Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Nancy, Unanue"'
Publikováno v:
Revista Médica Clínica Las Condes, Vol 26, Iss 4, Pp 470-482 (2015)
Las displasias esqueléticas son un grupo heterogéneo de enfermedades caracterizadas por la alteración primaria del tejido óseo y/o cartilaginoso. La incidencia de muchas de estas entidades es desconocida, estimándose una incidencia general de 1
Externí odkaz:
https://doaj.org/article/b99427ad7012481c9f6989136f1e558a
Autor:
Mariana Aracena, Diana Ponce, Fernando Cassorla, Nancy Unanue, Francisco Garay, Carla Vallejos, Fernando Rodríguez, Victor M. Bolanos-Garcia
Publikováno v:
Journal of Pediatric Genetics. :158-163
We report the case of a 3-year-old girl, who is the third child of nonconsanguineous parents, with short stature, hypertrophic cardiomyopathy, and mild dysmorphic features; all suggestive of Noonan syndrome. In addition, the patient presents with fee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdf409d55780be2a90ae9f78624b8f03
https://doi.org/10.1055/s-0038-1653977
https://doi.org/10.1055/s-0038-1653977
Autor:
M. T. López, K. Arcos, Nancy Unanue, Carla Vallejos, Diana Ponce, S. Célis, Maria Isabel Hernandez, Fernando Rodríguez, F. Belmar, Fernando Cassorla
Publikováno v:
Andrology. 6:579-584
Cryptorchidism is one of the most common congenital disorders in boys, and several genetic, hormonal, and environmental factors have been proposed as possible causes for this genitourinary defect. Genetic factors have been intensively searched, but r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc9a51497dd40f4f3c799679afe95378
https://doi.org/10.1111/andr.12501
https://doi.org/10.1111/andr.12501
Autor:
Fernando Rodríguez, P. Godoy, S. Célis, F. Giraudo, Nancy Unanue, María Palomares-Bralo, Carla Vallejos, R. Martín-Arenas, Maria Isabel Hernandez, Karen E. Heath, Fernando Cassorla, M. T. López
Publikováno v:
Andrology. 5:923-930
Summary Cryptorchidism is the most common congenital disorder in boys, but the cause for most cases remains unknown. Patients with Noonan Syndrome are characterized by a typical face, growth retardation, congenital heart defects, learning disabilitie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91bcf10a014728a702191f969c36392c
https://doi.org/10.1111/andr.12390
https://doi.org/10.1111/andr.12390
Autor:
Jonathan, Kraus, Nancy, Unanue, Aníbal, Espinoza, German, Iniguez, Lournaris, Torres-Santiago, Ravinder, Singh, Nelly, Mauras, Veronica, Mericq
Publikováno v:
Pediatric endocrinology reviews : PER. 16(1)
Among patients with Turner Syndrome (TS), premature ovarian failure is a main feature. Recently published consensus guidelines recommend that transdermal (TD) estradiol is the preferred route for estrogen replacement. Studies related to ultrasound (U
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::048978b302111a88257e74887d438842
https://pubmed.ncbi.nlm.nih.gov/30371036
https://pubmed.ncbi.nlm.nih.gov/30371036
Publikováno v:
Revista Médica Clínica Las Condes, Vol 26, Iss 4, Pp 470-482 (2015)
ResumenLas displasias esqueléticas son un grupo heterogéneo de enfermedades caracterizadas por la alteración primaria del tejido óseo y/o cartilaginoso.La incidencia de muchas de estas entidades es desconocida, estimándose una incidencia general
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::181af45cec2ece840813e3490d38ae42
https://doi.org/10.1016/j.rmclc.2015.07.005
https://doi.org/10.1016/j.rmclc.2015.07.005
Autor:
Nancy Unanue, Judith L. Ross, Karen O Klein, Nelly Mauras, Jobayer Hossain, L. Torres-Santiago, Martha Taboada, Verónica Mericq, Ravinder J. Singh, Richard J. Santen
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 98:2716-2724
Context: The long-term effects of pure 17β-estradiol (E2) depending on route of administration have not been well characterized. Objective: Our objective was to assess metabolic effects of oral vs transdermal (TD) 17β-E2 replacement using estrogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3de8c868279a03cfb90406181fa8372
https://doi.org/10.1210/jc.2012-4243
https://doi.org/10.1210/jc.2012-4243
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 29
Background Menarche is the last stage of pubertal development, which coincides, with the completion of longitudinal growth. Our aim was to evaluate, post-menarcheal growth and clinical variables proposed to be associated with this growth. Methods In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54be620560a6bba53124601a2df35373
https://doi.org/10.1515/jpem-2016-0035
https://doi.org/10.1515/jpem-2016-0035
Autor:
James Troendle, Sofía Aros, Nancy Unanue, James L. Mills, Barbara Conca, Devon Kuehn, Mary Conley, María de los Angeles Avaria, Cecilia Henriquez, Fernando Cassorla, Karin Kleinsteuber, Tonia C. Carter, Alejandra Avila
Publikováno v:
Alcoholism: Clinical and Experimental Research. 36:1811-1819
Although prenatal exposure to alcohol is the most common environmental cause of intellectual impairment, the vast majority, 90 to 95%, of children exposed to large quantities of alcohol in utero do not develop fetal alcohol syndrome (FAS; Cronk and W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72f511888b2a1fc2081ec5a653b7dc52
https://doi.org/10.1111/j.1530-0277.2012.01794.x
https://doi.org/10.1111/j.1530-0277.2012.01794.x
Publikováno v:
American Journal of Medical Genetics Part A. :2665-2671
Growth faltering occurs frequently in infancy in the 22q11 Deletion syndrome (22q11 DS). The subsequent course of growth in childhood and outcome for final adult height lacks consensus. We analyzed 5,149 growth data points from 812 Caucasian subjects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9c489f56a18e228d39e7d9d1c041d4d
https://doi.org/10.1002/ajmg.a.35426
https://doi.org/10.1002/ajmg.a.35426