Results 11 to 20 of about 440,641 (258)
New England Journal of Medicine, 2018 Multiple sclerosis is a potentially progressive, autoimmune neurologic disorder of the central nervous system, resulting from an autoimmune attack on central nervous system white matter. It is a leading cause of neurologic symptoms in young adults, with no known cure.
Daniel S. Reich, Peter A Calabresi
exaly +9 more sources
Journal of the Royal Society of Medicine, 1991 Tuberous sclerosis (epiloia, Bourneville-Pringle syndrome) is an inherited disease with an autosomal pattern. Both sexes are affected equally with varied expression in successive generations. Two cases of this unusual disorder in siblings are reported. They illustrate heredofamilial nature, dissimilar expression, mutations, and oral manifestations.
H H, Tillman, F, De Caro
+8 more sources
Вестник урологии, 2022 Introduction. SARS-CoV-2 causes several negative processes in the body and complicates the course of chronic somatic diseases, causing dysfunction and having a negative effect on many organs and systems of the body, including organs of the reproductive ...
S. S. Todorov +3 more
doaj +1 more source
Plasma Cell Rich Osteomyelitis: A Rare Entity [PDF]
Journal of Clinical and Diagnostic Research, 2020 Plasma cell rich osteomyelitis is a rare finding characterised by a plethora of plasma cells localised in the affected bone without the typical clinical features of infection.
PRAKHAR MAHESHWARI +3 more
doaj +1 more source
Clinical Case Reports, 2022 Considerable calcification and stenosis frequently occur in the radial artery (RA) in diabetic nephropathy. PTA was performed successfully using a balloon to expand and restrictively tear the longitudinal axis of the RA.
Jing Xie +4 more
doaj +1 more source
Sternocostoclavicular Hyperostosis: Positive Clinical and Radiological Response on Pamidronate
Frontiers in Endocrinology, 2021 BackgroundSternocostoclavicular hyperostosis (SCCH) is a rare disease, constituting a chronic sterile osteomyelitis with elevated bone turnover in the axial skeleton, causing pain and shoulder dysfunction.
Anne T. Leerling +4 more
doaj +1 more source
A rare case report of intermediate osteopetrosis and review of literature
Journal of Cleft Lip Palate and Craniofacial Anomalies, 2014 Osteopetrosis also known as "marble bone disease" is a group of rare genetic disorders caused by osteoclast failure, which ranges widely in severity.
Priyanka Verma +3 more
doaj +1 more source
Journal of Head & Neck Physicians and Surgeons, 2023 Introduction: Osteoarthritis of temporomandibular joint (TMJ) is a chronic degenerative joint disease characterized by synovitis, cartilage destruction, and subchondral bone remodeling and it is an age-related disorder.
S. Pattugayathri +3 more
doaj +1 more source
Journal of Clinical Investigation, 2012 Multiple sclerosis (MS) is a chronic, complex neurological disease with a variable clinical course in which several pathophysiological mechanisms such as axonal/ neuronal damage, demyelination, inflammation, gliosis, remyelination and repair, oxidative injury and excitotoxicity, alteration of the immune system as well as biochemical disturbances and ...
Alyssa, Nylander, David A, Hafler
openaire +4 more sources
Primary Sclerosing Lipogranuloma: A Rare Cause of Scrotal Mass [PDF]
Journal of Clinical and Diagnostic Research, 2018 Sclerosing Lipogranuloma (SLG) is a rare disease that affects many organs, with male genitourinary system being the most common site. It is a benign disease which occurs due to a granulomatous reaction of fatty tissue in this area.
Smita Singh +3 more
doaj +1 more source