Topical Collection on Rare Bone Diseases
In this topical collection (21 articles)
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Rare Bone Disease (CB Langman and E Shore, Section Editors)
Advances in the Classification and Treatment of Osteogenesis Imperfecta
Inas H. Thomas, Linda A. DiMeglio Pages 1-9 -
Rare Bone Disease (C Langman and E Shore, Section Editors)
Enchondromatosis and Growth Plate Development
Hongyuan Zhang, Benjamin A. Alman Pages 40-49 -
Rare Bone Disease (C Langman and E Shore, Section Editors)
Current Care and Investigational Therapies in Achondroplasia
Sheila Unger, Luisa Bonafé, Elvire Gouze Pages 53-60 -
Rare Bone Disease (C Langman and E Shore, Section Editors)
Microcephalic Osteodysplastic Primordial Dwarfism, Type II: a Clinical Review
Michael B. Bober, Andrew P. Jackson Pages 61-69 -
Rare Bone Disease (C Langman and E Shore, Section Editors)
Aberrant Bone Regulation in Albright Hereditary Osteodystrophy dueto Gnas Inactivation: Mechanisms and Translational Implications
Patrick McMullan, Emily L. Germain-Lee Pages 78-89 -
Rare Bone Disease (CB Langman and E Shore, Section Editors)
Hyperphosphatemic Familial Tumoral Calcinosis: Genetic Models of Deficient FGF23 Action
Lisal J. Folsom, Erik A. Imel Pages 78-87 -
Rare Bone Disease (CB Langman and E Shore, Section Editors)
Multicentric Carpotarsal Osteolysis: a Contemporary Perspective on the Unique Skeletal Phenotype
Nina S. Ma, S. Mumm, S. Takahashi, M. A. Levine Pages 85-94 -
Rare Bone Disease (CB Langman and E Shore, Section Editors)
Hypophosphatemic Rickets: Lessons from Disrupted FGF23 Control of Phosphorus Homeostasis
Bracha K. Goldsweig, Thomas O. Carpenter Pages 88-97 -
RARE BONE DISEASE (CB LANGMAN AND E SHORE, SECTION EDITORS)
Hypophosphatasia
Agnès Linglart, Martin Biosse-Duplan Pages 95-105 -
Rare Bone Disease (CB Langman and E Shore, Section Editors)
Hajdu-Cheney Syndrome, a Disease Associated with NOTCH2 Mutations
Ernesto Canalis, Stefano Zanotti Pages 126-131 -
Rare Bone Diseases (C Langman and E Shore, Section Editors)
Hereditary Multiple Exostoses: New Insights into Pathogenesis, Clinical Complications, and Potential Treatments
Maurizio Pacifici Pages 142-152 -
Rare Bone Disease (CB Langman and E Shore, Section Editors)
GNAS Spectrum of Disorders
Serap Turan, Murat Bastepe Pages 146-158 -
Rare Bone Disease (C Langman and E Shore, Section Editors)
Generalized Arterial Calcification of Infancy: New Insights, Controversies, and Approach to Management
Alison M. Boyce, Rachel I. Gafni, Carlos R. Ferreira Pages 232-241 -
RARE BONE DISEASE (CB LANGMAN AND E SHORE, SECTION EDITORS)
SP7: from Bone Development to Skeletal Disease
Jialiang S. Wang, Nicha Tokavanich, Marc N. Wein Pages 241-252 -
ReviewPaper
Variable Bone Phenotypes in Patients with Pseudohypoparathyroidism
Yan Wang, Chunyan Lu, Xiang Chen Pages 311-321 -
Rare Bone Disease (C Langman and E Shore, Section Editors)
Melorheostosis: a Rare Sclerosing Bone Dysplasia
Anupam Kotwal, Bart L. Clarke Pages 335-342 -
Rare Bone Diseases (CB Langman and E Shore, Section Editors)
Stem Cell Therapy as a Treatment for Osteogenesis Imperfecta
Cecilia Götherström, Lilian Walther-Jallow Pages 337-343 -
Rare Bone Disease (CB Langman and E Shore, Section Editors)
The Rare Bone Disease TeleECHO Program: Leveraging Telehealth to Improve Rare Bone Disease Care
Laura L. Tosi, Elmer N. Rajah, Michael H. Stewart… Pages 344-349 -
Rare Bone Disease (C Langman and E Shore, Section Editors)
Bone Health in Pediatric Patients with IBD: What Is New?
Rebecca J. Gordon, Catherine M. Gordon Pages 429-435 -
Rare Bone Disease (C Langman and E Shore, Section Editors)
Modeling Rare Bone Diseases in Animals
Charles A. O’Brien, Roy Morello Pages 458-465
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