Publications by authors named "Karin Geleijns"

23Publications

When a child dies: a systematic review of well-defined parent-focused bereavement interventions and their alignment with grief- and loss theories.

BMC Palliat Care 2020 Mar 12;19(1):28. Epub 2020 Mar 12.

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Universiteitsweg 100, 3584 CG, Utrecht, The Netherlands.

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http://dx.doi.org/10.1186/s12904-020-0529-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068872PMC
March 2020

Defining and expanding the phenotype of -associated developmental epileptic encephalopathy.

Neurol Genet 2019 Dec 10;5(6):e373. Epub 2019 Dec 10.

Department of Epilepsy Genetics and Precision Medicine (K.J.M., E.G., G.R., R.S.M.), The Danish Epilepsy Centre Filadelfia, Dianalund, Denmark; Institute for Regional Health Services (K.J.M., E.G., R.S.M.), University of Southern Denmark, Odense; Institute of Human Genetics (D.M., R. Jamra, A.F., J.R.L.), University of Leipzig Medical Center, Germany; Institute of Structural Biology (R. Janowski, D.N.), Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany; Department of Paediatric Radiology (C.R.), University of Leipzig Medical Center, Germany; Department of Epilepsy, Sleep and Pediatric Neurophysiology (J.T.), Lyon University Hospital, France; Neuropediatric Unit (A.-L.P., D.M.V., G.L.), Lyon University Hospital, France; Department of Medical Genetics (N.C., G.L.), Lyon University Hospital, France; GenDev Team (N.C.), CNRS UMR 5292, INSERM U1028, CNRL and University of Lyon, France; Department of Genetics (E.B.), University Medical Center Utrecht, The Netherlands; Department of Child Neurology (K.G.), Brain Center Rudolf Magnus, University Medical Center Utrecht, The Netherlands; Department of Paediatrics (A.P.B.), Copenhagen University Hospital Rigshospitalet, Denmark; Baylor College of Medicine (S.M., K.N.), Children's Hospital of San Antonio; Undiagnosed Diseases Program (G.B., C.P.), Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth; Western Australian Register of Developmental Anomalies (G.B., D.G.), Australia; Telethon Kids Institute and the School of Paediatrics and Child Health (G.B.), University of Western Australia, Perth; Linear Clinical Research (L.D.), WA, Australia; Center of Human Genetics (S.S), Jena University Hospital, Germany; Department of Neuropediatrics (A.D.), Jena University Hospital, Germany; Division of Neurology (K.L.H.), Children's Hospital of Philadelphia, PA; Division of Neuropediatrics (A.M.), University of Leipzig Medical Center, Germany; Amplexa Genetics (H.H.), Odense, Denmark; Clinic for Children (H.H.), Værløse, Denmark; Center for Integrative Brain Research (G.M.), Seattle Children's Research Institute, WA; Department of Pediatrics (G.M.), University of Washington, Seattle; Medical Genetics Unit (F.B.), Department of Life, Health and Environmental Sciences, University of L'Aquila, Italy; Istituto Dermopatico dell'Immacolata (F.B.), IDI-IRCCS, Rome, Italy; Institute of Human Genetics (T.B., M.H.), University Medical Center Hamburg-Eppendorf, Germany; Childrens Hospital (J.D.), University Medical Center Hamburg-Eppendorf, Germany; University of Copenhagen (G.R.), Denmark; Institute for Human Genetics (P.M.), University Hospital Magdeburg, Germany; Children's Hospital A. Meyer (R.G., A.V.), University of Florence, Italy; and Institute of Pharmaceutical Biotechnology (D.N.), Ulm University, Germany.

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http://dx.doi.org/10.1212/NXG.0000000000000373DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927360PMC
December 2019

Why the TimeToStop trial failed to recruit: a survey on antiepileptic drug withdrawal after paediatric epilepsy surgery.

Epileptic Disord 2018 Oct;20(5):374-385

Department of Child Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht and Utrecht University, Member of the European Reference Network EpiCARE, Utrecht, the Netherlands.

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http://dx.doi.org/10.1684/epd.2018.1003DOI Listing
October 2018

Specific EEG markers in POLG1 Alpers' syndrome.

Clin Neurophysiol 2018 10 4;129(10):2127-2131. Epub 2018 Aug 4.

Brain Center Rudolf Magnus, University Medical Center Utrecht, Department of Neurology, PO Box 85500, 3508 GA Utrecht, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.clinph.2018.07.016DOI Listing
October 2018

Individualized prediction of seizure relapse and outcomes following antiepileptic drug withdrawal after pediatric epilepsy surgery.

Epilepsia 2018 03 15;59(3):e28-e33. Epub 2018 Feb 15.

Department of Child Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1111/epi.14020DOI Listing
March 2018

Risks and Benefits of Rituximab in the Treatment of Hashimoto Encephalopathy in Children: Two Case Reports and a Mini Review.

Pediatr Neurol 2017 01 20;66:28-31. Epub 2016 Sep 20.

Department of Pediatric Immunology and Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2016.09.002DOI Listing
January 2017

Innate Immunity to Campylobacter jejuni in Guillain-Barré Syndrome.

Ann Neurol 2015 Sep 30;78(3):343-54. Epub 2015 Jun 30.

Department of Immunology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1002/ana.24442DOI Listing
September 2015

Susceptibility to Guillain-Barré syndrome is not associated with CD1A and CD1E gene polymorphisms.

J Neuroimmunol 2008 Dec 5;205(1-2):110-2. Epub 2008 Oct 5.

Department of Neurology, Erasmus MC, 's-Gravendijkwal 230, 3015CE, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.jneuroim.2008.08.013DOI Listing
December 2008

Subclass IgG to motor gangliosides related to infection and clinical course in Guillain-Barré syndrome.

J Neuroimmunol 2008 Feb 21;194(1-2):181-90. Epub 2008 Feb 21.

Department of Neurology, Erasmus MC, P.O. BOX 2040, 3000 CA Rotterdam, The Netherlands.

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http://linkinghub.elsevier.com/retrieve/pii/S016557280700435
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http://dx.doi.org/10.1016/j.jneuroim.2007.11.017DOI Listing
February 2008

Genetic polymorphisms of macrophage-mediators in Guillain-Barré syndrome.

J Neuroimmunol 2007 Oct 30;190(1-2):127-30. Epub 2007 Aug 30.

Department of Neurology, Erasmus MC, 's-Gravendijkwal 230, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.jneuroim.2007.07.008DOI Listing
October 2007

Mannose-binding lectin contributes to the severity of Guillain-Barré syndrome.

J Immunol 2006 Sep;177(6):4211-7

Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.

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http://dx.doi.org/10.4049/jimmunol.177.6.4211DOI Listing
September 2006

Diagnostic value of anti-GM1 ganglioside serology and validation of the INCAT-ELISA.

J Neurol Sci 2005 Dec 8;239(1):37-44. Epub 2005 Sep 8.

Department of Neurology, Erasmus Medical Center, Dr. Molewaterplein 50, 3015 GE, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.jns.2005.07.009DOI Listing
December 2005

Functional polymorphisms in LPS receptors CD14 and TLR4 are not associated with disease susceptibility or Campylobacter jejuni infection in Guillain-Barré patients.

J Neuroimmunol 2004 May;150(1-2):132-8

Department of Immunology, Erasmus Medical Centre, Dr. Molewaterplein 50, 3015 GE Rotterdam, The Netherlands.

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http://dx.doi.org/10.1016/j.jneuroim.2004.01.003DOI Listing
May 2004

Anti-GM1 IgG antibodies induce leukocyte effector functions via Fcgamma receptors.

Ann Neurol 2003 May;53(5):570-9

Department of Neurology and Immunology, University Medical Centre Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1002/ana.10503DOI Listing
May 2003

Screening for anti-ganglioside antibodies in hypocretin-deficient human narcolepsy.

Neurosci Lett 2003 Apr;341(1):13-6

Department of Neurology, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, The Netherlands.

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http://dx.doi.org/10.1016/s0304-3940(03)00085-5DOI Listing
April 2003