Novel <i>SIM1</i> Variants Expanding the Spectrum of SIM1-Related Obesity. [PDF]
Mohammed I +5 more
europepmc +1 more source
Psychometric evaluation of novel hyperphagia questionnaires in a real-world setting for patients with a rare MC4R pathway disease. [PDF]
Pomeroy J +6 more
europepmc +1 more source
Long-term intranasal oxytocin therapy in patients with hypothalamic syndrome: case series and literature review. [PDF]
Wang Y +8 more
europepmc +1 more source
Rare Presentation of Heterozygous PCSK1 Deficiency in an Adolescent Male. [PDF]
Metzger T, Jalal A, Duran SR.
europepmc +1 more source
Barriers, Limitations, and Experiences with Clinical Trials-Treatment in Rare Diseases with Prader-Willi Syndrome as an Example. [PDF]
Butler MG, Silvey S, van Bosse HJP.
europepmc +1 more source
Exploring cannabinoid receptor CB1 autophagy and the obesity phenotype of p62-deficient mice. [PDF]
Keller C +5 more
europepmc +1 more source
Treatment Priorities in Craniopharyngioma: Perspectives of Survivors and Caregivers. [PDF]
Kayadjanian N, Hsu EA.
europepmc +1 more source
Central nervous system adaptation mechanism of obesity induced by high-fat high-sucrose diet: Differences in brain function between obese and obese resistant rats based on fMRI. [PDF]
Fang Q +7 more
europepmc +1 more source
Case Report: Schaaf-Yang Syndrome Milder Phenotype Due to Potential Pathogenic Novel Missense Variant as an Unusual Cause of Obesity in a Pediatric Patient. [PDF]
Pastucha D +6 more
europepmc +1 more source
A proof-of-concept study of pitolisant for excessive daytime sleepiness in patients with Prader-Willi syndrome. [PDF]
Revana A +11 more
europepmc +1 more source

