|
|
Volumn 2012, Issue , 2012, Pages
|
|
Neonatal stroke associated with de novo antiphospholipid antibody and homozygous 1298C/C methylenetetrahydrofolate reductase mutation.
|
|
Author keywords
[No Author keywords available]
|
|
Indexed keywords
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
PHOSPHOLIPID ANTIBODY;
PLASMINOGEN ACTIVATOR INHIBITOR 1;
ANTIPHOSPHOLIPID SYNDROME;
ARTICLE;
BIOSYNTHESIS;
BLOOD;
BRAIN ISCHEMIA;
CASE REPORT;
CEREBROVASCULAR ACCIDENT;
FEMALE;
GENETIC POLYMORPHISM;
GENETICS;
HOMOZYGOTE;
HUMAN;
MUTATION;
NEWBORN;
ANTIBODIES, ANTIPHOSPHOLIPID;
ANTIPHOSPHOLIPID SYNDROME;
BRAIN ISCHEMIA;
FEMALE;
HOMOZYGOTE;
HUMANS;
INFANT, NEWBORN;
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
MUTATION;
PLASMINOGEN ACTIVATOR INHIBITOR 1;
POLYMORPHISM, GENETIC;
STROKE;
MLCS;
MLOWN;
|
|
EID: 84878461122
PISSN: None
EISSN: 1757790X
Source Type: Journal
DOI: 10.1136/bcr-2012-006451 Document Type: Article |
|
Times cited : (8)
|
|
References (0)
|
