Results 11 to 20 of about 922,760 (302)
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 grounded theory analysis of the occupational impact of caring for a partner who has multiple sclerosis [PDF]
, 2006 Chronic progressive conditions such as multiple sclerosis impact engagement in and orchestration of daily occupations by people with the condition, and their family members.
Gough, B, Heward, K, Molineaux, M
core +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
A longitudinal study of abnormalities on MRI and disability from multiple sclerosis [PDF]
, 2002 Background: In patients with isolated syndromes that are clinically suggestive of multiple sclerosis, such as optic neuritis or brain-stem or spinal cord syndromes, the presence of lesions as determined by T2-weighted magnetic resonance imaging (MRI) of ...
Brex, P.A. +5 more
core +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
Review: ‘Gimme five’: future challenges in multiple sclerosis. ECTRIMS Lecture 2009 [PDF]
, 2010 This article is based on the ECTRIMS lecture given at the 25th ECTRIMS meeting which was held in Düsseldorf, Germany, from 9 to 12 September 2009. Five challenges have been identified: (1) safeguarding the principles of medical ethics; (2) optimizing the
Bartholomaus I. +44 more
core +1 more source