While social withdrawal is a normal defense mechanism displayed by infants to regulate interactions, it can negatively impact infant development when it becomes chronic, leading to delays in motor, cognitive, and communication difficulties in later development. Infant withdrawal was associated with low levels of parental sensitivity (i.e.
View Article and Find Full Text PDFBackground: Father involvement, defined in terms of both the quantity and quality of ways in which fathers may be involved, affects the child's development. How specifically father involvement links to emotion regulation during early childhood (0-5 years) is, however, less clear.
Methods: This literature review synthesizes research on the links between father involvement and emotion regulation during early childhood, as well as the measurement methods used to assess them.
Borderline Personal Disord Emot Dysregul
July 2024
Background: Families and significant others of people with borderline personality disorder (BPD) show increased levels of psychological distress. Family Connections®, a 12-week group intervention based on the principles of Dialectical Behavior Therapy, was designed to provide families with both information about the disorder and emotion regulation skills. It has been progressively implemented in French-speaking European countries.
View Article and Find Full Text PDFThe purpose of this study was to assess the factor structure and the measurement invariance of the Coparenting Relationship Scale (CRS) across 10 countries based on the seven-factor coparenting model (i.e., Coparenting Agreement, Coparenting Closeness, Exposure to Conflict, Coparenting Support, Endorsement of Partner's Parenting; Division of Labor) proposed by Feinberg (2003).
View Article and Find Full Text PDFPurpose: The study of cell-free DNA (cfDNA) enables sequential analysis of tumor cell-specific genetic alterations in patients with neuroblastoma.
Experimental Design: Eighteen patients with relapsing neuroblastoma having received lorlatinib, a third-generation ALK inhibitor, were identified (SACHA national registry and/or in the institution). cfDNA was analyzed at relapse for nine patients and sequentially for five patients (blood/bone marrow plasma) by performing whole-genome sequencing library construction followed by ALK-targeted ddPCR of the hotspot mutations [F1174L, R1275Q, and I1170N; variant allele fraction (VAF) detection limit 0.