标题
Rare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestations
作者
关键词
-
出版物
JOURNAL OF DENTAL RESEARCH
Volume 93, Issue 7_suppl, Pages 7S-19S
出版商
SAGE Publications
发表日期
2014-04-04
DOI
10.1177/0022034514529150
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- The Rachitic Tooth
- (2014) Brian L. Foster et al. ENDOCRINE REVIEWS
- Clinical spectrum of hypophosphatasia diagnosed in adults
- (2013) Kathryn E. Berkseth et al. BONE
- Bisphosphonate-related osteonecrosis of the jaws and its relevance to children - a review
- (2013) Joanna Christou et al. International Journal of Paediatric Dentistry
- Dental perspectives in fibrous dysplasia and McCune–Albright syndrome
- (2013) Sunday O. Akintoye et al. Oral Surgery Oral Medicine Oral Pathology Oral Radiology
- Recessively Inherited Forms of Osteogenesis Imperfecta
- (2012) Peter H. Byers et al. Annual Review of Genetics
- Tooth root dentin mineralization defects in a mouse model of hypophosphatasia
- (2012) BL Foster et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Enzyme-Replacement Therapy in Life-Threatening Hypophosphatasia
- (2012) Michael P. Whyte et al. NEW ENGLAND JOURNAL OF MEDICINE
- The surgical management of fibrous dysplasia of bone
- (2012) Robert P Stanton et al. Orphanet Journal of Rare Diseases
- Gorham-Stout syndrome of the facial bones: a review of pathogenesis and treatment modalities and report of a case with a rare cutaneous manifestations
- (2012) Jamil Al-Jamali et al. Oral Surgery Oral Medicine Oral Pathology Oral Radiology
- Changing pattern of femoral fractures in osteogenesis imperfecta with prolonged use of bisphosphonates
- (2012) N. Nicolaou et al. Journal of Childrens Orthopaedics
- Craniofacial morphology in patients with hypophosphatemic rickets: A cephalometric study focusing on differences between bone of cartilaginous and intramembranous origin
- (2011) Hans Gjørup et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Hyperphosphatemic familial tumoral calcinosis (FGF23, GALNT3 and αKlotho)
- (2011) Emily G. Farrow et al. BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY
- Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta
- (2011) Víctor Martínez-Glez et al. HUMAN MUTATION
- Fassier–Duval femoral rodding in children with osteogenesis imperfecta receiving bisphosphonates: functional outcomes at one year
- (2011) Joanne Ruck et al. Journal of Childrens Orthopaedics
- Wormian bones in osteogenesis imperfecta: Correlation to clinical findings and genotype
- (2010) Oliver Semler et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study
- (2010) ALESSANDRA MAJORANA et al. International Journal of Paediatric Dentistry
- Vanishing Bone Disease: A Review
- (2010) D.N. Kiran et al. JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY
- Treatment of Gorham-Stout Disease With Zoledronic Acid and Interferon-α: A Case Report and Literature Review
- (2010) Dawn K. Kuriyama et al. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
- Gorham–Stout disease: the experience of the Rizzoli Institute and review of the literature
- (2010) Pietro Ruggieri et al. SKELETAL RADIOLOGY
- Familial Tumoral Calcinosis Caused by a Novel FGF23 Mutation: Response to Induction of Tubular Renal Acidosis with Acetazolamide and the Non-Calcium Phosphate Binder Sevelamer
- (2009) Juan Javier Lammoglia et al. HORMONE RESEARCH
- X-Linked Hypophosphatemic Rickets and Craniosynostosis
- (2009) Ananth S. Murthy JOURNAL OF CRANIOFACIAL SURGERY
- Orodental phenotype and genotype findings in all subtypes of hypophosphatasia
- (2009) Amélie Reibel et al. Orphanet Journal of Rare Diseases
- Neurosurgical aspects of childhood hypophosphatasia
- (2008) H. Collmann et al. CHILDS NERVOUS SYSTEM
- Age-Dependent Demise ofGNAS-Mutated Skeletal Stem Cells and “Normalization” of Fibrous Dysplasia of Bone
- (2008) Sergei A Kuznetsov et al. JOURNAL OF BONE AND MINERAL RESEARCH
- A case of familial tumoral calcinosis/hyperostosis–hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features
- (2008) C. E. Dumitrescu et al. OSTEOPOROSIS INTERNATIONAL
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