A new look at craniometaphyseal dysplasia

The Journal of Pediatrics

Volumn 112, Issue 4, 1988, Pages 577-579

  Cole, David E C ^a   Cohen Jr , M Michael ^a  

^a Izaak Walton Killam Hospital for Children   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CALCITONIN; CALCITRIOL;

CHILD; CRANIOMETAPHYSEAL DYSPLASIA; EDITORIAL; HUMAN; INFANT; PRIORITY JOURNAL;

BONE DISEASES, DEVELOPMENTAL; CALCITONIN; CALCITRIOL; DIAGNOSIS, DIFFERENTIAL; HUMAN; SKULL;

EID: 0023908262     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(88)80172-0     Document Type: Editorial

References (18)

1. Paget's disease of bone: etiology and therapeutic aspects
2. Healing of the bones in juvenile Paget's disease treated by human calcitonin
3. Hereditary bone dysplasia with hyperphosphatasemia: response to synthetic human calcitonin
4. Panostotic fibrous dysplasia: a congential disorder of bone with unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemia
5. Therapy of osteogenesis imperfecta with synthetic salmon calcitonin
6. Systemic treatment of osteogenesis imperfecta
7. Osteogenesis imperfecta: update and perspective
8. Calcitonin: physiology and pathophysiology
9. Axial and appendicular bone mineral density in patients with long-term deficiency or excess of calcitonin
10. 2-vitamin D concentrations in healthy men
11. 3 causes formation of multinucleated cells with several osteoclast characteristics in cultures of primate marrow
12. Osteopetrosis and the immune deficiency syndrome
13. Treatment of congenital osteopetrosis with high dose calcitriol
14. Genetic craniotubular bone dysplasia and hyperostoses: a critical analysis
15. Autosomal dominant craniometaphyseal dysplasia: clinical variability
16. Dominantly inherited craniodaphyseal dysplasia: a new craniotubular dysplasia
17. The evolution of craniometaphyseal dysplasia