Disease: Bardet-Biedl syndrome 6
- A Case of Laurence Moon Bardet Biedl Syndrome
- An evaluation of setmelanotide injection for chronic weight management in adult and pediatric patients with obesity due to Bardet-Biedl syndrome
- Bardet-Biedl syndrome associated with novel compound heterozygous variants in BBS12 gene
- Bardet-Biedl Syndrome Overview
- Bardet-Biedl Syndrome Presenting in Adulthood
- Behavioral Phenotyping of Bbs6 and Bbs8 Knockout Mice Reveals Major Alterations in Communication and Anxiety
- Burden of hyperphagia and obesity in Bardet-Biedl syndrome: a multicountry survey
- Caregiver burden in Bardet-Biedl syndrome: findings from the CARE-BBS study
- Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees
- Genetic Obesity Disorders: Body Mass Index Trajectories and Age of Onset of Obesity Compared with Children with Obesity from the General Population
- IL-6 ameliorates defective leptin sensitivity in DIO ventromedial hypothalamic nucleus neurons
- Interview-Based Patient- and Caregiver-Reported Experiences of Hunger and Improved Quality of Life with Setmelanotide Treatment in Bardet-Biedl Syndrome
- Multiple Independent Gene Disorders Causing Bardet-Biedl Syndrome, Congenital Hypothyroidism, and Hearing Loss in a Single Indian Patient
- Nonsyndromic Retinitis Pigmentosa Overview
- Novel multi-allelic variants, two BBS2 and one PKD1 variant, of renal ciliopathies: A case report and literature review
- Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein
- Outcomes in children of women with type 2 diabetes exposed to metformin versus placebo during pregnancy (MiTy Kids): a 24-month follow-up of the MiTy randomised controlled trial
- Phenotypic diversity observed in a Chinese patient cohort with biallelic variants in Bardet-Biedl syndrome genes
- Quality of life improvements following one year of setmelanotide in children and adult patients with Bardet-Biedl syndrome: phase 3 trial results
- The actin-bundling protein Fascin-1 modulates ciliary signalling