Literature DB >> 1464265

Validation of a questionnaire for clinical seizure diagnosis.

D C Reutens1, R A Howell, K E Gebert, S F Berkovic.   

Abstract

A detailed questionnaire has been devised for diagnosis of seizure type. It is suitable for administration by trained interviewers, either directly or by telephone. A comparison of physician-based and questionnaire-based diagnoses showed almost perfect agreement in classification of patients into those with seizures of either generalized or focal origin. Substantial to almost-perfect agreement was reached in diagnosis of patients with most individual seizure types. Disagreement in differentiation between simple and complex partial seizures (CPS) probably reflects the limitations of the clinical method rather than of the questionnaire itself. The questionnaire should be of value in large-scaled clinical and epidemiologic studies.

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Year:  1992        PMID: 1464265     DOI: 10.1111/j.1528-1157.1992.tb01760.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  28 in total

1.  Familial clustering of seizure types within the idiopathic generalized epilepsies.

Authors:  M R Winawer; C Marini; B E Grinton; D Rabinowitz; S F Berkovic; I E Scheffer; R Ottman
Journal:  Neurology       Date:  2005-08-23       Impact factor: 9.910

Review 2.  Copy number variants are frequent in genetic generalized epilepsy with intellectual disability.

Authors:  Saul A Mullen; Gemma L Carvill; Susannah Bellows; Marta A Bayly; Holger Trucks; Dennis Lal; Thoman Sander; Samuel F Berkovic; Leanne M Dibbens; Ingrid E Scheffer; Heather C Mefford
Journal:  Neurology       Date:  2013-09-25       Impact factor: 9.910

3.  The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures.

Authors:  Rosemary Burgess; Shuyu Wang; Amy McTague; Katja E Boysen; Xiaoling Yang; Qi Zeng; Kenneth A Myers; Anne Rochtus; Marina Trivisano; Deepak Gill; Lynette G Sadleir; Nicola Specchio; Renzo Guerrini; Carla Marini; Yue-Hua Zhang; Heather C Mefford; Manju A Kurian; Annapurna H Poduri; Ingrid E Scheffer
Journal:  Ann Neurol       Date:  2019-12       Impact factor: 10.422

4.  Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy.

Authors:  Mark A Corbett; Susannah T Bellows; Melody Li; Renée Carroll; Silvana Micallef; Gemma L Carvill; Candace T Myers; Katherine B Howell; Snezana Maljevic; Holger Lerche; Elena V Gazina; Heather C Mefford; Melanie Bahlo; Samuel F Berkovic; Steven Petrou; Ingrid E Scheffer; Jozef Gecz
Journal:  Neurology       Date:  2016-10-12       Impact factor: 9.910

5.  PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.

Authors:  Sarah E Heron; Bronwyn E Grinton; Sara Kivity; Zaid Afawi; Sameer M Zuberi; James N Hughes; Clair Pridmore; Bree L Hodgson; Xenia Iona; Lynette G Sadleir; James Pelekanos; Eric Herlenius; Hadassa Goldberg-Stern; Haim Bassan; Eric Haan; Amos D Korczyn; Alison E Gardner; Mark A Corbett; Jozef Gécz; Paul Q Thomas; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer; Leanne M Dibbens
Journal:  Am J Hum Genet       Date:  2012-01-13       Impact factor: 11.025

6.  Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsy.

Authors:  Lynette G Sadleir; Guillem de Valles-Ibáñez; Chontelle King; Matthew Coleman; Stuart Mossman; Sarah Paterson; John Nguyen; Samuel F Berkovic; Saul Mullen; Melanie Bahlo; Michael S Hildebrand; Heather C Mefford; Ingrid E Scheffer
Journal:  Epilepsia       Date:  2020-03-12       Impact factor: 5.864

7.  De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.

Authors: 
Journal:  Am J Hum Genet       Date:  2016-07-28       Impact factor: 11.025

8.  Diagnostic reference frames for seizures: A validation study.

Authors:  J F van Ast; W O Renier; J L Talmon; J M A Roos; A Hasman
Journal:  J Neurol       Date:  2005-11-14       Impact factor: 4.849

9.  Mutations in DEPDC5 cause familial focal epilepsy with variable foci.

Authors:  Leanne M Dibbens; Boukje de Vries; Simona Donatello; Sarah E Heron; Bree L Hodgson; Satyan Chintawar; Douglas E Crompton; James N Hughes; Susannah T Bellows; Karl Martin Klein; Petra M C Callenbach; Mark A Corbett; Alison E Gardner; Sara Kivity; Xenia Iona; Brigid M Regan; Claudia M Weller; Denis Crimmins; Terence J O'Brien; Rosa Guerrero-López; John C Mulley; Francois Dubeau; Laura Licchetta; Francesca Bisulli; Patrick Cossette; Paul Q Thomas; Jozef Gecz; Jose Serratosa; Oebele F Brouwer; Frederick Andermann; Eva Andermann; Arn M J M van den Maagdenberg; Massimo Pandolfo; Samuel F Berkovic; Ingrid E Scheffer
Journal:  Nat Genet       Date:  2013-03-31       Impact factor: 38.330

10.  PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures.

Authors:  Ingrid E Scheffer; Bronwyn E Grinton; Sarah E Heron; Sara Kivity; Zaid Afawi; Xenia Iona; Hadassa Goldberg-Stern; Maria Kinali; Ian Andrews; Renzo Guerrini; Carla Marini; Lynette G Sadleir; Samuel F Berkovic; Leanne M Dibbens
Journal:  Neurology       Date:  2012-10-17       Impact factor: 9.910

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