5 results match your criteria: "Erasmus Medical Center and Sophia Children's Hospital[Affiliation]"
Prenat Diagn
July 2019
Department of Child and Adolescent Psychiatry/Psychology, Unit of Psychosocial Care, Erasmus Medical Center and Sophia Children's Hospital, Rotterdam, The Netherlands.
Objective: To investigate, from the perspective of women and partners, at what stage of a termination of pregnancy (TOP) for fetal anomalies psychosocial care (PSC) is most meaningful, what topics should be discussed, and who should provide PSC.
Method: A cross-sectional retrospective cohort study was conducted with a consecutive series of 76 women and 36 partners, who completed a semi-structured online questionnaire.
Results: Overall, women expressed a greater need for PSC than their partners.
World Neurosurg
December 2018
Department of Radiology and Nuclear Medicine, Erasmus Medical Center, Erasmus Medical Center and Sophia Children's Hospital, Rotterdam, The Netherlands.
Background: Fibrous dysplasia (FD) is most often a slowly progressive benign disease in which the normal bone structure is replaced by fibrous and osteoid tissue.
Case Description: A 16-year-old adolescent, known with FD in the sphenoid bone, suffered an acute decreased visual acuity with papilledema on the left eye. The radiologic images were best compatible with cystic degeneration of the known FD with optic nerve compression in the optic canal.
J Clin Endocrinol Metab
November 2018
Department of Internal Medicine, Erasmus Medical Center, GE Rotterdam, Netherlands.
Context: Although the skeleton is a well-known thyroid hormone target organ, very little data are available on the association of thyroid function with bone outcomes during childhood.
Objective: To study the association of thyroid function with bone mass during childhood.
Design, Setting, And Participants: Population-based prospective cohort including 4204 children with TSH and free T4 (FT4) measured at the age of 6 years.
J Clin Endocrinol Metab
May 2018
Nemours Children's Health System, Jacksonville, Florida.
Context: Most girls with Turner syndrome (TS) have hypergonadotropic hypogonadism and need hormonal replacement for induction of puberty and then for maintaining secondary sex characteristics, attaining peak bone mass, and uterine growth. The optimal estrogen replacement regimen is still being studied.
Evidence Acquisition: We conducted a systematic search of PubMed for studies related to TS and puberty.
Eur J Endocrinol
December 2010
Subdivision of Endocrinology, Department of Internal Medicine, Erasmus Medical Center and Sophia Children's Hospital, Rotterdam, The Netherlands.
Objective: Smaller size at birth has been associated with an increased risk of metabolic and cardiovascular disorders in adult life. Fetal programming of the hypothalamic-pituitary-adrenal axis has been suggested as a possible explanation. Fetal glucocorticoid (GC) overexposure has effects that suggest a role of GCs in this programming.
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