Zobrazeno 1 - 10
of 15
pro vyhledávání: '"M. J. Martínez-Aedo"'
Autor:
Juan Pedro López-Siguero, R. Espigares, J. M. Rial, A. Fernández-Nistal, A. Gutiérrez-Macías, F. J. Arroyo, Luis Fernando López-Canti, Vicente Barrios, A. Escribano, V. Martínez, Rafael Espino, M. J. Martínez-Aedo, S. Rico, J. L. Lechuga, S. Bernal, M. Núñez, Jesús Argente, J. Gentil, F. Macías, J. Guillén, I. Rodríguez, J. M. Fernández-García, E. Caro, Gabriel Á. Martos-Moreno, J. L. Barrionuevo
Publikováno v:
Journal of Endocrinological Investigation. 34:300-306
Background: Treatment with GH promotes linear growth and decreases body fat in patients with isolated GH deficiency (GHD). However, few studies have analyzed how GH replacement modifies ghrelin levels and the adipokine profile and the relationship of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f89ed499f35bcc5666c1d8c897f904f
https://doi.org/10.1007/bf03347090
https://doi.org/10.1007/bf03347090
Autor:
I Díez, López, A de Arriba, Muñoz, J Bosch, Muñoz, P Cabanas, Rodríguez, E Gallego, Gómez, M J Martínez-Aedo, Ollero, J M Rial, Rodríguez, A C Rodríguez, Dehlia, R Cañete, Estrada, L Ibáñez, Toda
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 76(2)
In this document the Small for Gestational Age (SGA) Child Working Group of the Spanish Society for Paediatric Endocrinology proposes the guidelines for the management and follow-up of SGA children, highlighting the potential morbidity arising from t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b5d646764992e712d3f5b6441702a70
https://pubmed.ncbi.nlm.nih.gov/22015052
https://pubmed.ncbi.nlm.nih.gov/22015052
Autor:
Mónica Fernández-Cancio, J. Martínez-Mora, E. Vicens-Calvet, M. Carrera, M. Andrade, M. Gussinyé, Antonio Perez-Aytes, Emilio Suárez García, C. Piró, Teresa Vendrell, G. Lledó, M. Del Campo, Laura Audí, Pablo Lapunzina, L. Castaño, Diego Yeste, J. Sánchez del Pozo, José Luis Arroyo, Andrés Blanco Blanco, Maria Clemente, José I Labarta, A. Carrascosa, I. Hernández de la Calle, J. A. Bermúdez de la Vega, J. Forn, Joaquim Calaf, Pilar Andaluz, J. del Valle, E. Mayayo, Nuria Toran, E. Vilaró, Isabel Salinas, M. Beneyto, O. Angerri, Ángel Segura, María Caimari, Ricardo Gracia-Bouthelier, María Angeles Albisu, M. J. Martínez-Sopena, Elisabeth Gabau, V. Borrás, M. J. Martínez-Aedo, María Luisa Granada, Antonio M. Rodríguez
Publikováno v:
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Universitat Politècnica de Catalunya (UPC)
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Universitat Politècnica de Catalunya (UPC)
Background: Androgen receptor (AR) gene mutations are the most frequent cause of 46, XY disorders of sex development (DSD) and are associated with a variety of phenotypes, ranging from phenotypic women [complete androgen insensitivity syndrome (CAIS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee95fe3c9ea372221848db8eb441771e
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=12781
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=12781
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 68(4)
Noonan syndrome, characterized by short stature, facial anomalies, heart disease and cryptorchidism in males, is an autosomal dominant, genetically heterogeneous disease. Approximately 50 % of Noonan syndrome cases are caused by gain-of-function muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ea8ec804cadb4880f8d391126077853b
https://pubmed.ncbi.nlm.nih.gov/18394382
https://pubmed.ncbi.nlm.nih.gov/18394382
Autor:
L, Tapia Ceballos, J P, López Siguero, G, del Río Camacho, L, Audí Parera, A, Martín Torrecillas, M J, Martínez Aedo
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 67(1)
Diagnosis of ambiguous genitalia in a newborn is an emergency that can be difficult to manage, not only because salt wasting entities must be ruled out, but also due to the importance of gender assignment before psychological gender is established. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ee22ce02cd8d6848c485bd5dd76a36d
https://pubmed.ncbi.nlm.nih.gov/17663907
https://pubmed.ncbi.nlm.nih.gov/17663907
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 13(9)
Idiopathic short stature (ISS) includes a heterogeneous group of patients with common characteristics to those of familial short stature and constitutional delay. Some authors state that these children can often respond to GH treatment, thus increasi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d70b3a0b5dbc261bbac74778c9467a2d
https://pubmed.ncbi.nlm.nih.gov/11154155
https://pubmed.ncbi.nlm.nih.gov/11154155
Publikováno v:
Anales espanoles de pediatria. 52(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a8cae642df5700266bda207fc0d3324
https://pubmed.ncbi.nlm.nih.gov/11003885
https://pubmed.ncbi.nlm.nih.gov/11003885
Publikováno v:
Anales espanoles de pediatria. 53(1)
Some children grow normally or excessively after extirpation of a craniopharyngioma, despite growth hormone deficiency. We report a 4-year-old girl with suprasellar craniopharyngioma. Removal of the tumor resulted in panhypopituitarism. For the next
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::05eb038b2e12d7b7c2f4a3ccc33a7b53
https://pubmed.ncbi.nlm.nih.gov/10998409
https://pubmed.ncbi.nlm.nih.gov/10998409
Publikováno v:
Anales espanoles de pediatria. 48(3)
Idiopathic short stature is a common pediatric problem that has a heterogeneous nature and an unknown outcome concerning adult height (AH).The main objective of this study was to assess the spontaneous adult height and the influence of several pre an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9140f6b0ecb46c65309988a311c02697
https://pubmed.ncbi.nlm.nih.gov/9608086
https://pubmed.ncbi.nlm.nih.gov/9608086
Autor:
J P, López Siguero, M J, Martínez-Aedo Ollero, J A, Moreno Molina, A, Lora Espinosa, A, Martínez Valverde
Publikováno v:
Anales espanoles de pediatria. 47(1)
A prospective study was conducted to assess the evolution of the incidence of type 1 diabetes mellitus (insulin-dependent) in Málaga among children less than 14 years of age between 1982 and 1993.The capture-recapture method was chosen for estimatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::69d824723308ff9dda9629cefcb5fcbc
https://pubmed.ncbi.nlm.nih.gov/9382324
https://pubmed.ncbi.nlm.nih.gov/9382324