Publications by authors named "C Ceuterick-De Groote"
Introduction: Beyond the memory deficits classically observed in individuals with alcohol use disorder (IwAUD), research has recently focused on the study of autobiographical memory (AM) processes in IwAUD by analysing the content of AM narratives, and the implications for self-conception have been discussed. However, little is known about how IwAUD subjectively experience autobiographical recall.
Methods: Thirty-seven IwAUD and 37 control participants were invited to perform an AM task that involved recalling memories for 4 life periods (2 important memories per period).
Background: People with Parkinson's disease (PwPD) exhibit various sexual difficulties (SDs) that may be due to motor and/or nonmotor symptoms or the use of antiparkinsonian medication. SDs are often underreported by PwPD and underexplored by physicians.
Objective: This study aimed to explore the SDs experienced by PwPD and create a scale for assessing them.
Article Synopsis
- * This study analyzed the genetic, clinical, and neuropathological characteristics of 21 patients with MPZ mutations and found distinct features across different neuropathy subtypes, such as congenital hypomyelinating neuropathy and demyelinating Charcot-Marie-Tooth disease.
- * The research revealed significant differences in nerve structure and regeneration, especially in demyelinating types, along with new gene variants, highlighting that MPZ mutations impact both myelinated and non-myelinated nerve fibers.
The study examined the personal sense of identity in alcohol use disorder (AUD) through the relation between autobiographical memories and individuals' self-conception. The AUD detoxified patients and control participants were asked to create a list of self-statements to which they associated for the three main autobiographical memories illustrating them. The group variable was not associated with the number of positive self-statements, but it was associated with the number of negative self-statements.
View Article and Find Full Text PDFNeurofibromatosis type 1 (NF1) is an autosomal dominant disorder affecting approximately 1 in 2,000 newborns. Up to 5% of NF1 patients suffer from pseudarthrosis of a long bone (NF1-PA). Current treatments are often unsatisfactory, potentially leading to amputation.
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