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The Netherlands Journal of Medicine|December 15, 2007
Changing aspects of HFE-related hereditary haemochromatosis and endeavours to early diagnosisE M G Jacobs, A L M Verbeek, H G Kreeftenberg, et al.
Gastrointestinal Endoscopy|April 13, 2010
The staging of gastritis with the OLGA system by using intestinal metaplasia as an accurate alternative for atrophic gastritisLisette G Capelle, Annemarie C de Vries, Jelle Haringsma, et al.
Clinical Epigenetics|November 11, 2025
A frameshift variant in activity-dependent neuroprotective protein (ADNP) causes nucleocytoskeletal alterations in a dizygotic male twin: a case studyClaudio Peter D'Incal, Anke Van Dijck, Dale John Annear, et al.
Helicobacter|November 6, 2009
Serum levels of leptin as marker for patients at high risk of gastric cancerLisette G Capelle, Annemarie C de Vries, Jelle Haringsma, et al.
Disability and Rehabilitation|January 29, 2025
Associations of environmental and personal factors, participation and health-related quality of life with physical activity and sedentary behavior in people with subarachnoid hemorrhage: a cross-sectional accelerometer-based studyElisabeth A de Vries, Majanka H Heijenbrok-Kal, Fop van Kooten, et al.
Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
Cardiovascular and Interventional Radiology|December 25, 2014
Percutaneous Irreversible Electroporation of a Large Centrally Located Hepatocellular Adenoma in a Woman with a Pregnancy WishHester J Scheffer, Marleen C A M Melenhorst, Aukje A J M van Tilborg, et al.
The Netherlands Journal of Medicine|May 24, 2007
Heterozygous alpha-I antitrypsin deficiency as a co-factor in the development of chronic liver disease: a reviewK F Kok, P J Wahab, R H J Houwen, et al.
Developmental Medicine and Child Neurology|May 11, 2007
A novel microdeletion in 1(p34.2p34.3), involving the SLC2A1 (GLUT1) gene, and severe delayed developmentSascha Vermeer, David A Koolen, Gepke Visser, et al.
European Journal of Medical Genetics|July 16, 2013
An update on ECARUCA, the European Cytogeneticists Association Register of Unbalanced Chromosome AberrationsAnneke T Vulto-van Silfhout, Conny M A van Ravenswaaij, Jayne Y Hehir-Kwa, et al.
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