COL4A1 mutations should not be a contraindication for epilepsy surgery

Severe Hemolytic Jaundice in a Neonate with a Novel COL4A1 Mutation

Allelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutations

COL4A1 Mutation Revealed by an Isolated Brain Hemorrhage

Variants of Anterior Segment Dysgenesis and Cerebral Involvement in a Large Family With a Novel COL4A1 Mutation

Phenotypic Spectrum of COL4A1 Mutations: Porencephaly to Schizencephaly

Recognizable phenotypes associated with intracranial calcification

Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency

COL4A1-Related Disease: Raised Creatine Kinase and Cerebral Calcification as Useful Pointers.

Fetal intracerebral hemorrhage and COL4A1 mutation: promise and uncertainty.

Prenatal genetic confirmation of a COL4A1 mutation presenting with sonographic fetal intracranial hemorrhage.

A new family with autosomal dominant porencephaly with a novel COL4A1 mutation. Are arachnoid cysts related to COL4A1 mutations?

COL4A2 mutation associated with familial porencephaly and small-vessel disease.

Intracerebral Hemorrhage and COL4A1 and COL4A2 Mutations, from Fetal Life into Adulthood.

COL4A2 Mutations Impair COL4A1 and COL4A2 Secretion and Cause Hemorrhagic Stroke.

De Novo and Inherited Mutations in COL4A2, Encoding the Type IV Collagen a2 Chain Cause Porencephaly

Atypical timing and presentation of periventricular haemorrhagic infarction in preterm infants: the role of thrombophilia.

COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans.

Fetal Origin of Brain Damage in 2 Infants with a COL4A1 Mutation: Fetal and Neonatal MRI.

ANTI-A B AUTOANTIBODIES IN THE CSF OF A PATIENT WITH CAA-RELATED INFLAMMATION: A CASE REPORT.