(Q33157223)

23 July 2017

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title

The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizures (English)

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23 July 2017

Douglas E Crompton

1

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Samuel Berkovic

object named as

Samuel F Berkovic

series ordinal

2

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publication date

1 April 2009

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23 July 2017

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23 July 2017

volume

8

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23 July 2017

issue

4

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23 July 2017

page(s)

370-381

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Human epilepsies: interaction of genetic and acquired factors

23 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Navigating the channels and beyond: unravelling the genetics of the epilepsies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Voltage‐gated potassium channel antibodies in limbic encephalitis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

The neurobiology of antiepileptic drugs

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Epileptogenesis in experimental models.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Selective changes in single cell GABA(A) receptor subunit expression and function in temporal lobe epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Mechanisms of seizure-induced 'transcriptional channelopathy' of hyperpolarization-activated cyclic nucleotide gated (HCN) channels

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

On the cellular and network bases of epileptic seizures.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Cellular and network mechanisms of spike-wave seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Basic mechanisms of partial epilepsies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Orthostatic intolerance and tachycardia associated with norepinephrine-transporter deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Mutations in the dopamine beta-hydroxylase gene are associated with human norepinephrine deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Tissue-specific reduction in splicing efficiency of IKBKAP due to the major mutation associated with familial dysautonomia.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Cardiac channelopathies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Diagnostic value of history in patients with syncope with or without heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Risk stratification of patients with syncope

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Historical criteria that distinguish syncope from seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Diagnostic criteria for vasovagal syncope based on a quantitative history

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Syncope: a videometric analysis of 56 episodes of transient cerebral hypoxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Electro-encephalographic study of syncope; its differentiation from epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Electrocerebral accompaniments of syncope associated with malignant ventricular arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Electroencephalographic and clinical study of anoxic convulsions in children; their location within the group of infantile convulsions and their differenciation from epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Video-electrographic and clinical features in patients with ictal asystole

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

A sodium-channel mutation causes isolated cardiac conduction disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Mechanisms of disease: ion channel remodeling in the failing ventricle

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

The Visual Aura Rating Scale (VARS) for Migraine Aura Diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

A nosographic analysis of the migraine aura in a general population.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Elementary visual hallucinations, blindness, and headache in idiopathic occipital epilepsy: differentiation from migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Occipital epilepsies: identification of specific and newly recognized syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Parietal and occipital lobe epilepsy: a review.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Multi-center study on post-ictal headache in patients with localization-related epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Neurobiology of migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Analysis of the propagation of disinhibition-induced after-discharges along the guinea-pig hippocampal slice in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Comorbidity of migraine and epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Mitochondrial disorders in the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Benign occipital epilepsies of childhood: clinical features and genetics.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Epilepsy as part of the phenotype associated with ATP1A2 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Na(v)1.1 sodium channels

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Divergent sodium channel defects in familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Ictal clinical and scalp-EEG findings differentiating temporal lobe epilepsies from temporal 'plus' epilepsies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

BENIGN PAROXYSMAL VERTIGO OF CHILDHOOD. (A VARIETY OF VESTIBULAR NEURONITIS)

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Pediatric migraine equivalents: occurrence and clinical features in practice

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Benign paroxysmal vertigo in childhood: a long-term follow-up

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Primary episodic ataxias: diagnosis, pathogenesis and treatment

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

1 reference

7 January 2021

Paroxysmal motor disorders of sleep: the clinical spectrum and differentiation from epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Nocturnal frontal lobe epilepsy. A clinical and polygraphic overview of 100 consecutive cases.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Distinguishing sleep disorders from seizures: diagnosing bumps in the night

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Central pattern generators for a common semiology in fronto-limbic seizures and in parasomnias. A neuroethologic approach.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

The motor infrastructure: from ion channels to neuronal networks

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Narcolepsy with cataplexy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Seizures and enhanced cortical GABAergic inhibition in two mouse models of human autosomal dominant nocturnal frontal lobe epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Nicotine-induced dystonic arousal complex in a mouse line harboring a human autosomal-dominant nocturnal frontal lobe epilepsy mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Pathophysiology of REM sleep behaviour disorder and relevance to neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Myoclonus: current concepts and recent advances.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Electrophysiological studies of myoclonus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Electrophysiological studies of myoclonus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Benign sleep myoclonus in infancy mistaken for epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Pathogenesis of giant somatosensory evoked potentials in progressive myoclonic epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Cortical myoclonus in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

The myoclonus in corticobasal degeneration. Evidence for two forms of cortical reflex myoclonus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Focal subcortical reflex myoclonus. A clinical and neurophysiological study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Clinical and physiological features of epilepsia partialis continua. Cases ascertained in the UK.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Psychogenic nonepileptic seizures: review and update

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Paroxysmal kinesigenic choreoathetosis (PKC): confirmation of linkage to 16p11-q21, but unsuccessful detection of mutations among 157 genes at the PKC-critical region in seven PKC families

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Paroxysmal non-kinesigenic dyskinesia is caused by mutations of the MR-1 mitochondrial targeting sequence

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Seizure Characterization and Electroencephalographic Features in Glut‐1 Deficiency Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Defective Glucose Transport across the Blood-Brain Barrier as a Cause of Persistent Hypoglycorrhachia, Seizures, and Developmental Delay

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Ictal (99m)Tc ECD SPECT in paroxysmal kinesigenic choreoathetosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

1 reference

7 January 2021

Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Glycine receptors: recent insights into their structural organization and functional diversity

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Association of gephyrin and glycine receptors in the human brainstem and spinal cord: an immunohistochemical analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Glycine receptors in the striatum, globus pallidus, and substantia nigra of the human brain: an immunohistochemical study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB)

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Structure and functions of inhibitory and excitatory glycine receptors.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Retrospective study of concussive convulsions in elite Australian rules and rugby league footballers: phenomenology, aetiology, and outcome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

From genes to pain: Na v 1.7 and human pain disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2809%2970059-6

7 January 2021

10.1016/S1474-4422(09)70059-6

Identifiers

DOI

1 reference

23 July 2017

1 reference