Effects of long-term transcutaneous auricular vagus nerve stimulation on circadian vagal activity in people with Prader-Willi Syndrome: A case-series.

Autor: Schmausser M; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Cologne, Germany., Holland A; Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom., Beresford-Webb J; Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom., Eglen SJ; Department of Applied Mathematics and Theoretical Physics, University of Cambridge, UK., Manning K; Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom., Aman L; Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom., Kronhaus D; Department of Applied Mathematics and Theoretical Physics, University of Cambridge, UK., Koenig J; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Cologne, Germany. Electronic address: julian.koenig@uk-koeln.de.

Publikováno v: Research in developmental disabilities [Res Dev Disabil] 2024 Nov; Vol. 154, pp. 104855. Date of Electronic Publication: 2024 Oct 13.

The relationship between cardiac activity, behaviour and endogenous oxytocin and vasopressin in Prader-Willi Syndrome: An exploratory study.

Autor: Rice LJ; Faculty of Medicine and Health, Brain and Mind Centre, The University of Sydney, New South Wales, Australia; Faculty of Medicine and Health, Specialty of Child and Adolescent Health, The University of Sydney Children's Hospital Westmead Clinical School, Westmead, New South Wales, Australia. Electronic address: lauren.rice@sydney.edu.au., Agu J; Faculty of Medicine and Health, Specialty of Child and Adolescent Health, The University of Sydney Children's Hospital Westmead Clinical School, Westmead, New South Wales, Australia., Carter CS; Department of Psychology, University of Virginia; Kinsey Institute, Indiana University, Bloomington, IN, USA., Cho YH; Faculty of Medicine and Health, Specialty of Child and Adolescent Health, The University of Sydney Children's Hospital Westmead Clinical School, Westmead, New South Wales, Australia; Institute of Endocrinology and Diabetes, The Children's Hospital at Westmead, Westmead, New South Wales, Australia., Harris J; Department of Psychiatry and Behavioural Sciences and Paediatrics, Johns Hopkins University, Baltimore, MD, USA., Heilman K; Department of Psychiatry, University of North Carolina, Chapel Hill, NC, USA., Nazarloo HP; Department of Psychology, University of Virginia., Naanai H; Faculty of Medicine and Health, Specialty of Child and Adolescent Health, The University of Sydney Children's Hospital Westmead Clinical School, Westmead, New South Wales, Australia., Porges S; Kinsey Institute, Indiana University, Bloomington, IN, USA; Department of Psychiatry, University of North Carolina, Chapel Hill, NC, USA., Einfeld SL; Faculty of Medicine and Health, Brain and Mind Centre, The University of Sydney, New South Wales, Australia.

Publikováno v: International journal of psychophysiology : official journal of the International Organization of Psychophysiology [Int J Psychophysiol] 2024 Nov; Vol. 205, pp. 112429. Date of Electronic Publication: 2024 Sep 03.

Relationship of thyroid function with genetic subtypes and treatment with growth hormone in Prader-Willi syndrome.

Autor: Schmok T; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California, USA.; Idaho College of Osteopathic Medicine, Meridian, Idaho, USA., Surampalli A; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California, USA., Khare M; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California, USA.; Division of Pediatric Hospital Medicine, Department of Pediatrics, University of California, San Diego, California, USA., Zandihaghighi S; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California, USA., Baghbaninogourani R; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California, USA., Patolia B; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California, USA., Gold JA; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California, USA.; Department of Pediatrics, Division of Medical Genetics, University of Loma Linda, Loma Linda, California, USA.; Children's Hospital of Orange County, Orange, California, USA., Naidu A; Department of Pediatrics, Division of Endocrinology, University of California, Irvine, California, USA., Cassidy SB; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California, USA.; Division of Medical Genetics, Department of Pediatrics, University of California San Francisco, San Francisco, California, USA., Kimonis VE; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California, USA.; Children's Hospital of Orange County, Orange, California, USA.; Department of Neurology, University of California, Irvine, California, USA.; Department of Pathology, University of California, Irvine, California, USA.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Oct; Vol. 194 (10), pp. e63724. Date of Electronic Publication: 2024 Jun 04.

Implication of locus coeruleus dysfunction in Prader-Willi syndrome: Insights from a mouse model.

Autor: Tsai LP; Department of Pediatrics, Taipei Tzu Chi Hospital, Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan; School of Medicine, Tzu Chi University, Hualien 97071, Taiwan; Department of Pediatrics, Heping Fuyou Branch, Taipei City Hospital, Taipei 100027, Taiwan., Luo DZ; Department of Psychology, National Taiwan University, Taipei 10617, Taiwan., Chan H; Department of Pediatrics, Taipei Tzu Chi Hospital, Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan; Department of Life Science, College of Life Science, National Taiwan University, Taipei 10617, Taiwan., Hung WC; Department of Pediatrics, Taipei Tzu Chi Hospital, Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan; Department of Life Science, College of Life Science, National Taiwan University, Taipei 10617, Taiwan., Lai WS; Department of Psychology, National Taiwan University, Taipei 10617, Taiwan., Min MY; Department of Life Science, College of Life Science, National Taiwan University, Taipei 10617, Taiwan., Wong SB; Department of Pediatrics, Taipei Tzu Chi Hospital, Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan; School of Medicine, Tzu Chi University, Hualien 97071, Taiwan. Electronic address: wongshibing@tzuchi.com.tw.

Publikováno v: Experimental neurology [Exp Neurol] 2024 Nov; Vol. 381, pp. 114927. Date of Electronic Publication: 2024 Aug 17.

Genotype-phenotype characteristics of 57 patients with Prader-Willi syndrome: a single-center experience from Turkey.

Autor: Torun D; Departments of Medical Genetics., Akin O; Pediatric Endocrinology, Gülhane Faculty of Medicine, University of Health Sciences, Ankara, Turkey.

Publikováno v: Clinical dysmorphology [Clin Dysmorphol] 2024 Oct 01; Vol. 33 (4), pp. 145-151. Date of Electronic Publication: 2024 Jun 18.