Rare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestations

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