Results 101 to 110 of about 13,284 (234)
Clinical Challenges in Transition to Adult Care for Young People With Endocrinopathies
ABSTRACT The complexity of transition of pediatric patients to adult care is well recognized, with a multidisciplinary approach widely agreed to be essential. Despite extensive existing literature in this area, practical guidance as to the management of specific medical aspects and how to address these with patients and families is lacking, with little
Margaret Zacharin, Quynh‐Nhu Nguyen
wiley +1 more source
First two cases of craniomaxillofacial fibrous dysplasia from Nepal – case series
Neha Mishra,1 Sourav Kumar Rout2 1Department of Oral and Maxillofacial Pathology and Microbiology, Chitwan Medical College and Teaching Hospital, Bharatpur-10, Chitwan, Nepal; 2Department of Oral and Maxillofacial Surgery, Chitwan Medical College and ...
Rout SK, Mishra N
core
Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple +30 more
wiley +1 more source
Letter to the Editor - Fibrous Dysplasia of the Temporal Bone
We would like to report a case of fibrous dysplasia of the temporal bone in a 15 year female, who presented with occipital headache for four months. On examination there was deviation of the angle of the mouth towards the right side and partial closure ...
A. K. Sood +3 more
core +1 more source
A multifunctional heparinized polyamide membrane embedded with graphene quantum dots (GQDs) and hyperbranched polyethyleneimine (HPEI) is engineered for efficient bilirubin removal via a one‐step anticoagulation–adsorption process. The membrane demonstrates enhanced hemocompatibility, prolonged clotting times, and high bilirubin adsorption capacity ...
Abdur Rehman Mushtaq Ahmad +6 more
wiley +1 more source
Fibrous Dysplasia of Bone [PDF]
Brenda L, Nelson, Lester D R, Thompson
openaire +2 more sources
ABSTRACT The ciliopathies are a group of genetic disorders caused by defective function of either the primary cilia (a large number) or the motile cilia (a much smaller number). These have been defined as diseases with mutations in genes encoding individual ciliary or cilia‐associated proteins.
Robert P. Erickson +1 more
wiley +1 more source
A rare complication of craniofacial fibrous dysplasia
Fibrous dysplasia is a rare disease, the cause of which in not entirely known. The most common clinical manifestations of fibrous dysplasia of the temporal bone are the presence of two different pathologic disorders: morphologic and functional.
CASCONE, PIERO +3 more
core +1 more source
Maxillofacial Cemento‐Ossifying Fibroma: A Rare Case Report
ABSTRACT Cemento‐ossifying fibroma is a relatively rare lesion affecting the jaws, especially the anterior mandible. The most common clinical presentation is swelling. Diagnosis based on clinical observation only is challenging. Radiological images and histological findings can be misleading due to similitudes with other osteo‐fibrous lesions.
Alix N. Kamina +5 more
wiley +1 more source
This review highlights six genetic diseases of the bone, aiming to provide clinicians and researchers with updated information on their diagnosis and treatment. It also includes an assessment of common clinical and radiographic findings, along with pathophysiology related to diseases.
Colin Jones, Ambalangodage C. Jayasuriya
wiley +1 more source

