Disease: Osteopetrosis
- A Case of Osteopetrosis with Orbital Inflammation Secondary to Maxillary Osteomyelitis
- A novel compound heterozygous mutation of the <em>CLCN7</em> gene is associated with autosomal recessive osteopetrosis
- A novel compound heterozygous mutation of the CLCN7 gene is associated with autosomal recessive osteopetrosis
- A very rare case of bacteraemia in a 4-year-old girl with osteopetrosis with probable <em>Leuconostoc lactis</em> infection
- A very rare case of bacteraemia in a 4-year-old girl with osteopetrosis with probable Leuconostoc lactis 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
- Autosomal Dominant Osteopetrosis (ADO) caused by a Missense Variant in the TCIRG1 Gene
- Bone marrow Adipoq-lineage progenitors are a major cellular source of M-CSF that dominates bone marrow macrophage development, osteoclastogenesis, and bone mass
- Bone Turnover Marker for the Evaluation of Skeletal Remodelling in Autosomal Recessive Osteopetrosis after Haematopoietic Stem Cell Transplantation: A Case Report
- Brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS): new cases, systematic literature review, and associations with CSF1R-ALSP
- Carbonic Anhydrase II Activators in Osteopetrosis Treatment: A Review
- Carbonic anhydrase II deficiency
- 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: Gene mutations and clinical characteristics of four patients with osteopetrosis
- 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
- Characterization of Oral Pathology in Cats Affected by Patellar Fracture and Dental Anomaly Syndrome (PADS)
- Chloride transporter ClC-7 is essential for phagocytic clearance by microglia
- Clinical and genetic diagnosis of autosomal dominant osteopetrosis type II in a Chinese family: A case report
- Clinical and Osteopetrosis-Like Radiological Findings in Patients with Leukocyte Adhesion Deficiency Type III
- 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
- 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
- Distinct ClC-6 and ClC-7 Cl<sup>-</sup> sensitivities provide insight into ClC-7's role in lysosomal Cl<sup>-</sup> homeostasis
- Drug-induced osteopetrosis
- 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 Roflumilast, a Selective PDE4 Inhibitor, on Bone Phenotypes in ADO2 Mice
- Evaluation of polysomnography findings in children with genetic skeletal disorders
- 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 Turkiye's National Registry
- 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
- Histology, Osteoclasts
- 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
- Identifying bioactive phytoconstituents as C-terminal Src kinase inhibitors: a virtual screening and molecular simulation approach
- Idiopathic Osteosclerosis in Orthodontic Patients: A Report of Two Cases
- Impaired Autophagic Clearance with a Gain-of-Function Variant of the Lysosomal Cl<sup>-</sup>/H<sup>+</sup> Exchanger ClC-7
- Infantile osteopetrosis with delayed development, organomegaly and wandering eyes: case report
- Inhibition of non-canonical NF-κB signaling suppresses periodontal inflammation and bone loss
- Kisspeptin-10 binding to Gpr54 in osteoclasts prevents bone loss by activating Dusp18-mediated dephosphorylation of Src
- Leucine Repeat Rich Kinase 1 Controls Osteoclast Activity by Managing Lysosomal Trafficking and Secretion
- LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low-Density Lipoprotein Receptor-Related Protein 6
- Management of perinatal cervical spine injury using custom-fabricated external orthoses: design considerations, narrative literature review, and experience from the Hospital for Sick Children. Illustrative cases
- MARBLE DISEASE (CASE REPORT)
- Maxillary osteomyelitis in a young female with osteopetrosis: unveiling an uncommon connection
- Minimally Invasive Direct Coronary Artery Bypass in a Patient with Osteopetrosis and Symptomatic Ischemic Heart Disease:Report of a Case
- Molecular and functional mapping of Plekhm1-Rab7 interaction in osteoclasts
- Molecular Mechanisms of Craniofacial and Dental Abnormalities in Osteopetrosis
- Novel hybrid silicon-lipid nanoparticles deliver a siRNA to cure autosomal dominant osteopetrosis in mice. Implications for gene therapy in humans
- One half-century of advances in the evaluation and management of disorders of bone and mineral metabolism in children and adolescents
- Osteoclast Methods in Protein Phosphatase Research
- Osteomyelitis Possibly Caused by Exfoliation of Primary Teeth in a Patient with Osteopetrosis
- Osteopetrorickets: two contradictory patterns-one unifying diagnosis
- Osteopetrosis
- 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: Discovery and early history of "marble bone disease"
- 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
- Outlining the Clinical Profile of <em>TCIRG1 14 Variants</em> including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families
- 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<sup>mi/+</sup></em> Mice
- 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
- RhoA promotes osteoclastogenesis and regulates bone remodeling through mTOR-NFATc1 signaling
- 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
- Severe hypophosphataemia can be an early sign of osteopetrorickets: a case report
- Successful complete oral rehabilitation of a patient with osteopetrosis with extensive pre-treatments, bone grafts, dental implants and fixed bridges: a multidisciplinary 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 chromosome-level genome and key genes associated with mud-dwelling behavior and adaptations of hypoxia and noxious environments in loach (Misgurnus anguillicaudatus)
- The Cl- transporter ClC-7 is essential for phagocytic clearance by microglia
- 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
- 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 Leukoerythroblastic Reaction in a Newborn with Rh-Incompatibility and Hemolysis: Case Report and Literature Review
- Worth Syndrome-Patient Report, Diagnostic Work-Up, and Surgical Management of a Rare Craniofacial Entity