• <em>FKBP14</em> kyphoscoliotic Ehlers-Danlos syndrome misdiagnosed as Larsen syndrome: a case report
• 50 Years Ago in TheJournalofPediatrics: 50 Years Ago Today: The Expanding Phenotype of Larsen Syndrome
• A 360-Degree Surgical Approach for Correction of Cervical Kyphosis and Atlantoaxial Dislocation in the Case of Larsen Syndrome
• A case study of atypical Larsen syndrome with absent hallmark joint dislocations
• Advanced ossification of the carpal bones, and monkey wrench appearance of the femora, features suggestive of a propable mild form of desbeqious dysplasia: a case report and review of the literature
• An orthodontic perspective on Larsen syndrome
• Anesthetic challenges in the management of Larsen syndrome: A rare congenital anomaly
• Antenatal diagnosis of Larsen syndrome
• Anterior mediastinal tracheostomy with a median mandibular splitting approach in a Larsen syndrome patient with posterior cervical arthrodesis
• Association of Self-reported Systemic Reactions Following SARS-CoV-2 Vaccination With Immunological Response in the Danish National Cohort Study of Effectiveness and Safety of SARS-CoV-2 Vaccines (ENFORCE)
• Atlantoaxial dislocation adjacent to kyphotic deformity in a case of adult Larsen syndrome
• B3GALT6-linkeropathy: Three illustrative patients spanning the disease spectrum
• Cell-Dependent Pathogenic Roles of Filamin B in Different Skeletal Malformations
• Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
• Cervicothoracic dislocation due to congenital and bone-dysplasia-related vertebral malformations
• Clinical diagnosis of Larsen syndrome, Stickler syndrome and Loeys-Dietz syndrome in a 19-year old male: a case report
• Clinicopathologic Spectrum of Lysozyme-Associated Nephropathy
• Comparative analysis of the two extremes of <em>FLNB</em>-mutated autosomal dominant disease spectrum: from clinical phenotypes to cellular and molecular findings
• Congenital dislocation of the knee (CDK)
• Congenital dislocation of the knee at birth - Part I: Clinical signs and classification
• Congenital dislocation of the knee in a three-year-old-child with Larsen syndrome: Treatment with a hexapod-type external fixator
• Congenital Dislocation of the Knee in the Delivery Room
• Congenital dislocation of the knee: a protocol for management based on degree of knee flexion
• Congenital knee dislocation in Larsen syndrome treated by arthroplasty
• Congenital knee dislocation, case report and review of the literature
• Craniosynostosis: a previously unreported association with CHST3-related skeletal dysplasia (autosomal recessive Larsen syndrome)
• Craniovertebral junction instability in Larsen syndrome: An institutional series and review of literature
• Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach
• Developmental Foot Deformities in Patients with Connective Tissue Disorders
• Dural ectasia in a child with Larsen syndrome
• Endonasal Exposure of Lateral Recess of the Sphenoid Sinus: Significance of Pterygoid Process Pneumatization
• Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)
• Expanding the clinical spectrum of B4GALT7 deficiency: homozygous p.R270C mutation with founder effect causes Larsen of Reunion Island syndrome
• Fast and early mandibular osteogenetic distraction in a 24-day-old female newborn with Larsen syndrome
• FEVR findings in patients with Loeys-Dietz syndrome type II
• Filamin B: The next hotspot in skeletal research?
• FKBP14 kyphoscoliotic Ehlers-Danlos syndrome misdiagnosed as Larsen syndrome: a case report
• FLNB haploinsufficiency-related short stature: a new syndrome or an expanded spectrum of Larsen syndrome
• Further Defining the Phenotypic Spectrum of B3GAT3 Mutations and Literature Review on Linkeropathy Syndromes
• Germline Genetic NBN Variation and Predisposition to B-cell Acute Lymphoblastic Leukemia in Children
• GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome
• Hybrid repair of a giant left subclavian artery aneurysm and arch coarctation in a patient with Larsen syndrome
• Identification of 2-Sulfonyl/Sulfonamide Pyrimidines as Covalent Inhibitors of WRN Using a Multiplexed High-Throughput Screening Assay
• Knee arthrodesis for a congenital luxation with Larsen syndrome
• Larsen Syndrome and Associated Spinal Deformities
• Larsen syndrome and malignant hyperthermia
• Larsen syndrome in a newborn with genu recurvatum
• Larsen syndrome with C3-C4 spondyloptosis and atlantoaxial dislocation in an adult
• Larsen syndrome: a review of the literature and case report
• Larsen-syndrome: final diagnosis following multiple surgical interventions
• Long-term Outcomes of Surgically Treated Congenital Dislocation of the Knee
• Malignant hyperthermia in Larsen syndrome
• Malignant hyperthermia-like episode in a child with Larsen syndrome
• Management Dilemma of a Neuropathic Knee in a Known Case of Larsen Syndrome: A Case Report
• Management of joint dislocations of the lower limb in Larsen syndrome: practical approach
• Management of upper cervical kyphosis in an adolescent with Larsen's syndrome
• Mutations in Biosynthetic Enzymes for the Protein Linker Region of Chondroitin/Dermatan/Heparan Sulfate Cause Skeletal and Skin Dysplasias
• Neutrophil-Enriched Biomarkers and Long-Term Prognosis in Acute Coronary Syndrome: a Systematic Review and Meta-analysis
• Novel GZF1 pathogenic variants identified in two Chinese patients with Larsen syndrome
• Novel in-frame <em>FLNB</em> deletion causes Larsen syndrome in a three-generation pedigree
• Novel in-frame FLNB deletion causes Larsen syndrome in a three-generation pedigree
• One Stage Bilateral Total Hip Arthroplasty in Siblings with Larsen Syndrome
• One-stage release by double surgical approach for neglected congenital vertical talus: results in a series of walking children in Tanzania
• Ossicular malposition in Larsen syndrome: a case report
• Otologic manifestations of Larsen syndrome
• Pediatric cervical kyphosis in the MRI era (1984-2008) with long-term follow up: literature review
• Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients
• Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: congenital dislocations and vertebral changes as principal diagnostic features
• Pneumoperitoneum in a patient with Larsen syndrome
• Precocious appearance of the capital femoral ossific nucleus in Larsen syndrome
• Predictors of post traumatic growth in allogeneic hematopoietic stem cell transplantation survivors: a cross-sectional survey
• Prenatal and neonatal phenotype of Larsen of La Réunion Island syndrome (B4GALT7- linkeropathy)
• Prenatal and neonatal phenotype of Larsen of La Réunion Island syndrome (B4GALT7-linkeropathy)
• Prenatal diagnosis and postnatal outcome of fetal congenital knee dislocation: systematic review of literature
• Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene
• Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue
• Presumed Larsen syndrome in a child: a case with a 12-year follow-up
• Quantification of transmission risk in a male patient with a FLNB mosaic mutation causing Larsen syndrome: Implications for genetic counseling in postzygotic mosaicism cases
• Quiz answer. Young men with bilateral pain in the lower part of patella
• Reduced susceptibility to COVID-19 associated with ABO blood group and pre-existing anti-A and anti-B antibodies
• Review of cervical spine anomalies in genetic syndromes
• Seven additional families with spondylocarpotarsal synostosis syndrome with novel biallelic deleterious variants in FLNB
• Severe Aortic Root Dilatation in a Patient With Larsen Syndrome
• Severe Cervical Kyphosis and Spondyloptosis with Myelopathy in Larsen Syndrome: A Report of 2 Cases
• Significant traumatic atrophy of the spinal cord in connection with severe cervical vertebral body hypoplasia in a boy with Larsen syndrome: a case report and review of the literature
• Skeletal Dysplasia Families: A Stepwise Approach to Diagnosis
• Skeletal Dysplasia Mutations Effect on Human Filamins' Structure and Mechanosensing
• Spine deformities in rare congenital syndromes: clinical issues
• Spine malformation complex in 3 diverse syndromic entities: Case reports
• Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic or Hall type: report of a case with normal face and literature review
• Staged Bilateral Total Hip Arthroplasty in a Patient With Larsen Syndrome
• Structural Analysis of G1691S Variant in the Human Filamin B Gene Responsible for Larsen Syndrome: A Comparative Computational Approach
• Supraglottic airway and caudal epidural for anesthetic management of a child with Larsen syndrome
• Surgical management of cervical kyphosis in larsen syndrome. Case report and review of literature
• Surgical Treatment of Congenital and Obligatory Dislocation of the Patella in Children
• The management of knee dislocation in a child with Larsen syndrome
• Transcaval aortic valve implantation in a patient with Larsen syndrome: technical and anesthetic challenges
• Two Somali half-siblings with CHST3-related chondrodysplasia illustrating the phenotypic spectrum and intrafamilial variability
• Two-Staged Surgery for Kyphoscoliosis in Larsen Syndrome with A 30-Year Follow-Up: A Case Report
• Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion