[Bespreking van: A. van Wieringen, H. Rikhof (2013) De Zeven Sacramenten. Een bijbeltheologische en systematisch-theologische studie]

Autor: Smit, P.B.A.

Publikováno v: Smit, P B A 2014, ' [Bespreking van: A. van Wieringen, H. Rikhof (2013) De Zeven Sacramenten. Een bijbeltheologische en systematisch-theologische studie] ', Kerk en Theologie, pp. 198 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0ff38022a2e5b76720a487e4d006b0fa
https://research.vu.nl/en/publications/9db77f40-a9e6-423a-9fcc-0a58684cecbe

Clinical practice - latest insights in optimizing the care of children with Down syndrome.

Autor: van Gameren-Oosterom HBM; Department of Pediatrics, Groene Hart Ziekenhuis, P.O. Box 1098, 2800 BB, Gouda, The Netherlands. helma.gameren@ghz.nl., Weijerman ME; Department of Pediatrics, Alrijne, Leiderdorp, The Netherlands., van Wieringen H; Department of Pediatrics, St. Antonius, Utrecht, The Netherlands., de Winter JP; Department of Pediatrics, Spaarne Gasthuis, Haarlem/Hoofddorp, The Netherlands.; Leuven Child and Health Institute, KU Leuven, Leuven, Belgium.; Department of Development and Regeneration, KU Leuven, Leuven, Belgium., van Wermeskerken AM; Department of Pediatrics, Flevoziekenhuis, Almere, The Netherlands.

Publikováno v: European journal of pediatrics [Eur J Pediatr] 2023 May; Vol. 182 (5), pp. 2027-2039. Date of Electronic Publication: 2023 Mar 10.

Theoretical Studies in Nuclear Structure. IV. Wave Functions for the Nuclear p-Shell Part A. $\langle $ p n |p n-1 p $\rangle $ Fractional Parentage Coefficients

Autor: Jahn, H. A., van Wieringen, H.

Publikováno v: Proceedings of the Royal Society of London. Series A, Mathematical and Physical Sciences, 1951 Nov . 209(1099), 502-524.

Externí odkaz: https://www.jstor.org/stable/98832

The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations.

Autor: van Woerden GM; Department of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.; Department of Clinical Genetics, The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands., Senden R; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands., de Konink C; Department of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Clinical Genetics, The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands., Trezza RA; Department of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.; Department of Clinical Genetics, The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands., Baban A; Pediatric Cardiology and Cardiac Arrhythmias Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Bassetti JA; Division of Medical Genetics, Weill Cornell Medicine, New York City, New York, USA., van Bever Y; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.; Department of Clinical Genetics, The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands., Bird LM; Department of Pediatrics, University of California San Diego, San Diego, California, USA.; Division of Genetics/Dysmorphology, Rady Children's Hospital San Diego, San Diego, California, USA., van Bon BW; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Brooks AS; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.; Department of Clinical Genetics, The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands., Guan Q; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA., Klee EW; Division of Computational Biology, Department of Quantitative Health Sciences, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA., Marcelis C; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Rosado JM; Division of Computational Biology, Department of Quantitative Health Sciences, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA., Schimmenti LA; Department of Otorhinolaryngology Head and Neck Surgery, Ophthalmology, Clinical Genomics, and Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, USA., Shikany AR; The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Terhal PA; Department of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands., Nicole Weaver K; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA., Wessels MW; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands., van Wieringen H; Department of Pediatrics, St. Antonius Hospital, Nieuwegein, The Netherlands., Hurst AC; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA., Gooch CF; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA., Steindl K; Institute of Medical Genetics, University of Zürich, Schlieren, Switzerland., Joset P; Department of Medical Genetics, Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland., Rauch A; Institute of Medical Genetics, University of Zürich, Schlieren, Switzerland., Tartaglia M; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy., Niceta M; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.; Department of Pediatrics, Sapienza University, Rome, Italy., Elgersma Y; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.; Department of Clinical Genetics, The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands., Demirdas S; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.

Publikováno v: Human mutation [Hum Mutat] 2022 Oct; Vol. 43 (10), pp. 1377-1395. Date of Electronic Publication: 2022 Jul 29.

IgG1 glycosylation highlights premature aging in Down syndrome.

Autor: Streng, Bianca M. M.¹ (AUTHOR), Van Coillie, Julie^2,3 (AUTHOR), Wildenbeest, Joanne G.¹ (AUTHOR), Binnendijk, Rob S.⁴ (AUTHOR), Smits, Gaby⁴ (AUTHOR), den Hartog, Gerco⁴ (AUTHOR), Wang, Wenjun⁵ (AUTHOR), Nouta, Jan⁵ (AUTHOR), Linty, Federica^2,3 (AUTHOR), Visser, Remco^2,3 (AUTHOR), Wuhrer, Manfred⁵ (AUTHOR), Vidarsson, Gestur^2,3 (AUTHOR), Bont, Louis J.¹ (AUTHOR) l.bont@umcutrecht.nl

Publikováno v: Aging Cell. Jul2024, Vol. 23 Issue 7, p1-10. 10p.