Results 41 to 50 of about 4,486 (202)

A cephalometric method to diagnosis the craniovertebral junction abnormalities in osteogenesis imperfecta patients [PDF]

, 2015
Osteogenesis imperfecta (OI) is a hereditary bone fragility disorder that in most patients is caused by mutations affecting collagen type I. Their typical oral and craneofacial characteristics (Dentinogenesis imperfecta type I and class III malocclusion),
de Nova García, Joaquín, Feijóo, Gonzalo, Garcilazo, Mario, Gutiérrez Díez, María Pilar, Mourelle Martínez, Mª Rosa, Ortega Aranegui, Ricardo, Ríos Rodenas, Mercedes   +6 more
core   +2 more sources

Saul Wilson Syndrome: A Case Report With New Features in Saudi Arabia

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Saul Wilson syndrome is an extremely rare genetic disorder caused by heterozygous de novo mutations in the COG4 gene. We report the first case from Saudi Arabia with previously unreported facial dysmorphic features, expanding the known phenotypic spectrum and emphasizing the importance of recognizing phenotypic variability in rare disorders.
Saad A. Bin Owaimer, Fatimah H. Abusrair, May R. Mutlaq, Eissa A. Faqeih, Leen Abu‐Safieh   +4 more
wiley   +1 more source

The natural history of type II odontoid fractures in the elderly population. A retrospective study over a 14 years period. [PDF]

, 2014
Odontoid fractures are the most common cervical fractures in the adult population. They represent 9 to 18 % of all cervical fractures and the type II is the most common.
BIKFALVI, A.
core  

Combined anterior and posterior surgery for treatment of cervical fracture-dislocation in patients with ankylosing spondylitis [PDF]

, 2009
ObjectiveTo discuss the pathological characteristics of cervical spinal fracture complicating ankylosing spondylitis (AS) and the effect of combined anterior and posterior operation.MethodsEighteen AS patients with traumatic cervical fracture-dislocation
LO, Guo-huagm, WANG, Bing, KANG, Yi-jun, LU, Chang, MA, Ze-min, DENG, You-wen   +5 more
core   +1 more source

Insights Into Late‐Onset Rheumatoid Arthritis (LORA): Characteristics (Clinical and Imaging), Comorbidities, and Therapeutic Targets

Geriatrics &Gerontology International, Volume 26, Issue 2, February 2026.
The main features of late‐onset rheumatoid arthritis (LORA), manifesting after age 65, are acute onset, higher disease activity, systemic involvement, and less presence of autoantibodies. Management requires individualized strategies, balancing aggressive treat‐to‐target therapy in robust patients with frailty‐focused approaches to prevent geriatric ...
Fausto Salaffi, Marina Carotti, Sonia Farah, Francesca Bandinelli, Luca Ceccarelli, Andrea Di Matteo, Marco Di Carlo   +6 more
wiley   +1 more source

Percutaneous anterior C1/2 transarticular screw fixation: salvage of failed percutaneous odontoid screw fixation for odontoid fracture

Journal of Orthopaedic Surgery and Research, 2017
Background The objective of this study is to investigate the outcomes and safety of using percutaneous anterior C1/2 transarticular screw fixation as a salvage technique for odontoid fracture if percutaneous odontoid screw fixation fails. Methods Fifteen
Ai-Min Wu, Hai-Ming Jin, Zhong-Ke Lin, Yong-Long Chi, Xiang-Yang Wang   +4 more
doaj   +1 more source

New C2 Synchondrosal Fracture Classification System [PDF]

, 2015
Health Professions - Clinical (The Ohio State University Denman Undergraduate Research Forum)Background. Excessive cervical flexion-extension accompanying mild to severe impact injuries can lead to C2 synchondrosal fractures in young children. Objective.
Daulton, Robert
core   +1 more source

Properties of commonly used calcium phosphate cements in trauma and orthopaedic surgery [PDF]

, 2013
Introduction Half of the population sustains at least one fracture during their lifetime, and the majority of these fractures heal successfully.
Kops, N. (Nicole), Lieshout, E.M.M. (Esther) van, Patka, P. (Peter), Siebelt, M. (Michiel), Stok, J. (Johan) van der, Weinans, H.H. (Harrie)   +5 more
core   +3 more sources

From Molecule to Meaning: Neuronopathic Biomarkers and Clinical Relevance in GM1

Journal of Inherited Metabolic Disease, Volume 49, Issue 1, January 2026.
ABSTRACT GM1 gangliosidosis is a rare, progressively neurodegenerative lysosomal storage disorder characterized by profound central nervous system involvement and substantial clinical heterogeneity. The development of reliable biomarkers is essential for tracking disease progression, stratifying patients, and advancing clinical trial readiness. Primary
Krista Casazza, Roberto Giugliani, Debra S. Regier, Jeanine Jarnes   +3 more
wiley   +1 more source

Bisphosphonate's and Intermittent Parathyroid Hormone's Effect on Human Spinal Fusion: A Systematic Review of the Literature. [PDF]

, 2017
There has been a conscious effort to address osteoporosis in the aging population. As bisphosphonate and intermittent parathyroid hormone (PTH) therapy become more widely prescribed to treat osteoporosis, it is important to understand their effects on ...
Acosta, Frank L, Hah, Raymond, Hsieh, Patrick C, Iorio, Justin A, Jakoi, Andre M, Liu, John C, Patel, Neil N, Pham, Martin H, Stone, Michael A, Wang, Jeffrey C   +9 more
core   +2 more sources