Disease: Apert syndrome
- <em>De novo</em> variants of dominant monogenic disorders in Vietnam detected by a noninvasive prenatal test: a case series
- <em>Drosophila</em> Homolog of the Human Carpenter Syndrome Linked Gene, <em>MEGF8</em>, Is Required for Synapse Development and Function
- 3D Imaging Reveals Changes in the Neurovascular Architecture of the Murine Calvarium with Aging
- A case of Pfeiffer syndrome caused by FGFR2 gene variation
- A Complex Case of Clino-Syndactyly with Fourth Metacarpal Aplasia
- A European multicenter outcome study on the different perioperative airway management policies following midface surgery in syndromic craniosynostosis: a proposal for a Standard Operating Procedure
- A Twist-Box domain of the C. elegans Twist homolog, HLH-8, plays a complex role in transcriptional regulation
- Alterations in Sphenoid Anatomy in Craniosynostosis: Implications for Fronto-Orbital Advancement
- Anatomical study of first palmar intermetacarpal flap in cadavers and application for congenital first web contracture in a child with Apert's syndrome
- Apert Syndrome
- Apert Syndrome
- Apert Syndrome - caveats of squint management
- Apert Syndrome Type III Hand: Prevalence and Outcomes
- Apert syndrome: a rare clinical image
- Apert Syndrome: Dental management considerations and objectives
- Apert Syndrome: Selection Rationale for Midface Advancement Technique
- Apical expansion of calvarial osteoblasts and suture patency is dependent on fibronectin cues
- 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
- Bacterial Sepsis among Children with Congenital Heart Disease in Tikur Anbessa Specialized Hospital, Addis Ababa, Ethiopia
- Cleft Palate in Apert Syndrome
- Cleft Palate in Apert Syndrome: A Descriptive Study of Incidence and Surgical Outcome
- Clinical and Genetic Studies of the First Monozygotic Twins with Pfeiffer Syndrome
- Clinical and operative risk factors for complications after Apert hand syndactyly reconstruction
- Clinical manifestations of Apert syndrome
- Clinical-Epidemiological Study of a Cohort of 35 Patients with Craniosynostosis
- Coexistence of Two Rare Conditions Complicating the Other's Management: Propionic Acidemia and Apert Syndrome
- Comparison of Internal and External Distraction in Frontofacial Monobloc Advancement: A Three-Dimensional Quantification
- Cranial Morphology Associated With Syndromic Craniosynostosis: A Potential Detection of Abnormality in Patient's Cranial Growth Using Angular Statistics
- Craniofacial morphology in Apert syndrome: a systematic review and meta-analysis
- Craniofacial syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis
- Delayed Postnatal Synostosis without Spheno-occipital Synchondrosis Fusion: A Curious Case of Apert Syndrome
- Developments in the Diagnosis and Therapeutic Strategy of the Apert Hand
- 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?
- Drosophila Homolog of the Human Carpenter Syndrome Linked Gene, MEGF8, Is Required for Synapse Development and Function
- Evaluation of polysomnography findings in children with genetic skeletal disorders
- 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
- Factors Affecting Optic Nerve Damage in Le Fort III Osteotomy: A Retrospective Study
- Frontofacial Monobloc Advancement With Internal Distraction: Surgical Technique and Osteotomy Guide
- Frontofacial Reconstruction Technique Modification With Preservation of Blood Supply to the Monobloc Segment
- Genetic Subtypes of Apert Syndrome Are Associated With Differences in Airway Morphology and Early Upper Airway Obstruction
- Growth charts in <em>FGFR2</em>- and <em>FGFR3</em>-related faciocraniosynostoses
- Impact of Anterior and Posterior Vault Distraction Osteogenesis (A-PVDO) and 3D-Printed Positioning/Shaping Templates in Apert Syndrome: A Case Series Study
- Impact of paternal age on assisted reproductive technology outcomes and offspring health: a systematic review
- Introduction of Spring-Assisted Cranioplasty for Bicoronal Synotosis in India: Description of First Case and Our Learning Experience
- Left Ophthalmic Segment Internal Carotid Artery Aneurysm Treated with Flow Diversion in a Child with Apert Syndrome: Technical Note
- Male reproductive ageing: a radical road to ruin
- Measurement of the Neutrophils Count and Oxidative Burst in Neutrophils of Patients with Sanjad Sakati Syndrome
- Molecular Mechanisms Involved in Craniosynostosis
- Molecular Scalpels: The Future of Pediatric Craniofacial Surgery?
- Mother and Daughter Carrying of the Same Pathogenic Variant in <em>FGFR2</em> with Discordant Phenotype
- Noninvasive Ventilation in Pediatric Acute Respiratory Distress Syndrome: "Another Dogma Bites the Dust"
- Open-wedge osteotomy for thumb radial angulation in Apert syndrome using a bone-graft substitute
- Optic Nerve Atrophy in Syndromic Craniosynostosis
- Orbital and Eyelid Characteristics, Strabismus, and Intracranial Pressure Control in Apert Children Treated by Endoscopic Strip Craniectomy versus Fronto-Orbital Advancement
- Orthognathic Surgery in Patients with Syndromic Craniosynostosis
- Outcome of Bilateral Hand Reconstruction in a Child Presenting Late With Apert Syndrome: A Case Report and Literature Review
- Outcomes of Apert Syndrome Hand Reconstruction With Tilapia Skin: A Prospective Study
- Patient Tailored Surgery in Saethre-Chotzen Syndrome: Analysis of Reoperation for Intracranial Hypertension
- Persistent falcine sinus in the newborn: 3 case reports of associated anomalies
- Pfeiffer Syndrome
- Pfeiffer Syndrome
- Plantar intermetatarsal perforator flap for first web skin-graftless syndactyly release: Anatomical study and clinical application
- Posterior Cranial Distraction in Craniosynostosis: A Systematic Review of the 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
- Presentation and Treatment of a Patient With Jacobs Syndrome and Metopic Craniosynostosis
- Processes and patterns: Insights on cranial covariation from an Apert syndrome mouse model
- Role of sperm DNA damage in creating de-novo mutations in human offspring: the 'post-meiotic oocyte collusion' hypothesis
- Ruptured Sinus of Valsalva Aneurysm in Apert Syndrome: Case report
- 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
- SEVERE INFANTILE ASTHMA TREATED WITH LONG-ACTING MUSCARINIC ANTAGONIST: A CASE SERIES
- Skeletal changes after midface surgery in patients with craniofacial deformities: a three-dimensional quantification method
- Subcranial Midface Advancement in Patients with Syndromic Craniosynostosis
- Successful reverse total shoulder replacement in a patient with Apert syndrome
- Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis
- Syndactyly
- Syndactyly
- Syndromic Craniofacial Disorders
- Syndromic Craniosynostosis: A Comprehensive Review
- The Apert Foot: Anatomical Changes, Classification, Thoughts on surgical Treatment
- The influence of orbital architecture on strabismus in craniosynostosis
- The Kaleidoscope of Midface Management in Apert Syndrome: A 23-Year Single-Institution Experience
- The Role of Airway Management on Feeding Difficulties in Children With Pfeiffer Syndrome
- The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4
- Thirty-year Experience Treating Syndromic Craniosynostosis: Long-term Outcomes Following Cranial Expansions
- Three-dimensional analysis of the palatal morphology in growing patients with Apert syndrome and Crouzon syndrome
- Three-Dimensional Evaluation of Dental Arches in Individuals with Syndromic Craniosynostosis
- TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse
- Two-Center Review of Posterior Vault Expansion following a Staged or Expectant Treatment of Crouzon and Apert Craniosynostosis
- Two-stage surgical treatment for medially angulated great toes in Apert feet by wedged corrective osteotomy with distraction of the inter-metatarsal space: A case report
- Unraveling the Complexity of Apert Syndrome: Genetics, Clinical Insights, and Future Frontiers
- Variations in Paranasal Sinus Anatomy in Children With Apert Syndrome: A Radiological Analysis
- Virtual Reality and Mixed Reality-Assisted Endoscopic DCR in Extremely Complex Lacrimal Obstructions
- Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports