Results 171 to 180 of about 24,669 (243)

A questionnaire-based survey on hyperphagia in individuals with Prader-Willi syndrome in Japan. [PDF]

Endocr J
Tachibana M, Oto Y, Kashimada K, Ishii T, Takahashi Y, Muroya K, Aoki Y, Kurosawa K, Ogata T, Kawai M.   +9 more
europepmc   +1 more source

A scoping review of dietary interventions to treat obesity among Prader-Willi syndrome individuals. [PDF]

Intractable Rare Dis Res
Aman M, Hamid HA, Rajikan R.
europepmc   +1 more source

Sensorineural deafness in a child with Prader-Willi Syndrome-A rare case report. [PDF]

J Family Med Prim Care
Saikrishna P, Tripathy SK, Medhagopal RG, Das S, Bharti B, Malik A.   +5 more
europepmc   +1 more source

The burden of illness in Prader-Willi syndrome: a systematic literature review. [PDF]

Orphanet J Rare Dis
Dempsey D, Hall M, Lanning B, Barron-Millar B, Huang M, Cowen N, Nagao M, Gandhi R, Bhatnagar A.   +8 more
europepmc   +1 more source

Effects of probiotics on patients with Prader-Willi syndrome: a systematic review and meta-analysis of randomized controlled trials. [PDF]

Front Nutr
Toh QY, Kang YN, Chee SY, Chiu HH.
europepmc   +1 more source

Hyperactive Catatonia in an Adolescent With Prader-Willi Syndrome. [PDF]

Cureus
Alharbi R, Shaaban SS, MacMaster E.
europepmc   +1 more source

GABAergic regulation of Locus coeruleus activity in necdin-deficient mice, an animal model of Prader-Willi syndrome. [PDF]

J Neurodev Disord
Tsai LP, Chan H, Hung WC, Min MY, Cheng SJ, Yang CE, Yu CH, Wong SB.   +7 more
europepmc   +1 more source

Dual Genetic Diagnosis of Prader-Willi Syndrome and TMC1-Related Severe Congenital Hearing Loss: Diagnostic Challenges and Cochlear Implant Outcomes. [PDF]

Diagnostics (Basel)
Samara P, Athanasopoulos M, Koudoumnaki E, Markatos N, Athanasopoulos I.   +4 more
europepmc   +1 more source