Disease: Prosencephaly cerebellar dysgenesis
- A case of tubulinopathy presenting with porencephaly caused by a novel missense mutation in the TUBA1A gene
- A new family with autosomal dominant porencephaly with a novel Col4A1 mutation. Are arachnoid cysts related to Col4A1 mutations?
- Abnormalities of the Fetal Central Nervous System: Prenatal US Diagnosis with Postnatal Correlation
- An Iatrogenic Model of Brain Small-Vessel Disease: Post-Radiation Encephalopathy
- Case Report: Complex Congenital Brain Anomaly in a BBxHF Calf-Clinical Signs, Magnetic Resonance Imaging, and Pathological Findings
- CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study
- COL4A2 mutation associated with familial porencephaly and small-vessel disease
- Magnetic resonance imaging of intracranial malformations in dogs and cats
- Molecular and phenotypic spectrum of ASPM-related primary microcephaly: Identification of eight novel mutations
- Ovine and Bovine Congenital Abnormalities Associated With Intrauterine Infection With Schmallenberg Virus
- Porencephaly and cortical dysplasia as cause of seizures in a dog
- Porencephaly and hydranencephaly in six dogs
- Single forebrain ventricle without prosencephaly: agenesis of the corpus callosum with dehiscent fornices
- Sporadic COL4A1 mutations with extensive prenatal porencephaly resembling hydranencephaly
- The spectrum of brain malformations and disruptions in twins
- Uterine perforation by a cystoperitoneal shunt, an unusual cause of recurrent vaginal discharge