(Q35811060)

10 August 2017

1 reference

title

Fever, genes, and epilepsy (English)

1 reference

10 August 2017

Stéphanie Baulac

1

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Michel Baulac

7

object named as

Michel Baulac

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10 August 2017

Isabelle Gourfinkel-An

2

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10 August 2017

Rima Nabbout

3

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10 August 2017

Gilles Huberfeld

4

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10 August 2017

Jose Serratosa

5

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10 August 2017

Eric Leguern

6

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10 August 2017

1 July 2004

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10 August 2017

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10 August 2017

3

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10 August 2017

421-430

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10 August 2017

7

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Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

10 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Monogenic idiopathic epilepsies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

The prevalence and incidence of convulsive disorders in children

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Descriptive epidemiology of epilepsy: contributions of population-based studies from Rochester, Minnesota

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Epidemiology of febrile and afebrile convulsions in children in Japan

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Convulsions among the Chamorro people of Guam, Mariana islands. II. Febrile convulsions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

1 reference

7 January 2021

The risk of epilepsy following febrile convulsions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Factors prognostic of unprovoked seizures after febrile convulsions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Febrile seizures and epilepsy: the contributions of epidemiology

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Predictors of epilepsy in children who have experienced febrile seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Risk of epilepsy after febrile convulsions: a national cohort study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Unprovoked seizures in children with febrile seizures: short-term outcome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Epilepsy diagnosis and localization in patients with antecedent childhood febrile convulsions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Risk factors for complex partial seizures: a population-based case-control study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Delineation of cryptogenic Lennox-Gastaut syndrome and myoclonic astatic epilepsy using multiple correspondence analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Familial occurrence of epilepsy in children with newly diagnosed multiple seizures: Dutch Study of Epilepsy in Childhood

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Hippocampal neuron loss in temporal lobe epilepsy: correlation with early childhood convulsions.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Characteristics of medial temporal lobe epilepsy: I. Results of history and physical examination

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

The occurrence of epilepsy and febrile seizures in Virginian and Norwegian twins

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Pedigree analysis in families with febrile seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Hereditary febrile seizures: phenotype and evidence for a chromosome 19p locus.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

A locus for febrile seizures (FEB3) maps to chromosome 2q23-24

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

A locus for simple pure febrile seizures maps to chromosome 6q22-q24.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Significant evidence for linkage of febrile seizures to chromosome 5q14-q15.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Evidence favoring genetic heterogeneity for febrile convulsions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Genetics of the febrile seizure susceptibility trait.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Childhood-onset epilepsy with and without preceding febrile seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Phenotypic features of familial febrile seizures: case-control study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Complex febrile seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Lack of SCN1A mutations in familial febrile seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Failure to find causal mutations in the GABA(A)-receptor gamma2 subunit (GABRG2) gene in Japanese febrile seizure patients

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

The lack of association between febrile convulsions and polymorphisms in SCN1A

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Generalized epilepsy with febrile seizures plus: A common childhood-onset genetic epilepsy syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS)

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

1 reference

7 January 2021

Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Generalized epilepsy with febrile seizures plus: further heterogeneity in a large family

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Clinical and genetic analysis of a new multigenerational pedigree with GEFS+ (Generalized Epilepsy with Febrile Seizures Plus)

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

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%2804%2900808-7

7 January 2021

A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in man

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

An update on GABAA receptors

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Altered kinetics and benzodiazepine sensitivity of a GABAA receptor subunit mutation [gamma 2(R43Q)] found in human epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Two different mechanisms of disinhibition produced by GABAA receptor mutations linked to epilepsy in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB)

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Severe infantile epilepsies: molecular genetics challenge clinical classification.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

1 reference

7 January 2021

Hippocampal sclerosis revisited

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Febrile convulsions. Is seizure duration the most important predictor of temporal lobe epilepsy?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Febrile seizures and mesial temporal sclerosis: No association in a long-term follow-up study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Interleukin (IL)1beta, IL-1alpha, and IL-1 receptor antagonist gene polymorphisms in patients with temporal lobe epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Increased frequency of interleukin-1beta-511T allele in patients with temporal lobe epilepsy, hippocampal sclerosis, and prolonged febrile convulsion.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Prodynorphin Gene Promoter Polymorphism and Temporal Lobe Epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Lack of association between an interleukin 1 beta (IL-1beta) gene variation and refractory temporal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Association Analysis of a Polymorphism of Interleukin 1β (IL‐1β) Gene with Temporal Lobe Epilepsy in a Chinese Population

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Prodynorphin gene promoter polymorphism and temporal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Mutation analysis of the leucine-rich, glioma inactivated 1 gene (LGI1) in Japanese febrile seizure patients

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Familial temporal lobe epilepsy: a common disorder identified in twins

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Familial temporal lobe epilepsy: a clinically heterogeneous syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Seizure outcome and hippocampal atrophy in familial mesial temporal lobe epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Hippocampal malformation as a cause of familial febrile convulsions and subsequent hippocampal sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Familial temporal lobe epilepsy with febrile seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Paroxysms of excitement: sodium channel dysfunction in heart and brain

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

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%2804%2900808-7

7 January 2021

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Genome search for susceptibility loci of common idiopathic generalised epilepsies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Febrile seizures: treatment and prognosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Distribution of seizure precipitants among epilepsy syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Hyperthermia-induced seizures in the rat pup: a model for febrile convulsions in children

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Febrile seizures: an appropriate-aged model suitable for long-term studies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Seizure-induced neuronal injury: vulnerability to febrile seizures in an immature rat model

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Temperature dependence of intrinsic membrane properties and synaptic potentials in hippocampal CA1 neurons in vitro.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

The effects of temperature on synaptic transmission in hippocampal tissue slices.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Three types of hyperthermic seizures in rats

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Hyperthermia induces age-dependent changes in rat hippocampal excitability

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Increased plasma levels of pro- and anti-inflammatory cytokines in patients with febrile seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Powerful anticonvulsant action of IL-1 receptor antagonist on intracerebral injection and astrocytic overexpression in mice

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Glutamate release in the nucleus tractus solitarius induced by peripheral lipopolysaccharide and interleukin-1 beta.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

B7-H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin-10 secretion

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Persistently modified h-channels after complex febrile seizures convert the seizure-induced enhancement of inhibition to hyperexcitability

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Brugada-like electrocardiographic pattern induced by fever

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

Cold induces shifts of voltage dependence in mutant SCN4A, causing hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2804%2900808-7

7 January 2021

10.1016/S1474-4422(04)00808-7

Identifiers

DOI

1 reference

release_zqqnjk64njabbfnf6bo23xw6mi

10 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/zqqnjk64njabbfnf6bo23xw6mi

24 November 2022

mapped directly with Wikidata item

1 reference