Mostrando 8 resultados de: 8
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Journal of Pediatric Endocrinology and Metabolism(2)
Application of Clinical Genetics(1)
Clinical Epigenetics(1)
Diabetes, Metabolic Syndrome and Obesity(1)
International Journal of Molecular Sciences(1)
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Enfermedades(7)
Fisiología humana(6)
Ginecología, obstetricia, pediatría, geriatría(2)
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Anthropometric variables as cardiovascular risk pbkp_redictors in a cohort of adult subjects with Turner syndrome
ArticleAbstract: Background and purpose: Excessive adiposity is associated with cardiometabolic complications in TurnPalabras claves:Anthropometric indexes, Body Composition, cardiometabolic risk, Metabolic syndrome, obesity, Overweight, Turner syndromeAutores:Francisco Álvarez-Nava, Jéssica Guarderas, Julia Witt, Lanes R., Marcia Racines, María EstévezFuentes:scopusGH/IGF-1 signaling and current knowledge of epigenetics; A review and considerations on possible therapeutic options
ReviewAbstract: Epigenetic mechanisms play an important role in the regulation of the Growth Hormone- Insulin-like GPalabras claves:Epigenetic drugs, Epigenetics, Gene regulation, Growth hormone, Insulin-like growth factor I, Intrauterine growth retardation, metabolism, Postnatal growthAutores:Francisco Álvarez-Nava, Lanes R.Fuentes:googlescopusGHR and VDR genes do not contribute to the growth hormone (GH) response in GH deficient and turner syndrome patients
ArticleAbstract: We have prospectively assessed the influence of GHR and VDR gene polymorphisms on the response to rhPalabras claves:GHR and VDR polymorphisms, Growth hormone deficiency, Growth hormone therapy, Turner syndromeAutores:Francisco Álvarez-Nava, Gunczler P., Lanes R., Marcano H., Paoli M., Pardo T., Soto-Quintana M., Villalobos J.Fuentes:googlescopusFemale pseudohermaphroditism with phallic urethra in the offspring of a mother with an adrenal tumor
ArticleAbstract: Background: Female pseudohermaphroditism is a disorder in which 46,XX females with ovaries do not dePalabras claves:Differential Diagnosis, Female pseudohermaphroditism, Maternal adrenal tumorAutores:Álvarez Z., Francisco Álvarez-Nava, Lanes R., Soto-Quintana M., Temponi A.Fuentes:googlescopusElevated second-trimester maternal serum β-human chorionic gonadotropin and amniotic fluid alpha-fetoprotein as indicators of adverse obstetric outcomes in fetal Turner syndrome
ArticleAbstract: Aim The objective of this study was to determine the ability of biochemical analytes to identify advPalabras claves:adverse pregnancy outcome, biochemical screening, Prenatal diagnosis, Turner syndromeAutores:Bracho A., Francisco Álvarez-Nava, Lanes R., Morales-Machin A., Pons H., Soto M.Fuentes:googlescopusEpigenetics in Turner syndrome
ReviewAbstract: Background: Monosomy of the X chromosome is the most frequent genetic abnormality in human as it isPalabras claves:Aneuploidy, Chromatin, DNA methylation, Embryonic stem cells, Epigenetics, Gene Expression, Mouse models, Turner syndromeAutores:Francisco Álvarez-Nava, Lanes R.Fuentes:googlescopusMetabolic syndrome as a risk factor for sensorineural hearing loss in adult patients with turner syndrome
ArticleAbstract: Background and purpose: Metabolic syndrome (MetS) is a disorder associated with an increased risk ofPalabras claves:hearing loss, Metabolic syndrome, RISK FACTORS, Turner syndromeAutores:Francisco Álvarez-Nava, Jéssica Guarderas, Julia Witt, Lanes R., Marcia Racines-Orbe, María Estévez, Yosselin VicuñaFuentes:scopusMolecular analysis in Turner syndrome
ArticleAbstract: Objective: The frequency of Y-chromosome material is high in Turner syndrome (TS), but the ocurrencePalabras claves:Autores:Fernández E., Francisco Álvarez-Nava, Lanes R., Sánchez M.A., Soto-Quintana M.Fuentes:googlescopus