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English
Genetics of migraine
scientific article published on February 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
review article
1 reference
stated in
Europe PubMed Central
title
Genetics of migraine
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
main subject
migraine
1 reference
based on heuristic
inferred from title
author
Michel Ferrari
series ordinal
3
object named as
Ferrari MD
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
author name string
Haan J
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
Terwindt GM
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
publication date
1 February 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
published in
Neurologic Clinics
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
volume
15
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
page(s)
43-60
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
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Evidence for mitochondrial dysfunction in patients with alternating hemiplegia of childhood
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A study of hereditary essential tremor
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Familial periodic cerebellar ataxia: a problem of cerebellar intracellular pH homeostasis.
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Tourette's syndrome and migraine
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7 January 2021
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Abnormal brain and muscle energy metabolism shown by 31P magnetic resonance spectroscopy in patients affected by migraine with aura
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7 January 2021
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Migraine and epilepsy.
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7 January 2021
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The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1
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7 January 2021
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Alternating hemiplegia of childhood
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7 January 2021
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Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p
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Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patient.
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7 January 2021
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Possible linkage of Tourette syndrome to markers on short arm of chromosome 3 (C3p21-14)
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7 January 2021
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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
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Familial paroxysmal kinesigenic ataxia and continuous myokymia.
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Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus
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7 January 2021
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Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
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MELAS: clinical features, biochemistry, and molecular genetics
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On Recurrent Motor Paralysis in Migraine, with Report of a Family in which Recurrent Hemiplegia Accompanied the Attacks
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7 January 2021
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Linkage analysis with chromosome 9 markers in hereditary essential tremor
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7 January 2021
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Lack of association between mitochondrial tRNALeu(UUR) point mutation and cluster headache
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7 January 2021
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The first report of cluster headache in identical twins
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7 January 2021
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Mitochondrial encephalomyopathy: variable clinical expression within a single kindred
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7 January 2021
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Migraine and epilepsy with infantile onset and electroencephalographic findings of occipital spike-wave complexes
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Progress in mapping human epilepsy genes
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7 January 2021
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Familial cavernous malformations of the central nervous system and retina
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7 January 2021
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Gene location in Tourette syndrome
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7 January 2021
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A gene responsible for cavernous malformations of the brain maps to chromosome 7q
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7 January 2021
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Monozygotic twins discordant for familial hemiplegic migraine
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Crossref
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7 January 2021
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Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients
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7 January 2021
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Familial essential tremor and idiopathic torsion dystonia are different genetic entities
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7 January 2021
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Mitochondrial inheritance in a mitochondrially mediated disease
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7 January 2021
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Neuroexcitatory plasma amino acids are elevated in migraine.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Serotonin metabolism in migraine
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
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Autosomal dominant episodic ataxia: a heterogeneous syndrome
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with tourette syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine associated with focal cerebral edema, cerebrospinal fluid pleocytosis, and progressive cerebellar ataxia: MRI documentation.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
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Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
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The genetics of idiopathic generalized epilepsies of adolescent onset: differences between juvenile myoclonic epilepsy and epilepsy with random grand mal and with awakening grand mal
1 reference
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https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
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Episodic ataxias as channelopathies
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
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Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
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inferred from DOI database lookup
Hereditary hemorrhagic telangiectasia
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Crossref
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Hereditary cerebral haemorrhage with amyloidosis--Dutch type. Magnetic resonance imaging findings in 7 cases.
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Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group
1 reference
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Crossref
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based on heuristic
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Is familial hemiplegic migraine a hereditary form of basilar migraine?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
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inferred from DOI database lookup
Mitochondrial myopathy: a genetic study of 71 cases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
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Familial paroxysmal ataxia: report of a family
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine and concomitant symptoms among 8167 adult twin pairs.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Alternating hemiplegia: complicated migraine of infancy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Migraine: Exclusion of the Susceptibility Gene from the Reported Locus of Familial Hemiplegic Migraine on 19p
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for familial hemiplegic migraine maps to chromosome 19
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Inheritance of cluster headache and its possible link to migraine
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Bilineal transmission in Tourette's syndrome families
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign familial neonatal convulsions linked to genetic markers on chromosome 20.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine in twins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A locus for cerebral cavernous malformations maps to chromosome 7q in two families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Headache syndromes and psychiatric disorders: association and familial transmission
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine and depression: Association and familial transmission
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Testing Models for Genetic Determination in Migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
31P-magnetic resonance spectroscopy in migraine without aura.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial abnormalities in migraine. Preliminary findings
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic heterogeneity of familial hemiplegic migraine
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comorbidity of migraine and epilepsy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Validity of family history data on severe headache and migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of a gene for partial epilepsy to chromosome 10q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic markers: association study in migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioural disorders: lessons in linkage.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adult onset familial hemiplegic migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cluster headache in twins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant cerebellar phenotypes: the genotype has settled the issue
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical intra- and interfamilial variability of cluster headache.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genetics of migraine without aura and migraine with aura
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Increased familial risk and evidence of genetic factor in migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial occurrence of cluster headache
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial occurrence of migraine without aura and migraine with aura.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Partial epilepsy: chinks in the armour
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Point mutation in platelet mitochondrial tRNA(Leu(UUR)) in patient with cluster headache
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alternating hemiplegia of childhood: a study of 10 patients and results of flunarizine treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The hereditary syndrome of thrombocytopathia, bleeding tendency, extreme miosis, muscular fatigue, asplenia, headache, etc. ("Stormorken's syndrome"): I. The headache
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cluster headache in identical twins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial cluster headache: Occurrence in three generations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An association between migrainous aura and hereditary haemorrhagic telangiectasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new syndrome: thrombocytopathia, muscle fatigue, asplenia, miosis, migraine, dyslexia and ichthyosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An autosomal locus predisposing to deletions of mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
9p monosomy in a patient with Gilles de la Tourette's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifying complex disease genes: progress and paradigms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign infantile familial convulsions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial cerebral amyloid angiopathy presenting as recurrent cerebral haemorrhage.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of genes predisposing to idiopathic generalized epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2805%2970294-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0733-8619(05)70294-2
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
PubMed ID
9058396
1 reference
stated in
Europe PubMed Central
PubMed ID
9058396
retrieved
30 September 2017
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