• Acquired resistance to pamidronate treated effectively with zoledronate in juvenile Paget's disease
• An histologic and histochemical study of familial osteoectasia. (Chronic idiopathic hyperphosphatasia)
• Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget 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
• Denosumab treatment for juvenile Paget's disease: results from two adult patients with osteoprotegerin deficiency ("Balkan" mutation in the TNFRSF11B gene)
• FAMILIAL OSTEOECTASIA WITH MACROCRANIUM
• Genotype-phenotype correlation in juvenile Paget disease: role of molecular alterations of the TNFRSF11B gene
• Global loss of bone, muscle, and fat mass in a patient with juvenile Paget disease (hereditary hyperphosphatasia)
• Hyperostosis corticalis deformans juvenilis: unfamiliar generalized osteopathy in 2 siblings
• Infantile cortical hyperostosis and COL1A1 mutation in four generations
• 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 with heterozygous duplication within TNFRSF11A encoding RANK
• Juvenile Paget's Disease: Report of a successful treatment throughout the complete growth of a patient with a missense TNFRSF11B mutation
• Loss of Functional Osteoprotegerin: More Than a Skeletal Problem
• Novel homozygous mutations in the osteoprotegerin gene TNFRSF11B in two unrelated patients with juvenile Paget's disease
• OSTEOCHALASIA DESMALIS FAMILIARIS. (HYPEROSTOSIS CORTICALIS DEFORMANS JUVENILIS, CHRONIC IDIOPATHIC HYPERPHOSPHATASIA, OSTEOECTASIA AND MACROCRANIUM)
• Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome)
• Polymorphisms of CSF1 and TM7SF4 genes in a case of mild juvenile Paget's disease found using next-generation sequencing
• Profound hypocalcemia following effective response to zoledronic acid treatment in a patient with juvenile Paget's disease
• Response to parathyroid hormone and 1,25-dihydroxyvitamin D3 of bone-derived cells isolated from normal children and children with abnormalities in skeletal development
• Rhizomelia and Impaired Linear Growth in a Girl with Juvenile Paget Disease: The Natural History of the Condition
• Unanticipated difficult intubation in a patient with juvenile Paget disease