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tooth mobility/phosphatase

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記事臨床試験特許
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Chronic periodontitis is a multifactorial disease resulting in the inflammation and destruction of the supporting structures around the teeth, leading to tooth mobility and subsequent loss of tooth. Metabolic disorders, such as diabetes mellitus, play a crucial role in the progression

Development of Thymol microsponges loaded In situ gel for the treatment of Periodontitis

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Objective: Periodontitis is an oral disease categorized by disturbance of periodontal tissue and creation of periodontal pockets. Thymol (TH) loaded microsponge in situ gelling system was formulated for local action in the periodontal

Knockout of NRAGE promotes autophagy related gene expression and the periodontitis process in mice

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Background and objective: Neurotrophin receptor-interacting MAGE homologue (NRAGE) plays a crucial role in the regulation of bone metabolism. The present study investigated the regulation role of NRAGE on autophagy activation and

Congenital adrenal hyperplasia: a case report with premature teeth exfoliation and bone resorption.

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Congenital adrenal hyperplasia (CAH) is an inherited autosomal recessive disorder characterized by insufficient production of cortisol. The aim of this case report was to present a child with CAH, premature exfoliation of primary teeth and accelerated eruption of his permanent teeth related to bone

Brown tumor of secondary hyperparathyroidism: surgical approach and clinical outcome.

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BACKGROUND Secondary hyperparathyroidism is a frequent complication of chronic renal failure. The brown tumor is an unusual presentation of fibrous osteitis that represents a serious complication of renal osteodystrophy, affecting predominantly the hands, feet, skull, and facial bones. METHODS The

Surgery-first accelerated orthognathic surgery: postoperative rapid orthodontic tooth movement.

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OBJECTIVE Clinically, we have observed the phenomenon of postoperatively accelerated orthodontic tooth movement in patients who had orthognathic surgery. This phenomenon lasts for a period of 3 to 4 months. However, the underlying mechanisms of this phenomenon have not been well studied yet. The

Odontohypophosphatasia treated with asfotase alfa enzyme replacement therapy in a toddler: a case report

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Hypophosphatasia (HPP) is a rare skeletal disorder caused by loss-of-function mutations in Alkaline Phosphatase, Biomineralization associated (ALPL) gene that encodes tissue-nonspecific alkaline phosphatase. Odontohypophosphatasia (odonto-HPP), a mild form of HPP, is characterized only by
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