Results 91 to 100 of about 15,656 (183)

Circulating microRNA signatures reveal core and reversible dysregulation in obesity via machine learning

The Journal of Physiology, EarlyView.
Abstract figure legend Machine learning analysis of circulating microRNA (miRNA) profiles identified a minimal set of biomarkers that distinguish individuals with obesity from lean individuals both before and after weight‐loss intervention. Comparative analyses revealed heterogeneous molecular responses to weight reduction, with some miRNAs showing ...
Yuan Yue, Rajesh Katare, Jeremiah Deng, Daniel Alencar Da Costa, Patrick Manning   +4 more
wiley   +1 more source

PRADER-WILLI SYNDROME AND DEVELOPMENTAL TRAJECTORIES: ANALYSIS OF A CLINICAL CASE [PDF]

openLa sindrome di Prader-Willi rappresenta una condizione genetica rara, ma significativa, che colpisce circa un individuo su 15-30.000 e si caratterizza per una complessa presentazione clinica che coinvolge diversi aspetti del funzionamento fisico ...
PROFUMO, MADDALENA
core  

Pituitary-Adrenal Axis in Prader Willi Syndrome [PDF]

, 2016
Purpose: Prader Willi syndrome (PWS) is a rare genetic condition that has concurrent endocrinological insufficiencies. The presence of growth hormone deficiency has been well documented, but adrenal insufficiency (AI) is not widely reported. A review was
Angela K. Lucas-Herald, Mohamad Guftar Shaikh, Shaikh, Mohamad Guftar, Edgar, Olivia S., Mohamad Shaikh, Olivia Edgar, Olivia S. Edgar, Lucas-Herald, Angela K., Angela Lucas-Herald   +8 more
core   +1 more source

A clinical follow-up of 35 Brazilian patients with Prader-Willi Syndrome

Clinics, 2012
OBJECTIVE: Prader-Willi Syndrome is a common etiology of syndromic obesity that is typically caused by either a paternal microdeletion of a region in chromosome 15 (microdeletions) or a maternal uniparental disomy of this chromosome.
Caio Robledo D'Angioli Costa Quaio, Tatiana Ferreira de Almeida, Lilian Maria José Albano, Israel Gomy, Debora Romeo Bertola, Monica Castro Varela, Celia P. Koiffmann, Chong Ae Kim   +7 more
doaj   +1 more source

Use of Glucagon‐Like Peptide‐1 Receptor Agonists in Danish Adolescents and Young Adults 2018–2025

Obesity, Volume 34, Issue 8, Page 1551-1557, August 2026.
ABSTRACT Objective Use of glucagon‐like peptide‐1 receptor agonists (GLP‐1RAs) has increased rapidly following approval for obesity treatment, but data on their use in younger populations remain limited. We examined trends in GLP‐1RA use among 12– to 24‐year‐olds in Denmark during 2018–2025.
Helene Kildegaard, Jacob Harbo Andersen, Rebecca Kofod Vinding, Julie Tonsgaard Kloppenborg, Anton Pottegård   +4 more
wiley   +1 more source

Prader-Willi Critical Region, a Non-Translated, Imprinted Central Regulator of Bone Mass: Possible Role in Skeletal Abnormalities in Prader-Willi Syndrome. [PDF]

, 2016
Prader-Willi Syndrome (PWS), a maternally imprinted disorder and leading cause of obesity, is characterised by insatiable appetite, poor muscle development, cognitive impairment, endocrine disturbance, short stature and osteoporosis.
Lee, NJ ; https://orcid.org/, Natalie K Wee, Purtell, Louise, Qi, Y, Zolotukhin, Sergei, Sergei Zolotukhin, Nicola J Lee, Lee, Nicola J., Herzog, Herbert, Croucher, Peter I, Herzog, H ; https://orcid.org/, Wee, NK, Louise Purtell, Ronaldo F Enriquez, Ee-Cheng Khor, Baldock, Paul A., Rishikesh N Kulkarni, Kulkarni, Rishikesh N, Paul A Baldock, Baldock, PA, Kulkarni, Rishikesh N., Baldock, Paul A, Wee, Natalie K, Enriquez, Ronaldo F, Fanshawe, Bruce, Campbell, Lesley, Zolotukhin, S, Croucher, Peter I., Lesley Campbell, Purtell, L, Lee, Nicola J, Enriquez, Ronaldo F., Campbell, L ; https://orcid.org/, Enriquez, RF, Wee, Natalie K., Yue Qi, Khor, Ee-Cheng, Croucher, PI, Fanshawe, B, Peter I Croucher, Kulkarni, RN, Khor, EC, Bruce Fanshawe, Herbert Herzog, Qi, Yue   +44 more
core   +2 more sources

Periodontal disease in a patient with Prader-Willi syndrome: a case report

Journal of Medical Case Reports, 2011
Introduction Prader-Willi syndrome is a complex genetic disease caused by lack of expression of paternally inherited genes on chromosome 15q11-q13. The prevalence of Prader-Willi syndrome is estimated to be one in 10,000 to 25,000.
Kitamura Masahiro, Yamada Satoru, Nozaki Takenori, Kobashi Mariko, Hirano Hiroyuki, Yanagita Manabu, Murakami Shinya   +6 more
doaj   +1 more source

Mandibular Movement Monitoring in Children With Neurodisability

Pediatric Pulmonology, Volume 61, Issue 8, August 2026.
ABSTRACT Background Obstructive sleep apnoea (OSA) in children is diagnosed using polysomnography (PSG), but children with neurodisability are >3 times more likely to not tolerate leads and sensors. The diagnostic accuracy of Sunrise, a small sensor applied to the chin, has not been assessed in this special population.
Andrew J. Collaro, Kiara D. Sclip, Lydia R. Penny, Laura R. Mead, Ajay Kevat, Jasneek K. Chawla   +5 more
wiley   +1 more source

Autonomic Function in Fragile X Syndrome: A Systematic Review

Journal of Intellectual Disability Research, Volume 70, Issue 8, Page 773-787, August 2026.
ABSTRACT Background Fragile X syndrome (FXS) is a monogenic X‐linked cause of intellectual disability and autism. Individuals with FXS often have high levels of anxiety and sometimes display challenging behaviours. Autonomic dysfunction has been suggested to be one physiological mechanism that may contribute to these.
Sydni Weissgold, Sarah E. A. Eley, Damien Wright, Andrew G. McKechanie, Andrew C. Stanfield   +4 more
wiley   +1 more source

Health Supervision for Children With Prader-Willi Syndrome [PDF]

, 2011
This set of guidelines was designed to assist the pediatrician in caring for children with Prader-Willi syndrome diagnosed by clinical features and confirmed by molecular testing. Prader-Willi syndrome provides an excellent example of how early diagnosis
null null, Shawn E. McCandless
core   +1 more source