相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Diagnostic and therapeutic aspects of hemiplegic migraine
Vincenzo Di Stefano et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2020)
Teaching NeuroImages: Transient cytotoxic edema in a child with a novelATP1A2mutation
Alexandra B. Kornbluh et al.
NEUROLOGY (2020)
Migraine as a Cortical Brain Disorder
Picro Barbanti et al.
HEADACHE (2020)
Novel missense mutation in the ATP1A2 gene associated with atypical sporadic hemiplegic migraine
Marianna Gabriella Rispoli et al.
BMJ CASE REPORTS (2019)
Headache Classification Committee of the International Headache Society (IHS) The International Classification of Headache Disorders, 3rd edition
Jes Olesen
CEPHALALGIA (2018)
Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation
Nadine Pelzer et al.
NEUROLOGY (2018)
Current Aura Without Headache
Divya R. Shah et al.
CURRENT PAIN AND HEADACHE REPORTS (2018)
Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation
N. Pelzer et al.
CEPHALALGIA (2017)
Clinical and electroencephalographic abnormalities during the full duration of a sporadic hemiplegic migraine attack
Nathalie Chastan et al.
NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY (2016)
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Sue Richards et al.
GENETICS IN MEDICINE (2015)
Case Definitions, Diagnostic Algorithms, and Priorities in Encephalitis: Consensus Statement of the International Encephalitis Consortium
A. Venkatesan et al.
CLINICAL INFECTIOUS DISEASES (2013)
Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults
Eleni Panagiotakaki et al.
BRAIN (2010)
Familial basilar migraine associated with a new mutation in the ATP1A2 gene
A Ambrosini et al.
NEUROLOGY (2005)
Rare missense variants in ATP1A2 in families with clustering of common forms of migraine
U Todt et al.
HUMAN MUTATION (2005)
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood
MT Bassi et al.
JOURNAL OF MEDICAL GENETICS (2004)
Alternating hemiplegia of childhood or familial hemiplegic migraine?:: A novel ATP1A2 mutation
KJ Swoboda et al.
ANNALS OF NEUROLOGY (2004)
Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait
E Kanavakis et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2003)
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2
M De Fusco et al.
NATURE GENETICS (2003)
An epidemiological survey of hemiplegic migraine
LL Thomsen et al.
CEPHALALGIA (2002)
Alternating hemiplegia of childhood: Clinical manifestations and long-term outcome
MA Mikati et al.
PEDIATRIC NEUROLOGY (2000)