Results 11 to 20 of about 8,062 (235)
Intravitreal triamcinolone for management of idiopathic juxtafoveolar telangiectasis
Oman Journal of Ophthalmology, 2010 Nitin Nema, Michael S Ip
doaj +2 more sources
BMC Ophthalmology, 2018 Background To evaluate the structural changes associated with visual acuity (VA) in patients with idiopathic macular telangiectasia (MT) type 1 using multimodal imaging modalities.
Jingli Guo +6 more
doaj +2 more sources
Route of Delivery in a Patient with Vaginal Stenosis from Stevens-Johnson Syndrome and Review of the Management of Genital Complications [PDF]
Women's Health ReportsBackground: Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe dermatological conditions, predominantly affecting women with mortality rates of 4.8–48%. Antibiotics are common triggers.
Meng-Chen Tsai +2 more
doaj +2 more sources
Hereditary multiple telangiectasis
, 1927 (l) The cause of the disease is unknown. (2) It has a hereditary nature, and appears in both sexes. It can be transmitted by both male and female. (3) There is a tendency to increase in severity with advancing years. (4) Recovery is rare. (5) It is rarely a primary cause of death. (6) There is no satisfactory treatment.
Hilton T. Smith
openaire +2 more sources
Ataxia Telangiectasia: A Single Center Experience in a Decade [PDF]
Pediatric Sciences Journal, 2022 Background: Ataxia Telangiectasia (A-T) is a rare neurodegenerative disorder that affects a number of different systems of the body. Aim of the work: To identify the spectrum of clinical presentations of children with A-T.
Lobna Mansour +5 more
doaj +1 more source
Clinical Presentation and Pathological Effects of a Hydrozoan Bloom on Farmed Atlantic Salmon. [PDF]
J Fish DisABSTRACT Largely unpredictable, gelatinous plankton blooms are a growing concern for the ever‐expanding mariculture industry. Recently, a bloom of a colonial hydrozoan known as Apolemia sp. was detected via a citizen‐science initiative, Nye.dugnadforhavet.no, in mid‐Norway in July 2023.
Madaro A +5 more
europepmc +2 more sources
Case Report: TEMPI syndrome: Report of three cases and treatment follow-up
Frontiers in Oncology, 2022 The TEMPI syndrome is a novel and rare disease with five distinct clinical features: Telangiectasis, Erythrocytosis, Monoclonal gammopathy, Perinephric fluids collection, and Intrapulmonary shunting.
Zhuo-Fan Xu +11 more
doaj +1 more source
Idiopathic Juxtafoveolar Retinal Telangiectasis
Delhi Journal of Ophthalmology, 2010 Idiopathic juxtafoveolar retinal telangiectasis (IJRT), also known as idiopathic macular telangiectasia (IMT), refers to a heterogeneous group of well recognized clinical entities characterized by telangiectatic alterations of the juxtafoveolar capillary
Neha Goel +4 more
doaj +3 more sources