C Harden
Overview
Explore the profile of C Harden including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
218
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Recent Articles
1.
Kumar-Pelayo M, Oller-Cramsie M, Mihu N, Harden C
Epilepsy Behav
. 2013 Jul;
28(3):501-3.
PMID: 23892581
Our video-EEG monitoring (VEEG) unit is part of a typical metropolitan tertiary care center that services a diverse patient population. We aimed to determine if the specific clinical reason for...
2.
Pugh M, Berlowitz D, Montouris G, Bokhour B, Cramer J, Bohm V, et al.
Neurology
. 2007 Oct;
69(21):2020-7.
PMID: 17928576
Background: Providers are increasingly being held accountable for the quality of care provided. While quality indicators have been used to benchmark the quality of care for a number of other...
3.
Labar D, Dilone L, Solomon G, Harden C
Seizure
. 2002 Jan;
10(8):570-2.
PMID: 11792158
The aim of this study was to determine if there is cerebral cortical hemispheral asymmetry in human epileptogenesis. We studied 75 epilepsy patients using electroencephalograms, neuroimaging, ictal semiology and physical...
4.
Harden C
Epilepsia
. 2001 Sep;
42 Suppl 4:36-9.
PMID: 11564124
Levetiracetam was approved in November 1999 as add-on therapy for the treatment of partial-onset seizures in adults (age 16 years and older). This review focuses on recently published data from...
5.
Durner M, Keddache M, Tomasini L, Shinnar S, Resor S, Cohen J, et al.
Ann Neurol
. 2001 Mar;
49(3):328-35.
PMID: 11261507
Idiopathic generalized epilepsy (IGE) is a common, complex disease with an almost exclusively genetic etiology but with variable phenotypes. Clinically, IGE can be divided into different syndromes. Varying lines of...
6.
Hosain S, Nikalov B, Harden C, Li M, Fraser R, Labar D
J Child Neurol
. 2000 Aug;
15(8):509-12.
PMID: 10961788
Lennox-Gastaut syndrome is a severe age-specific epilepsy syndrome that presents with medication-resistant seizures in childhood. Antiepileptic drugs are the mainstay of treatment. Nonpharmacologic treatments include corpus callosum section and the...
7.
Greenberg D, Durner M, Keddache M, Shinnar S, Resor S, Moshe S, et al.
Am J Hum Genet
. 2000 Mar;
66(2):508-16.
PMID: 10677311
Evidence for genetic influences in epilepsy is strong, but reports identifying specific chromosomal origins of those influences conflict. One early study reported that human leukocyte antigen (HLA) markers were genetically...
8.
Durner M, Shinnar S, Resor S, Moshe S, Rosenbaum D, Cohen J, et al.
Am J Med Genet
. 2000 Feb;
96(1):49-52.
PMID: 10686551
Juvenile myoclonic epilepsy (JME) is a distinct epileptic syndrome with a complex mode of inheritance. Several studies found evidence for a locus involved in JME on chromosome 6 near the...
9.
Faught E, Morris G, Jacobson M, French J, Harden C, Montouris G, et al.
Epilepsia
. 1999 Aug;
40(8):1135-40.
PMID: 10448828
Purpose: Valproate (VPA) triples the half-life of lamotrigine (LTG), and combined use may be difficult. The adverse effect (AE) profile of this combination needs clarification. Methods: We prospectively recorded our...
10.
Durner M, Zhou G, Fu D, Abreu P, Shinnar S, Resor S, et al.
Am J Hum Genet
. 1999 Apr;
64(5):1411-9.
PMID: 10205274
Several loci and candidate genes for epilepsies or epileptic syndromes map or have been suggested to map to chromosome 8. We investigated families with adolescent-onset idiopathic generalized epilepsy (IGE), for...