• <em>COL4A1</em> gene mutations and perinatal intracranial hemorrhage in neonates: case reports and literature review
• <em>Col4a2</em> Mutations Contribute to Infantile Epileptic Spasm Syndrome and Neuroinflammation
• "I Do not know them" - Capgras syndrome associated with porencephaly and agenesis of the Splenium
• A case of a surviving co-twin diagnosed with porencephaly and renal hypoplasia after a single intrauterine fetal death at 21 weeks of gestation in a monochorionic monoamniotic twin pregnancy
• A case of left congenital homonymous hemianopia associated with right occipital porencephaly
• A case of tubulinopathy presenting with porencephaly caused by a novel missense mutation in the TUBA1A gene
• A Giant Porencephaly: A Rare Etiology of Pediatric Seizures
• A porencephalic cyst formation in a 6-year-old female with a functioning ventriculoperitoneal shunt: a case-based review
• Abnormalities of the Fetal Central Nervous System: Prenatal US Diagnosis with Postnatal Correlation
• Aggressive Pyogenic Spondylitis Caused by <em>S. constellatus</em>: A Case Report
• An Atypical Porencephalic Cyst Manifesting as a Simple Partial Seizure: A Case Report and Literature Review
• An Iatrogenic Model of Brain Small-Vessel Disease: Post-Radiation Encephalopathy
• Are postnatal traumatic events an underestimated cause of porencephalic lesions in dogs and cats?
• Asymmetry of the bilateral bispectral index in a hemiparetic patient with porencephaly
• Basement membrane collagen IV: Isolation of functional domains
• Biallelic Variants in the <em>COLGALT1</em> Gene Causes Severe Congenital Porencephaly: A Case Report
• Biallelic Variants in the COLGALT1 Gene Causes Severe Congenital Porencephaly: A Case Report
• Case Report: Complex Congenital Brain Anomaly in a BBxHF Calf-Clinical Signs, Magnetic Resonance Imaging, and Pathological Findings
• Case report: Temporal alterations in vascular function during the first 2 weeks of pediatric septic shock
• Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
• Clinical Features, Imaging Characteristics, and Long-term Outcome of Dogs with Cranial Meningocele or Meningoencephalocele
• COL4A1 Mutation in a Neonate With Intrauterine Stroke and Anterior Segment Dysgenesis
• COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans
• COL4A1 mutations in two infants with congenital cataracts and porencephaly: an ophthalmologic perspective
• COL4A1 MUTATIONS IN TWO INFANTS WITH CONGENITAL CATARACTS AND PORENCEPHALY: AN OPHTHALMOLOGIC PERSPECTIVE
• COL4A1-related disorder as a mimic of congenital TORCHES infection-Expanding the clinical, neuroimaging and genotype spectrum
• Collagen glycosylation
• Congenital cerebral and cerebellar anomalies in relation to bovine viral diarrhoea virus and Akabane virus in newborn calves
• Discordant electroencephalogram epileptiform activity and hemispherectomy in children with refractory epilepsy and encephaloclastic lesions: a case series
• Edge-to-edge repair of the systolic anterior motion of mitral valve and cardiac myectomy of the abnormally positioned papillary muscles in an infant with <em>COL4A1</em> mutation
• Expanding Ventricular Diverticulum Overlying the Cerebral Hemisphere through an Open-Lip Schizencephalic Cleft: A Report of Two Pediatric Cases
• Expression of Concern: A Giant Porencephaly: A Rare Etiology of Pediatric Seizures
• Fetal cytomegalovirus infection
• Fetal stroke and cerebrovascular disease: Advances in understanding from lenticulostriate and venous imaging, alloimmune thrombocytopaenia and monochorionic twins
• Fetopathic effects of experimental Schmallenberg virus infection in pregnant goats
• Further refinement of COL4A1 and COL4A2 related cortical malformations
• Hemispheric surgery in children: perisylvian technique
• Hypodipsic hypernatremia after long-standing polydipsia in a cat with suspect neonatal head trauma
• Identification of fibronectin 1 as a candidate genetic modifier in a Col4a1 mutant mouse model of Gould syndrome
• Increased Susceptibility to Postoperative PCA Morphine-Induced Respiratory Depression in a Patient with an Undiagnosed Traumatic Porencephalic Cyst - A Case Report
• Infantile hemiparesis and porencephaly due to a COL4A1 mutation: Gould syndrome
• Intraparenchymal hemorrhage and cerebral venous thrombosis in an adult with congenital porencephalic cyst presenting for generalized tonic-clonic seizures
• Intravenous Alteplase for Acute Stroke and Pulmonary Embolism in a Patient With Recent Abdominoplasty
• Leukoencephalopathy with spot-like calcifications caused by recessive COL4A2 variants
• Life-threatening muscle complications of COL4A1-related disorder
• Multilobar Epilepsy Surgery in Childhood and Adolescence: Predictors of Long-Term Seizure Freedom
• Multiorgan manifestations of COL4A1 and COL4A2 variants and proposal for a clinical management protocol
• Neuroimaging Perspectives of Perinatal Arterial Ischemic Stroke
• Neuropsychological presentation of colpocephaly and porencephaly with symptom onset in adulthood
• Novel <em>COL4A1</em> mutation in a fetus with early prenatal onset of schizencephaly
• Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations
• Novel COL4A2 mutation causing familial malformations of cortical development
• Novel COL4A2 variant in a large pedigree: Consequences and dilemmas
• Novel Variant in COL4A1 Causes Extensive Prenatal Intracranial Hemorrhage and Porencephaly
• Optic Nerve Hypoplasia, Corpus Callosum Agenesis, Cataract, and Lissencephaly in a Neonate with a Novel<em>COL4A1</em> Mutation
• p.Gly743Val Mutation in COL4A1 Is Responsible for Familial Porencephaly and Severe Hypermetropia
• Phenotypic characterization of COL4A1-related West syndrome
• Phentermine Use During First and Second Trimesters Associated with Fetal Stroke
• Phenytoin-induced dyskinesia: a case report
• Polysulfone tailor-made implant for the surgical correction of a frontoparietal meningoencephalocoele in a cat
• Porencephalic cyst in adult
• Porencephalic cyst: a rare cause of new-onset seizure in an adult
• Porencephaly and Intracranial Calcifications in a Neonate
• Porencephaly and Periventricular Encephalitis in a 4-month-old Puppy: Detection of Canine Parvovirus Type 2 and Potential Role in Brain Lesions
• Porencephaly causing limb size asymmetry
• Porencephaly in an Italian neonate with foetal alcohol spectrum disorder: A case report
• Porencephaly may Present even in Elderly
• Porencephaly with an optic organ abnormality in a beagle dog
• Post-traumatic cysts detected by ultrasound in infant presented with first-time seizures: Case report
• Potential risks associated with laparoscopic gastrostomy in patients with the COL4A1 variant: Two case reports
• Prenatal clinical manifestations in individuals with <em>COL4A1/2</em> variants
• Prenatal Diagnosis of <em>COL4A1</em> Mutations in Eight Cases: Further Delineation of the Neurohistopathological Phenotype
• Prenatal diagnosis of familial porencephaly associated with fetal stroke
• Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesions
• Progressive cerebral atrophies in three children with COL4A1 mutations
• Pseudo-porencephaly Mimicking Multiple Intracerebral Hemorrhages
• Pseudo-porencephaly With Structural Epilepsy After Perinatal Intracerebral Bleeding
• Psychosis Associated with Acquired Porencephaly-Cause or Incidental Finding? Case Report and Review of Literature
• Relationships among clinic, home, and ambulatory blood pressures with small vessel disease of the brain and functional status in older people with hypertension
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• Retraction: A Giant Porencephaly: A Rare Etiology of Pediatric Seizures
• Risk factors and results of hemispherotomy reoperations in children
• Schizencephaly and Porencephaly Due to Fetal Intracranial Hemorrhage: A Report of Two Cases
• Schizencephaly in Hereditary Hemorrhagic Telangiectasia
• Schmallenberg virus affects T-bet, Gata3, RoRrγt, Foxp3 and Eomes in mice brain
• Sonographic spectrum and postnatal outcomes of early-onset versus late-onset fetal cerebral ventriculomegaly
• Spectrum of Fetal Intraparenchymal Hemorrhage in COL4A1/A2-Related Disorders
• Successful hemispherotomy in two refractory epilepsy patients with cerebral hemiatrophy and contralateral EEG abnormalities
• Surgical management of pediatric patients with encephalopathy due to electrical status epilepticus during sleep (ESES)
• Surgical strategy for refractory epilepsy secondary to porencephaly: ictal SPECT may obviate the need for intracranial electroencephalography. Patient series
• Targeted re-sequencing in pediatric and perinatal stroke
• Teaching NeuroImage: Porencephaly and Hemorrhage in Infantile COL4A2-Related Cerebral Microangiopathy
• Teratogenic bluetongue and related orbivirus infections in pregnant ruminant livestock: timing and pathogen genetics are critical
• The <em>Col4a2^{em1(IMPC)Wtsi}</em> mouse line: lessons from the Deciphering the Mechanisms of Developmental Disorders program
• The spectrum of brain malformations and disruptions in twins
• Trends in the prevalence and characteristics of unilateral spastic cerebral palsy in patients born between 1988 and 2007 in Okinawa, Japan
• Vasospasm Following Hemispherectomy: A Case Report of a Novel Complication
• Vein of Galen Aneurysmal Malformation
• Ventriculoperitoneal shunt for giant porencephaly: a case report and literature review
• Whole genome sequencing unveils genetic heterogeneity in optic nerve hypoplasia