Disease: Osteopetrosis autosomal dominant type 1
- A case of autosomal dominant osteopetrosis type II with a novel TCIRG1 gene mutation
- A Mild Case of Autosomal Recessive Osteopetrosis Masquerading as the Dominant Form Involving Homozygous Deep Intronic Variations in the CLCN7 Gene
- Anterior cruciate ligament rupture in a patient with Albers-Schonberg disease
- Autosomal recessive osteopetrosis type I: description of pathogenic variant of TCIRG1 gene
- Chloroquine increases osteoclast activity in vitro but does not improve the osteopetrotic bone phenotype of ADO2 mice
- Clinical and genetic diagnosis of autosomal dominant osteopetrosis type II in a Chinese family: A case report
- Clinical Significance of DXA and HR-pQCT in Autosomal Dominant Osteopetrosis (ADO II)
- Genotyping, generation and proteomic profiling of the first human autosomal dominant osteopetrosis type II-specific induced pluripotent stem cells
- Identification of the first deletion in the LRP5 gene in a patient with autosomal dominant osteopetrosis type I
- Interferon Gamma-1b Does Not Increase Markers of Bone Resorption in Autosomal Dominant Osteopetrosis
- Locking plate osteosynthesis for a femoral fracture and subsequent nonunion in a patient with osteopetrosis
- Maxillary osteomyelitis associated with osteopetrosis: Systematic review
- Multiomics landscape of the autosomal dominant osteopetrosis type II disease-specific induced pluripotent stem cells
- Natural History of Type II Autosomal Dominant Osteopetrosis: A Single Center Retrospective Study
- Phenotypic severity of autosomal dominant osteopetrosis type II (ADO2) mice on different genetic backgrounds recapitulates the features of human disease
- Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review
- Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized Osteosclerosis