• <em>Drosophila</em> Homolog of the Human Carpenter Syndrome Linked Gene, <em>MEGF8</em>, Is Required for Synapse Development and Function
• 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
• Absence of the RING domain in <em>MID1</em> results in patterning defects in the developing human brain
• Acute and long-term exercise adaptation of adipose tissue and skeletal muscle in humans: a matched transcriptomics approach after 8-week training-intervention
• Advances in genetic research on Non-syndromic congenital joint synostosis
• An Uncommon Cause of Recurrent Presyncope, Dizziness, and Tachycardia: A Case Report of Diffuse, Adult-Onset Nesidioblastosis/Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome (NIPHS)
• Analysis of High Flow Nasal Cannula Utilization During Pediatric Critical Care Transport
• Andexanet alfa and heparin resistance in cardiac surgery: Experiences and risks associated with the reversal of direct oral anticoagulants
• 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
• Approaches to ventriculoperitoneal shunt scalp erosion: countersinking into the calvarium. Illustrative case
• 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
• Case report: A girl with witnessed sleep apnea
• Changes in the Proteome of Platelets from Patients with Critical Progression of COVID-19
• Characterization of subdural collections in initial neuroimaging of abusive head trauma: Implications for forensic age diagnostics and clinical decision-making
• Clinical and Genetic Studies of the First Monozygotic Twins with Pfeiffer Syndrome
• Clinical and operative risk factors for complications after Apert hand syndactyly reconstruction
• Cohort profile: evaluation of immune response and household transmission of SARS-CoV-2 in Costa Rica: the RESPIRA study
• Comparison of Internal and External Distraction in Frontofacial Monobloc Advancement: A Three-Dimensional Quantification
• Continuation of fluoropyrimidine treatment with S-1 after cardiotoxicity on capecitabine- or 5-fluorouracil-based therapy in patients with solid tumours: a multicentre retrospective observational cohort study
• De Novo Heterozygous Mutation in FGFR2 Causing Type II Pfeiffer Syndrome
• Diffuse, Adult-Onset Nesidioblastosis/Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome (NIPHS): Review of the Literature of a Rare Cause of Hyperinsulinemic Hypoglycemia
• 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
• Early Outcomes of SARS-CoV-2 Infection in a Multisite Prospective Cohort of Inpatient Veterans
• Ectrodactyly-Ectodermal Dysplasia-Cleft Syndrome: Ocular Findings and Surgical Treatment
• Evaluating the efficacy and safety of neoadjuvant pembrolizumab in patients with stage I-III MMR-deficient colon cancer: a national, multicentre, prospective, single-arm, phase II study protocol
• Examining the prevalence of sleep disturbances in patients seeking physical therapy services
• Exosome-mediated small interfering RNA delivery inhibits aberrant osteoblast differentiation in Apert syndrome model mice
• Expression and subcellular localization of USH1C/harmonin in human retina provides insights into pathomechanisms and therapy
• 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
• Family burden after critical illness: the forgotten caregivers
• Fluoropyrimidine-induced hand-foot syndrome and cardiotoxicity: recommendations for the use of the oral fluoropyrimidine S-1 in metastatic colorectal cancer
• Frontofacial Reconstruction Technique Modification With Preservation of Blood Supply to the Monobloc Segment
• High prevalence of venous thrombotic events in Cushing's syndrome: data from ERCUSYN and details in relation to surgery
• Identification and characterization of two novel KCNH2 mutations contributing to long QT syndrome
• Immunogenicity and safety of a fourth homologous dose of NVX-CoV2373
• Immunogenicity of Monovalent mRNA-1273 and BNT162b2 Vaccines in Children &lt;5 Years of Age
• Incidence and risk factors for postintensive care syndrome in a cohort of critically ill patients
• Increased Sphingomyelin and Free Sialic Acid in Cerebrospinal Fluid of Kearns-Sayre Syndrome: New Findings Using Untargeted Metabolomics
• Iodine Images in Dual-energy CT: Detection of Hepatic Steatosis by Quantitative Iodine Concentration Values
• Lectin-Based Affinity Enrichment and Characterization of N-Glycoproteins from Human Tear Film by Mass Spectrometry
• Left Ophthalmic Segment Internal Carotid Artery Aneurysm Treated with Flow Diversion in a Child with Apert Syndrome: Technical Note
• Liver Fat Scores for Noninvasive Diagnosis and Monitoring of Nonalcoholic Fatty Liver Disease in Epidemiological and Clinical Studies
• Measurement of Retrobulbar Blood Flow and Vascular Reactivity-Relevance for Ocular and Cardiovascular Diseases
• 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?
• Mortality Risks after Two Years in Frail and Pre-Frail Older Adults Admitted to Hospital
• Mother and Daughter Carrying of the Same Pathogenic Variant in <em>FGFR2</em> with Discordant Phenotype
• Mystery of the Muenke midface: spheno-occipital synchondrosis fusion and craniofacial skeletal patterns
• 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
• Posoleucel, an Allogeneic, Off-the-Shelf Multivirus-Specific T-Cell Therapy, for the Treatment of Refractory Viral Infections in the Post-HCT Setting
• Precise in vivo RNA base editing with a wobble-enhanced circular CLUSTER guide RNA
• Precision RNA base editing with engineered and endogenous effectors
• Prenatal imaging of a fetus with the rare combination of Pfeiffer syndrome and hypoplastic left heart syndrome
• Preoperative Imaging in Patients with 22q11 Deletion Syndrome Undergoing Velopharyngeal Surgery
• Preprocedural Electrophysiological Monitoring in Craniofacial Surgery for a Patient with Chiari Malformation
• Prolonged cytopenias after immune effector cell therapy and lymphodepletion in patients with leukemia, lymphoma and solid tumors
• Quantitative assay to analyze neutralization and inhibition of authentic Middle East respiratory syndrome coronavirus
• 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
• Serological survey of avian metapneumovirus in vaccinated and unvaccinated broiler chickens in Hong Kong
• Severe anal intraepithelial neoplasia trends and subsequent invasive anal cancer in the United States
• Subcranial Midface Advancement in Patients with Syndromic Craniosynostosis
• Survival by sex and HIV status in patients with anal cancer in the USA between 2001 and 2019: a retrospective cohort study
• Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis
• Syndromic Craniofacial Disorders
• Syndromic Craniosynostosis: A Comprehensive Review
• The association of low birthweight and prematurity on outcomes in children and adults with nephrotic syndrome-a NEPTUNE cohort study
• The Effects of the Mediterranean Diet on Health and Gut Microbiota
• The influence of orbital architecture on strabismus in craniosynostosis
• The Longitudinal Association of Cardiorespiratory Fitness and Adiposity With Clustered Cardiometabolic Risk: A Mediation Analysis
• 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 immunotherapy in the treatment of colorectal cancer
• Therapy with pembrolizumab in treatment-naïve patients with nonmetastatic, mismatch repair deficient colorectal cancer
• Thirty-year Experience Treating Syndromic Craniosynostosis: Long-term Outcomes Following Cranial Expansions
• Treatment of acute knee dislocations
• Trends and risk of lung cancer among people living with HIV in the USA: a population-based registry linkage study
• TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse
• Type II Pfieffer misdiagnosed as Crouzon syndrome with additional features of supernumerary teeth and localized symmetrical gigantism: a case report
• Ultrasound examination of nerves of the upper extremities
• Ultrasound of nerves of the lower extremities
• Unique Genomic Epidemiology of COVID-19 in the White Mountain Apache Tribe, April to August 2020, Arizona
• 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