Manifestations of systemic diseases and conditions that affect the periodontal attachment apparatus: Case definitions and diagnostic considerations

JM Albandar, C Susin… - Journal of clinical …, 2018 - Wiley Online Library
Objectives This review proposes case definitions and diagnostic considerations of systemic
disorders and conditions that affect the periodontal attachment apparatus. Importance …

The role of biomineralization in disorders of skeletal development and tooth formation

CS Kovacs, C Chaussain, P Osdoby… - Nature Reviews …, 2021 - nature.com
The major mineralized tissues are bone and teeth, which share several mechanisms
governing their development and mineralization. This crossover includes the hormones that …

Mitigating osteonecrosis of the jaw (ONJ) through preventive dental care and understanding of risk factors

JT Wan, DM Sheeley, MJ Somerman, JS Lee - Bone research, 2020 - nature.com
It is well established that alterations in phosphate metabolism have a profound effect on
hard and soft tissues of the oral cavity. The present-day clinical form of osteonecrosis of the …

Bone tissue regeneration in the oral and maxillofacial region: a review on the application of stem cells and new strategies to improve vascularization

V Wu, MN Helder, N Bravenboer… - Stem cells …, 2019 - Wiley Online Library
Bone tissue engineering techniques are a promising alternative for the use of autologous
bone grafts to reconstruct bone defects in the oral and maxillofacial region. However, for …

Nanotechnology-based materials as emerging trends for dental applications

T Barot, D Rawtani, P Kulkarni - Reviews on Advanced Materials …, 2021 - degruyter.com
Nanomaterials have unique and superior properties such as high surface area and
nanoscale size, makes them highly advanced and vital for rapid diagnosis and beneficial in …

[HTML][HTML] Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa

PS Kishnani, ET Rush, P Arundel, N Bishop… - Molecular genetics and …, 2017 - Elsevier
Hypophosphatasia (HPP) is a rare, inherited, systemic, metabolic disorder caused by
autosomal recessive mutations or a single dominant-negative mutation in the gene …

X-linked hypophosphatemia: a new era in management

K Dahir, MS Roberts, S Krolczyk… - Journal of the …, 2020 - academic.oup.com
X-linked hypophosphatemia (XLH) is a rare, hereditary, progressive musculoskeletal
disease that often causes pain and short stature, as well as decreased physical function …

High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes

R Brommage, J Liu, GM Hansen, LL Kirkpatrick… - Bone research, 2014 - nature.com
Screening gene function in vivo is a powerful approach to discover novel drug targets. We
present high-throughput screening (HTS) data for 3 762 distinct global gene knockout (KO) …

Phenotypic and genotypic characterization and treatment of a cohort with familial tumoral calcinosis/hyperostosis‐hyperphosphatemia syndrome

MS Ramnitz, P Gourh… - Journal of bone and …, 2016 - academic.oup.com
Familial tumoral calcinosis (FTC)/hyperostosis‐hyperphosphatemia syndrome (HHS) is a
rare disorder caused by mutations in the genes encoding fibroblast growth factor‐23 …

Hypophosphatasia: diagnosis and clinical signs–a dental surgeon perspective

A Bloch‐Zupan - International journal of paediatric dentistry, 2016 - Wiley Online Library
Background Hypophosphatasia (HPP) is a rare inherited metabolic disease in which
mutations in the ALPL gene (encoding tissue‐nonspecific alkaline phosphatase) result in …