Results 151 to 160 of about 264,137 (313)

Caregiver support in home care: a literature review on the role of the community nurse

openAbstract L’invecchiamento della popolazione e l’aumento delle cronicità hanno reso l’assistenza domiciliare un modello centrale nei sistemi sanitari, affidando un ruolo cruciale ai caregiver familiari.
BIANCHI, TANIA
core  

Factors Associated With Caregiver Burden in Family Caregivers of Older Adults: A Cross-Sectional Study

Aim: This study aimed to assess caregiver burden and identify factors associated with caregiver burden among family caregivers of older adults. Method: This cross-sectional study included 140 older adults and their family caregivers.
Nesrin İlhan, Hande Kaya Akdoğan
core   +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

Psychiatric and Cognitive Features in Italian Women With the FMR1 Premutation: A Comprehensive Assessment Using SCID‐5 and Standardized Cognitive Measures

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Women with the FMR1 premutation (PM) are at increased risk for fragile X‐associated conditions (FXPAC), including cognitive and psychiatric features collectively termed fragile X‐associated neuropsychiatric disorders (FXAND). This study is the first to systematically investigate cognitive and psychiatric features in Italian female premutation ...
Federica Alice Maria Montanaro, Randi J. Hagerman, Giuseppina Spano, Flora Tassone, Giancarlo Logroscino, Andrea Bosco   +5 more
wiley   +1 more source

Factors Related to the Caregiver Burden on Families Caring for Clients with Schizophrenia: Scoping Review

Psychology Research and Behavior Management
Iwan Shalahuddin,1 Fernanda Mahardiani,2 Efri Widianti,3 Indra Maulana3 1Department of Community Nursing, Faculty of Nursing, Universitas Padjadjaran, Sumedang, Jawa Barat, Indonesia; 2Faculty of Nursing, Universitas Padjadjaran, Sumedang, Jawa Barat ...
Shalahuddin I, Mahardiani F, Widianti E, Maulana I   +3 more
doaj  

Caregiver Burden, Social Support, and Depressive Symptoms Among Caregivers of Patients With Heart Failure. [PDF]

J Nurs Res
Kim DY, Choi J, Son YJ.
europepmc   +1 more source

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source

Factors linked to informal caregiver burden in dementia across Latin America and the Caribbean: A systematic review and meta-analysis. [PDF]

Alzheimers Dement
Quintero-Cardona P, Tangarife MA, Blandon J, Arango-Lasprilla JC, Ibanez A, Baez S.   +5 more
europepmc   +1 more source

Emerging needs and critical issues of the caregiver figure: a case study on the care of the elderly in Veneto

reservedCaregiver, letteralmente ‘prestatore di cura.’ Una parola, molteplici gesti, sentimenti, interazioni e valori che si traducono in una pratica complessa innestata sulla relazione.
FIACCHI, CARLOTTA
core  

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source