Results 121 to 130 of about 122,915 (293)
Paediatric Respiratory Reviews, 2019 Paediatric sarcoidosis is an extremely rare disease characterized by a granulomatous inflammation. The estimated incidence is 0.6-1.02/100,000 children, but in the absence of international registers, the disease is probably under-reported. Its pathophysiologic basis is not clearly understood but the current hypothesis is a combination of a genetic ...
Nathan, Nadia +8 more
openaire +8 more sources
Journal of Internal Medicine, 2016 : Cardiac sarcoidosis is a rare but life-threatening condition, requiring a high degree of clinical suspicion and low threshold for investigation to make the diagnosis.
B. T. Costello +2 more
semanticscholar +1 more source
Cryptococcal meningitis complicating sarcoidosis
Medicine, 2016 Background:Cryptococcal meningitis is an uncommon but severe complication of sarcoidosis. Methods:We present 2 patients with cryptococcal meningitis complicating sarcoidosis and compared findings with 38 cases reported in the literature.
S. Leonhard +3 more
semanticscholar +1 more source
World Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.ABSTRACT Spasmodic dysphonia is a laryngeal dystonia that can present as adductor, abductor, or mixed types, with or without tremor. The etiology is not understood fully. Comprehensive evaluation is required to establish the diagnosis. Treatments include voice therapy, medications, botulinum toxin injection, laryngeal surgery, deep brain stimulation ...
Aaron J. Jaworek, Robert T. Sataloff
wiley +1 more source
Calcium Metabolism and Bone Changes in Sarcoidosis [PDF]
, 1957 Gordon Mather
openalex +1 more source
American Journal of Respiratory and Critical Care Medicine, 2016 RATIONALE Pulmonary sarcoidosis is classically defined by T-helper (Th) cell type 1 inflammation (e.g., IFN-γ production by CD4(+) effector T cells). Recently, IL-17A-secreting cells have been found in lung lavage, invoking Th17 immunity in sarcoidosis ...
Joris Ramstein +15 more
semanticscholar +1 more source
The Journal of Dermatology, EarlyView.ABSTRACT HLA‐B51 is well‐established as a genetic risk factor for the development of Behçet's disease (BD), and its association with certain clinical manifestations has been documented. However, there is a lack of comprehensive research examining its role in the overall symptom completeness and full clinical expression of the disease.
Bo Hyun Lee +4 more
wiley +1 more source
Editorial: Interstitial Lung Disease Around the World
Frontiers in Medicine, 2022 Marlies Wijsenbeek +4 more
doaj +1 more source