CADASIL - Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Journal Title: Sultan Qaboos University Medical Journal - Year 2011, Vol 11, Issue 2
Abstract
Authors and Affiliations
Ramachandiran Nandhagopal| Department of Medicine, Sultan Qaboos University Hospital, Muscat, Oman; Former afliation: Department of Neurology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India
Keywords
Related Articles
- EP ID EP14058
- DOI -
- Views 290
- Downloads 9
Efficacy of OK-432 Therapy for the Incisionless Treatment of Head and Neck Cystic Masses Case series
Head and neck masses can present in different pathologies that usually vary according to the age of the patient. We report five cases of benign head or neck masses occurring among patients of different ages who were ma...
Histological Evaluation of Hydroxyapatite Granules with and without Platelet-Rich Plasma versus an Autologous Bone Graft Comparative study of biomaterials used for spinal fusion in a New Zealand white rabbit model
Objectives: Hydroxyapatite (HA) has osteoconductive properties and is widely used as a bone graft substitute. Platelet-rich plasma (PRP) is an autologous product with osteoinductive effects. Hypothetically, a combinat...
Cushing’s Disease Sustained remission in fve cases induced by medical therapy with the dopamine agonist cabergoline
We report fve cases of Cushing’s disease where the patients were given a therapeutic trial of cabergoline. Morning serum cortisol, adrenocorticotrophic hormone (ACTH), and sleeping cortisol concentrations were signif...
What are Patients’ Concerns about Medical Errors in an Emergency Department?
Objectives: Concerns about medical errors have recently increased. An understanding of how patients conceptualise medical error would help health care providers to allay safety concerns and increase patient satisfaction...
An Adolescent with Progressive Enlargement of Digits: Case report and proposed diagnostic criteria for macrodystrophia lipomatosa
Macrodystrophia lipomatosa (ML) is a rare congenital non-hereditary condition caused by an increase in all mesenchymal elements. We report a 14-year-old girl who presented to the Medical Outpatient Department, Kunhitharu...