Benign Childhood Epilepsy with Centrotemporal Spikes and Electroencephalography Trait are Not Linked to EBN1 and EBN2 of Benign Neonatal Familial Convulsions

No abstract is available for this paper.

• Publication year

  1997

• Venue

  Epilepsia

• Publication date

  1997-07-01

• Fields of study

  Medicine, Psychology

• Identifiers
  DOI 10.1111/j.1528-1157.1997.tb01465.xPMID 9579905
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  1996cited by this paper
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  1992cited by this paper
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  1992cited by this paper
• Benign childhood epilepsy with centrotemporal spikes.

  1989cited by this paper
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  1989cited by this paper
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  1988cited by this paper
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  1987cited by this paper
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  1987cited by this paper
• Strategies for multilocus linkage analysis in humans.

  1984cited by this paper
• [Electroclinical and developmental aspects of epilepsy in the aphasia-epilepsy syndrome].

  1983cited by this paper
• Benign Epilepsy of Childhood with Centrotemporal EEG Foci: A Genetic Study

  1975cited by this paper
• The Development of the Electroencephalogram in Normal Children from the Age of 1 Through 15 Years – Paroxysmal activity

  1971cited by this paper
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  1965cited by this paper
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  1964cited by this paper

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  2003cites this paper
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  2002cites this paper
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  2002cites this paper
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  2002cites this paper
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  2001cites this paper
• [Idiopathic partial epilepsy syndromes].

  2001cites this paper
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  2000cites this paper
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  2000cites this paper
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  2000cites this paper
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  2000cites this paper
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  1999cites this paper
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