Results 11 to 20 of about 488 (159)
Subclinical varicose vein recurrence: modern approaches in aesthetic phlebology [PDF]
Background Recurrence after varicose vein treatment is usually framed as varices on a previously treated limb, potentially overlooking patients with cosmetic C0–C1 concerns who still experience duplex Doppler ultrasound-verified reflux.
Serhii Shchukin
doaj +2 more sources
Oral and periodontal manifestations associated with systemic sclerosis: A case series and review
Systemic sclerosis is a rare connective tissue disorder with a wide range of oral manifestations. This case series reports significant oral and periodontal changes and also makes an attempt to correlate oral and systemic findings in these patients which ...
Rekha Jagadish +2 more
doaj +1 more source
Purpose: To present a case of vaso-vagal syncope (VVS) after mydriatic eye drops in a patient with cutaneous hemangioma and intracerebral vascular abnormalities.
Sarah A Alowedi +3 more
doaj +3 more sources
INVESTIGATIONS ON AN OUTBREAK OF OVINE INFECTIOUS NECROTIC HEPATITIS AT SOHAG GOVERNORATE [PDF]
A herd of 78 raising sheep at Sohag Governorate appeared suffering from drowsiness, rapid shallow respiration and 9 % mortality rate. The necropsy findings were frothy fluid from the mouth and nose, subcutaneous congestion and haemorrhages ...
Shahera M.R. Abdel Haseeb +2 more
doaj +1 more source
Optical coherence tomography characteristics of group 2A idiopathic parafoveal telangiectasis [PDF]
PURPOSE: To describe the optical coherence tomography (OCT) characteristics of patients with group 2A idiopathic parafoveal telangiectasis (IPFT) and to correlate them with biomicroscopic and fluorescein angiographic (FA) findings based on Gass and Blodi
SANCHEZ, JUAN G. +11 more
core +1 more source
Hereditary hemorrhagic telangiectasis with juvenile polyposis syndrome: a case report
Hereditary hemorrhagic telangiectasis (HHT) and juvenile polyposis syndrome (JPS) are both relatively rare hereditary disorders. It has been reported that patients with SMAD4 mutations may suffer from both HHT and JPS, defined as JPS/HHT.
Meng-Yu Tao +7 more
doaj +1 more source
Adult onset coats disease in a 56-year-old male: An atypical presentation
Coats disease is a congenital retinal vascular disease, which is seen commonly in childhood and remits and exacerbates throughout life. However, it is not rare for coats disease to present in adulthood for the first time.
Bodhraj Dhawan +3 more
doaj +1 more source
Triple Therapy Management of Macular Telangiectasia
We report the case of a 65 year old lady presenting with sudden diminution of vision in her right eye (RE) with the best corrected visual acuity (BCVA) being counting fingers at 1 metre.
Hammad Rashid Nasti +3 more
doaj +1 more source
Bilateral juxtafoveolar telangiectasis in monozygotic twins
PURPOSE: To report the clinical and angiographic features of two monozygotic twins affected by bilateral group 2 idiopathic juxtafoveolar telangiectasis. METHOD: Case reports.
Rapizzi E +7 more
core +1 more source

