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
BACKGROUND: Hemiplegic migraine (HM) and alternating hemiplegia of childhood (AHC) are rare episodic...
BACKGROUND Pathogenic heterozygous variants in the ATP1A2 gene have most commonly been associated...
BACKGROUND: The mechanisms of genotype-phenotype interaction in Familiar Hemiplegic migraine type 2 ...
Introduction. Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attack...
Introduction Familial hemiplegic migraine (FHM) is a rare subtype of migraine with transient hemipl...
Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura with an autosomal dominan...
Hemiplegic migraine (HM) is a rare form of migraine characterized by severe attacks of unilateral an...
Hemiplegic migraine (HM) is a rare form of migraine characterized by severe attacks of unilateral an...
Abstract Familial hemiplegic migraine (FHM) is an autosomal dominant form of migraine with aura. Th...
Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutat...
Mutations in the ATP1A2 gene, encoding the alpha2-subunit of the Na+,K+-ATPase, are associated with ...
BACKGROUND Pathogenic heterozygous variants in the ATP1A2 gene have most commonly been associated wi...
Familial hemiplegic migraine (FHM) is a severe dominant form of migraine with aura associated with t...
[Introduction]: Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine atta...
Contains fulltext : 51118.pdf (publisher's version ) (Closed access
BACKGROUND: Hemiplegic migraine (HM) and alternating hemiplegia of childhood (AHC) are rare episodic...
BACKGROUND Pathogenic heterozygous variants in the ATP1A2 gene have most commonly been associated...
BACKGROUND: The mechanisms of genotype-phenotype interaction in Familiar Hemiplegic migraine type 2 ...
Introduction. Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attack...
Introduction Familial hemiplegic migraine (FHM) is a rare subtype of migraine with transient hemipl...
Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura with an autosomal dominan...
Hemiplegic migraine (HM) is a rare form of migraine characterized by severe attacks of unilateral an...
Hemiplegic migraine (HM) is a rare form of migraine characterized by severe attacks of unilateral an...
Abstract Familial hemiplegic migraine (FHM) is an autosomal dominant form of migraine with aura. Th...
Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutat...
Mutations in the ATP1A2 gene, encoding the alpha2-subunit of the Na+,K+-ATPase, are associated with ...
BACKGROUND Pathogenic heterozygous variants in the ATP1A2 gene have most commonly been associated wi...
Familial hemiplegic migraine (FHM) is a severe dominant form of migraine with aura associated with t...
[Introduction]: Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine atta...
Contains fulltext : 51118.pdf (publisher's version ) (Closed access
BACKGROUND: Hemiplegic migraine (HM) and alternating hemiplegia of childhood (AHC) are rare episodic...
BACKGROUND Pathogenic heterozygous variants in the ATP1A2 gene have most commonly been associated...
BACKGROUND: The mechanisms of genotype-phenotype interaction in Familiar Hemiplegic migraine type 2 ...
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