Results 91 to 100 of about 31,040 (260)
Sjögren: unique surname, two men, four syndromes and one disease
Arquivos de Neuro-PsiquiatriaHenrik and Torsten Sjögren (/ˈʃoʊɡrən/ or SHOH–grən) were two Swedish physicians living in the same period, but completely unrelated, except for their notable contributions to Medicine. The first one described keratoconjunctivitis sicca, afterward called
José Vitor Alécio Rodrigues +7 more
doaj +1 more source
Você conhece esta síndrome? Do you know this syndrome?
Anais Brasileiros de Dermatologia, 2010 Relatamos um caso típico, em um paciente masculino de 20 anos, da síndrome de Sjögren-Larsson, que é uma doença neurocutânea, autossômica recessiva e incapacitante, caracterizada por ictiose congênita, plegia espástica e retardo mental.
Marcela Duarte Villela Benez +3 more
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Clinical and laboratorial profile and histological features on minor salivary glands from patients under investigation for Sjögren's syndrome [PDF]
, 2014 Diagnosis of Sjögren's syndrome (SS) is complex and the usefulness of labial minor salivary glands biopsy in this process remains controversial. Objectives: to evaluate the clinical and laboratorial profile and histological features on labial minor ...
dos-Santos, Teresa-Cristina-Ribeiro-Bartholomeu +3 more
core +1 more source
Salivary gland scintigraphy in sjögren syndrome
Revista Ciencias Biomédicas, 2011 Sjögren syndrome is a systemic autoimmune disease that mainly affects exocrineglands, such as the salivary and lacrimal glands, causing a decline in their secretions.This disease is also known as Sicca Syndrome.
Betancourt-Piñeres Aiken Felipe +6 more
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Autoimmune hyperphosphatemic tumoral calcinosis in a patient with FGF23 autoantibodies [PDF]
, 2018 Hyperphosphatemic familial tumoral calcinosis (HFTC)/hyperostosis-hyperphosphatemia syndrome (HHS) is an autosomal recessive disorder of ectopic calcification due to deficiency of or resistance to intact fibroblast growth factor 23 (iFGF23). Inactivating
Burbelo +14 more
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Characterization of Pulmonary Functional Abnormalities in Systemic Sclerosis Using Xenon MRI
Journal of Magnetic Resonance Imaging, EarlyView.ABSTRACT Background Xenon MRI is increasingly used to evaluate patients with interstitial lung disease (ILD) and pulmonary hypertension (PH), both of which are common manifestations of systemic sclerosis (SSc). As such, Xe‐MRI may be suited to interrogate lung function impairment in SSc.
Dawson Shaver +11 more
wiley +1 more source
Caspian Journal of Neurological Sciences, 2015 Sjogren-Larsson Syndrome (SLS) is an inherited autosomal recessive neurocutaneous disorder with congenital ichthyosis, spastic diplegia or quadriplegia and mental retardation.
Karim Nikkhah +2 more
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New Aspects of Thromboangiitis obliterans (von Winiwarter-Buerger's Disease) [PDF]
, 1984 The existence of thromboangiitis obliterans as a clinical entity has been a matter of debate for many years. In contrast to other immunovasculitides there is no organ involvement while peripheral vessels are affected.
Berlit, Peter +3 more
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Ocular facial myositis and sialadenitis presenting with new onset ulcerative colitis
JPGN Reports, EarlyView.Abstract Extra‐intestinal manifestations of inflammatory bowel disease (IBD) can involve most organ systems, although the immunologic underpinnings are not well understood. Most patients who present with an extra‐intestinal manifestation have a single site of extra‐intestinal involvement; however, a small cohort presents with multiple different sites ...
Nicole Du, Nicole Mendez, Anil Darbari
wiley +1 more source
Computed tomographic imaging characteristics of the normal canine lacrimal glands. [PDF]
, 2014 BackgroundThe canine lacrimal gland (LG) and accessory lacrimal gland of the third eyelid (TEG) are responsible for production of the aqueous portion of the precorneal tear film.
Murphy, Christopher J +2 more
core +2 more sources