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H Stroink

Showing results (31-40 of 47) with videos related to

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Epilepsia|May 1, 1997
The diagnostic yield of a second EEG after partial sleep deprivation: a prospective study in children with newly diagnosed seizuresJ A Carpay, A W de Weerd, R J Schimsheimer, et al.
Neurology|June 30, 2005
Four-year outcome after early withdrawal of antiepileptic drugs in childhood epilepsyA T Geerts, J M F Niermeijer, A C B Peters, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 27, 2004
Interrater agreement of the diagnosis and classification of a first seizure in childhood. The Dutch Study of Epilepsy in ChildhoodH Stroink, C A van Donselaar, A T Geerts, et al.
Epilepsia|February 1, 1997
Evolution of epilepsy and EEG findings in Angelman syndromeL A Laan, W O Renier, W F Arts, et al.
Pediatrics|October 2, 1997
Endocrinologic disorders and optic pathway gliomas in children with neurofibromatosis type 1M H Cnossen, E N Stam, L C Cooiman, et al.
Human Mutation|April 24, 1999
Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. OnlineQ Wang, S Verhoef, A M Tempelaars, et al.
AJNR. American Journal of Neuroradiology|March 10, 2001
Alexander disease: diagnosis with MR imagingM S van der Knaap, S Naidu, S N Breiter, et al.
Archives of Disease in Childhood|July 11, 1998
A prospective 10 year follow up study of patients with neurofibromatosis type 1M H Cnossen, A de Goede-Bolder, K M van den Broek, et al.
Clinical and Experimental Immunology|March 26, 2003
Immunoglobulins in children with epilepsy: the Dutch Study of Epilepsy in ChildhoodP M C Callenbach, C M Jol-Van Der Zijde, A T Geerts, et al.
Prenatal Diagnosis|March 10, 2001
First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysisW J Kleijer, O P van Diggelen, J L Keulemans, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Epilepsia|May 1, 1997
The diagnostic yield of a second EEG after partial sleep deprivation: a prospective study in children with newly diagnosed seizuresJ A Carpay, A W de Weerd, R J Schimsheimer, et al.
Neurology|June 30, 2005
Four-year outcome after early withdrawal of antiepileptic drugs in childhood epilepsyA T Geerts, J M F Niermeijer, A C B Peters, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 27, 2004
Interrater agreement of the diagnosis and classification of a first seizure in childhood. The Dutch Study of Epilepsy in ChildhoodH Stroink, C A van Donselaar, A T Geerts, et al.
Epilepsia|February 1, 1997
Evolution of epilepsy and EEG findings in Angelman syndromeL A Laan, W O Renier, W F Arts, et al.
Pediatrics|October 2, 1997
Endocrinologic disorders and optic pathway gliomas in children with neurofibromatosis type 1M H Cnossen, E N Stam, L C Cooiman, et al.
Human Mutation|April 24, 1999
Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. OnlineQ Wang, S Verhoef, A M Tempelaars, et al.
AJNR. American Journal of Neuroradiology|March 10, 2001
Alexander disease: diagnosis with MR imagingM S van der Knaap, S Naidu, S N Breiter, et al.
Archives of Disease in Childhood|July 11, 1998
A prospective 10 year follow up study of patients with neurofibromatosis type 1M H Cnossen, A de Goede-Bolder, K M van den Broek, et al.
Clinical and Experimental Immunology|March 26, 2003
Immunoglobulins in children with epilepsy: the Dutch Study of Epilepsy in ChildhoodP M C Callenbach, C M Jol-Van Der Zijde, A T Geerts, et al.
Prenatal Diagnosis|March 10, 2001
First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysisW J Kleijer, O P van Diggelen, J L Keulemans, et al.
Pageof 5