Publications by authors named "Maartje Boon"

17Publications

Thoracoscopic sympathicotomy for the treatment of intolerable palmar and axillary hyperhidrosis in children is associated with high recurrence rates.

Authors:
Arjan J F P Verhaegh Michiel Kuijpers Maartje Boon Mike J L DeJongste Wobbe Bouma Massimo A Mariani Theo J Klinkenberg

Pediatr Dermatol 2020 Sep 16;37(5):987-992. Epub 2020 Jul 16.

Department of Cardiothoracic Surgery, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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September 2020

Coreflooding data on nine sandstone cores to measure CO residual trapping.

Authors:
Hailun Ni Maartje Boon Charlotte Garing Sally M Benson

Data Brief 2019 Aug 12;25:104249. Epub 2019 Jul 12.

Department of Energy Resources Engineering, Stanford University, Stanford, CA, USA.

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August 2019

Neurofibromatosis type 1 associated low grade gliomas: A comparison with sporadic low grade gliomas.

Authors:
Jelte Helfferich Ronald Nijmeijer Oebele F Brouwer Maartje Boon Annemarie Fock Eelco W Hoving Lisethe Meijer Wilfred F A den Dunnen Eveline S J M de Bont

Crit Rev Oncol Hematol 2016 Aug 21;104:30-41. Epub 2016 May 21.

Department of Paediatrics, Beatrix Children's Hospital, Paediatric Oncology/Hematology Division, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands. Electronic address:

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August 2016

Erratum to: Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach.

Authors:
Ragna S Boerma Kees P Braun Marcel P H van den Broek Frederique M C van Berkestijn Marielle E Swinkels Eveline O Hagebeuk Dick Lindhout Marjan van Kempen Maartje Boon Joost Nicolai Carolien G de Kovel Eva H Brilstra Bobby P C Koeleman

Neurotherapeutics 2016 Jan;13(1):238

Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

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January 2016

Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach.

Authors:
Ragna S Boerma Kees P Braun Marcel P H van den Broek Maarten P H van de Broek Frederique M C van Berkestijn Marielle E Swinkels Eveline O Hagebeuk Dick Lindhout Marjan van Kempen Maartje Boon Joost Nicolai Carolien G de Kovel Eva H Brilstra Bobby P C Koeleman

Neurotherapeutics 2016 Jan;13(1):192-7

Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

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January 2016

Application of the 2012 revised diagnostic definitions for paediatric multiple sclerosis and immune-mediated central nervous system demyelination disorders.

Authors:
E Daniëlle van Pelt Rinze F Neuteboom Immy A Ketelslegers Maartje Boon Coriene E Catsman-Berrevoets Rogier Q Hintzen

J Neurol Neurosurg Psychiatry 2014 Jul 5;85(7):790-4. Epub 2013 Dec 5.

Department of Neurology, Erasmus MC, Rotterdam, The Netherlands.

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July 2014

PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions.

Authors:
Rianne van Vliet Guido Breedveld Johanneke de Rijk-van Andel Eva Brilstra Nienke Verbeek Corien Verschuuren-Bemelmans Maartje Boon Johnny Samijn Karin Diderich Ingrid van de Laar Ben Oostra Vincenzo Bonifati Anneke Maat-Kievit

Neurology 2012 Aug 8;79(8):777-84. Epub 2012 Aug 8.

Department of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands.

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August 2012

Neurologic symptoms and diarrhea in a 15-year-old boy.

Authors:
Maaike Sietses Esther A N M Mooi-Kokenberg Maartje Boon Tina E Faber

Pediatr Infect Dis J 2012 Jun;31(6):659

Department of Pediatrics and Pediatric infectious Diseases, Medical Center Leeuwarden, Leeu-warden, The Netherlands.

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June 2012

The management of multiple sclerosis in children: a European view.

Authors:
Angelo Ghezzi Brenda Banwell Alexey Boyko Maria Pia Amato Banu Anlar Morten Blinkenberg Maartje Boon Massimo Filippi Sergiusz Jozwiak Immy Ketelslegers Barbara Kornek Ming Lim Eva Lindstrom Congor Nadj Rinze Neuteboom Maria A Rocca Kevin Rostasy Marc Tardieu Evangeline Wassmer Coriene Catsman-Berrevoets Rogier Hintzen

Mult Scler 2010 Oct 4;16(10):1258-67. Epub 2010 Aug 4.

Centro Studi SM, H S. Antonio Abate, Gallarate, VA, Italy.

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October 2010

Is hearing loss a feature of Joubert syndrome, a ciliopathy?

Authors:
Hester Y Kroes Bert G A Van Zanten Sander A De Ru Maartje Boon Grazia M S Mancini Marjo S Van der Knaap Bwee Tien Poll-The Dick Lindhout

Int J Pediatr Otorhinolaryngol 2010 Sep 29;74(9):1034-8. Epub 2010 Jun 29.

Dept. of Medical Genetics, University Medical Center Utrecht, The Netherlands.

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September 2010

Barkhof magnetic resonance imaging criteria predict early relapse in pediatric multiple sclerosis.

Authors:
Rinze F Neuteboom Immy A Ketelslegers Maartje Boon Coriene E Catsman-Berrevoets Rogier Q Hintzen

Pediatr Neurol 2010 Jan;42(1):53-5

Department of Neurology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.

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January 2010

Fatigue and depression in children with multiple sclerosis and monophasic variants.

Authors:
Immy A Ketelslegers Coriene E Catsman-Berrevoets Maartje Boon M Judith Eikelenboom Hans Stroink Rinze F Neuteboom Femke K Aarsen Elise M van de Putte Rogier Q Hintzen

Eur J Paediatr Neurol 2010 Jul 12;14(4):320-5. Epub 2009 Oct 12.

Department of Neurology, Erasmus MC, Rotterdam, the Netherlands.

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July 2010

A 649 kb microduplication in 1p34.1, including POMGNT1, in a patient with microcephaly, coloboma and laryngomalacia; and a review of the literature.

Authors:
Nicolien Hanemaaijer Trijnie Dijkhuizen Maaike Haadsma Margot Boeve Maartje Boon Roel Hordijk Klaas Kok Birgit Sikkema-Raddatz Conny M A van Ravenswaaij-Arts

Eur J Med Genet 2009 Mar-Jun;52(2-3):116-9

Department of Genetics, CB50, University Medical Centre Groningen, University of Groningen, PO Box 30.001, 9700 RB Groningen, The Netherlands.

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September 2009

Isolated elevated serum transaminases leading to the diagnosis of asymptomatic Pompe disease.

Authors:
Marieke Hoeksma Maartje Boon Klary E Niezen-Koning Lidy van Overbeek-van Gils Francjan J van Spronsen

Eur J Pediatr 2007 Aug 17;166(8):871-4. Epub 2006 Oct 17.

Section of Metabolic Diseases, Department of Paediatrics, Beatrix Children's Hospital, University Medical Centre Groningen, 9700 RB, Groningen, The Netherlands.

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August 2007

Plantar lipomatosis, unusual facies, and developmental delay: confirmation of Pierpont syndrome.

Authors:
Grétel G Oudesluijs Roel Hordijk Maartje Boon Paul E Sijens Raoul C M Hennekam

Am J Med Genet A 2005 Aug;137(1):77-80

Department of Clinical Genetics, University Medical Center Groningen, The Netherlands.

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August 2005

1H chemical shift imaging, MRI, and diffusion-weighted imaging in vanishing white matter disease.

Authors:
Paul E Sijens Maartje Boon Linda C Meiners Oebele F Brouwer Matthijs Oudkerk

Eur Radiol 2005 Nov 27;15(11):2377-9. Epub 2005 Apr 27.

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November 2005

Inheritance mode of multiple sclerosis: the effect of HLA class II alleles is stronger than additive.

Authors:
Maartje Boon Ilja M Nolte Jacques De Keyser Charles H C M Buys Gerard J te Meerman

Hum Genet 2004 Sep;115(4):280-4

Department of Neurology, University Hospital Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands.

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September 2004