Results 191 to 200 of about 14,270 (287)

Cross Sectional Study of Prenatal Diagnosis Uptake Among Individuals With Genetic Conditions

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Prenatal diagnostic genetic testing allows for early identification of significant fetal conditions and enables informed decision‐making regarding management options. The aim of this study was to assess prenatal testing practice among individuals with genetic conditions.
Ebunoluwa Ojo, Roni Zemet, Allyson Nevins, Katherine Abraham, April D. Adams   +4 more
wiley   +1 more source

Caring masculinities and the politics of feminist representation in the Portuguese media. [PDF]

Front Sociol
Santos SJ, Garraio J, Janiques de Carvalho B.   +2 more
europepmc   +1 more source

Understanding fathers' responses to breastfeeding as a "shared parental task": a realist evaluation of a Danish breastfeeding support intervention. [PDF]

Arch Public Health
Jacobsen MH, Gadeberg AK, Rossau HK, Nilsson IMS, Villadsen SF.   +4 more
europepmc   +1 more source

Building a theory of change to guide fatherhood programming to prevent family violence: a comparison of two programs. [PDF]

BMC Public Health
Kohli A, Doyle K, Uysal J, Ojamuge D, Karamage E, Lundgren R.   +5 more
europepmc   +1 more source

Relational contexts and men's responsibilities informing men's participation in antenatal care in rural sub-Saharan Africa: A scoping review. [PDF]

PLOS Glob Public Health
Musiwa AS, Mavhu W, Nyamwanza O, Nyambi A, Stevens-Uninsky M, Rehman N, Anni NS, Dine RD, Chadambuka E, Couban R, Mbuagbaw L.   +10 more
europepmc   +1 more source

Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Prenatal sequencing of fetuses with abnormalities detected on imaging is expanding globally. Debate continues over whether variants of uncertain significance (VUS) should be reported prenatally, with some recent national position statements opposing this.
A. Gibbs, R. Braham, V. Ramachandran, R. Roberts, C. Willison, T. Ashraf, J. Cobben, A. Gardham, M. Holder‐Espinasse, T. Homfray, S. G. Mehta, D. Tapon, P. Vasudevan, N. J. Chandler   +13 more
wiley   +1 more source

Between distance and duty: emotional labor in transnational fatherhood among Pakistani migrants in Italy. [PDF]

Front Sociol
Haider SI.
europepmc   +1 more source

Prenatal Genetic Testing for Beckwith‐Wiedemann Syndrome: Considerations, Challenges and Observations (A Real‐World Study)

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Prenatal genetic testing for imprinting disorders is rarely requested with the exception of Beckwith‐Wiedemann syndrome (BWS) which is associated with specific ultrasound findings (e.g., placental mesenchymal dysplasia, omphalocele). However, genetic testing for BWS is challenging as aberrant DNA methylation has to be addressed which
Melissa Connolly, Louise McClelland, Pierpaola Tannorella, Tanja Richter, Ester Mainini, Andreas Dufke, Annette Lischka, Matthias Begemann, Katja Eggermann, Thomas Eggermann, Silvia Russo   +10 more
wiley   +1 more source

Men's Experiences with Fatherhood in Heterosexual Relationships: A Narrative Analysis. [PDF]

Am J Mens Health
Gao N, Chan C, Darroch F, Broom A, McKenzie S, Mootz J, Oliffe JL.   +6 more
europepmc   +1 more source

Monogenic and syndromic obesity in children: Clinical recognition, genetics, and precision management

Pediatric Investigation, EarlyView.
Monogenic and syndromic obesity in children often arises from defects in the leptin–melanocortin pathway. Understanding these rare genetic causes not only clarifies mechanisms of appetite regulation but also enables precision therapies, offering hope beyond lifestyle interventions.
Hadel Khalil, Eugene Feigin, Hussein Zaitoon   +2 more
wiley   +1 more source