X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1310) 1310
Book Review (506) 506
Publication (101) 101
Book Chapter (33) 33
Book / eBook (11) 11
Conference Proceeding (9) 9
Data Set (1) 1
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
familial hemiplegic migraine (1170) 1170
index medicus (1008) 1008
humans (920) 920
clinical neurology (639) 639
migraine (592) 592
neurosciences (530) 530
male (401) 401
female (375) 375
animals (307) 307
mutation (273) 273
adult (251) 251
migraine disorders - genetics (231) 231
headache (202) 202
cortical spreading depression (199) 199
epilepsy (188) 188
migraine disorders - physiopathology (183) 183
middle aged (178) 178
aura (176) 176
genetic aspects (169) 169
genetics (162) 162
calcium channels - genetics (160) 160
neurology (153) 153
calcium-channel (151) 151
mutations (144) 144
migraine with aura - genetics (141) 141
adolescent (136) 136
child (121) 121
pedigree (118) 118
gene (117) 117
genetics & heredity (109) 109
mice (105) 105
ataxia (101) 101
episodic ataxia type-2 (100) 100
phenotype (100) 100
spreading depression (99) 99
analysis (98) 98
research (85) 85
abridged index medicus (82) 82
aged (82) 82
calcium channels (82) 82
risk factors (81) 81
biochemistry & molecular biology (79) 79
gene-related peptide (79) 79
migraine with aura - physiopathology (78) 78
genetic predisposition to disease (77) 77
genes (73) 73
type-2 (73) 73
mutation - genetics (72) 72
pharmacology & pharmacy (72) 72
sodium-potassium-exchanging atpase - genetics (72) 72
medicine & public health (70) 70
seizures (69) 69
cacna1a (68) 68
episodic ataxia (67) 67
migraine disorders - diagnosis (67) 67
migraine with aura (67) 67
migraine disorders - drug therapy (66) 66
brain (64) 64
child, preschool (62) 62
psychiatry (62) 62
atp1a2 (61) 61
prevalence (61) 61
epilepsy - genetics (60) 60
genome-wide association (60) 60
magnetic resonance imaging (60) 60
cluster headache (59) 59
genotype (59) 59
locus (58) 58
genetic research (57) 57
nerve tissue proteins - genetics (57) 57
channel (56) 56
genetic predisposition to disease - genetics (56) 56
headaches (56) 56
pediatrics (56) 56
disease models, animal (55) 55
dna mutational analysis (55) 55
migraine disorders - complications (55) 55
cerebellar-ataxia (54) 54
pain (54) 54
stroke (54) 54
hemiplegic migraine (51) 51
migraine disorders - epidemiology (51) 51
neurons (51) 51
brain-stem activation (50) 50
cacna1a gene (50) 50
diagnosis (50) 50
ion channels - genetics (49) 49
transcranial magnetic stimulation (49) 49
young adult (49) 49
care and treatment (48) 48
channelopathy (48) 48
linkage (47) 47
mechanisms (47) 47
typical migraine (47) 47
physiology (46) 46
ca2+ channels (45) 45
frontal-lobe epilepsy (45) 45
gene mutations (45) 45
potassium channel gene (45) 45
article (44) 44
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1258) 1258
German (28) 28
French (24) 24
Spanish (14) 14
Italian (11) 11
Japanese (5) 5
Polish (3) 3
Portuguese (3) 3
Persian (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Clinical Neurophysiology, ISSN 0736-0258, 01/2018, Volume 35, Issue 1, pp. e3 - e7
INTRODUCTION:Familial hemiplegic migraine (FHM) is a genetic disease with a variable clinical phenotype. The imaging and electroencephalogram (EEG) correlates... 
Familial hemiplegic migraine | ATP1A2 | EEG | Encephalopathy | NEUROSCIENCES | SPREADING DEPRESSION | CLINICAL NEUROLOGY | Index Medicus
Journal Article
Neurology, ISSN 0028-3878, 01/2018, Volume 90, Issue 7, pp. e575 - e582
OBJECTIVETo investigate whether the clinical characteristics of patients with hemiplegic migraine with and without autosomal dominant mutations in CACNA1A,... 
INDIVIDUALS | METAANALYSIS | CHANNEL | PRRT2 GENE | FAMILIAL MIGRAINE | SUSCEPTIBILITY LOCI | PAROXYSMAL KINESIGENIC DYSKINESIA | EPISODIC ATAXIA | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | PATHOPHYSIOLOGY
Journal Article
Headache: The Journal of Head and Face Pain, ISSN 0017-8748, 06/2019, Volume 59, Issue 6, pp. 917 - 923
Objective To explore the neuropsychological correlates and implications of familial hemiplegic migraines (FHMs). Background FMH is a rare, autosomal dominant... 
neuropsychology | familial hemiplegic migraine | baseline testing | CLINICAL NEUROLOGY | Case studies | Migraine | Cerebellum | Headache | Psychology | Cognitive ability | Information processing | Impairment | Measuring techniques
Journal Article
Cephalalgia, ISSN 0333-1024, 8/2014, Volume 34, Issue 9, pp. 708 - 711
Background Familial hemiplegic migraine (FHM) is a rare monogenic subtype of migraine with aura that includes motor auras. Prophylactic treatment of FHM often... 
familial hemiplegic migraine | ion transport | anticonvulsants | Migraine | neurogenetics | PROPHYLAXIS | ATTACKS | AURA | NEUROSCIENCES | CLINICAL NEUROLOGY
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 09/2018, Volume 392, pp. 22 - 27
Familial hemiplegic migraine (FHM) is a rare monogenic form of migraine with aura with three distinct genetic subtypes (FHM1-3). Imaging studies during acute... 
Familial hemiplegic migraine | ATP1A2 | MRI | Perfusion | FHM2 | CT | HYPERPERFUSION | MECHANISMS | NEUROSCIENCES | CLINICAL NEUROLOGY | PATHOPHYSIOLOGY | ENCEPHALOPATHY | EDEMA | MUTATION | BIPHASIC NEUROVASCULAR CHANGES | AURA | COMA | CT imaging | Genetic aspects | Diagnostic imaging | Migraine | Index Medicus
Journal Article
Cephalalgia, ISSN 0333-1024, 11/2017, Volume 37, Issue 13, pp. 1294 - 1298
Background Familial hemiplegic migraine (FHM) is a rare type of migraine with aura that is characterized by transient hemiparesis. Mutations in three genes... 
familial hemiplegic migraine | SCN1A gene | China | Migraine | NEUROSCIENCES | CLINICAL NEUROLOGY | Young Adult | Migraine Disorders - genetics | Pedigree | Humans | Middle Aged | NAV1.1 Voltage-Gated Sodium Channel - genetics | Adolescent | Asian Continental Ancestry Group - genetics | Adult | Female | Male | Mutation, Missense | Index Medicus
Journal Article
Cephalalgia, ISSN 0333-1024, 11/2014, Volume 34, Issue 13, pp. 1062 - 1069
Background Familial hemiplegic migraine (FHM) is a rare monogenic subtype of migraine with aura, characterized by motor auras. The majority of FHM families... 
familial hemiplegic migraine | SCN1A gene | Migraine | ion channel defects | Amino Acid Sequence | Humans | Middle Aged | NAV1.1 Voltage-Gated Sodium Channel - genetics | Molecular Sequence Data | Male | Young Adult | DNA Mutational Analysis | Pedigree | Adolescent | Age of Onset | Adult | Female | Aged | Migraine with Aura - genetics | Mutation | Child | Index Medicus
Journal Article
CEPHALALGIA, ISSN 0333-1024, 11/2014, Volume 34, Issue 13, pp. 1062 - 1069
Background Familial hemiplegic migraine (FHM) is a rare monogenic subtype of migraine with aura, characterized by motor auras. The majority of FHM families... 
GENE-MUTATIONS | familial hemiplegic migraine | Migraine | SCNIA gene | MECHANISMS | NEUROSCIENCES | ion channel defects | CLINICAL NEUROLOGY | NA+-CHANNEL | INACTIVATION | PRRT2 MUTATIONS | SODIUM-CHANNEL SCN1A | SEVERE MYOCLONIC EPILEPSY | INFANTILE CONVULSIONS | PAROXYSMAL KINESIGENIC DYSKINESIA | EPISODIC ATAXIA
Journal Article