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Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|December 18, 2007
Absence of nodular regenerative hyperplasia after low-dose 6-thioguanine maintenance therapy in inflammatory bowel disease patientsN K H de Boer, P E Zondervan, L P L Gilissen, et al.
Human Molecular Genetics|April 18, 2003
The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndromeRob Willemsen, Marianne Hoogeveen-Westerveld, Surya Reis, et al.
Plos One|October 26, 2023
Correction: Global TALES feasibility study: Personal narratives in 10-year-old children around the worldMarleen F Westerveld, Rena Lyons, Nickola Wolf Nelson, et al.
JAMA|October 18, 2000
Regional brain volume abnormalities and long-term cognitive outcome in preterm infantsB S Peterson, B Vohr, L H Staib, et al.
International Journal of Radiation Oncology, Biology, Physics|October 3, 2022
GEC-ESTRO (ACROP)-ABS-CBG Consensus Brachytherapy Target Definition Guidelines for Recurrent Endometrial and Cervical Tumors in the VaginaMitchell Kamrava, Eric Leung, Francois Bachand, et al.
European Journal of Human Genetics : EJHG|July 14, 2016
Genotype and brain pathology phenotype in children with tuberous sclerosis complexIris E Overwater, Rob Swenker, Emma L van der Ende, et al.
Stroke|August 28, 2004
Genome-wide linkage in a large Dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13Y B W E M Roos, G Pals, P M Struycken, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|January 22, 2022
Dose-effect relationship between vaginal dose points and vaginal stenosis in cervical cancer: An EMBRACE-I sub-studyHenrike Westerveld, Kathrin Kirchheiner, Remi A Nout, et al.
Experimental Cell Research|May 1, 2019
Modelling the neuropathology of lysosomal storage disorders through disease-specific human induced pluripotent stem cellsJulianna Kobolák, Kinga Molnár, Eszter Varga, et al.
Clinical Genetics|February 22, 2011
Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co-segregates with tuberous sclerosis complex in mildly affected kindredsM Wentink, M Nellist, M Hoogeveen-Westerveld, et al.
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