Results 211 to 220 of about 37,133 (259)

A novel <i>SLC2A10</i> gain-of-function variant links glycolytic macrophage polarization to chronic nonbacterial osteomyelitis. [PDF]

Life Sci Alliance
Li X, Shen L, Jia K, Chen S, An J.
europepmc   +1 more source

Effect of Pre-Orthodontic CGF-Assisted GTR for Class II Furcation Lesions After Orthodontic Treatment: 5-Year Observation. [PDF]

Int Dent J
Qiao J, Peng L, Wang X, Zhang Y, Duan J, An N, Ouyang X.   +6 more
europepmc   +1 more source

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Surgical Diseases of the Temporo-Mandibular Joint

Acta Odontologica Scandinavica, 1956
During the past 25 years or so disorders of the temporomandibular joint have received considerable and steadily increasing attention, not the least in relation to odontological research and clinical problems. The significance of bite defects on the development of mandibular joint disorders has especially been a subject for detailed discussions, as ...
exaly   +2 more sources

Systemic bone disease in patients with mandibular atrophy

Journal of Oral and Maxillofacial Surgery, 1982
Abstract Although the etiology of alveolar ridge resorption is unclear, the labile alveolar bone may be highly sensitive to changes in systemic bone mineral content. Ten patients presenting with severe mandibular atrophy were studied by photon absorption densitometry. Four patients exhibited a significant reduction in radial midshaft mineral content.
R A, Bays, R S, Weinstein
openaire   +2 more sources

Gaucher's disease: Case report of mandibular trauma

Oral Surgery, Oral Medicine, Oral Pathology, 1992
Gaucher's disease is a disturbance of lipid storage that results in the accumulation of histiocytes filled with glucosyl ceramide in various organs and bones. Clinical features include history of epistaxis, hemoptysis, and spontaneous gingival hemorrhage.
G R, Regenye, B A, Huberman, A B, Itkin
openaire   +2 more sources

Mandibular Reconstruction in a Patient With Rosai–Dorfman Disease

Journal of Craniofacial Surgery, 2016
The Rosai-Dorfman disease (RDD) is a rare disorder known as sinus histiocytosis with massive lymphadenopathy which affects other organs besides the lymphatic nodes. The most frequent clinical presentation is the skin involvement, but the most serious one is when the central nervous system is compromised.
Jorge Ernesto Cantini, Ardila, Tulio, Torres, Carlos, Torres, Giovanni, Montealegre, Alejandra, García, Susana, Correa, Viviana, Gómez-Ortega   +6 more
openaire   +2 more sources

Reconstruction of Mandibular Diseases with Salvageable Joint

Yang Chi, Chi Yang, Minjie Chen
exaly   +2 more sources

Congenital mandibular coronoid process hyperplasia and associated diseases

Oral Diseases, 2022
Abstract Coronoid process hyperplasia (CPH) is an oral and maxillofacial surgical disease that can result in restricted jaw movement due to an enlarged and elongated mandibular coronoid process. It is characterized by the painless progressive restriction of unilaterally or bilaterally mouth opening.
openaire   +2 more sources

Morbidity and mortality of mandibular resection for malignant disease

The American Journal of Surgery, 1977
Twenty-nine per cent of patients undergoing mandibular resection had an entirely uncomplicated postoperative course. Local complications occurred in 54 per cent and systemic complication in 35 per cent. Increasing the extent of resection or an additional procedure, such as radical neck dissection, increased the local complication rate.
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Mandibular osteotomies in patients with juvenile rheumatoid arthritic disease

Scandinavian Journal of Rheumatology, 2003
This retrospective study evaluates the results after orthognathic surgery in a group of patients with juvenile rheumatoid arthritis.The material comprised sixteen patients where genioplasty with or without bilateral sagittal split (BSSO) had been performed during a 10-year period between 1991 and 2000.
F, Oye, T, Bjørnland, G, Støre
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