• A Twist-Box domain of the C. elegans Twist homolog, HLH-8, plays a complex role in transcriptional regulation
• Apert Syndrome Type III Hand: Prevalence and Outcomes
• Apert syndrome: a rare clinical image
• Apert syndrome: craniofacial challenges and clinical implications
• Apert syndrome: neurosurgical outcomes and complications following posterior vault distraction osteogenesis
• Apert Syndrome: Selection Rationale for Midface Advancement Technique
• Automated three-dimensional analysis of facial asymmetry in patients with syndromic coronal synostosis: A retrospective study
• Case report: A third variant in the 5' UTR of <em>TWIST1</em> creates a novel upstream translation initiation site in a child with Saethre-Chotzen syndrome
• Clinical and operative risk factors for complications after Apert hand syndactyly reconstruction
• Comparison of Internal and External Distraction in Frontofacial Monobloc Advancement: A Three-Dimensional Quantification
• Discussion of "Does the Mutation Type Affect the Response to Cranial Vault Expansion in Children With Apert Syndrome?"
• Discussion: Two-Center Review of Posterior Vault Expansion following a Staged or Expectant Treatment of Crouzon and Apert Craniosynostosis
• Does the Mutation Type Affect the Response to Cranial Vault Expansion in Children With Apert Syndrome?
• Exosome-mediated small interfering RNA delivery inhibits aberrant osteoblast differentiation in Apert syndrome model mice
• Facial Fat Graft Injection Reduces Asymmetry and Improves Forehead Contour in Early Infancy Apert Syndrome Patients
• Genetic Heterogeneity, Craniofacial Surgical Burden, and Surgical Techniques in Patients With Saethre-Chotzen Syndrome
• Left Ophthalmic Segment Internal Carotid Artery Aneurysm Treated with Flow Diversion in a Child with Apert Syndrome: Technical Note
• Measurement of the Neutrophils Count and Oxidative Burst in Neutrophils of Patients with Sanjad Sakati Syndrome
• Molecular Scalpels: The Future of Pediatric Craniofacial Surgery?
• Patient Tailored Surgery in Saethre-Chotzen Syndrome: Analysis of Reoperation for Intracranial Hypertension
• Perinatal imaging findings of a fetus with Pfeiffer syndrome and a heterozygous c.1019A>G, p.Tyr340Cys (Y340C) mutation in FGFR2 presenting a cloverleaf skull, craniosynostosis and short limbs on prenatal ultrasound mimicking thanatophoric dysplasia ty
• Pfeiffer Syndrome
• Pfeiffer Syndrome
• Sensitivity, specificity and cutoff identifying optic atrophy by macular ganglion cell layer volume in syndromic craniosynostosis
• Sensitivity, Specificity, and Cutoff Identifying Optic Atrophy by Macular Ganglion Cell Layer Volume in Syndromic Craniosynostosis
• Ser252Trp mutation in fibroblast growth factor receptor 2 promotes branching morphogenesis in mouse salivary glands
• Skull progenitor cell-driven meningeal lymphatic restoration improves neurocognitive functions in craniosynostosis
• Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis
• Syndromic Craniofacial Disorders
• Syndromic Craniosynostosis: A Comprehensive Review
• The influence of orbital architecture on strabismus in craniosynostosis
• The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients
• The Role of Airway Management on Feeding Difficulties in Children With Pfeiffer Syndrome
• The role of pathogenic TCF12 variants in children with coronal craniosynostosis-a systematic review with addition of two novel cases
• Webplasty using an external fixator for complex syndactyly caused by Apert syndrome
• Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports