Results 91 to 100 of about 26,036 (310)

Maxillofacial fibrous dysplasia

open access: yesIndian Journal of Dental Research, 2005
Fibrous dysplasia is a non- neoplastic hamartomatous developmental fibro osseous lesion of bone. This paper provides a brief overview of fibrous dysplasia in a historic perspective and highlights the controversies in fibrous dysplasia seen in the cranio-
Mahajan Sumita, Kamboj Mala, Baoz Karen
doaj  

A Rare Case of Radiculopathy: Monostotic Fibrous Dysplasia of the Sacrum

open access: yesActa Médica Portuguesa, 2019
Fibrous dysplasia is a bone disease characterized by an osteoblastic dysfunction resulting in a fibrous replacement of the normal medullary bone. We describe the case of a 33-year-old who presented with low back pain irradiating to her right leg.
Joaquim Cruz Teixeira   +3 more
doaj   +1 more source

Benign fibro-osseous lesions of the maxillas : analysis of 11 cases [PDF]

open access: yes, 2008
Introduction: A study is made of the principal characteristics of the oral lesions biopsied in our Service of Oral Surgery and histologically diagnosed as corresponding to fibro-osseous lesions of the maxillas.
Berini Aytés, Leonardo   +3 more
core  

Continuous decompression treatment of unicameral bone cyst in a small‐breed dog: A case report

open access: yesVeterinary Surgery, EarlyView.
Abstract Objective To report the long‐term outcomes of continuous decompression for repairing a unicameral bone cyst in a dog. Study design Case report. Animal A 1‐year‐old Maltese‐Poodle mixed breed dog presented with left forelimb lameness. Methods A well‐defined cyst in the left humeral condyle was detected on radiography and computed tomography.
Eun‐Sun Lee   +4 more
wiley   +1 more source

Monostotic fibrous dysplasia of the spine: report of a case involving a cervical vertebra [PDF]

open access: yes, 2018
Monostotic fibrous dysplasia of the spine is a rare entity. Only 26 cases, of which 11 were located in the cervical spine, are to be found in the literature.
Heini, P.   +3 more
core  

Aortic and cardiovascular remodelling after thoracic endovascular aortic repair for blunt traumatic aortic injury in younger patients: A narrative review of physiological and clinical outcomes

open access: yesExperimental Physiology, EarlyView.
Abstract Blunt traumatic aortic injury (BTAI) is severe, often fatal in younger populations due to high‐energy deceleration mechanisms. Thoracic endovascular aortic repair (TEVAR) has revolutionised BTAI treatment, surpassing the previously standard open surgical repair in mortality and complication rates.
Marco David Bokobza De la Rosa   +8 more
wiley   +1 more source

Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report

open access: yesEuropean Journal of Radiology Open, 2020
The fibrous dysplasia of bone is painless, benign, and slowly progressive bone lesion. It may rarely become aggressive by compression of adjacent organs or malignant transformation.
Lynda N. Bile-Gui   +2 more
doaj   +1 more source

Benign fibro-osseous lesions of the maxillas: analysis of 11 cases [PDF]

open access: yes, 2014
Introduction: A study is made of the principal characteristics of the oral lesions biopsied in our Service of Oral Surgery and histologically diagnosed as corresponding to fibro-osseous lesions of the maxillas.
Berini Aytés, Leonardo   +3 more
core  

Condylar Hyperplasia: An Updated Review of the Literature [PDF]

open access: yes, 2015
Condylar hyperplasia (CH) is a rare disorder characterized by excessive bone growth that almost always presents unilaterally, resulting in facial asymmetry. Classification of the different types of CH can differ depending on the authors.
Almeida, Luis Eduardo   +2 more
core   +2 more sources

Massive reduction of RyR1 in muscle spindles of mice carrying recessive Ryr1 mutations alters proprioception and causes scoliosis

open access: yesThe Journal of Physiology, EarlyView.
Abstract figure legend Intrafusal muscles contained within muscle spindles are endowed with ryanodie receptor 1 (RyR1) calcium channels and participate in proprioceptor function. Mutations in RyR1 linked to severe RYR1‐congenital myopathies affect calcium release from both extrafusal as well as intrafusal muscles.
Alexis Ruiz   +8 more
wiley   +1 more source

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