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Neurobiology of Disease|January 12, 2011
Innate and adaptive immunity in amyotrophic lateral sclerosis: evidence of complement activationM Sta, R M R Sylva-Steenland, M Casula, et al.
Neuropathology and Applied Neurobiology|May 12, 2005
Distribution, characterization and clinical significance of microglia in glioneuronal tumours from patients with chronic intractable epilepsyE Aronica, J A Gorter, S Redeker, et al.
AIDS (London, England)|April 13, 1999
Nitric oxide synthase expression and apoptotic cell death in brains of AIDS and AIDS dementia patientsV A Vincent, C J De Groot, P J Lucassen, et al.
International Journal of Cardiology|December 3, 2014
Uncertain diagnosis of Fabry disease: consensus recommendation on diagnosis in adults with left ventricular hypertrophy and genetic variants of unknown significanceB E Smid, L van der Tol, F Cecchi, et al.
Neuropathology and Applied Neurobiology|August 13, 2004
Immunohistochemical localization of vascular endothelial growth factor receptors-1, -2 and -3 in human spinal cord: altered expression in amyotrophic lateral sclerosisW G M Spliet, E Aronica, M Ramkema, et al.
Epilepsy Research|March 15, 2001
Glioneuronal tumors and medically intractable epilepsy: a clinical study with long-term follow-up of seizure outcome after surgeryE Aronica, S Leenstra, C W van Veelen, et al.
Pigment Cell Research|June 1, 1996
Foetal human melanocytes: in situ detection, in vitro culture and differentiation characteristics at 6-11 weeks EGAI C Le Poole, R M Van den Wijngaard, R P Verkruisen, et al.
Journal of Neuro-Oncology|November 23, 2001
High concentration of Daunorubicin and Daunorubicinol in human malignant astrocytomas after systemic administration of liposomal DaunorubicinK W Albrecht, P C de Witt Hamer, S Leenstra, et al.
Oncogene|October 16, 2007
The genomic profile of human malignant glioma is altered early in primary cell culture and preserved in spheroidsP C De Witt Hamer, A A G Van Tilborg, P P Eijk, et al.
Acta Neuropathologica|February 17, 2005
Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathologyE Aronica, A A M W van Kempen, M van der Heide, et al.
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