Alternating hemiplegia of childhood

Known as: alternating hemiplegia childhood, alternating childhood hemiplegia, Alternating hemiplegia syndrome 
 

Topic mentions per year

Topic mentions per year

1999-2018
051019992018

Papers overview

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2015
2015
OBJECTIVE Mutations in ATP1A3, the gene that encodes the α3 subunit of the Na(+)/K(+) ATPase, are the primary cause of… (More)
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2015
2015
OBJECTIVES Mutations in the ATP1α3 subunit of the neuronal Na+/K+-ATPase are thought to be responsible for seizures, hemiplegias… (More)
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2015
2015
Alternating hemiplegia of childhood is a rare disorder caused by de novo mutations in the ATP1A3 gene, expressed in neurons and… (More)
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2014
2014
BACKGROUND AND OBJECTIVE Alternating hemiplegia in childhood (AHC) is a disease characterized by recurrent episodes of hemiplegia… (More)
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2014
2014
Alternating hemiplegia of childhood (AHC) is a rare neurodevelopmental disorder characterized by early-onset recurrent… (More)
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2014
2014
BACKGROUND AND PURPOSE Alternating hemiplegia of childhood (AHC) is a rare neurological disease characterized by recurrent… (More)
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2014
2014
De novo mutations in ATP1A3, the gene encoding the α3-subunit of Na(+),K(+)-ATPase, are associated with the neurodevelopmental… (More)
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Review
2014
Review
2014
A syndrome of alternating hemiplegia of childhood (AHC) is a rare disorder first presented in 1971. AHC is characterized by… (More)
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2010
2010
Jeffrey R. Tenney, MD, PhD Mark B. Schapiro, MD Alternating hemiplegia of childhood (AHC) is a rare disorder characterized by… (More)
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Review
1999
Review
1999
Alternating hemiplegia of childhood (AHC) is a very rare disease characterized by recurrent attacks of loss of muscular tone… (More)
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