Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
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The Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation MedicineTherapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug DiscoveryThe genetic variants in 3' untranslated region of voltage-gated sodium channel alpha 1 subunit gene affect the mRNA-microRNA interactions and associate with epilepsy.A Data Fusion Approach to Enhance Association Study in Epilepsy.Temperature-dependent changes in neuronal dynamics in a patient with an SCN1A mutation and hyperthermia induced seizuresSchizophrenia Associated with Epileptiform Discharges without Seizures Successfully Treated with Levetiracetam.Precision physiology and rescue of brain ion channel disorders.Headache and Epilepsy.Erythromelalgia: a cutaneous manifestation of neuropathy?Association of epilepsy and asthma: a population-based retrospective cohort study.
P2860
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P2860
Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Genetic neurological channelopathies: molecular genetics and clinical phenotypes
@nl
Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
@ast
Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
@en
type
label
Genetic neurological channelopathies: molecular genetics and clinical phenotypes
@nl
Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
@ast
Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
@en
prefLabel
Genetic neurological channelopathies: molecular genetics and clinical phenotypes
@nl
Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
@ast
Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
@en
P2860
P3181
P356
P1476
Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
@en
P2093
P2860
P3181
P356
10.1136/JNNP-2015-311233
P407
P5008
P577
2015-11-11T00:00:00Z
2016-01-01T00:00:00Z