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European Journal of Human Genetics : EJHG|October 22, 1998
Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24A J van der Vleuten, C M van Ravenswaaij-Arts, C J Frijns, et al.
Brain Injury|May 9, 2017
Outpatient follow-up after mild traumatic brain injury: Results of the UPFRONT-studyM E de Koning, M E Scheenen, H J van der Horn, et al.
Clinical Neurology and Neurosurgery|September 11, 2007
Cardiac responses of vagus nerve stimulation: intraoperative bradycardia and subsequent chronic stimulationJ J Ardesch, H P J Buschman, P H van der Burgh, et al.
SN Comprehensive Clinical Medicine|June 28, 2021
SARS-CoV-2-Induced Multisystem Inflammatory Syndrome in a Young Adult: Case ReportHaldun Bulut, Alexandra H E Herbers, Ilse M G Hageman, et al.
Clinical Genetics|April 29, 2005
Refinement of the chromosome 16 locus for benign familial infantile convulsionsP M C Callenbach, E H van den Boogerd, R F M de Coo, et al.
Human Molecular Genetics|January 12, 2001
Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humorN Jacobson, M Andrews, A R Shepard, et al.
Diabetes, Obesity & Metabolism|January 10, 2018
Dapagliflozin for prednisone-induced hyperglycaemia in acute exacerbation of chronic obstructive pulmonary diseaseMaaike C Gerards, Gerdien E Venema, Kornelis W Patberg, et al.
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