Results 21 to 30 of about 383,904 (242)
ABSTRACT Women with the FMR1 premutation (FXpm) are at heightened genetic vulnerability for depression, with risk compounded by the stressors of parenting a disabled child. Although risk factors persist as FXpm women age, depression in FXpm mothers during midlife and old age is poorly characterized. This study used an accelerated longitudinal design to
Jessica Klusek+8 more
wiley +1 more source
Genomics Review of Selective RET Inhibitors Sensitivity in Thyroid Cancer Clinical Trials
ABSTRACT RET gene is a driver of thyroid cancer (TC) tumorigenesis. The incidence of TC has increased worldwide in the last few decades, both in medullary and follicular‐derived subtypes. Several drugs, including multikinase and selective inhibitors, have been explored.
Sara Gil‐Bernabé+5 more
wiley +1 more source
Creating a Dialogue: Bringing Anthropology to the University Campus [PDF]
Traditional academic anthropology centers on fieldwork and the production of publications that contribute to a growing body of scholarship. In the past several decades, this collective knowledge has primarily circulated only within the discipline itself;
Moison, Madeline
core +1 more source
The Position of Audiovisual Anthropology: Professional Spaces and Participative Methodologies [PDF]
Este texto se publicó originalmente en Íconos. Revista de Ciencias Sociales n°44, sección Temas, 147-162, 2012La Antropología audiovisual conecta de modo directo con la esencia misma de la Antropología sociocultural, la cual pretende vincularse a la ...
Robles Picón, Juan Ignacio
core +2 more sources
ABSTRACT Patients with Turner Syndrome (TS) and those exposed to high concentrations of glucocorticoids have a number of characteristics in common, including an increased risk of cardiovascular disease. Pediatric TS patients underwent studies of salivary cortisol (SC) and cortisone (SCn), body composition, continuous glucose monitoring, vascular ...
Lily Jones+6 more
wiley +1 more source
ABSTRACT Turner Syndrome (TS) is a sex chromosomal disorder associated with karyotype heterogeneity. Although TS can be associated with severe prenatal findings, most often linked to the 45, X karyotype, the majority of TS fetuses have no overt phenotype, resulting in delayed diagnosis and management.
Ivonne Bedei+10 more
wiley +1 more source
A Critical Analysis of the Medical Model as used in the Study of Pregnancy and Childbirth [PDF]
One key concept in medical sociology/anthropology for the analysis of approaches to health and illness is the medical model. However, this medical model is not only applied at the analytical level, i.e.
van Teijlingen, Edwin
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ABSTRACT Rare diseases impact approximately 1 in 10 people worldwide, and yet, less than 5% of all rare diseases currently have an approved treatment option available. This is due to many challenges unique to rare diseases, including small, diverse patient populations, the cost of drug development that is not proportionate to the number of patients who
Caleb P. Bupp+7 more
wiley +1 more source
St. Thomas Aquinas and the development natural law in economics thought [PDF]
Building on the system of reason provided for by the Greek philosopher and specifically Aristotle, St. Thomas Aquinas built a comprehensive system and theory of natural law which has lasted through the ages.
Rashid, Muhammad
core
Parental Decision‐Making Following a Prenatal Diagnosis of Turner Syndrome: A Systematic Review
ABSTRACT This systematic review investigates factors influencing parental decision‐making following a prenatal diagnosis (PND) of Turner syndrome (TS), aiming to enhance the foundation for tailored and supportive genetic counseling. A comprehensive literature search was conducted in the medical databases PubMed, Embase, and CINAHL.
Inger Lily Hjuler Dorf+2 more
wiley +1 more source