Familial Hemiplegic Migraine With ATP1A2 Mutations

J Gordon Millichap

doi:10.15844/pedneurbriefs-21-5-7

Familial Hemiplegic Migraine With ATP1A2 Mutations

Pediatric Neurology Briefs

Volume 21 (2007): Issue 5

By: J Gordon Millichap

Open Access

|May 2007

Abstract

Three children with prolonged hemiplegia following severe unilateral headache and having mutations in ATP1A2 are reported from UCLA School of Medicine, Los Angeles, CA; University Children’s Hospital, Zurich, Switzerland; and Wake Forest University School of Medicine, Winston-Salem, NC.

References

Jen JC Klein A Boltshauser E Cartwright MS Roach ES Mamsa H Prolonged hemiplegic episodes in children due to mutations in ATP1A2 J Neurol Neurosurg Psychiatry 2007 May 78 5 523 6 10.1136/jnnp.2006.103267 17435187
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Vanmolkot FH Van Bortel LM de Hoon JN Altered arterial function in migraine of recent onset Neurology 2007 May 8 68 19 1563 70 10.1212/01.wnl.0000260964.28393.ed 17460157
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Tietjen GE Migraine as a systemic disorder Neurology 2007 May 8 68 19 1555 6 10.1212/01.wnl.0000265415.18382.fb 17485641
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-21-5-7 | Journal eISSN: 2166-6482

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Language: English

Page range: 38 - 39

Published on: May 1, 2007

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Hemiplegic Migraine,

ATP1A2 Mutations,

Hemiparesis

© 2007 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 21 (2007): Issue 5