Results 41 to 50 of about 3,824 (214)

Kraniofasiyal Tutulum Gösteren Poliostatik Fibröz Displazi: Olgu Sunumu

open access: yesCumhuriyet Dental Journal, 2015
Fibröz displazi kemiğin, nedeni bilinmeyen, kanselöz kemiğin tüm bileşenlerinin yerini, farklı oranda anormal görünümlü kemik içeren fibröz dokunun almasıyla sonuçlanan iskelet lezyonudur.
Elif Kaya
doaj   +1 more source

Fibrous dysplasia of the temporal bone secondary to ear surgery: A case report [PDF]

open access: yes, 2015
Introduction: In this report, we describe the clinical course, diagnostic features and management of a patient with fibrous dysplasia of the temporal bone 7 years after middle ear surgery on the same side.
Gavilan, Javier   +5 more
core   +2 more sources

Polyostotic Fibrous Dysplasia Complicated by Pathological Fracture of Right Femoral Shaft with Nonunion: A Case Report

open access: yesFrontiers in Surgery, 2022
IntroductionFibrous dysplasia is a benign fibrous bone tumor that accounts for 5% to 10% of benign bone tumors. It can manifest as simple fibrous dysplasia (70%–80%), polyostotic fibrous dysplasia (20%–30%), with approximately the same incidence in men ...
Qifan Yang   +4 more
doaj   +1 more source

Legius syndrome: Case report and review of literature [PDF]

open access: yes, 2015
A 8-month-old child was referred to our Dermatologic Unit for suspected Neurofibromatosis type 1 (NF 1), because of the appearance, since few days after birth, of numerous caf\ue9-au-lait spots (seven larger than 5 mm); no other sign evocative of NF 1 ...
Belcaro, Chiara   +4 more
core   +2 more sources

Management of post‐implant fibrous dysplasia in the maxilla: A case study

open access: yesClinical Advances in Periodontics, Volume 16, Issue 1, Page 41-47, March 2026.
Abstract Background Fibrous dysplasia is generally rare, and even rarer in older adults. Special care is needed when altering the alveolar bone in these cases, especially if an implant is involved. This case study highlights such a scenario. Methods This case study details the experience of a 63‐year‐old African American female who presented with a ...
Yousef Taha Y. Amrou   +4 more
wiley   +1 more source

PAGET’S DISEASE OF THE BONE: AN UNUSUAL CAUSE OF LOW BACK PAIN IN AN ADULT MALE [PDF]

open access: yesRomanian Journal of Rheumatology, 2016
Paget’s disease of the bone (PDB) or osteitis deformans is a chronic metabolic bone disorder, characterized by focal increase in bone resorption, followed by a rapid and abnormal bone repair with a disorganized and excessive bone formation, leading to ...
Iulian Resmerita   +2 more
doaj   +1 more source

Characterization of an FTLD-PDB family with the coexistence of SQSTM1 mutation and hexanucleotide (G4C2) repeat expansion in C9orf72 gene [PDF]

open access: yes, 2016
The C9orf72 expansion is considered a major genetic cause of familial frontotemporal dementia (FTD) in several patients' cohorts. Interestingly, C9orf72 expansion carriers, present also abundant neuronal p62-positive inclusions.
Almeida, MR   +8 more
core   +1 more source

The Scientific Case for Animal Models: A Perspective From Musculoskeletal Researchers

open access: yesFASEB BioAdvances, Volume 8, Issue 2, February 2026.
ABSTRACT The National Institutes of Health (NIH) has launched a major initiative to expand human‐based New Approach Methodologies (NAMs) in biomedical research and reduce reliance on animal models. While NAMs offer powerful complementary tools, animal‐based research remains indispensable in musculoskeletal science for understanding complex cellular and
Michael Hadjiargyrou   +4 more
wiley   +1 more source

Clinicopathologic Analysis of Sarcomas in the Oral and Maxillofacial Region: A Systematic Review

open access: yesOral Diseases, Volume 32, Issue 2, Page 338-349, February 2026.
ABSTRACT Objective This study aimed to systematically review primary sarcomas in the oral and maxillofacial region, focusing on patient demographics and sarcoma‐specific characteristics, including clinical presentation, histopathology, treatment approaches, outcomes, and survival rates.
Iara Vieira Ferreira   +7 more
wiley   +1 more source

Radioiodine treatment in McCune-Albright syndrome with hyperthyroidism

open access: yesIndian Journal of Endocrinology and Metabolism, 2012
McCune-Albright syndrome (MAS) is a sporadic disease characterized by polyostotic fibrous dysplasia, "café-au-lait" spots and hyperfunctional endocrinopathies.
Dhritiman Chakraborty   +5 more
doaj   +1 more source

Home - About - Disclaimer - Privacy