PubRank

Samuel F Berkovic

Author PubWeight™ 265.10‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009. Epilepsia 2010 18.28
2 De novo mutations in epileptic encephalopathies. Nature 2013 7.42
3 KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy. Ann Neurol 2012 4.12
4 Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. Nat Genet 2013 3.64
5 Prediction of seizure likelihood with a long-term, implanted seizure advisory system in patients with drug-resistant epilepsy: a first-in-man study. Lancet Neurol 2013 3.22
6 Somatic mutations in cerebral cortical malformations. N Engl J Med 2014 3.13
7 Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy. Nat Genet 2012 2.98
8 Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study. Lancet Neurol 2007 2.88
9 A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome. Am J Hum Genet 2008 2.58
10 Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6. Am J Hum Genet 2011 2.49
11 Sodium-channel defects in benign familial neonatal-infantile seizures. Lancet 2002 2.43
12 Navigating the channels and beyond: unravelling the genetics of the epilepsies. Lancet Neurol 2008 2.39
13 SCN1A mutations and epilepsy. Hum Mutat 2005 2.34
14 SRPX2 mutations in disorders of language cortex and cognition. Hum Mol Genet 2006 2.34
15 Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus. Am J Hum Genet 2001 2.32
16 GABRA1 and STXBP1: novel genetic causes of Dravet syndrome. Neurology 2014 2.30
17 The spectrum of SCN1A-related infantile epileptic encephalopathies. Brain 2007 2.30
18 Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study. Lancet Neurol 2010 2.23
19 Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. Hum Mol Genet 2009 2.12
20 Mutations in DEPDC5 cause familial focal epilepsy with variable foci. Nat Genet 2013 2.10
21 Temporal lobectomy: long-term seizure outcome, late recurrence and risks for seizure recurrence. Brain 2004 2.08
22 Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage. Am J Hum Genet 2012 2.07
23 Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants. Ann Neurol 2007 2.00
24 Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Brain 2013 1.95
25 X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. Nat Genet 2008 1.95
26 Epilepsy and mental retardation limited to females: an under-recognized disorder. Brain 2008 1.94
27 Paroxysmal motor disorders of sleep: the clinical spectrum and differentiation from epilepsy. Epilepsia 2006 1.94
28 Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1. Ann Neurol 2009 1.94
29 PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome. Am J Hum Genet 2012 1.91
30 Rare copy number variants are an important cause of epileptic encephalopathies. Ann Neurol 2011 1.88
31 GRIN2A mutations cause epilepsy-aphasia spectrum disorders. Nat Genet 2013 1.85
32 Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy. Proc Natl Acad Sci U S A 2007 1.82
33 Seizure-associated hippocampal volume loss: a longitudinal magnetic resonance study of temporal lobe epilepsy. Ann Neurol 2002 1.82
34 Tramadol and new-onset seizures. Med J Aust 2005 1.77
35 Mechanisms of human inherited epilepsies. Prog Neurobiol 2008 1.75
36 Distinguishing sleep disorders from seizures: diagnosing bumps in the night. Arch Neurol 2006 1.73
37 Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations. Brain 2006 1.72
38 Copy number variants are frequent in genetic generalized epilepsy with intellectual disability. Neurology 2013 1.72
39 Is benign rolandic epilepsy genetically determined? Ann Neurol 2004 1.68
40 Sodium channels and the neurobiology of epilepsy. Epilepsia 2012 1.66
41 GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies. Hum Mol Genet 2004 1.65
42 Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations. Ann Neurol 2014 1.62
43 Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients. Brain 2010 1.61
44 Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorder. Brain 2004 1.54
45 Genetic association studies in epilepsy: "the truth is out there". Epilepsia 2004 1.51
46 Channelopathies in idiopathic epilepsy. Neurotherapeutics 2007 1.49
47 A focal epilepsy and intellectual disability syndrome is due to a mutation in TBC1D24. Am J Hum Genet 2010 1.48
48 Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis. Neurology 2012 1.48
49 Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Hum Mol Genet 2012 1.48
50 Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline. Dev Med Child Neurol 2013 1.44
51 Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1. Brain 2008 1.41
52 Epilepsy in offspring of whom both parents have idiopathic generalized epilepsy: biparental inheritance. Epilepsia 2003 1.40
53 SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum. Epilepsia 2007 1.40
54 Changes in cortical excitability differentiate generalized and focal epilepsy. Ann Neurol 2007 1.35
55 PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures. Neurology 2012 1.35
56 Channelopathies as a genetic cause of epilepsy. Curr Opin Neurol 2003 1.32
57 Timing of de novo mutagenesis--a twin study of sodium-channel mutations. N Engl J Med 2010 1.28
58 Brivaracetam as adjunctive treatment for uncontrolled partial epilepsy in adults: a phase III randomized, double-blind, placebo-controlled trial. Epilepsia 2013 1.25
59 Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis. Hum Mol Genet 2013 1.23
60 SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis. Epilepsia 2009 1.23
61 Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus. J Clin Invest 2010 1.21
62 Recent advances in the molecular genetics of epilepsy. J Med Genet 2013 1.21
63 Hippocampal pathology in refractory temporal lobe epilepsy: T2-weighted signal change reflects dentate gliosis. Neurology 2002 1.20
64 MR imaging and spectroscopic study of epileptogenic hypothalamic hamartomas: analysis of 72 cases. AJNR Am J Neuroradiol 2004 1.18
65 The genetics of human epilepsy. Trends Pharmacol Sci 2003 1.17
66 Susceptibility genes for complex epilepsy. Hum Mol Genet 2005 1.17
67 KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidine. Ann Neurol 2014 1.15
68 Altered kinetics and benzodiazepine sensitivity of a GABAA receptor subunit mutation [gamma 2(R43Q)] found in human epilepsy. Proc Natl Acad Sci U S A 2002 1.14
69 Genetic variation of CACNA1H in idiopathic generalized epilepsy. Ann Neurol 2004 1.14
70 Occipital epilepsies: identification of specific and newly recognized syndromes. Brain 2003 1.13
71 Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy. Arch Neurol 2011 1.11
72 A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia. Am J Hum Genet 2011 1.11
73 SCN1A testing for epilepsy: application in clinical practice. Epilepsia 2013 1.10
74 Does variation in NIPA2 contribute to genetic generalized epilepsy? Hum Genet 2014 1.10
75 Axon initial segment dysfunction in epilepsy. J Physiol 2010 1.10
76 Assessment of the role of FDG PET in the diagnosis and management of children with refractory epilepsy. Eur J Nucl Med Mol Imaging 2005 1.08
77 Progressive gait deterioration in adolescents with Dravet syndrome. Arch Neurol 2012 1.08
78 Exploration of the genetic architecture of idiopathic generalized epilepsies. Epilepsia 2006 1.07
79 Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore. Mol Pharmacol 2008 1.07
80 Mutations in TNK2 in severe autosomal recessive infantile onset epilepsy. Ann Neurol 2013 1.07
81 GENETICS. The Human Variome Project. Science 2008 1.07
82 Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation. Brain 2003 1.07
83 Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability. Epilepsia 2008 1.05
84 NREM arousal parasomnias and their distinction from nocturnal frontal lobe epilepsy: a video EEG analysis. Sleep 2009 1.05
85 Glucose transporter 1 deficiency in the idiopathic generalized epilepsies. Ann Neurol 2012 1.02
86 Multidrug-resistant genotype (ABCB1) and seizure recurrence in newly treated epilepsy: data from international pharmacogenetic cohorts. Epilepsia 2009 1.02
87 Predicting seizure control: cortical excitability and antiepileptic medication. Ann Neurol 2010 1.02
88 Efficacy and safety of levetiracetam 1000-3000 mg/day in patients with refractory partial-onset seizures: a multicenter, open-label single-arm study. Epilepsy Res 2005 1.02
89 Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients. J Med Genet 2010 1.01
90 A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel. Mol Cell Neurosci 2007 1.01
91 Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene. Brain 2013 1.00
92 Benign mesial temporal lobe epilepsy. Nat Rev Neurol 2011 1.00
93 Clinical genetic study of the epilepsy-aphasia spectrum. Epilepsia 2013 0.99
94 Intracortical hyperexcitability in humans with a GABAA receptor mutation. Cereb Cortex 2007 0.98
95 Augmented currents of an HCN2 variant in patients with febrile seizure syndromes. Ann Neurol 2010 0.98
96 Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families. Epilepsia 2004 0.98
97 A GABAA receptor mutation causing generalized epilepsy reduces benzodiazepine receptor binding. Neuroimage 2006 0.98
98 A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy. Epilepsia 2007 0.98
99 Developmental impact of a familial GABAA receptor epilepsy mutation. Ann Neurol 2008 0.97
100 Chromosomal abnormalities and epilepsy: a review for clinicians and gene hunters. Epilepsia 2002 0.97
101 Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance. Brain 2010 0.96
102 Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families. J Med Genet 2009 0.96
103 Vaccination, seizures and 'vaccine damage'. Curr Opin Neurol 2007 0.96
104 The Epilepsy Genetic Association Database (epiGAD): analysis of 165 genetic association studies, 1996-2008. Epilepsia 2010 0.96
105 Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum. Epilepsia 2012 0.96
106 Multiple molecular mechanisms for a single GABAA mutation in epilepsy. Neurology 2013 0.95
107 EEG in adult-onset idiopathic generalized epilepsy. Epilepsia 2003 0.95
108 Update on pharmacogenetics in epilepsy: a brief review. Lancet Neurol 2006 0.94
109 Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. Epilepsia 2012 0.94
110 Neonatal seizures and long QT syndrome: a cardiocerebral channelopathy? Epilepsia 2009 0.94
111 New hyperekplexia mutations provide insight into glycine receptor assembly, trafficking, and activation mechanisms. J Biol Chem 2013 0.93
112 Is focal cortical dysplasia sporadic? Family evidence for genetic susceptibility. Epilepsia 2014 0.93
113 Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaboration. Epilepsia 2006 0.93
114 Prediction by modeling that epilepsy may be caused by very small functional changes in ion channels. Arch Neurol 2009 0.93
115 Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome. Epilepsia 2013 0.92
116 Low blood glucose precipitates spike-and-wave activity in genetically predisposed animals. Epilepsia 2010 0.92
117 TBC1D24 mutation associated with focal epilepsy, cognitive impairment and a distinctive cerebro-cerebellar malformation. Epilepsy Res 2013 0.92
118 Nicotine-induced dystonic arousal complex in a mouse line harboring a human autosomal-dominant nocturnal frontal lobe epilepsy mutation. J Neurosci 2007 0.92
119 Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes. Epilepsia 2012 0.91
120 The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizures. Lancet Neurol 2009 0.91
121 Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3. Epilepsia 2010 0.91
122 Genetics of febrile seizure subtypes and syndromes: a twin study. Epilepsy Res 2013 0.91
123 Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy. Epilepsy Res 2007 0.90
124 Sandifer syndrome misdiagnosed as refractory partial seizures in an adult. Epileptic Disord 2004 0.89
125 Risk factors for sudden unexpected death in epilepsy: a controlled prospective study based on coroners cases. Seizure 2003 0.89
126 Endozepine stupor: disease or deception? A critical review. Sleep 2004 0.88
127 Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency. Epilepsia 2012 0.88
128 Glioneuronal tumours in neurofibromatosis type 1: MRI-pathological study. J Clin Neurosci 2004 0.87
129 Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation. Epilepsia 2014 0.87
130 'North Sea' progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation. Brain 2013 0.86
131 Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy. Epilepsia 2003 0.86
132 The Role of Seizure-Related SEZ6 as a Susceptibility Gene in Febrile Seizures. Neurol Res Int 2011 0.86
133 Long-term follow-up of febrile infection-related epilepsy syndrome. Epilepsia 2011 0.86
134 Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies. Epilepsia 2013 0.86
135 Mutation of SCARB2 in a patient with progressive myoclonus epilepsy and demyelinating peripheral neuropathy. Arch Neurol 2011 0.85
136 A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy. Epilepsia 2010 0.85
137 De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin. J Med Genet 2009 0.85
138 Copy number variants--an unexpected risk factor for the idiopathic generalized epilepsies. Brain 2010 0.85
139 Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations. Epilepsia 2011 0.85
140 A twin study of genetic influences on epilepsy outcome. Twin Res 2003 0.85
141 Mutation in the Na+ channel subunit SCN1B produces paradoxical changes in peripheral nerve excitability. Brain 2005 0.85
142 TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features. Neurology 2016 0.85
143 Transcallosal resection of hypothalamic hamartomas in patients with intractable epilepsy. Epileptic Disord 2003 0.85
144 Early seizures after temporal lobectomy predict subsequent seizure recurrence. Ann Neurol 2005 0.84
145 In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission. Brain 2012 0.84
146 Evidence for genetic factors in vasovagal syncope: a twin-family study. Neurology 2012 0.83
147 Etiology of hippocampal sclerosis: evidence for a predisposing familial morphologic anomaly. Neurology 2013 0.83
148 Is variation in the GABA(B) receptor 1 gene associated with temporal lobe epilepsy? Epilepsia 2005 0.83
149 Verbal memory in left temporal lobe epilepsy: evidence for task-related localization. Ann Neurol 2002 0.83
150 Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsy. Am J Med Genet A 2013 0.83
151 Treatment of new-onset epilepsy: seizures beget discussion. Lancet 2005 0.83
152 Cortical excitability and refractory epilepsy: a three-year longitudinal transcranial magnetic stimulation study. Int J Neural Syst 2012 0.83
153 Genetics of epilepsy syndromes in families with photosensitivity. Neurology 2013 0.83
154 Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus. Arch Neurol 2012 0.83
155 Impaired verbal associative learning after resection of left perirhinal cortex. Brain 2007 0.83
156 Reduced variance in monozygous twins for multiple MR parameters: implications for disease studies and the genetic basis of brain structure. Neuroimage 2009 0.82
157 Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+). Epilepsia 2005 0.82
158 Networks underlying paroxysmal fast activity and slow spike and wave in Lennox-Gastaut syndrome. Neurology 2013 0.82
159 Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: is there overlap? Brain 2004 0.82
160 Mild adolescent/adult onset epilepsy and paroxysmal exercise-induced dyskinesia due to GLUT1 deficiency. Epilepsia 2010 0.82
161 Long-term seizure outcome and risk factors for recurrence after extratemporal epilepsy surgery. Epilepsia 2012 0.82
162 Detection of microchromosomal aberrations in refractory epilepsy: a pilot study. Epileptic Disord 2010 0.81
163 Glucose metabolism transporters and epilepsy: only GLUT1 has an established role. Epilepsia 2014 0.81
164 Gene expression analysis in absence epilepsy using a monozygotic twin design. Epilepsia 2008 0.81
165 Are myotonia and epilepsy linked by a chloride channel? Neurology 2013 0.81
166 Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26. Neurology 2013 0.81
167 The psychological impact of a newly diagnosed seizure: losing and restoring perceived control. Epilepsy Behav 2007 0.80
168 Subtle microscopic abnormalities in hippocampal sclerosis do not predict clinical features of temporal lobe epilepsy. Epilepsia 2004 0.80
169 Hypothalamic hamartoma and epilepsy: the pathway of discovery. Epileptic Disord 2003 0.80
170 A retrospective population-based study on seizures related to childhood vaccination. Epilepsia 2011 0.80
171 Do mutations in SCN1B cause Dravet syndrome? Epilepsy Res 2012 0.80
172 Personality development in the context of intractable epilepsy. Arch Neurol 2009 0.80
173 Benign occipital epilepsies of childhood: clinical features and genetics. Brain 2008 0.80
174 Increased serotonin receptor availability in human sleep: evidence from an [18F]MPPF PET study in narcolepsy. Neuroimage 2005 0.79
175 Proconvulsant-induced seizures in alpha(4) nicotinic acetylcholine receptor subunit knockout mice. Neuropharmacology 2002 0.79
176 Hippocampal sclerosis: MR prediction of seizure intractability. Epilepsia 2007 0.79
177 Can changes in cortical excitability distinguish progressive from juvenile myoclonic epilepsy? Epilepsia 2010 0.79
178 New therapeutic opportunities in epilepsy: a genetic perspective. Pharmacol Ther 2010 0.79
179 Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsy. Epilepsy Behav 2010 0.78
180 Weight and fat distribution in patients taking valproate: a valproate-discordant gender-matched twin and sibling pair study. Epilepsia 2014 0.78
181 Overcoming barriers to successful epilepsy management. Epilepsy Curr 2012 0.78
182 Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes. Epilepsia 2011 0.78
183 Exercise-induced temporal lobe epilepsy. Neurology 2002 0.78
184 Concepts and controversies of juvenile myoclonic epilepsy: still an enigmatic epilepsy. Expert Rev Neurother 2014 0.77
185 Profiles of psychosocial outcome after epilepsy surgery: the role of personality. Epilepsia 2009 0.77
186 Founder effect with variable age at onset in Arab families with Lafora disease and EPM2A mutation. Epilepsia 2007 0.77
187 Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+? Epilepsia 2009 0.77
188 Balance impairment in chronic antiepileptic drug users: a twin and sibling study. Epilepsia 2009 0.77
189 Small temporal pole encephaloceles: a treatable cause of "lesion negative" temporal lobe epilepsy. Epilepsia 2010 0.76
190 Transcranial magnetic stimulation and epilepsy. J Clin Neurophysiol 2002 0.76
191 GEFS+ where focal seizures evolve from generalized spike wave: video-EEG study of two children. Epileptic Disord 2007 0.76
192 Association of a nicotinic receptor mutation with reduced height and blunted physostigmine-stimulated growth hormone release. J Clin Endocrinol Metab 2007 0.76
193 Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations. Epilepsy Res 2012 0.76
194 Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations. Epilepsy Res 2013 0.76
195 A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2. Mov Disord 2012 0.76
196 Direct and indirect measures of verbal relational memory following anterior temporal lobectomy. Neuropsychologia 2002 0.76
197 Cognitive complaints after a first seizure in adulthood: Influence of psychological adjustment. Epilepsia 2008 0.75
198 Is photosensitive epilepsy less common in males due to variation in X chromosome photopigment genes? Epilepsia 2007 0.75
199 Key epilepsy gene gets further phenotypic delineation. Neurology 2010 0.75
200 Prediction of drug resistance in epilepsy: not as easy as ABC. Lancet Neurol 2006 0.75
201 Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria. Epilepsia 2010 0.75
202 Abnormal Processing of Autophagosomes in Transformed B Lymphocytes from SCARB2-Deficient Subjects. Biores Open Access 2013 0.75
203 New driving guidelines: ethical and legal uncertainties. Med J Aust 2003 0.75
204 Invited comments on the Shostak and Ottman review. Epilepsia 2006 0.75
205 Inter-session repeatability of cortical excitability measurements in patients with epilepsy. Epilepsy Res 2011 0.75
206 Psychological trajectories in the year after a newly diagnosed seizure. Epilepsia 2012 0.75
207 Clinical features of seizures associated with parahippocampal/inferior temporal lesions compared to those with hippocampal sclerosis. Epilepsia 2010 0.75
208 Temporal lobe dysembryoplastic neuroepithelial tumour: significance of discordant interictal spikes. Epileptic Disord 2004 0.75
209 Action to improve awareness, participation, care and support for people with epilepsy. Med J Aust 2011 0.75
210 Multifocal epilepsy: the role of palliative resection - intractable frontal and occipital lobe epilepsy secondary to radiotherapy for acute lymphoblastic leukaemia. Epileptic Disord 2008 0.75
211 Adjunctive therapy of uncontrolled partial seizures with levetiracetam in Australian patients. Epilepsy Behav 2007 0.75
212 Parahippocampal epilepsy with subtle dysplasia: A cause of "imaging negative" partial epilepsy. Epilepsia 2009 0.75
213 What happens now? Ongoing outcome after post-temporal lobectomy seizure recurrence. Neurology 2006 0.75
214 Significance of post-operative auras after temporal lobectomy: a surprising methodological trap. Epilepsy Behav 2012 0.75
215 Association studies and functional validation or functional validation alone? Epilepsy Res 2007 0.75
216 Rare protein sequence variation in SV2A gene does not affect response to levetiracetam. Epilepsy Res 2012 0.75
217 Siblings with refractory occipital epilepsy showing localized network activity on EEG-fMRI. Epilepsia 2013 0.75
218 Obstetric events as a risk factor for febrile seizures: a community-based twin study. Twin Res Hum Genet 2008 0.75