Results 51 to 60 of about 4,398 (211)

Analysis of Nicotine Toxicity and Mechanisms of Senescence in Nucleus Pulposus Cells Using Network Toxicology and Molecular Docking Technique

open access: yesJOR SPINE, Volume 8, Issue 2, June 2025.
The current study improves cyber toxicology as a method of evaluating environmental toxicity and molecular biological qualities in addition to clarifying the possible molecular pathways of nicotine‐induced senescence in IVDD. ABSTRACT Aim Through the use of network toxicology, the research sought to determine whether cellular senescence and associated ...
Chen Jiang   +8 more
wiley   +1 more source

Giant aneurysmal bone cyst of the mandible with unusual presentation [PDF]

open access: yes, 2009
Aneurysmal bone cysts are rare benign lesions of bone tissue, infrequent in craneofacial skeleton with regard to other structures like long bones or the spine.
Acero Sanz, Julio   +5 more
core  

Chondromyxoid fibroma management: a single institution experience of 22 cases [PDF]

open access: yes, 2014
Background: Several different strategies have been reported for the treatment of chondromyxoid fibromas, all with variable outcomes and high recurrence rates.
Al-Khateeb, H   +9 more
core   +1 more source

Patellar aneurysmal bone cyst in children: a case report

open access: yesThe Pan African Medical Journal, 2012
An aneurysmal bone cyst is a benign aggressive bone lesion first described by Jaffe and Lichtenstein in 1942 [1]. It is typically an expansile osteolytic lesion consisting of blood-filled spaces and channels that are divided by connective tissue septa ...
Mounir Arroud   +3 more
doaj   +1 more source

Aneurysmal Bone Cyst: An Uncommon Secondary Event in Calcaneal Chondroblastoma [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Chondroblastoma is an uncommon benign bone tumour, involvement of epiphysis of long bones is typical. Chondroblastoma of the calcaneum is uncommon and its association with secondary aneurysmal bone cyst is even rarer.
Sandip Barman   +4 more
doaj   +1 more source

Life Beyond Childhood: Insight Into the Lived Experience of 91 Adults With KBG Syndrome Through an Online Patient/Caregiver‐Reported Co‐Produced Questionnaire

open access: yesBrain and Behavior, Volume 15, Issue 5, May 2025.
KBG syndrome (KBGS) is one of the most common monogenic causes of ID alongside short stature, macrodontia, and other variable features. Phenotypes in childhood are well documented, but data are lacking about adulthood and how best to support individuals. This study provides essential data on the lived experience of KBGS in adulthood.
Karen J. Low   +8 more
wiley   +1 more source

Bone and soft tissue tumors of hip and pelvis [PDF]

open access: yes, 2012
Objective is to identify epidemiologic and radiologic criteria allowing specific diagnoses of tumors and tumor-like lesions in the hip region and pelvis, and to optimize pre-operative staging.Patients with pelvic tumors are usually older, and their ...
Bloem, Johan L., Reidsma, Inge I.
core   +1 more source

Solid variant of aneurysmal bone cist on the distal extremity of the radius in a child

open access: yesRevista Brasileira de Ortopedia, 2016
The solid variant of aneurismal bone cysts (ABC) is considered rare. It occurs with greater frequency in pediatric patients and in the tibia, femur, pelvis and humerus. We present a case of a metaphyseal lytic lesion on the distal extremity of the radius
Adriano Jander Ferreira   +5 more
doaj   +1 more source

Synchronization of Calcifying Odontogenic Cyst and Aneurysmal Bone Cyst: A Case Report [PDF]

open access: yesJournal of Dental Materials and Techniques, 2017
Although aneurysmal bone cysts and calcifying odontogenic cysts accompanied with other lesions are reported in the literature, the simultaneous occurrence of these two distinct lesions has not been reported.
Jahanshah Salehinejad   +3 more
doaj   +1 more source

Neonatal Cholestasis Progressing to a Multisystem Syndrome With Liver Cirrhosis in Two Siblings With FARSA Deficiency: An Evolving Hepatological Phenotype

open access: yesJIMD Reports, Volume 66, Issue 3, May 2025.
ABSTRACT Biallelic variants in FARSA or FARSB are associated with reduced cytoplasmic phenylalanyl‐tRNA synthetase (FARS1) activity and underlie a multisystem syndrome characterized by growth limitation, developmental delay, brain calcifications, interstitial lung disease (ILD), and liver involvement.
Y. Aelvoet   +11 more
wiley   +1 more source

Home - About - Disclaimer - Privacy