Nerve enlargement in patients with Noonan syndrome: A retrospective cohort study.

Autor: Draaisma F; Department of Pediatrics, Radboud Institute for Health Sciences, Radboud University Medical Center, Amalia Children's Hospital, Nijmegen, The Netherlands., Leenders EKSM; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands., Erasmus CE; Department of Pediatric Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen Medical Center, Amalia Children's Hospital, Nijmegen, The Netherlands., Braakman HMH; Department of Pediatric Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen Medical Center, Amalia Children's Hospital, Nijmegen, The Netherlands., Burgers MCJ; Department of Pediatrics, Radboud Institute for Health Sciences, Radboud University Medical Center, Amalia Children's Hospital, Nijmegen, The Netherlands., Coppens CH; Department of Pediatrics, Radboud Institute for Health Sciences, Radboud University Medical Center, Amalia Children's Hospital, Nijmegen, The Netherlands., Rinne T; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands., Zenker M; Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany., Tartaglia M; Molecular Genetics and Functional Genomics, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy., Reintjes W; Department of Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands., Voermans NC; Department of Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands., van Engelen BGM; Department of Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands., van Alfen N; Department of Neurology, Clinical Neuromuscular Imaging Group, Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands., Draaisma JMT; Department of Pediatrics, Radboud Institute for Health Sciences, Radboud University Medical Center, Amalia Children's Hospital, Nijmegen, The Netherlands.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Nov; Vol. 194 (11), pp. e63810. Date of Electronic Publication: 2024 Jul 03.

The characteristics of eating, drinking and oro-pharyngeal swallowing difficulties associated with repaired oesophageal atresia/tracheo-oesophageal fistula: a systematic review and meta-proportional analysis.

Autor: Stewart, Alexandra^1,2 (AUTHOR) Alex.stewart@gosh.nhs.uk, Govender, Roganie^3,4 (AUTHOR), Eaton, Simon⁵ (AUTHOR), Smith, Christina H.¹ (AUTHOR), De Coppi, Paolo^2,5 (AUTHOR), Wray, Jo² (AUTHOR)

Publikováno v: Orphanet Journal of Rare Diseases. 7/4/2024, Vol. 19 Issue 1, p1-15. 15p.

A comprehensive assessment of oral health, swallowing difficulty, and nutritional status in older nursing home residents.

Autor: Chou, Kuei-Ru^1,2,3,4,5 (AUTHOR), Huang, Mao-Suan⁶ (AUTHOR), Chiu, Wan-Chun^7,8,9 (AUTHOR), Chen, Yi-Hsiu⁷ (AUTHOR), Chen, Yu-Yoh¹⁰ (AUTHOR), Xiao, Qian⁷ (AUTHOR), Yang, Suh-Ching^7,8,11,12 (AUTHOR) sokei@tmu.edu.tw

Publikováno v: Scientific Reports. 11/14/2023, Vol. 13 Issue 1, p1-9. 9p.

Swallowing-related quality of life in children with oesophageal atresia: a national cohort study.

Autor: Bergmann, Sandra¹ sandra.bergmann@med.uni-muenchen.de, Ritz, Laura Antonia², Widenmann-Grolig, Anke³, Jechalke, Stephan³, von Schweinitz, Dietrich¹, Hubertus, Jochen⁴, Lurz, Eberhard⁵ eberhard.lurz@med.uni-muenchen.de

Publikováno v: European Journal of Pediatrics. Jan2023, Vol. 182 Issue 1, p275-283. 9p. 2 Charts, 1 Graph.

Factors of family impact in a Swedish-German cohort of children born with esophageal atresia.

Autor: Dellenmark-Blom, Michaela¹ (AUTHOR) michaela.dellenmark.blom@gu.se, Abrahamsson, Kate^1,2 (AUTHOR), Dingemann, Jens³ (AUTHOR), Witt, Stefanie⁴ (AUTHOR), Dingemann, Carmen³ (AUTHOR), Jönsson, Linus^1,2 (AUTHOR), Gatzinsky, Vladimir^1,2 (AUTHOR), Bullinger, Monika⁴ (AUTHOR), Ure, Benno M.³ (AUTHOR), Chaplin, John E.² (AUTHOR), Quitmann, Julia H.⁴ (AUTHOR)

Publikováno v: Orphanet Journal of Rare Diseases. 5/21/2022, Vol. 17 Issue 1, p1-11. 11p.