Transient nonverbal learning disorder in a child suffering from Familial Hemiplegic Migraine. (Q51854426)

14 April 2018

title

Transient nonverbal learning disorder in a child suffering from Familial Hemiplegic Migraine. (English)

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14 April 2018

Non-Verbal Learning Disorder

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Barbara Podestà

1

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Eleonora Briatore

2

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14 April 2018

Andrea Boghi

3

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Daniela Marenco

4

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Stefano Calzolari

5

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language of work or name

English

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publication date

9 September 2011

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14 April 2018

published in

Cephalalgia

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14 April 2018

volume

31

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issue

14

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14 April 2018

page(s)

1497-1502

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14 April 2018

A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria.

cites work

1 reference

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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

21 January 2018

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Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

21 January 2018

1 reference

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Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

21 January 2018

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1H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1.

21 January 2018

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Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

21 January 2018

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Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity

21 January 2018

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Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation

21 January 2018

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A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.

21 January 2018

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Prolonged hemiplegic episodes in children due to mutations in ATP1A2.

21 January 2018

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A novel ATP1A2 mutation in a family with FHM type II

21 January 2018

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Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.

21 January 2018

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Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation

21 January 2018

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A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation.

21 January 2018

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Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation

21 January 2018

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Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2

21 January 2018

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Reversible cognitive decline accompanies migraine and cluster headaches.

21 January 2018

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Functional neuroimaging of headaches

21 January 2018

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MRS shows abnormalities before symptoms in familial Alzheimer disease

21 January 2018

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Recurrent Episodes of Coma: An Unusual Phenotype of Familial Hemiplegic Migraine with Linkage to Chromosome 1

21 January 2018

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21 January 2018

Identifiers

DOI

10.1177/0333102411418260

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14 April 2018

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14 April 2018