Results 161 to 170 of about 491,052 (313)

Emotional and Caregiver Burden in Adults with Glaucoma-Related Blindness at a Chinese Tertiary Center. [PDF]

Clin Ophthalmol
Luo Z, Konatsu K, Yang Y, Cheng L, He Y, Zhang Y, Han Y, Huang J.   +7 more
europepmc   +1 more source

High‐Resolution Genomic Characterization of WAGR Spectrum Disorder: Insights From a Novel Cohort and Literature Synthesis, and Validation of Patient‐Reported Data

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT WAGR spectrum disorder (WAGRSD) is an ultra‐rare congenital disorder caused by heterozygous deletion of chromosome 11p13. While classically associated with Wilms tumor, Aniridia, Genitourinary anomalies, and a Range of developmental delays, accurate delineation of the deletion is critical for prognosis because the phenotypic spectrum extends ...
Andrew M. George, Bamelak T. Duki, Zoe S. Katz, Aravind Viswanathan, Suzanne P. MacFarland, Evan R. Hathaway, Caitlin Monahan, John Morris, Kelly L. Trout, Shari M. Krantz, Arupa Ganguly, Jennifer M. Kalish   +11 more
wiley   +1 more source

Advancing Knowledge Translation Through Cultural Adaptation of an Intervention for Latino Family Caregivers of Persons Living With Dementia Using Participatory Action Research. [PDF]

Int J Nurs Pract
White CL, Shieu B, Peacock KS, Delgado RE, Neidre DB, Luy LP.   +5 more
europepmc   +1 more source

Interdisciplinary Team Based Pastoral Care: A Potentially Adaptable Model for Estonian Healthcare

, 2017
This article aims to build a potentially adaptable model of clinical pastoral care for Estonia’s healthcare institutions. To help the development of spiritual support provision in Estonian healthcare institutions, we are currently working on creating a ...
Lehtsaar, Tõnu, Meel, Liidia
core  

Patient Perspectives on Psychiatric Polygenic Risk Scores in Reproductive Decision‐Making and Polygenic Embryo Screening

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Polygenic risk scores (PRS) estimate individuals' genetic risk for developing multifactorial conditions. Recent genome‐wide association studies have enabled development of psychiatric PRS, which hold potential to streamline diagnosis and treatment of psychiatric conditions.
Lauren A. Ginn, Amanda R. Merner, Page M. Trotter, Kaitlynn P. Craig, Abigail C. Martinez, Ana Lucía Battaglino, Dorit Barlevy, Daphne M. Ayton, Takahiro Soda, Eric A. Storch, Gabriel Lázaro‐Muñoz, Stacey Pereira   +11 more
wiley   +1 more source

Factors influencing the caregiver burden on primary family caregivers of stroke survivors: a scoping review. [PDF]

Qual Life Res
Hongwei Y, Juan W, Hui J, Zhongjian L, Xuechun L, Yaqiong A, Mingyue Z, Lingmei R, Xiaoqian W.   +8 more
europepmc   +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

Additive effect of patient anosognosia and theory of mind deficit on dementia caregiver distress. [PDF]

Front Neurol
Eslami-Amirabadi M, Scheffler A, Kramer JH, Gorno-Tempini ML, Seeley WW, Rosen H, Rabinovici GD, Miller BL, Chiong W, Rankin KP.   +9 more
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

Caregiver Qualities and Resident Satisfaction in Long-Term Care: Mediating Roles of Spending Time and Environment. [PDF]

Healthcare (Basel)
Li X, Yin C, Mpofu E.
europepmc   +1 more source