Pathogenesis of cerebral malformations in human fetuses with meningomyelocele
نویسندگان
چکیده
منابع مشابه
Exome Sequencing in Fetuses with Structural Malformations
Prenatal diagnostic testing is a rapidly advancing field. An accurate diagnosis of structural anomalies and additional abnormalities in fetuses with structural anomalies is important to allow "triage" and designation of prognosis. This will allow parents to make an informed decision relating to the pregnancy. This review outlines the current tests used in prenatal diagnosis, focusing particular...
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چکیده ندارد.
15 صفحه اولImmune response in human cerebral cavernous malformations.
BACKGROUND AND PURPOSE Preliminary observations suggesting the presence of B and plasma cells and oligoclonality of immunoglobulin (Ig) G in cerebral cavernous malformations (CCM) have motivated a systematic study correlating the infiltration of the immune cells with clinical activity and antigen-triggered immune response in surgically excised lesions. METHODS Infiltration of plasma, B, T, an...
متن کاملPediatric cerebral cavernous malformations: Genetics, pathogenesis, and management
Case 1 A 2‐year‐old Hispanic girl presented with a 3‐day history of vomiting followed by a sudden onset of right facial droop and right eye ptosis. She had achieved normal developmental milestones until then. In retrospect, she had several months of occasional left leg weakness causing falls. There was no history of seizures. She had a family history with two second‐degree relatives with cerebr...
متن کاملGenetic Malformations of the Human Cerebral Cortex
This review outlines human genetic disorders that proIf flies had a cerebral cortex, figuring out how it develduce a morphologically abnormal cerebral cortex. Other oped would be relatively simple. You could perform dedisorders are associated with a grossly normal cortex liberate, random mutagenesis and screen flies for cortithat nonetheless does not function properly—such as cal abnormalities ...
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ژورنال
عنوان ژورنال: Cerebrospinal Fluid Research
سال: 2008
ISSN: 1743-8454
DOI: 10.1186/1743-8454-5-4