Mónica Arancibia
YOU?
Author Swipe
View article: Fetal Hyperthyroidism Secondary to Maternal Basedow–Graves' Disease
Fetal Hyperthyroidism Secondary to Maternal Basedow–Graves' Disease Open
Fetal hyperthyroidism is a rare prenatal disease and can be life-threatening. The diagnosis is based on ultrasound in mothers with a history of Basedow–Graves' disease and elevation of thyrotropin receptor antibodies (TRAbs) levels. The tr…
View article: Variación estacional de 25-hidroxi-vitamina D3, hormona paratiroidea y fosfatasa alcalina en niños escolares
Variación estacional de 25-hidroxi-vitamina D3, hormona paratiroidea y fosfatasa alcalina en niños escolares Open
El principal rol de la vitamina D es la regulación del metabolismo del calcio, cuya principal fuente es la vitamina D3 que se obtiene principalmente por la acción de la luz ultravioleta (UV) en la piel.Objetivo: Evaluar las diferencias est…
View article: Variación estacional de 25-hidroxi-vitamina D3, hormona paratiroidea y fosfatasa alcalina en niños escolares
Variación estacional de 25-hidroxi-vitamina D3, hormona paratiroidea y fosfatasa alcalina en niños escolares Open
El principal rol de la vitamina D es la regulación del metabolismo del calcio, cuya principal fuente es la vitamina D3 que se obtiene principalmente por la acción de la luz ultravioleta (UV) en la piel.Objetivo: Evaluar las diferencias est…
View article: SUN-099 Seasonal Variations of 25-Hydroxy Vitamin D3, Parathyroid Hormone, and Alkaline Phosphatase in School-Aged Children
SUN-099 Seasonal Variations of 25-Hydroxy Vitamin D3, Parathyroid Hormone, and Alkaline Phosphatase in School-Aged Children Open
BACKGROUND: The central role of Vitamin D is the homeostasis of calcium and phosphorus, affecting bone metabolism directly. The principal source of Vitamin D is the synthesis by the skin in response to its exposure to ultraviolet B radiati…
View article: Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and Arthrogryposis
Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and Arthrogryposis Open
Context Congenital hypopituitarism (CH) is rarely observed in combination with severe joint contractures (arthrogryposis). Schaaf-Yang syndrome (SHFYNG) phenotypically overlaps with Prader-Willi syndrome, with patients also manifesting art…