Results 131 to 140 of about 4,014,458 (336)

Stress, Health, and Injury Among Illinois Farmers

American Journal of Industrial Medicine, EarlyView.
ABSTRACT Objectives The goal of this cross‐sectional study was to characterize stress, injury, and chronic health conditions among agricultural producers in Illinois. The objectives were to: (1) describe the prevalence and nature of work‐related injuries; (2) describe chronic health conditions, stress, and symptoms of mental health conditions; and (3 ...
Josie M. Rudolphi, Salah Issa, Courtney Cuthbertson, Kaleigh Barnett   +3 more
wiley   +1 more source

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The interstitial 6p microdeletion syndrome is characterized by dysmorphic facies and structural heart, kidney, brain, and musculoskeletal differences. RREB1 haploinsufficiency and consequent abnormal RAS‐MAPK pathway signaling have been proposed as a driver of the disease phenotype; however, apart from a single case report, the phenotype of ...
Alanna Strong, Caoimhe McKenna, Karen Stals, Antonio Vitobello, Mathilde Renaud, Claudine Rieubland, Michel Guipponi, Christophe Philippe, Paul Vrana, Alisa Gaskell, A. Micheil Innes, Alyssa L. Rippert, Rebecca Ahrens‐Nicklas, Elizabeth Bhoj, Kiersten Keller, Bimal P. Chaudhari, Brandon S. Stone   +16 more
wiley   +1 more source

Association of Electroconvulsive Therapy With Psychiatric Readmissions in US Hospitals

JAMA psychiatry, 2017
E. Slade, D. Jahn, W. Regenold, B. Case
semanticscholar   +1 more source

An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical Recommendations

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Natural History Studies can help inform clinician and caregiver expectations, form the basis of management guidelines, and provide a comparator for therapeutic intervention. In rare conditions, where collection of prospective longitudinal data is untimely and impractical, quasi‐natural history data—from multiple individuals of different ages ...
E. Woods, N. Holmes, A. S. Denommé‐Pichon, M. Vincent, N. Belova, C. Gooch, B. Isidor, C. W. Ockeloen, E. Pavlidou, H. Stewart, V. J. M. Verhoeven, A. Ververi, A. Dixit, A. Sarkar, R. Legg, E. Reid, M. Balasubramanian   +16 more
wiley   +1 more source

Psychiatric Disorders and Trends in Resource Use in Pediatric Hospitals

Pediatrics, 2016
B. Zima, Jonathan Rodean, M. Hall, Naomi S. Bardach, Tumaini R. Coker, J. Berry   +5 more
semanticscholar   +1 more source

Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genetic disorders commonly share features such as developmental delays, cognitive impairment, and behavioral challenges, yet many conditions also present unique dysmorphic features that distinguish them. Performing a thorough medical and family history and a detailed physical exam with attention to dysmorphic features is often the first step ...
Natasha L. Rudy, Adriana Gomes, Tinatin Tkemaladze, Omar Abdul‐Rahman, Drew Cratsenberg, Giulia Pascolini, Giovanni Di Zenzo, Daniele Castiglia, Emily Black, Camerun Washington, Lauren Chad, Cynthia Curry, Miguel Del Campo, Nicole Fleischer, Lynne M. Bird, Anna C. E. Hurst   +15 more
wiley   +1 more source

Advances and challenges of psychiatric reform in Brazil 22 years after the Caracas declaration

Medwave, 2012
The authors present the psychiatric reform in Brazil (PRB) against the backdrop of the ideological and technical crisis of the care model previous to redemocratization and the Unified Healthcare System (SUS) creation.
Domingos Sávio Nascimento Alves, Paulo Roberto Fagundes da Silva   +1 more
doaj   +1 more source

Genome Sequencing Uncovers Additional Findings in Phelan‐McDermid Syndrome

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Phelan‐McDermid syndrome (PMS) is a genetic condition caused by deletions of chromosome 22q13.3 or pathogenic variants in the SHANK3 gene. Neurologic features typically include intellectual disability, autism spectrum disorder, hypotonia, and absent speech, though there is considerable variability even among individuals with the same molecular
Rachel Gore Moses, Morgan Similuk, Alexandra Hehn, Rylee Duncan, Margaret Pekar, Eliza Gordon‐Lipkin, Maria T. Acosta, Deena Zeltser, Nadjalisse Reynolds‐Lallement, Latha Soorya, Mustafa Sahin, Tess Levy, Alexander Kolevzon, Joseph D. Buxbaum, Elizabeth Berry‐Kravis, Craig M. Powell, Jonathan A. Bernstein, Mari Tokita, Bryce A. Seifert, Rajarshi Ghosh, Magdalena A. Walkiewicz, Audrey Thurm   +21 more
wiley   +1 more source

Comparison of Religious Teaching with Muscle Relaxation Methods on Anxiety Patients

Caspian Journal of Neurological Sciences, 2019
Background: Anxiety in psychiatric patients is more prevalent than the general population. Non-pharmacological methods for the treatment of anxiety are beneficial to the health of the patient, but it is not clear which of these approaches are more ...
Fateme Attar Ghasbe, Naema Khodadadi-Hassankiadeh, Shahrokh Yousefzadeh-Chabok, Anita Reihanian, Samaneh Ghorbani Shirkouhi   +4 more
doaj  

Learning From History: Deinstitutionalization of People with Mental Illness as Precursor to Long-Term Care Reform [PDF]

, 2007
Considers the deinstitutionalization of state mental hospital patients over the past fifty years, and uses this as a model for evaluating reform efforts of custodial and long-term care services for the ...
Chris Koyanagi
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