|
|
Volumn 23, Issue 1, 2002, Pages 7-10
|
|
Familial hemiplegic migraine: Clinical features and probable linkage to chromosome 1 in an Italian family
a
a
a
a
b
a
c
a
|
|
Author keywords
Cerebellar disease; Familial hemiplegic migraine; Linkage analysis
|
|
Indexed keywords
CALCIUM CHANNEL P TYPE;
CALCIUM CHANNEL Q TYPE;
ADULT;
ARTICLE;
CASE REPORT;
CEREBELLAR ATAXIA;
CEREBELLUM DISEASE;
CHROMOSOME 19P;
CHROMOSOME 1Q;
CHROMOSOME MARKER;
CLINICAL FEATURE;
CONTROLLED STUDY;
EPILEPSY;
FAMILIAL DISEASE;
FEMALE;
GENE MUTATION;
GENETIC HETEROGENEITY;
GENETIC LINKAGE;
HEAD INJURY;
HEMIPLEGIA;
HUMAN;
ITALY;
LINKAGE ANALYSIS;
MALE;
MENTAL DEFICIENCY;
MIGRAINE;
NEUROLOGIC EXAMINATION;
NYSTAGMUS;
PEDIGREE ANALYSIS;
RELATIVE;
SPEECH DISORDER;
ADULT;
APOLIPOPROTEIN A-II;
CALCIUM CHANNELS;
CEREBELLAR ATAXIA;
CEREBELLUM;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 1;
CHROMOSOMES, HUMAN, PAIR 19;
DNA MUTATIONAL ANALYSIS;
FEMALE;
GENE FREQUENCY;
GENETIC MARKERS;
GENETIC PREDISPOSITION TO DISEASE;
GENETIC SCREENING;
HUMANS;
ITALY;
LINKAGE (GENETICS);
MALE;
MIDDLE AGED;
MIGRAINE WITH AURA;
PEDIGREE;
PENETRANCE;
|
|
EID: 0036274795
PISSN: 15901874
EISSN: None
Source Type: Journal
DOI: 10.1007/s100720200016 Document Type: Article |
|
Times cited : (31)
|
|
References (10)
|
