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index medicus (193) 193
humans (181) 181
episodic ataxia type-2 (176) 176
familial hemiplegic migraine (118) 118
clinical neurology (116) 116
neurosciences (101) 101
animals (80) 80
male (77) 77
calcium channels - genetics (74) 74
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epilepsy (36) 36
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middle aged (34) 34
mice (31) 31
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phenotype (29) 29
ataxia - genetics (28) 28
analysis (27) 27
cacna1a gene (27) 27
cacna1a (26) 26
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type-2 (26) 26
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gene (24) 24
genetics (24) 24
migraine with aura - genetics (24) 24
mutations (24) 24
cerebellar-ataxia (23) 23
child (23) 23
cortical spreading depression (23) 23
vertigo (23) 23
adolescent (20) 20
hemiplegic migraine (20) 20
hypokalemic periodic paralysis (20) 20
cerebellum (19) 19
downbeat nystagmus (19) 19
frontal-lobe epilepsy (19) 19
mutation - genetics (19) 19
aged (18) 18
biochemistry & molecular biology (18) 18
genetics & heredity (18) 18
medicine & public health (18) 18
migraine disorders - physiopathology (18) 18
abridged index medicus (17) 17
research (17) 17
channelopathies (16) 16
clinical spectrum (16) 16
disease models, animal (16) 16
dna mutational analysis (16) 16
gene mutations (16) 16
idiopathic generalized epilepsy (16) 16
magnetic resonance imaging (16) 16
molecular sequence data (16) 16
potassium channel gene (16) 16
acetazolamide (15) 15
channelopathy (15) 15
childhood absence epilepsy (15) 15
dizziness (15) 15
ion channels - genetics (15) 15
menieres-disease (15) 15
migraine disorders - complications (15) 15
missense mutation (15) 15
progressive ataxia (15) 15
spinocerebellar ataxia (15) 15
aura (14) 14
calcium channel (14) 14
calcium channels, n-type - genetics (14) 14
cerebellar ataxia - genetics (14) 14
epilepsy - genetics (14) 14
genes (14) 14
pharmacology & pharmacy (14) 14
physiological aspects (14) 14
calcium channels - physiology (13) 13
genotype (13) 13
headache (13) 13
nystagmus (13) 13
vestibular migraine (13) 13
amino acid sequence (12) 12
ca2+ channels (12) 12
calcium (12) 12
cerebellar ataxia (12) 12
ion channels (12) 12
ion channels - physiology (12) 12
migraine disorders - diagnosis (12) 12
migraine with aura - physiopathology (12) 12
mutation, missense (12) 12
severe myoclonic epilepsy (12) 12
synaptic-transmission (12) 12
acetazolamide - therapeutic use (11) 11
ataxia - physiopathology (11) 11
calcium channels - metabolism (11) 11
diagnosis (11) 11
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Cancer Research, ISSN 0008-5472, 04/2005, Volume 65, Issue 8, pp. 3299 - 3306
Cells exposed to hypoxia respond by increasing the level of hypoxia-inducible factor-1 (HIF-1). This factor then activates a number of genes by binding to... 
HEMIPLEGIC MIGRAINE | ANDROGEN RECEPTOR | FACTOR 1-ALPHA | DNA-BINDING | ONCOLOGY | EPISODIC ATAXIA TYPE-2 | SARCOMA-ASSOCIATED HERPESVIRUS | ENDOTHELIAL-CELLS | TUMOR-SUPPRESSOR PROTEIN | FACTOR-I | TRANSCRIPTION FACTOR
Journal Article
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, ISSN 0031-6768, 07/2010, Volume 460, Issue 2, pp. 375 - 393
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 10/2015, Volume 23, Issue 11, pp. 1505 - 1512
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CEPHALALGIA, ISSN 0333-1024, 10/2014, Volume 34, Issue 12, pp. 959 - 967
Aim:The aim of this study was to assess biochemical changes in the brain of patients with hemiplegic migraine in between attacks. Methods:Eighteen patients... 
ATROPHY | Migraine | magnetic resonance spectroscopy | DISORDERS | FHM | imaging | NEUROSCIENCES | CLINICAL NEUROLOGY | genetics | MAGNETIC-RESONANCE-SPECTROSCOPY | GENE | EPISODIC ATAXIA TYPE-2 | HEADACHES | MUTATIONS | SPECTRUM | CALCIUM-CHANNEL | HYPOTHALAMUS
Journal Article
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, ISSN 0167-4889, 07/2016, Volume 1863, Issue 7, pp. 1791 - 1798
During the past two decades, many pathological genetic variants in SCN5A, the gene encoding the pore-forming subunit of the cardiac (monomeric) sodium channel... 
BRUGADA-SYNDROME | EPISODIC ATAXIA TYPE-2 | PROTEIN-QUALITY CONTROL | VENTRICULAR-TACHYCARDIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRUNCATED CONSTRUCTS | SEVERE MYOCLONIC EPILEPSY | ENDOPLASMIC-RETICULUM | BETA-SUBUNITS | LONG-QT SYNDROME | CALCIUM-CHANNEL | CELL BIOLOGY
Journal Article
PLoS Genetics, ISSN 1553-7390, 07/2017, Volume 13, Issue 7, pp. e1006905 - e1006905
Journal Article
European Journal of Neurology, ISSN 1351-5101, 01/2019, Volume 26, Issue 1, pp. 66 - e7
Background and purpose CACNA1A encodes the alpha 1 subunit of the neuronal calcium channel P/Q. CACNA1A mutations underlie three allelic disorders: familial... 
episodic ataxia type 2 | neuropsychological testing | CACNA1A | developmental delay | familial hemiplegic migraine type 1 | SPORADIC HEMIPLEGIC MIGRAINE | DELAYED CEREBRAL EDEMA | CEREBELLAR DYSFUNCTION | MENTAL-RETARDATION | COGNITIVE IMPAIRMENT | MINOR HEAD TRAUMA | NEUROSCIENCES | CLINICAL NEUROLOGY | SPINOCEREBELLAR ATAXIA | EPISODIC ATAXIA TYPE-2 | CALCIUM-CHANNEL | EPILEPTIC ENCEPHALOPATHY | Psychomotor Performance | Comorbidity | Humans | Nervous System Diseases - psychology | Child, Preschool | Genotype | Male | Educational Status | Nervous System Diseases - genetics | Mental Disorders - psychology | Neuropsychological Tests | Young Adult | Mental Disorders - genetics | Phenotype | Cerebellar Ataxia - genetics | Migraine Disorders - genetics | Adolescent | Adult | Female | Retrospective Studies | Ataxia - genetics | Calcium Channels - genetics | Child | Spinocerebellar Ataxias - genetics | Medicine, Experimental | Medical research | Calcium channels | Genetic aspects | Analysis | Migraine | Headache | Calcium | Mental disorders | Psychology | Memory | Disorders | Cognitive ability | Data bases | Delay | Literature reviews | Databases | Spinocerebellar ataxia | Ataxia | Genetics | Differential diagnosis | Children | Genotypes | Phenotypes | Case reports | Measuring techniques | Patients | Neurology | Psychomotor performance | Mutation | Index Medicus
Journal Article
NEUROLOGY, ISSN 0028-3878, 09/2010, Volume 75, Issue 10, pp. 937 - 938
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