Jamal Ali Teir

ORCID: 0000-0003-0810-0965
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About
Contact & Profiles
Research Areas
  • Systemic Lupus Erythematosus Research
  • Skin Diseases and Diabetes
  • Systemic Sclerosis and Related Diseases
  • Facial Nerve Paralysis Treatment and Research
  • Blood disorders and treatments
  • Muscle and Compartmental Disorders
  • Vasculitis and related conditions
  • Atherosclerosis and Cardiovascular Diseases
  • Peripheral Neuropathies and Disorders
  • Protein Tyrosine Phosphatases
  • Trigeminal Neuralgia and Treatments
  • Ear Surgery and Otitis Media
  • Neurological and metabolic disorders
  • Blood groups and transfusion
  • Platelet Disorders and Treatments
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Sarcoidosis and Beryllium Toxicity Research
  • Connective tissue disorders research
  • Dermatologic Treatments and Research

Shaikh Khalifa Medical City
2022-2023

Al Ain Hospital
2014-2021

Objective. Accelerated atherosclerosis and premature coronary heart disease (CHD) are recognized complications of systemic lupus erythematosus (SLE), but the exact etiology remains unclear is likely to be multifactorial. We hypothesized that SLE patients with CHD have increased exposure traditional risk factors as well differing phenotype therapy-related compared free CHD. Our aim was examine for development clinical in setting. Methods. In a UK-wide multicenter retrospective case-control...

10.3899/jrheum.090306 article EN The Journal of Rheumatology 2009-12-01

Systemic sclerosis is an autoimmune condition characterized by a wide range of clinical presentations. Registries may serve to expand understanding about systemic and aid in patient care follow-up. The objective this study was analyze the prevalence large cohort from United Arab Emirates Sclerosis Registry find significant similarities differences between different subsets. All scleroderma patients were included multicenter national retrospective analysis. Data on demographics,...

10.1177/23971983221145788 article EN Journal of Scleroderma and Related Disorders 2023-01-05

Granulomatosis with polyangiitis (formerly called Wegener's granulomatosis) is a systemic autoimmune disease, which can lead to necrotizing vasculitis affecting small vessels and cause inflammation of blood in the nose, sinuses, throat, lungs, kidneys. In rare instances, it has shown involvement brain cranial nerves as well. We are reporting case granulomatosis polyangiitis, complicated by bilateral facial palsy due lower motor neuron nerve, responded well immunosuppressive treatment,...

10.1155/2021/9963564 article EN cc-by Case Reports in Rheumatology 2021-08-04

A 55-year-old woman with an 8-year history of type 2 diabetes was admitted to the cardiology department symptoms suggestive congestive cardiac failure. She had also severe left thigh pain for past 12 days. found have a muscle infarction (diabetic myonecrosis), which

10.7861/clinmedicine.14-3-319 article EN cc-by-nc-nd Clinical Medicine 2014-06-01

Vascular disease is integral to the pathogenesis of connective tissue diseases. Small vessel vasculitis underlies many clinical manifestations systemic lupus erythematosus and complicates rheumatoid arthritis other In contrast, in sclerosis, abnormal vasomotor activity a proliferative arterial vasculopathy are prominent. Disorders angiogenesis have been implicated diseases, thromboembolic common antiphospholipid antibody syndrome Behçets disease, association between chronic inflammatory...

10.2174/157339706778019656 article EN Current Rheumatology Reviews 2006-08-01

Anti-phospholipid antibody syndrome (APS) has a broad spectrum of thrombotic and nonthrombotic clinical manifestations. The diagnosis requires set criteria thrombosis along with persistently positive anti-phospholipid tests. In this report, we are presenting case APS, who is 38-year-old male, presented complains seizures found to have stroke, which on further investigation revealed been caused possibly from left atrial mass. Therefore, high index suspicion required for the APS in young...

10.1155/2020/8877445 article EN cc-by Case Reports in Medicine 2020-11-16
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