Literature DB >> 14570825

Enteroviruses in chronic fatigue syndrome: "now you see them, now you don't".

M C Dalakas.   

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Year:  2003        PMID： 14570825      PMCID： PMC1757390          DOI： 10.1136/jnnp.74.10.1361

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  43 in total

1.  APOE epsilon4 genotype is associated with an earlier onset of chronic temporal lobe epilepsy.

Authors:  R S Briellmann; Y Torn-Broers; B E Busuttil; B J Major; R M Kalnins; M Olsen; G D Jackson; A G Frauman; S F Berkovic
Journal:  Neurology       Date:  2000-08-08       Impact factor: 9.910

2.  Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.

Authors:  Sergey Kalachikov; Oleg Evgrafov; Barbara Ross; Melodie Winawer; Christie Barker-Cummings; Filippo Martinelli Boneschi; Chang Choi; Pavel Morozov; Kamna Das; Elita Teplitskaya; Andrew Yu; Eftihia Cayanis; Graciela Penchaszadeh; Andreas H Kottmann; Timothy A Pedley; W Allen Hauser; Ruth Ottman; T Conrad Gilliam
Journal:  Nat Genet       Date:  2002-01-28       Impact factor: 38.330

3.  Idiopathic familial temporal lobe epilepsy with febrile convulsions.

Authors:  N Ward; J Evanson; O C Cockerell
Journal:  Seizure       Date:  2002-01       Impact factor: 3.184

4.  Familial temporal lobe epilepsy: a common disorder identified in twins.

Authors:  S F Berkovic; A McIntosh; R A Howell; A Mitchell; L J Sheffield; J L Hopper
Journal:  Ann Neurol       Date:  1996-08       Impact factor: 10.422

5.  Seizure outcome and hippocampal atrophy in familial mesial temporal lobe epilepsy.

Authors:  E Kobayashi; I Lopes-Cendes; C A Guerreiro; S C Sousa; M M Guerreiro; F Cendes
Journal:  Neurology       Date:  2001-01-23       Impact factor: 9.910

6.  Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy.

Authors:  José M Morante-Redolat; Ana Gorostidi-Pagola; Salomé Piquer-Sirerol; Amets Sáenz; Juan J Poza; Juan Galán; Stefan Gesk; Theologia Sarafidou; Victor-F Mautner; Simona Binelli; Eike Staub; Bernd Hinzmann; Lisa French; Jean-F Prud'homme; Daniela Passarelli; Paolo Scannapieco; Carlo A Tassinari; Giuliano Avanzini; José F Martí-Massó; Lan Kluwe; Panagiotis Deloukas; Nicholas K Moschonas; Roberto Michelucci; Reiner Siebert; Carlo Nobile; Jordi Pérez-Tur; Adolfo López de Munain
Journal:  Hum Mol Genet       Date:  2002-05-01       Impact factor: 6.150

7.  A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy.

Authors:  Elisabeth Stögmann; Alexander Zimprich; Christoph Baumgartner; Susanne Aull-Watschinger; Volker Höllt; Fritz Zimprich
Journal:  Ann Neurol       Date:  2002-02       Impact factor: 10.422

Review 8.  Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease.

Authors:  David Botstein; Neil Risch
Journal:  Nat Genet       Date:  2003-03       Impact factor: 38.330

9.  Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism.

Authors:  Antonio Pizzuti; Elisabetta Flex; Carlo Di Bonaventura; Tania Dottorini; Gabriella Egeo; Mario Manfredi; Bruno Dallapiccola; Anna Teresa Giallonardo
Journal:  Ann Neurol       Date:  2003-03       Impact factor: 10.422

10.  Febrile convulsions. Is seizure duration the most important predictor of temporal lobe epilepsy?

Authors:  J Maher; R S McLachlan
Journal:  Brain       Date:  1995-12       Impact factor: 13.501
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