• 'Distraction Vaginogenesis': Preliminary Results Using a Novel Method for Vaginal Canal Expansion in Rats
• <em>ADAMTS18</em>-related anterior segment dysgenesis mistaken as Axenfeld-Rieger syndrome
• "Multisystem Inflammatory Syndrome in Children" (MIS-C) after COVID-19 Infection in the Metropolitan Area of Nuremberg-Erlangen, Germany-Expectations and Results of a Two-Year Period
• 4q25 Microdeletion with Axenfeld-Rieger Syndrome and Developmental Delay
• A case of Axenfeld-Rieger syndrome with retinal detachment
• A novel missense mutation of FOXC1 in an Axenfeld-Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature review
• A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome
• A patient with concurrent Axenfeld-Rieger and Stickler syndromes verified by molecular genetics
• A PITX2 splice-site mutation in a family with Axenfeld-Rieger syndrome leads to decreased expression of nuclear PITX2 protein
• A rare case of unilateral Axenfeld-Rieger anomaly associated with optic disc coloboma: A multimodal imaging canvas
• ADAMTS18-related anterior segment dysgenesis mistaken as Axenfeld-Rieger syndrome
• Adjunctive orthodontic therapy for prosthetic rehabilitation in a growing child with Axenfeld-Rieger syndrome: A case report
• Ahmed glaucoma implant and augmented MicroPulse transscleral cyclophotocoagulation in a monocular Axenfeld-Rieger syndrome patient with glaucoma
• Alternative Genetic Diagnoses in Axenfeld-Rieger Syndrome Spectrum
• Axenfeld anomaly with persistent pupillary membrane
• Axenfeld-Reiger syndrome: A search for the missing links
• Axenfeld-Rieger anomaly with slit pupils
• Axenfeld-Rieger Syndrome
• Axenfeld-Rieger Syndrome
• Axenfeld-Rieger Syndrome and Possible Airway Complications
• Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report
• Axenfeld-Rieger syndrome combined with ectropion uveae and pigment dispersion syndrome: A case report
• Axenfeld-Rieger syndrome in monozygotic twin brothers: Case report
• Axenfeld-Rieger syndrome in the pediatric population: A review
• Axenfeld-Rieger syndrome: a novel histopathologic finding associated with corneal abnormalities
• Axenfeld-Rieger syndrome: A systematic review examining genetic, neurological, and neurovascular associations to inform screening
• Axenfeld-Rieger syndrome: more than meets the eye
• Axenfeld-Rieger syndrome: ophthalmological and dental diagnostic and therapeutic options
• Axenfeld-Rieger syndrome: orthopedic and orthodontic management in a pediatric patient: a case report
• Bitot-like spots in children with normal vitamin A levels
• Cardiac anomalies in Axenfeld-Rieger syndrome
• Case report of the rare Peters' anomaly complicated with Axenfeld-Rieger syndrome: A case report and brief review of the literature
• Case report: Congenital mitral and tricuspid valve insufficiency in a patient with Axenfeld-Rieger syndrome
• Case Report: Congenital Pseudoacorea in an Ocular Axenfeld-Rieger Syndrome: What is it?
• Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome
• Characteristics of Corneal Endothelium in Axenfeld Rieger Spectrum
• Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features
• Clinical and Genetic Correlation in Neurocristopathies: Bridging a Precision Medicine Gap
• Commercial Gene Panels for Congenital Anterior Segment Anomalies: Are They All the Same?
• Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants
• Complete detachment of the Schwalbe's line in a case of Axenfeld-Reiger anomaly - A rare presentation
• Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger Syndrome
• Craniofacial and dental features of Axenfeld-Rieger syndrome patients with PITX2 mutations
• Dental and Craniofacial Manifestation of Axenfeld-Rieger Syndrome: A Case Report
• Dental and Maxillofacial Manifestations of Axenfeld-Rieger Syndrome: Presentation of a Case in a 5-Year-Old Girl
• Detection of metabolic syndrome with ATR-FTIR spectroscopy and chemometrics in blood plasma
• Distinct Roles of Histone Lysine Demethylases and Methyltransferases in Developmental Eye Disease
• Early-Onset Glaucoma in <em>egl1</em> Mice Homozygous for <em>Pitx2</em> Mutation
• Enamel defects of Axenfeld-Rieger syndrome and the role of PITX2 in its pathogenesis
• Evanescent, episodic salmon-colored macules in a young woman
• Extraocular muscle hypoplasia associated with Axenfeld-Rieger syndrome
• Familial 4p Interstitial Deletion Provides New Insights and Candidate Genes Underlying This Rare Condition
• First XEN implantation in Axenfeld- Rieger syndrome: A case report and literature review
• Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome
• Glaucoma drainage device implantation in a pregnant woman with axenfeld-rieger syndrome
• Glaucoma Syndromes: Insights into Glaucoma Genetics and Pathogenesis from Monogenic Syndromic Disorders
• Heterogeneity of Axenfeld-Rieger Syndrome: Molecular and Clinical Findings in Chinese Patients
• Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling
• Hyperproliferative embryotoxon simulating double cornea
• Identification and functional study of FOXC1 variants in Chinese families with glaucoma
• In Silico Characterization of Pathogenic Homeodomain Missense Mutations in the PITX2 Gene
• In Vivo Assessment of Retinal Phenotypes in Axenfeld-Rieger Syndrome
• Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2
• Intracranial injection of NK cells engineered with a HER2-targeted chimeric antigen receptor in patients with recurrent glioblastoma
• Intragenic FOXC1 deletion in a Vietnamese child with Axenfeld-Rieger syndrome: case report and review of literature
• Iris Ectropion Syndrome
• Laser corepraxy in mesodermal iris dysgenesis (Axenfeld-Rieger syndrome) (case report)
• Leukoencephalopathy with spot-like calcifications caused by recessive COL4A2 variants
• Loss of FOXC1 contributes to the corneal epithelial fate switch and pathogenesis
• Mechanistic Insights into Axenfeld-Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants
• Megalocornea
• Megalocornea
• Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delay
• Microspherophakia
• Microspherophakia: A clinical approach and mini review with a case report
• Modified horizontal muscle transposition without tenotomy and splitting for a case of inferior rectus and inferior oblique muscles aplasia with hemifacial microsomia
• Neuroimaging Findings in Axenfeld-Rieger Syndrome: A Case Series
• Oligodontia in the Clinical Spectrum of Syndromes: A Systematic Review
• Ophthalmological Manifestations of Axenfeld-Rieger Syndrome: Current Perspectives
• Penetrating Keratoplasty in Congenital Glaucoma
• Peripheral Anterior Synechiae as a Manifestation of Axenfeld-Rieger Anomaly
• Peters Anomaly
• Posterior embryotoxon as the initial ophthalmological sign of Axenfeld-Rieger syndrome
• Posterior segment findings in Axenfeld-Rieger syndrome
• Primary Cilium in Neural Crest Cells Crucial for Anterior Segment Development and Corneal Avascularity
• Progressive Vision Loss in a Patient With Axenfeld-Rieger Syndrome
• Refining medical clearance protocol for patients with primary psychiatric complaints in the emergency department
• Retropharyngeal Abscess With Mediastinal Extension: A Case Series and Review of the Literature
• SHORT Syndrome: an Update on Pathogenesis and Clinical Spectrum
• Speech Motor Profiles in Primary Progressive Aphasia
• Subcutaneous Sweet Syndrome Successfully Treated With Ustekinumab in a Patient With Ulcerative Colitis
• Surgical Outcomes of Glaucoma Drainage Device Implantation in Refractory Glaucoma Patients in Thailand
• The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning
• The clinical and genetic findings in a Chinese family with Axenfeld-Rieger syndrome
• The clinical outcomes of keratoplasty in irreversible corneal decompensation secondary to Axenfeld-Rieger syndrome
• The management of a Moroccan family with Axenfeld-Rieger syndrome
• The morphology of angle dysgenesis assessed by ultrasound biomicroscopy and its relationship with glaucoma severity and mutant genes in Axenfeld-Rieger syndrome
• The Ocular Neural Crest: Specification, Migration, and Then What?
• UNC-30/PITX coordinates neurotransmitter identity with postsynaptic GABA receptor clustering
• Whole genome sequencing in families with oligodontia