• "Creation of the Scaphocephalic Index: Measurement of Global and Regional Severity in Scaphocephaly"
• A Systematic Review of Idiopathic Secondary Stenosis Following Index Surgery for Craniosynostosis
• Apert Syndrome - caveats of squint management
• Are patients with syndromic craniosynostosis at greater risk for epilepsy than patients with non-syndromic craniosynostosis?
• Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
• Cognitive Outcomes of Children With Sagittal Craniosynostosis Treated With Either Endoscopic or Open Calvarial Vault Surgery
• Combined Dynamic Osteotomies for Craniosynostosis
• Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosis
• Craniosynostosis in primary metabolic bone disorders: a single-institution experience
• Does the participation of a senior plastic surgeon improve conditions of hospitalisation in craniosynostosis repair surgery?
• Dog breeds and conformations in the UK in 2019: VetCompass canine demography and some consequent welfare implications
• Effect of continuous positive airway pressure helmet on respiratory function following surgical procedures in brachycephalic dogs: A randomized controlled trial
• Endoscopic surgery for craniosynostosis: a bibliometric analysis of primary studies
• Evaluation of neurocognitive and social developments after craniosynostosis surgery
• Evaluation of risk factors for sleep-disordered breathing in dogs
• Exosome-mediated small interfering RNA delivery inhibits aberrant osteoblast differentiation in Apert syndrome model mice
• Experiences of surgical complications and reoperations in nonsyndromic sagittal synostosis patients in Oulu
• Frequency and predictors of concurrent complications in multi-suture release for syndromic craniosynostosis
• Geometric growth of the normal human craniocervical junction from 0 to 18 years old
• Hypophosphatasia
• Implementation of an Enhanced Recovery After Surgery Protocol for Cranial Vault Remodeling Procedures
• Incidence of Nonsynostotic Plagiocephaly and Developmental Disorders
• Intracranial Pressure, Autoregulation, and Cerebral Perfusion in Infants With Nonsyndromic Craniosynostosis at the Time of Surgical Correction
• Long-term sequelae of normocephalic pansynostosis: a rare but insidious entity
• Low Prevalence of Clinically Significant Hyponatremia following Cranial Vault Reconstruction for Single-Suture Craniosynostosis
• Measurement of Upper Airway Volume in Children with Craniofacial Abnormalities
• Measuring coagulopathy in pediatric craniofacial surgery
• Minimal adverse events occur when inducing emesis with apomorphine in brachycephalic, mesocephalic, and dolichocephalic dogs
• Morphometric analysis and outcomes following posterior cranial vault distraction in syndromic and multisuture craniosynostosis
• Multicenter comparison of head shape outcomes for three minimally invasive strip craniectomy techniques for sagittal craniosynostosis
• Neurocognitive outcomes and associated clinical factors 5 years after surgery in children with craniosynostosis
• Neurosurgical Outcomes Among Non-English Speakers: A Systematic Review and a Framework for Future Research
• Optic neuropathy in craniosynostosis
• Oral health knowledge, attitude and practice among parents of children with craniofacial syndromes
• Outcomes of the early endoscopic-assisted suturectomy for treatment of multisuture craniosynostosis
• Pfeiffer Syndrome
• Photogrammetry Applied to Neurosurgery: A Literature Review
• Prevalence of craniosynostosis in Finland, 1987-2010: A population-based study
• Re-imagining early cloverleaf skull deformity management from front to back approach-30 years on
• Regulatory role and mechanism of primary cilia in craniofacial and dental development
• Safety, Pharmacokinetics, and Pharmacodynamics of Efzimfotase Alfa, a Second-generation Enzyme Replacement Therapy: Phase 1, Dose-escalation Study in Adults with Hypophosphatasia
• 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
• Sports participation after craniosynostosis repair: the critical role of post-operative guidance in parental decision-making
• Tendon-associated gene expression precedes osteogenesis in mid-palatal suture establishment
• The Craniofacial Collaboration UK: Developmental Outcomes in 7- and 10-Year-Old Children With Metopic Synostosis
• The Craniofacial Collaboration UK: Developmental Outcomes in 7- and 10-Year-Old Children With Sagittal Synostosis
• The influence of orbital architecture on strabismus in craniosynostosis
• The Outcome of Inferior Oblique Myectomy for Apparent Inferior Oblique Overaction Associated with Craniosynostosis
• The regulatory role and mechanism of primary cilia in craniofacial and dental development
• Tranexamic acid decreases transfusion requirements during the modified pi-plasty procedure for sagittal craniosynostosis
• Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes
• Treatment Delays in Nonsyndromic Craniosynostosis: A 30-Year Retrospective Case-Control Analysis of the Impact of Socioeconomic and Family Status on Access to Care
• Undiagnosed sagittal synostosis as cause of "idiopathic" intracranial hypertension
• Use of piezoelectric instrumentation in craniofacial surgery
• Vaulting further: cranial vault expansion for craniocerebral disproportion without primary craniosynostosis