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Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations.
Neurology. 2010 Sep 28;75(13):1159-65. doi: 10.1212/WNL.0b013e3181f4d7bf.
Neurology. 2010.
PMID: 20876469
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1.
Suls A, Mullen SA, Weber YG, Verhaert K, Ceulemans B, Guerrini R, Wuttke TV, Salvo-Vargas A, Deprez L, Claes LR, Jordanova A, Berkovic SF, Lerche H, De Jonghe P, Scheffer IE.
Suls A, et al. Among authors: verhaert k.
Ann Neurol. 2009 Sep;66(3):415-9. doi: 10.1002/ana.21724.
Ann Neurol. 2009.
PMID: 19798636
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Critical evaluation of four different seizure detection systems tested on one patient with focal and generalized tonic and clonic seizures.
Van de Vel A, Verhaert K, Ceulemans B.
Van de Vel A, et al. Among authors: verhaert k.
Epilepsy Behav. 2014 Aug;37:91-4. doi: 10.1016/j.yebeh.2014.06.014. Epub 2014 Jul 7.
Epilepsy Behav. 2014.
PMID: 25010322
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Cognitive outcomes following epilepsy in infancy: A longitudinal community-based study.
O'Reilly H, Eltze C, Bennett K, Verhaert K, Webb R, Merrett A, Scott RC, Whitney A, Helen Cross J, de Haan M.
O'Reilly H, et al. Among authors: verhaert k.
Epilepsia. 2018 Dec;59(12):2240-2248. doi: 10.1111/epi.14589. Epub 2018 Nov 5.
Epilepsia. 2018.
PMID: 30395354
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Gorlin-Goltz syndrome in a child: case report and clinical review.
Snoeckx A, Vanhoenacker FM, Verhaert K, Chappelle K, Parizel PM.
Snoeckx A, et al. Among authors: verhaert k.
JBR-BTR. 2008 Nov-Dec;91(6):235-9.
JBR-BTR. 2008.
PMID: 19202996
Review.
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Polyarthritis and humeral epiphysial separation in an infant with acute disseminated histoplasmosis.
Verhaert K, Rodriguez M, Mendoza G, Delgadillo JL, Casaer P.
Verhaert K, et al.
Pediatr Infect Dis J. 2002 Apr;21(4):352-3. doi: 10.1097/00006454-200204000-00020.
Pediatr Infect Dis J. 2002.
PMID: 12075772
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