Search Results - "Berrade, S."

Growth patterns and outcomes of growth hormone therapy in patients with acrodysostosis by Ertl, D.-A., Mantovani, G., de Nanclares, G. P., Elli, F. M., Pereda, A., Pagnano, A., Sanchis, A., Cueto-Gonzalez, A. M., Berrade, S., León, M. C., Rothenbuhler, A., Audrain, C., Berkenou, J., Knight, N., Dolman, K., Gleiss, A., Argente, J., Linglart, A.

“…Introduction Severe short stature is a feature of acrodysostosis, but data on growth are sparse. Treatment with recombinant human growth hormone (rhGH) is used…”
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Vitamin D status and response to growth hormone treatment in prepubertal children with growth hormone deficiency by Durá-Travé, T., Gallinas-Victoriano, F., Moreno-González, P., Urretavizcaya-Martinez, M., Berrade-Zubiri, S., Chueca-Guindulain, M. J.

“…Purpose To analyze whether vitamin D deficiency could condition the growth response to GH therapy, as well as to analyze if GH treatment modifies both seasonal…”
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Prevalence of hypovitaminosis D and associated factors in obese Spanish children by Durá-Travé, T, Gallinas-Victoriano, F, Chueca-Guindulain, M J, Berrade-Zubiri, S

“…Background/Objectives: Vitamin D deficiency may contribute to endocrine health and disease (diabetes, autoimmune thyroid diseases, polycystic ovarian syndrome,…”
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Incidence of type 1 diabetes in Navarre (2009-2016): higher in the southern regions of the autonomous community by Forga, L, Tamayo, I, Berrade, S, Ibañez, B, Rodríguez Erdozain, R M, Goñi, M J

“…Geographical and seasonal variations of type 1 diabetes (T1D) are useful for establishing the key ethio-pathogenic factors of the disease. The present work…”
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Low height and rare diseases by Chueca Guindulain, Mj, Berrade, S, Oyarzábal, M

“…Low stature is the main reason of consultation in paediatric endocrinology. In a high percentage of cases, its etiology is clear and fundamentally answers to…”
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Detection of Hypomethylation Syndrome among Patients with Epigenetic Alterations at the GNAS Locus by Perez-Nanclares, Gustavo, Romanelli, Valeria, Mayo, Sonia, Garin, Intza, Zazo, Celia, Fernandez-Rebollo, Eduardo, Martínez, Francisco, Lapunzina, Pablo, de Nanclares, Guiomar Pérez, the Spanish PHP Group

“…Context: Genomic imprinting is the modification of the genome so that genes from only one (rather than two) of the parental alleles are expressed. The…”
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What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis by Pereda, Arrate, Garin, Intza, Perez de Nanclares, Guiomar

“…Pseudohypoparathyroidism (PHP) is a rare disease whose phenotypic features are rather difficult to identify in some cases. Thus, although these patients may…”
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Gene–gene interaction between PPARγ2 and ADRβ3 increases obesity risk in children and adolescents by Ochoa, M C, Marti, A, Azcona, C, Chueca, M, Oyarzábal, M, Pelach, R, Patiño, A, Moreno-Aliaga, M J, Martínez-González, M A, Martínez, J A

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Prevalencia de hipovitaminosis D y factores asociados en la edad infantojuvenil by Durá-Travé, Teodoro, Gallinas-Victoriano, Fidel, Chueca-Guindulain, María Jesús, Berrade-Zubiri, Sara, Moreno-Gónzalez, Paula, Malumbres-Chacón, María

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Incidencia de diabetes tipo 1 en Navarra (2009-2016): mayor en la zona sur de la comunidad by Forga, L., Tamayo, I., Berrade, S., Ibáñez, B., Rodríguez Erdozain, R. M., Goñi, M. J.

“…RESUMEN Fundamento Las variaciones geográficas y estacionales en la incidencia de diabetes tipo 1 (DM1) son útiles para intentar conocer la etiopatogenia de la…”
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Talla baja y enfermedades raras by Chueca, M.J., Berrade, S., Oyarzábal, M.

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Andermann syndrome: presentation of a case by Gurtubay, I G, Yoldi, M E, Carrera, B, Morales, G, Berrade, S, Alvarez, M J

“…Peripheral neuropathy with agenesis of the corpus callosum (or Andermann's syndrome) is a hereditary autosomal recessive disorder rarely found outside certain…”
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Familial benign partial epilepsy of early infancy by Carrera, B, Berrade, S, Yoldi, M E, Gurtubay, I G, Carrero, I, Morales, G, Ibiricu, M A

“…We present two patients who at the ages of 5 and 17 months respectively presented with convulsive crises with motor signs, of partial onset and secondary…”
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Talla baja y enfermedades raras by Berrade Zubiri, Sara, Oyarzábal Irigoyen, Miren, Chueca Guinduláin, María Jesús

“…La baja talla constituye el primer motivo de consulta en endocrinología pediátrica. En un alto porcentaje su etiología es clara y obedece fundamentalmente a…”
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Nosocomial infections. Vascular catheters by Andueza, M P, Montes, C, Elarre, C, Gil, M J, Roncal, C, Berrade, S, Atin, I, Asiain, M C

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Change of position and the decrease in the cases of sudden infant death syndrome in Navarra by Olivera Olmedo, J E, Sánchez Valverde, F, Zabalza Pérez-Nievas, A, Berrade Zubiri, S, Olivera Urdiroz, A, Viguria Campistegui, D, Guillén Grimá, G

“…The prone position during sleep has been described as the most important risk factor in relationship to sudden infant death syndrome (SIDS). The prevalence of…”
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