Results 21 to 30 of about 62,523 (216)

Comorbid bipolar affective disorder and obsessive compulsive disorder in childhood: A case study and brief review

Indian Journal of Psychological Medicine, 2012
Obsessive compulsive disorder and bipolar affective disorder in the pediatric population show a bidirectional overlap. Few studies that have addressed this issue show that the prevalence of obsessive compulsive disorder in bipolar affective disorder ...
Amlan K Jana, Samir Kumar Praharaj, Vinod Kumar Sinha   +2 more
doaj   +1 more source

Efficiency of Nursing Intervention on Psychological Adjustment, Perfectionism and Symptoms among Patients with Obsessive Compulsive Disorder [PDF]

International Egyptian Journal of Nursing Sciences and Research, 2023
Background: Obsessive-compulsive disorder is a mental disorder in which a person experiences unwanted thoughts, and persistence ideas that patient perceives to be inappropriate. Aim: To evaluate efficiency of nursing intervention program on psychological
Abeer Ahmed, Manal Ali, Saida El-Azzab
doaj   +1 more source

The mediating role of fear of self and obsessive beliefs in the relationship between inferential confusion and obsessive-compulsive disorder symptoms [PDF]

مجله علوم روانشناختی, 2023
Background: Previous research has highlighted the potential role of inferential confusion in the development and maintenance of obsessive- compulsive disorder symptoms.
zahra khosravi roubiat, Mahmoud Najafi
doaj  

Childhood-Onset Obsessive Compulsive Disorder [PDF]

Psikiyatride Güncel Yaklaşımlar, 2011
Childhood-onset obsessive-compulsive disorder affects 1%-2% of children and adolescents. While symptoms reported by children and behavioral therapies and pharmacological interventions administered to children are similar to those seen among individuals ...
Murat Erdem, Ibrahim Durukan, Dursun Karaman   +2 more
doaj  

Developing a causal model of Body Dysmorphic Disorder with Obsessive-Compulsive Disorder: the mediating role of distress tolerance [PDF]

Journal of Research in Psychopathology
Considering the high coexistence of obsessive-compulsive disorder with body dysmorphic disorder, the present study aimed to develop a causal model of Body Dysmorphic Disorder Based on Obsessive-Compulsive Disorder symptoms with the mediating role of ...
Mohammad rasul Mufassery, Said Asadnia, Mansour Agashte, Naser Torabzade, Shaian Shahini, Parvaneh Shahini   +5 more
doaj   +1 more source

Problematic Internet Use in Frontotemporal Dementia: A Case Series

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The present study investigated problematic internet use (PIU) among 61 patients with frontotemporal dementia (FTD) compared to a cohort of 354 patients with mild cognitive impairment (MCI) and Alzheimer's dementia. PIU was identified in 22.9% of FTD patients compared to only 0.8% of AD patients (p < 0.001). Behaviors included compulsive social
Daniele Urso, Giuseppe Volpe, Agnese Valguarnera, Davide Vilella, Alessandra Vitulli, Valentina Gnoni, Alessia Giugno, Eleonora Rollo, Mark D. Griffiths, Giancarlo Logroscino   +9 more
wiley   +1 more source

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian, Tianjia Zhu, Hao Huang, Shavonne L. Massey, Mark P. Fitzgerald, Darshana Parikh, Arastoo Vossough, Ingo Helbig, Nicholas S. Abend   +8 more
wiley   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli, Stefania Della Vecchia, Patrizia Bergonzini, Elisa Caramaschi, Elisabetta Spezia, Claudia Parenti, Simona Filomena Madeo, Laura Lucaccioni, Cavalleri Francesca, Marisa Pugliese, Federico Raviglione, Clara Colonna, Olga Calabrese, Ilaria Stanghellini, Maria Carmen Marongiu, Enrico Biagioni, Anna Rita Ferrari, Roberta Battini, Lorenzo Iughetti   +18 more
wiley   +1 more source

Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy, Jesse Richards, Brooke R. Sweeney, Seema Kumar, Katie E. Queen, Joshua Zaritsky, Carl H. Cramer, Elias I. Traboulsi, Brittni A. Scruggs, Erica E. Davis, Ekaterina Keifer, Emma McGibbon, Timothy Ogden, Bendert De Graaf, Tonia Hymers, Elizabeth Forsythe, Philip Beales   +16 more
wiley   +1 more source

Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith–Magenis Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc, Christophe Nemos, Céline Bonnet, Mathilde Renaud, Sandra Chapuis, Pauline Boiroux, Marie‐Noëlle Babinet, Caroline Demily   +7 more
wiley   +1 more source