• A Case of Osteopetrosis with Orbital Inflammation Secondary to Maxillary Osteomyelitis
• A very rare case of bacteraemia in a 4-year-old girl with osteopetrosis with probable <em>Leuconostoc lactis</em> infection
• Adult Osteopetrosis Type 2
• Allogenic hematopoietic stem cell transplantation in an Iranian patient with osteopetrosis caused by carbonic anhydrase II deficiency: A case report
• Analysis of clinical presentation and genetic characteristics of malignant infantile osteopetrosis
• Application of femoral nail, reconstruction locked plate and bone morphogenic protein - 7 in an osteopetrosis patient with a recurrent femoral shaft fracture: A case report
• Atp6i deficient mouse model uncovers transforming growth factor-β1 /Smad2/3 as a key signaling pathway regulating odontoblast differentiation and tooth root formation
• Autosomal Dominant Osteopetrosis (ADO) caused by a Missense Variant in the TCIRG1 Gene
• Birefringence-induced phase delay enables Brillouin mechanical imaging in turbid media
• Brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS): new cases, systematic literature review, and associations with CSF1R-ALSP
• Carbonic anhydrase II deficiency syndrome with amelogenesis imperfecta linked to a homozygous <em>CA2</em> deletion
• Carbonic Anhydrase II Deficiency: Unusual Presentation of the Arabic Mutation. A Case Report
• Case Report: Osteosclerotic metaphyseal dysplasia with optic nerve involvement and progressive osteonecrosis of the jaw due to a novel LRRK1 mutation
• Centrosome clustering control in osteoclasts through CCR5-mediated signaling
• Challenges of Hip and Knee Arthroplasty in Patients With Osteopetrosis
• Characterization of a spontaneous osteopetrosis model using RANKL-dysfunctional mice
• Chloride transporter ClC-7 is essential for phagocytic clearance by microglia
• Clinical, genetic aspects and molecular pathogenesis of osteopetrosis
• Complications of surgical management of osteopetrosis. A case report of multiple surgeries performed on one patient
• Conditional Loss of MEF2C Expression in Osteoclasts Leads to a Sex-Specific Osteopenic Phenotype
• Conversion Total Hip Arthroplasty in Patients With Osteopetrosis: Insights From Two Unique Cases
• Cranial distraction osteogenesis for craniosynostosis associated with osteopetrosis: A case report
• CRISPR/Cas9-Mediated Gene Correction in Osteopetrosis Patient-Derived iPSCs
• Current knowledge of bone-derived factor osteocalcin: its role in the management and treatment of diabetes mellitus, osteoporosis, osteopetrosis and inflammatory joint diseases
• Defects in Bone and Bone Marrow in Inherited Anemias: the Chicken or the Egg
• Diagnosis and treatment process of femoral subtrochanteric fracture in patients with osteopetrosis (marble bone disease): A case report
• Distinct ClC-6 and ClC-7 Cl^- sensitivities provide insight into ClC-7's role in lysosomal Cl^- homeostasis
• Early Recovery of Physical Function After Total Hip Arthroplasty in a Patient With Osteopetrosis: A Case Report
• Early treatment principles of tooth replacement disorders associated with hereditary oral diseases
• Effect of Allele-Specific Clcn7^G213R siRNA Delivered Via a Novel Nanocarrier on Bone Phenotypes in ADO2 Mice on 129S Background
• Effect of Roflumilast, a Selective PDE4 Inhibitor, on Bone Phenotypes in ADO2 Mice
• Endoscopic endonasal optic nerve decompression in children younger than 2 years old with congenital optic canal stenosis: illustrative cases
• Fluconazole-Induced Protein Changes in Osteogenic and Immune Metabolic Pathways of Dental Pulp Mesenchymal Stem Cells of Osteopetrosis Patients
• Fosl2 Deficiency Predisposes Mice to Osteopetrosis, Leading to Bone Marrow Failure
• Fracture Patterns and Mortality in Osteopetrosis: A 7-year Retrospective Analysis from Türkiye's National Registry
• Gain-of-function variants in CLCN7 cause hypopigmentation and lysosomal storage disease
• Generation of an induced pluripotent stem cell line (SYSUSCi004-A) from a patient with Infantile Malignant Osteopetrosis
• Genotype-phenotype analysis of selective failure of tooth eruption-A systematic review
• GNAS gene mutations affecting XLαs and bone health: A long neglected relationship
• How to adapt orthodontic treatment for a patient with a general pathology? Review of the literature based on six scenarios that challenge the practitioner
• How to adapt orthodontic treatment for a patient with a general pathology? Review of the literature based on six scenarios that challenge the practitioner
• Identification of an novel genetic variant associated with osteoporosis: insights from the Taiwan Biobank Study
• Idiopathic Osteosclerosis in Orthodontic Patients: A Report of Two Cases
• Impact of the SIK3 Pathway Inhibition on Osteoclast Differentiation via Oxidative Phosphorylation
• Impaired Autophagic Clearance with a Gain-of-Function Variant of the Lysosomal Cl^-/H⁺ Exchanger ClC-7
• Impdh2 deficiency suppresses osteoclastogenesis through mitochondrial oxidative phosphorylation and alleviates ovariectomy-induced osteoporosis
• Infantile osteopetrosis with delayed development, organomegaly and wandering eyes: case report
• Investigating mechanical and inflammatory pathological mechanisms in osteoarthritis using MSC-derived osteocyte-like cells in 3D
• Involvement of Siglec-15 in regulating RAP1/RAC signaling in cytoskeletal remodeling in osteoclasts mediated by macrophage colony-stimulating factor
• Kisspeptin-10 binding to Gpr54 in osteoclasts prevents bone loss by activating Dusp18-mediated dephosphorylation of Src
• Management of Osteomyelitis in Autosomal Dominant Osteopetrosis: A Rare Case Report
• MARBLE DISEASE (CASE REPORT)
• Maxillary osteomyelitis in a young female with osteopetrosis: unveiling an uncommon connection
• Molecular and functional mapping of Plekhm1-Rab7 interaction in osteoclasts
• Molecular Heterogeneity of Osteopetrosis in India: Report of 17 Novel Variants
• Molecular Mechanisms of Craniofacial and Dental Abnormalities in Osteopetrosis
• Multisystem disorder associated with a pathogenic variant in CLCN7 in the absence of osteopetrosis
• Novel hybrid silicon-lipid nanoparticles deliver a siRNA to cure autosomal dominant osteopetrosis in mice. Implications for gene therapy in humans
• Osteoclast Methods in Protein Phosphatase Research
• Osteomyelitis and Pathologic Fracture of Mandible in Undiagnosed Osteopetrosis
• Osteopetrorickets: two contradictory patterns-one unifying diagnosis
• Osteopetrosis and related osteoclast disorders in adults: A review and knowledge gaps On behalf of the European calcified tissue society and ERN BOND
• Osteopetrosis and related osteoclast disorders in adults: A review and knowledge gapsOn behalf of the European calcified tissue society and ERN BOND
• Osteopetrosis complicated by multilevel spondylolysis
• Osteopetrosis in the pediatric patient: what the radiologist needs to know
• Osteopetrosis of Adulthood: A Condition of Bone Overgrowth
• Osteopetrosis with Arnold Chiari malformation type I
• Osteopetrosis-pseudoglioma syndrome
• Osteopetrosis: Gene-based nosology and significance
• Osteosclerotic Metaphyseal Dysplasia Due to a Likely Pathogenic LRRK1 Variant as a Cause of Recurrent Long Bone Fractures
• Osteosynthesis of an intertrochanteric fracture on osteopetrosis A case report
• Patient-Reported Outcomes in Autosomal Dominant Osteopetrosis: Findings from the Osteopetrosis Registry Study
• Portal Hypertension Refractory Ascites Caused by Secondary Hemochromatosis
• Progressive Cone-Rod Dystrophy and RPE Dysfunction in <em>Mitf^mi/+</em> Mice
• Rankl genetic deficiency and functional blockade undermine skeletal stem and progenitor cell differentiation
• Recurrent fractures in a teen with osteopetrosis
• Relative contributions of osteal macrophages and osteoclasts to postnatal bone development in CSF1R-deficient rats and phenotype rescue following wild-type bone marrow cell transfer
• Robotic arm-assisted total knee arthroplasty in a patient with osteopetrosis: a case report and review of literature
• Sensitivity Analysis of Upper Limb Musculoskeletal Models During Isometric and Isokinetic Tasks
• SNX10 regulates osteoclastogenic cell fusion and osteoclast size in mice
• Successful complete oral rehabilitation of a patient with osteopetrosis with extensive pre-treatments, bone grafts, dental implants and fixed bridges: a multidisciplinary case report
• Successful completion of orthodontic therapy in a patient with osteopetrosis: Case Report
• Surgical outcome of distal tibia Salter Harris II fracture in osteopetrosis patient
• The burden of hospital admissions for skeletal dysplasias in Sri Lanka: a population-based study
• The Cl- transporter ClC-7 is essential for phagocytic clearance by microglia
• The genome of African manatee <em>Trichechus senegalensis</em> reveals secondary adaptation to the aquatic environment
• The molecular spectrum of Turkish osteopetrosis and related osteoclast disorders with natural history (including a candidate gene, CCDC120)
• The molecular spectrum of Turkish osteopetrosis and related osteoclast disorders with natural history, including a candidate gene, CCDC120
• The PDE4 Inhibitors Roflumilast and Rolipram Rescue ADO2 Osteoclast Resorption Dysfunction
• The Variation in the Traits Ameliorated by Inhibitors of JAK1/2, TGF-β, P-Selectin, and CXCR1/CXCR2 in the <em>Gata1</em>^low Model Suggests That Myelofibrosis Should Be Treated by These Drugs in Combination
• Thickness of the hard palate : A new criterion for the diagnosis of osteoporosis?
• Total hip arthroplasty for the treatment of a hip disorder complicated by autosomal dominant osteopetrosis: a case report
• Total hip arthroplasty with monobloc press-fit acetabular components and large-diameter bearings for atypical acetabula is safe: a consecutive case series of 125 hips with mean follow-up of 9 years
• Tracheal stenosis in a yellow-crowned parrot (Amazona ochrocephala) due to diffuse ossification and osteopetrosis of tracheal rings
• Transient Generalized Osteosclerosis in a Newborn Mimicking Congenital Osteopetrosis with Negative Comprehensive Genetic Workup: A Case Report
• Transient Leukoerythroblastic Reaction in a Newborn with Rh-Incompatibility and Hemolysis: Case Report and Literature Review
• Transmembrane protein 53 craniotubular dysplasia (OMIM # 619727): The skeletal disease and consequent blindness of this new disorder