Disease: Juvenile Paget disease
- A Case Report of Bone Paget's Disease with Concurrent Psoriasis and Positive Celiac Serology
- Acquired resistance to pamidronate treated effectively with zoledronate in juvenile Paget's disease
- Benign transient hyperphosphatasemia: Two case reports
- Blockade of the angiotensin II type 1 receptor increases bone mineral density and left ventricular contractility in a mouse model of juvenile Paget disease
- Clinical course in two children with Juvenile Paget's disease during long-term treatment with intravenous bisphosphonates
- Denosumab in pediatric bone disorders and the role of RANKL blockade: a narrative review
- Dominant osteogenesis imperfecta with low bone turnover caused by a heterozygous SP7 variant
- Early identification of a 12-bp tandem duplication in TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK): Clinical characterization and response to bisphosphonate therapy
- Establishment of a TNFRSF11B knock-out human induced pluripotent stem cell line (KSCBi002-B-2) via CRISPR/Cas9 system
- Familial Paget's disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27)
- Genetic disorders associated with the RANKL/OPG/RANK pathway
- Global loss of bone, muscle, and fat mass in a patient with juvenile Paget disease (hereditary hyperphosphatasia)
- Juvenile Paget disease
- Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)
- Juvenile Paget's disease with compound heterozygous mutations in TNFRSF11B presenting with recurrent clavicular fractures and a mild skeletal phenotype
- Juvenile Paget's Disease: Report of a successful treatment throughout the complete growth of a patient with a missense TNFRSF11B mutation
- Mechanisms of Bone Fragility: From Osteogenesis Imperfecta to Secondary Osteoporosis
- Non-Odontogenic Tumors of the Jaws
- Off-label uses of denosumab in metabolic bone diseases
- Outliers of bone metabolic diseases
- Pediatric otosyphilis-An unusual cause of conductive hearing loss
- Rhizomelia and Impaired Linear Growth in a Girl with Juvenile Paget Disease: The Natural History of the Condition