Intracerebral hemorrhage and COL4A1 and COL4A2 mutations, from fetal life into adulthood
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.23544/fullpdf
Reference21 articles.
1. Cadasil;Chabriat;Lancet Neurol,2009
2. Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease;Hara;N Engl J Med,2009
3. C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy;Richards;Nat Genet,2007
4. COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage;Weng;Ann Neurol,2012
5. First prenatal genetic confirmation of a COL4A1 mutation presenting with sonographic fetal intracranial hemorrhage;Lichtenbelt;Ultrasound Obstet Gynecol,2012
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1. Perinatal and long‐term outcomes of fetal intracranial hemorrhage: systematic review and meta‐analysis;Ultrasound in Obstetrics & Gynecology;2021-09-16
2. Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesions;Ultrasound in Obstetrics & Gynecology;2021-05
3. Genetic Profiling of Idiopathic Antenatal Intracranial Haemorrhage: What We Know?;Genes;2021-04-15
4. Phenotypic characterization of COL4A1-related West syndrome;Epilepsy Research;2020-08
5. Venous pathologies in paediatric neuroradiology: from foetal to adolescent life;Neuroradiology;2019-11-09
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