• "Osteopetrosis" in the Fairbank Collection
• A boy with severe craniodiaphyseal dysplasia and apparently normal mother
• A case of craniodiaphyseal dysplasia
• A generalized disorders of the connective tissues with progeria, choanal atresia, symphalangism, hypoplasia of dentine and craniodiaphyseal hypostosis
• A recessive form of craniodiaphyseal dysplasia caused by a homozygous missense variant in SP7/Osterix
• Acquired Chiari malformation secondary to hyperostosis of the skull: a case report and literature review
• Activating the unfolded protein response in osteocytes causes hyperostosis consistent with craniodiaphyseal dysplasia
• BMP antagonists in tissue development and disease
• Bone scan findings in craniometaphyseal dysplasia
• Camurati-Engelmann disease (progressive hereditary craniodiaphyseal dysplasia). Case report
• Cranio-diaphyseal dysplasia (report of a case)
• Craniodiaphyseal dysplasia
• Craniodiaphyseal dysplasia
• Craniodiaphyseal dysplasia
• Craniodiaphyseal dysplasia, a disease or group of diseases?
• Craniodiaphyseal dysplasia, Lenz-Majewski type
• Craniodiaphyseal dysplasia; another cause of difficult intubation
• Craniodiaphyseal dysplasia: A Rare And Successful Bone-Anchored Hearing Aid Implantation
• Craniodiaphyseal dysplasia: an unusual cause of recurrent dacryocystitis
• Craniodiaphyseal dysplasia. Partial suppression of osteoblastic activity in the severe progressive form with calcitonin therapy
• Craniometaphyseal and craniodiaphyseal dysplasia, head and neck manifestations and management
• Craniotubular dysplasia with severe postnatal growth retardation, mental retardation, ectodermal dysplasia, and loose skin: Lenz-Majewski-like syndrome
• Deep Brain Stimulation for Craniocervical Dystonia (Meige Syndrome): A Report of Four Patients and a Literature-Based Analysis of Its Treatment Effects
• Dominantly inherited craniodiaphyseal dysplasia: a new craniotubular dysplasia
• Fractures in connection with an atypical form of craniodiaphyseal dysplasia: case report of a boy and his mother
• Histologic, microradiographic and electron microscopic investigations of bone tissue in a case of craniodiaphyseal dysplasia
• Hydrocephalus and craniodiaphyseal dysplasia (author's transl)
• Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia
• Intracranial and extracranial reduction osteoplasty for craniodiaphyseal dysplasia
• Lacrimo-auriculo-dento-digital syndrome with unilateral inner ear dysplasia and craniocervical osseous abnormalities: case report and review of literature
• Lenz-Majewski syndrome
• Leontiasis ossea: a symptom...!
• Long-term follow-up of severe autosomal recessive SP7-related bone disorder
• Macrocephaly and sclerosis of the tubular bones in an isolated patient: a mild case of craniodiaphyseal dysplasia?
• Management and outcome of two pregnancies in a woman with craniodiaphyseal dysplasia
• Miscellaneous Bone Disorders
• MR imaging features of craniodiaphyseal dysplasia
• Nasolacrimal obstruction and facial bone histopathology in craniodiaphyseal dysplasia
• Reversing LRP5-dependent osteoporosis and SOST deficiency-induced sclerosing bone disorders by altering WNT signaling activity
• Sclerosing bone dysplasias--a target-site approach
• Sclerostin: clinical insights in muscle-bone crosstalk
• Sclerostin: Intracellular mechanisms of action and its role in the pathogenesis of skeletal and vascular disorders
• Stenosis of the cervical canal in craniodiaphyseal dysplasia
• Temporal bone findings in craniodiaphyseal dysplasia
• The Camurati-Engelmann syndrome (progressive diaphyseal dysplasia)
• The Erlenmeyer flask bone deformity in the skeletal dysplasias
• The skull in metaphyseal chondrodysplasia type Jansen
• Unusual case of hyperostosis of the type "cranio-diaphyseal dysplasia"