Results 91 to 100 of about 1,165,403 (129)

Precision or Paradox? AI‐Driven Adiposity Imaging in Women With Overweight and Obesity: A Systematic Review and Meta‐Analysis

Obesity Reviews, Volume 27, Issue 9, September 2026.
ABSTRACT Artificial intelligence (AI) enables automated, high‐throughput adiposity quantification, offering refined risk stratification for women with overweight and obesity. We systematically reviewed and meta‐analyzed studies evaluating AI‐based segmentation of visceral, subcutaneous, and total fat in adult women populations (BMI: 25–29.9 and ≥ 30 kg/
Asefa Adimasu Taddese, Bjorn T. Tam
wiley   +1 more source

Altered neural electrophysiological properties in the anterior cingulate cortex in a mouse model of Prader‐Willi syndrome

The Journal of Physiology, Volume 604, Issue 17, Page 7313-7336, 1 September 2026.
Abstract figure legend Prader‐Willi syndrome (PWS) originates from deficiencies in chromosome 15q11‐13 region clustering around a critical region containing multiple‐repeat non‐coding RNA gene Snord116, resulting in metabolic and behavioural abnormalities leading to hyperphagia and obesity.
Volodymyr Rybalchenko, Ryan Butler
wiley   +1 more source

Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory

Orphanet Journal of Rare Diseases
Objective Prader-Willi syndrome (PWS) is a genetic neurodevelopmental disorder with a characteristic trajectory. Infants display hypotonia, poor social and feeding skills, and high risk of choking, which have been shown to improve after oxytocin (OT ...
Maithe Tauber, Gwenaelle Diene, Pascale Fichaux-Bourin, Graziella Pinto, Iva Gueorguieva, Marc Nicolino, Rachel Reynaud, Delphine Bernoux, Veronique Beauloye, Elin Malek Abrahimians, Cordula Kiewert, Pierre Payoux, Sophie Cabal, Catherine Molinas, Melanie Glattard, Sylvie Viaux-Savelon, Antoine Guedeney, David Cohen, Catherine Arnaud, Marion Valette   +19 more
doaj   +1 more source

Prader-Willi syndrome

, 1994
Title from Web page (viewed June 17, 2009).; "March 1, 1994."; Discusses Prader-Willi syndrome, including the relationship between IQ and services available to those with the syndrome in the state.; Harvested from the web on 6/17 ...
Kasprak, John.
core  

Behavioral Profile of Children and Adolescents with Prader-Willi Syndrome and Exogenous Obesity

Psicologia, 2009
The objective of present study was compared the behavioral profile of two different groups of children and adolescents with obesity. Ten subjects presented diagnoses of exogenous obesity and ten Prader-Willi syndrome.
Yara Garzuzi, Luiz Renato Rodrigues Carreiro, José Salomão Schwartzman, Maria Luiza Guedes de Mesquita, Domingos Palma, Fábio Ancona Lopez, Denise Ely Bellotto de Moraes, Elizeu Coutinho de Macedo, Maria Cristina Triguero Veloz Teixeira   +8 more
doaj  

PRADER-WILLI SYNDROME: WHAT IS THE GENERAL PEDIATRICIAN SUPPOSED TO DO? - A REVIEW

, 2018
Objective: To carry out a review about Prader-Willi Syndrome based on the most recent data about the subject and to give recommendation for the general pediatricians for early diagnoses and follow-up.
Hamilton Cabral Menezes-Filho (5884745), Celia Priszkulnik Koiffmann (5884733), Paula Lage Pasqualucci (5884715), Simone Sakura Ito (5884721), Durval Damiani (4829520), Larissa Baldini Farjalla Mattar (5884727), Leticia Azevedo Soster (5884739), Jorge David Aivazoglou Carneiro (5884742), Caroline Buff Gouveia Passone (5884712), Ruth Rocha Franco (4829526)   +9 more
core   +1 more source

Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype

Brazilian Journal of Medical and Biological Research, 2008
Monosomy 1p36 is the most common subtelomeric microdeletion syndrome with an incidence rate estimated to be 1 in 5000 births. A hypothesis of a similarity between patients with 1p36 deletion and those with Prader-Willi syndrome and the existence of two ...
V.R. Rodríguez, L.F. Mazzucato, J.M. Pina-Neto   +2 more
doaj  

Prader-Willi Syndrome: Diagnostic Criteria

, 1993
Diagnostic criteria for Prader-Willi syndrome (PWS), developed by consensus of seven clinicians in consultation with experts, are reported from the University of Washington, Seattle, and six additional ...
J Gordon Millichap
core   +1 more source

Perception of four intellectual and developmental disabilities based on search engine and news portrayal.

PLoS ONE
BackgroundFor people with intellectual and developmental disabilities, other's perceptions of them based on their condition often begin before birth and go on to impact relationships, opportunities, and self perception across the life course.
Lillian J Droscha, Sophia Chung, Zoe Li-Khan, Ashley Scott, Eric Rubenstein   +4 more
doaj   +1 more source

Prader-Willi-like phenotype in fragile X syndrome

, 1994
Prader-Willi-like phenotype in fragile X syndrome. Schrander-Stumpel C, Gerver WJ, Meyer H, Engelen J, Mulder H, Fryns JP. Department of Clinical Genetics, Maastricht University Hospital, The Netherlands.
Frijns, J.P., Gerver, W.J.M., Mulder, H., Schrander-Stumpel, C.T.R.M., Meyer, H., Engelen, J.J.M.   +5 more
core   +1 more source