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Pharmacology, Biochemistry, and Behavior|November 6, 2016
Nano-particle delivery of brain derived neurotrophic factor after focal cerebral ischemia reduces tissue injury and enhances behavioral recoveryNia M Harris, Rodney Ritzel, Nickolas S Mancini, et al.Journal of Thrombosis and Haemostasis : JTH|February 10, 2017
Clumping factor A, von Willebrand factor-binding protein and von Willebrand factor anchor Staphylococcus aureus to the vessel wallJ Claes, L Liesenborghs, M Peetermans, et al.American Journal of Medical Genetics. Part A|March 27, 2020
Human RAD50 deficiency: Confirmation of a distinctive phenotypeAviël Ragamin, Gökhan Yigit, Kristine Bousset, et al.Neurogenetics|December 11, 2012
Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutationsCathryn Poulton, Renske Oegema, Daphne Heijsman, et al.Journal of Medical Genetics|August 19, 2005
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephalyG Breedveld, I F de Coo, M H Lequin, et al.American Journal of Medical Genetics. Part A|April 2, 2010
Periventricular nodular heterotopia and distal limb deficiency: a recurrent associationMarie Claire Y de Wit, Irenaeus F M de Coo, Rachel Schot, et al.Journal of Hepatology|May 1, 1996
Epidemiological, clinical and therapeutic associations of hepatitis C types in western European patientsP Simmonds, J Mellor, A Craxi, et al.International Journal of Pediatric Otorhinolaryngology|July 2, 2010
Is hearing loss a feature of Joubert syndrome, a ciliopathy?Hester Y Kroes, Bert G A Van Zanten, Sander A De Ru, et al.Seizure|July 20, 2010
Absence epilepsy and periventricular nodular heterotopiaM C Y de Wit, H M Schippers, I F M de Coo, et al.Neurology. Genetics|April 30, 2021
Biallelic DAB1 Variants Are Associated With Mild Lissencephaly and Cerebellar HypoplasiaDaphne J Smits, Rachel Schot, Martina Wilke, et al.Pageof 44