• <em>Drosophila</em> Homolog of the Human Carpenter Syndrome Linked Gene, <em>MEGF8</em>, Is Required for Synapse Development and Function
• A case of Pfeiffer syndrome caused by FGFR2 gene variation
• A pediatric case of transient periictal MRI abnormalities after repeated seizures
• A Twist-Box domain of the C. elegans Twist homolog, HLH-8, plays a complex role in transcriptional regulation
• Absence of Bilateral Multiple Cyclovertical Muscle Insertions in a Patient With Pfeiffer Syndrome
• Apert Hand Reconstruction With Tilapia Skin
• Apert syndrome or acrocephalosyndactilia type I
• Apert Syndrome Outcomes: Comparison of Posterior Vault Distraction Osteogenesis Versus Fronto Orbital Advancement
• Apert Syndrome Type III Hand: Prevalence and Outcomes
• Apert syndrome: a rare clinical image
• Apert syndrome: an informative long-term dentofacial outcome
• 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
• Auricles Anomalies in Patients With a TCF12 Gene Mutation
• Automated three-dimensional analysis of facial asymmetry in patients with syndromic coronal synostosis: A retrospective study
• Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
• Clinical and Genetic Studies of the First Monozygotic Twins with Pfeiffer 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
• Complex Airway Management in Patients with Tracheal Cartilaginous Sleeves
• Complex craniosynostosis in the context of Carpenter's syndrome
• Computer-Assisted Frontofacial Monobloc Advancement and Facial Bipartition for Pfeiffer Syndrome: Surgical Technique
• Congenital inferior turbinate hypertrophy: an overlooked entity in newborns and review of the literature
• Considering the view from the inside of the maxillary sinus in Le Fort II osteotomy
• Cranial Morphology Associated With Syndromic Craniosynostosis: A Potential Detection of Abnormality in Patient's Cranial Growth Using Angular Statistics
• Craniofacial morphology and growth in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis
• Craniofacial morphology in Apert syndrome: a systematic review and meta-analysis
• Developments in the Diagnosis and Therapeutic Strategy of the Apert Hand
• Differential diagnosis of syndromic craniosynostosis: a case series
• 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
• Distraction Lengthening of the Apert Thumb
• Does different cranial suture synostosis influence orbit volume and morphology in Apert syndrome?
• Does the association between abnormal anatomy of the skull base and cerebellar tonsillar position also exist in syndromic craniosynostosis?
• Does the Mutation Type Affect the Response to Cranial Vault Expansion in Children With Apert Syndrome?
• Drosophila Homolog of the Human Carpenter Syndrome Linked Gene, MEGF8, Is Required for Synapse Development and Function
• Endoscopic strip craniectomy with orthotic helmeting for safe improvement of head growth in children with Apert syndrome
• Evaluation of dental maturity in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis
• Excessive osteoclast activation by osteoblast paracrine factor RANKL is a major cause of the abnormal long bone phenotype in Apert syndrome model mice
• Exosome-mediated small interfering RNA delivery inhibits aberrant osteoblast differentiation in Apert syndrome model mice
• Expansion of the phenotypic and mutational spectrum of Carpenter syndrome
• Facial Dysmorphology in Saethre-Chotzen Syndrome
• Facial Fat Graft Injection Reduces Asymmetry and Improves Forehead Contour in Early Infancy Apert Syndrome Patients
• Familial Pfeiffer Syndrome: Variable Manifestations and Role of Multidisciplinary Team Care
• Frontofacial Monobloc Advancement With Internal Distraction: Surgical Technique and Osteotomy Guide
• Frontofacial Reconstruction Technique Modification With Preservation of Blood Supply to the Monobloc Segment
• Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review
• Hearing, Speech, Language, and Communicative Participation in Patients With Apert Syndrome: Analysis of Correlation With Fibroblast Growth Factor Receptor 2 Mutation
• Hypertelorbitism Corrected by Facial Bipartition Improves Exotropia
• Influence of Nonsyndromic Bicoronal Synostosis and Syndromic Influences on Orbit and Periorbital Malformation
• Inner Ear Anomalies in Children With Apert Syndrome: A Radiological and Audiological Analysis
• Le Fort II Distraction with Simultaneous Zygomatic Repositioning
• Lefort II distraction with zygomatic repositioning versus Lefort III distraction: A comparison of surgical outcomes and complications
• Left Ophthalmic Segment Internal Carotid Artery Aneurysm Treated with Flow Diversion in a Child with Apert Syndrome: Technical Note
• Lipofilling of the lower eyelids: A craniofacial tool to postpone the facial advancement in craniofacial syndromes
• Local Soft Tissue and Bone Displacements Following Midfacial Bipartition Distraction in Apert Syndrome - Quantification Using a Semi-Automated Method
• Long-term Management of a Patient with Apert Syndrome
• Measurement of the Neutrophils Count and Oxidative Burst in Neutrophils of Patients with Sanjad Sakati Syndrome
• Molecular Scalpels: The Future of Pediatric Craniofacial Surgery?
• Monobloc Distraction and Facial Bipartition Distraction with External Devices
• Morphological Basis for Airway Surgical Intervention in Apert Syndrome
• Mother and Daughter Carrying of the Same Pathogenic Variant in <em>FGFR2</em> with Discordant Phenotype
• Open-wedge osteotomy for thumb radial angulation in Apert syndrome using a bone-graft substitute
• Optic canal characteristics in pediatric syndromic craniosynostosis
• Optic Nerve Atrophy in Syndromic Craniosynostosis
• Orbital and Periorbital Dysmorphology in Untreated Pfeiffer Syndrome
• 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
• Perioperative airway complications in infants and children with Crouzon and Pfeiffer syndromes: A single-center experience
• Pfeiffer syndrome type 3 with FGR2 c.1052C&gt;G (p.Ser351Cys) variant in West Africa: a case report
• Pfeiffer syndrome type 3 with FGR2 c.1052C>G (p.Ser351Cys) variant in West Africa: a case report
• Phenotypic variability of syndromic craniosynostosis caused by c.833G &gt; T in FGFR2: Clinical and genetic evaluation of eight patients from a five-generation family
• Postnatal Progressive Craniosynostosis in Syndromic Conditions: Two Patients With Saethre-Chotzen Due to <em>TWIST1</em> Gene Deletions and Review of the Literature
• Prenatal diagnosis of Pfeiffer syndrome and role of three-dimensional ultrasound: case report and review of literature
• Prenatal imaging of a fetus with the rare combination of Pfeiffer syndrome and hypoplastic left heart syndrome
• Preprocedural Electrophysiological Monitoring in Craniofacial Surgery for a Patient with Chiari Malformation
• Processes and patterns: Insights on cranial covariation from an Apert syndrome mouse model
• Psychological Adjustment in Apert Syndrome: Parent and Young Person Perspectives
• Quantitative Morphologic Analysis of Cranial Vault in Twist1+/- Mice: Implications in Craniosynostosis
• Respective Roles of Craniosynostosis and Syndromic Influences on Cranial Fossa Development
• Sanjad Sakati syndrome and sleep-disordered breathing: an undisclosed association
• Ser252Trp mutation in fibroblast growth factor receptor 2 promotes branching morphogenesis in mouse salivary glands
• Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis
• Syndrome-related outcomes following posterior vault distraction osteogenesis
• The Apert Foot: Anatomical Changes, Classification, Thoughts on surgical Treatment
• The association of Greig syndrome and mastocytosis reveals the involvement of the hedgehog pathway in advanced mastocytosis
• The developing mouse coronal suture at single-cell resolution
• The influence of orbital architecture on strabismus in craniosynostosis
• The limits of clinical findings in similar phenotypes, from Carpenter to ATRX syndrome using a whole exome sequencing approach: a case review
• 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
• Three-dimensional analysis of the palatal morphology in growing patients with Apert syndrome and Crouzon syndrome
• Treating Syndromic Craniosynostosis with Monobloc Facial Bipartition and Internal Distractor Devices: Destigmatizing the Syndromic Face
• TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse
• Variations in Paranasal Sinus Anatomy in Children With Apert Syndrome: A Radiological Analysis
• Visual outcomes in children with syndromic craniosynostosis: a review of 165 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
• Zygomatic repositioning and Le Fort II distraction with intraoral devices in Apert syndrome: A case report