Results 211 to 220 of about 16,134,108 (309)

Psychometric validation of the Patient Health Questionnaire-9 in Chinese adolescent and adult psychiatric inpatient populations. [PDF]

Front Psychiatry
Li W, Yin JY, Wang Q, Zhong J.
europepmc   +1 more source

Severe Headbanging Responsive to Levodopa in a Child With FOXP1 Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT We report a 9‐year‐old female with FOXP1 syndrome due to a de novo in‐frame deletion in the FOXP1 gene. The child has a severe neurodevelopmental disorder including global developmental delay and autism spectrum disorder. At age 2, she developed severe headbanging, which was progressive and did not respond to multidisciplinary, behavioral ...
Pamela Veale, Christopher Tiessen, Vithya Gnanakumar   +2 more
wiley   +1 more source

Psychometric properties and validity of a Mobile Patient Health Questionnaire-9 (MPHQ-9) for ecological momentary assessment in depressed adults. [PDF]

Psychol Assess
Haddox D, Mackin DM, Griffin TZ, Heinz MV, Nemesure MD, Collins AC, Price GD, Lekkas D, Pillai A, Nepal S, Campbell AT, Jacobson NC.   +11 more
europepmc   +1 more source

Patient and Family Reported Clinical Picture of IRF2BPL‐Related Disorders

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT IRF2BPL‐related disorder is a neurodevelopmental disorder caused by heterozygous variants in the IRF2BPL (Interferon Regulatory Factor 2 Binding Protein‐Like) gene. The few reports available in the literature suggest that common symptoms include developmental delay, intellectual disability, and developmental regression.
Zoe Goldstone‐Joubert, Danielle M. Pascual, Laurie Anne Bailey, Loren D. M. Peña, Paul C. Marcogliese   +4 more
wiley   +1 more source

Prevalence, predictors, and functional impact of postpartum depression using the Patient Health Questionnaire-9 (PHQ-9) among 830 women. [PDF]

BMC Pregnancy Childbirth
Keven MC, Yucel E, Savaş M, Salık EA, Yıldız S, Yeğen BD, Kılıç H, Güleç S, Dönmez KS, Uysak KÇ, Altay AY, Baştemur AG, Bütün Z, Bakır E, Karadağ A, Birge Ö, Keskin N, Tanaçan A.   +17 more
europepmc   +1 more source

Influence of Molecular Genetic Classes on Behavior in Prader‐Willi Syndrome

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT A wide range of behavioral phenotypes has been described in PWS patients including autism spectrum disorder (ASD). The prevalence of behavioral disorders was studied in 292 participants over 3 years with genetically confirmed PWS (N = 164 females and N = 128 males) with deletion (N = 182) and mUPD (maternal uniparental disomy) (N = 99).
Ranim Mahmoud, Merlin G. Butler, Wai Park, Jennifer L. Miller, Daniel J. Driscoll, June‐Anne Gold, Virginia Kimonis   +6 more
wiley   +1 more source

Uncovering the genetic overlap between the Patient Health Questionnaire-9 (PHQ-9), Patient Health Questionnaire-2 (PHQ-2) and Major Depressive Disorder (MDD)

Bentwood S, Adams M, Lu Y, McIntosh A, Kwong A.   +4 more
europepmc   +1 more source

Measurement properties of the Patient Health Questionnaire 15 (PHQ-15) and Somatic Symptom Disorder B-criteria scale (SSD-12), including revised 1-week versions. [PDF]

Sci Rep
Hybelius J, Af Winklerfelt Hammarberg S, Ahnlund Hoffmann A, Spansk E, Olsson A, Strand E, Söderström Winter L, Åkerlund T, Björkander D, Kosic A, Chahin G, Epstein M, Axelsson E.   +12 more
europepmc   +1 more source

Understanding Arthrogryposis Multiplex Congenita (AMC) Across the Lifespan: An Integrative Review of the Adult AMC Registry's Contributions With Lived Experience Partnerships

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT This reflective essay explores how collaborative work between researchers and adults living with Arthrogryposis Multiplex Congenita (AMC) has deepened and broadened our understanding of what it means to live with this rare condition. By intentionally integrating the lived experiences of individuals with AMC into research processes, the ...
Bonita J. Sawatzky, Megan K. MacGillivray, Tracey Schalk, William Bennett Mortenson   +3 more
wiley   +1 more source