochemical features, and perform molecular analysis for canPalabras claves:Autores:Fang P., Hwa V., Jaime Guevara-Aguirre, Kerns S.L., Marco Guevara-Aguirre, Ostrer H., Procel P., Rosenbloom A.L., Rosenfeld R.G., Saavedra J.Fuentes:scopusImmunoblot studies of the acid-labile subunit (ALS) in biological fluids, normal human serum and in children with GH deficiency and GH receptor deficiency before and after long-term therapy with GH or IGF-I respectively
ArticleAbstract: OBJECTIVE: The aims of this investigation were (a) to study the presence of immunoreactive forms ofPalabras claves:Autores:Argente J., Gargosky S.E., Jaime Guevara-Aguirre, Labarta J., Lee P., Rosenfeld R.G., Simpson D.Fuentes:scopus