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Medicine (United States), ISSN 0025-7974, 12/2017, Volume 96, Issue 50, p. e9209
Rationale: Van Buchem disease (VBD) is a very rare autosomal recessive disease. According to our review of the relevant literature, this article is the first... 
Hyperostosis | Van Buchem disease | hyperostosis | MEDICINE, GENERAL & INTERNAL | HYPEROSTOSIS CORTICALIS GENERALISATA | van Buchem disease | BONE | SCLEROSTEOSIS | CARRIERS | FEATURES | Diagnosis, Differential | Phenotype | Humans | Middle Aged | Taiwan | Female | Rare Diseases | Osteochondrodysplasias - diagnosis | Osteochondrodysplasias - therapy | Decompression, Surgical
Journal Article
Journal of the Royal College of Physicians of Edinburgh, ISSN 1478-2715, 2011, Volume 41, Issue 2, pp. 169 - 173
Egill Skallagrímsson, a tenth-century Viking, was a colourful warrior poet and an early anti-hero. The thickness and strength of his skull and his very ugly... 
Egill Skallagrímsson | Van Buchem disease | Paget's disease of bone | Diagnosis, Differential | Osteitis Deformans - history | History, Medieval | Humans | Mandible - pathology | Craniofacial Abnormalities - history | Male | Famous Persons | Iceland | Craniofacial Abnormalities - diagnosis | Skull - pathology | Adult | Craniofacial Abnormalities - pathology
Journal Article
Nature Reviews Molecular Cell Biology, ISSN 1471-0072, 01/2012, Volume 13, Issue 1, pp. 27 - 38
The past 15 years have witnessed tremendous progress in the molecular understanding of osteoblasts, the main bone-forming cells in the vertebrate skeleton. In... 
CLEIDOCRANIAL DYSPLASIA | TRANSCRIPTION FACTOR CBFA1 | WNT SIGNALING PATHWAYS | SYMPATHETIC-NERVOUS-SYSTEM | IN-VIVO | RECEPTOR-RELATED PROTEIN-5 | PARATHYROID-HORMONE | MESENCHYMAL STEM-CELLS | VAN-BUCHEM-DISEASE | HEMATOPOIETIC STEM | CELL BIOLOGY | Physiological aspects | Reports | Genetic aspects | Osteoblasts | Cellular control mechanisms
Journal Article
Skeletal Radiology, ISSN 0364-2348, 12/2003, Volume 32, Issue 12, pp. 708 - 718
Objective. The purpose of this study was to evaluate the lifetime evolution of the radioclinical features in a large family with van Buchem disease. Design and... 
Medicine | Bone dysplasia | Hyperostosis | Van Buchem disease | hyperostosis | bone dysplasia | HYPEROSTOSIS CORTICALIS GENERALISATA | GENE | CHROMOSOME 17Q12-Q21 | van Buchem disease | VANBUCHEMS DISEASE | SCLEROSTEOSIS | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Age Factors | Facial Nerve Diseases - diagnostic imaging | Humans | Middle Aged | Camurati-Engelmann Syndrome - genetics | Family Health | Male | Tomography, X-Ray Computed | Diaphyses | Hyperostosis, Cortical, Congenital - pathology | Statistics as Topic | Bone Diseases, Developmental - genetics | Sclerosis | Bone Diseases, Developmental - pathology | Craniofacial Abnormalities - diagnostic imaging | Camurati-Engelmann Syndrome - diagnostic imaging | Netherlands | Camurati-Engelmann Syndrome - pathology | Skull - pathology | Hearing Loss, Conductive - diagnostic imaging | Adult | Craniofacial Abnormalities - pathology | Female | Retrospective Studies | Child | Facial Nerve Diseases - genetics | Craniofacial Abnormalities - genetics | Hyperostosis, Cortical, Congenital - diagnostic imaging | Genetic Predisposition to Disease - genetics | Hearing Loss, Sensorineural - pathology | Metacarpus - diagnostic imaging | Hearing Loss, Conductive - pathology | Hearing Loss, Sensorineural - genetics | Hearing Loss, Sensorineural - diagnostic imaging | Hyperostosis, Cortical, Congenital - genetics | Bone Diseases, Developmental - diagnostic imaging | Pedigree | Skull - diagnostic imaging | Adolescent | Facial Nerve Diseases - pathology | Hearing Loss, Conductive - genetics | Metacarpus - pathology | Aged | Observer Variation | Evolution
Journal Article
JOURNAL OF BONE AND MINERAL RESEARCH, ISSN 0884-0431, 06/2008, Volume 23, Issue 6, pp. 860 - 869
Introduction: Sclerosteosis is a rare high bone mass genetic disorder in humans caused by inactivating mutations in SOST, the gene encoding sclerostin. Based... 
PROTEIN | 17Q12-Q21 | sclerosteosis | sclerostin | DENSITY | LRP5 GENE | HISTOMORPHOMETRY | BMP ANTAGONIST | MASS | ENDOCRINOLOGY & METABOLISM | bone formation | SOST | MUTATIONS | bone strength | VAN-BUCHEM-DISEASE
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 06/2006, Volume 21, Issue 6, pp. 934 - 945
Wnt/ beta -catenin signaling has been proven to play a central role in bone biology. Unexpectedly, the Wnt antagonist Dkk2 is required for terminal osteoblast... 
Journal Article
Journal Article