Results 31 to 40 of about 7,621 (203)
INTRACRANIAL TELANGIECTASIS [PDF]
Archives of Neurology & Psychiatry, 1921 The two following cases of probable cerebral telangiectasis seem to be of sufficient interest to warrant report. REPORT OF CASES Case 1.— History .—A merchant, aged 21 years, was referred by Dr. Ransom of Hancock, Minn., July 14, 1920. The patient's family history was negative except that his father died of diabetes.
openaire +1 more source
Incorporation of two terminology projects into a system for information retrieval using NLP for term expansion [PDF]
, 2007 In this paper, we will discuss two medical terminology projects at the University College of Ghent, Faculty of translation studies, and the benefits of combining them to provide Dutch professionals and laymen with better access to information in ...
Van Wiele, Kurt, Vanopstal, Klaar
core +1 more source
Transcriptomics in Venous Leg Ulcers (VLU): A Systematic Review
Wound Repair and Regeneration, Volume 34, Issue 2, March/April 2026.ABSTRACT Venous leg ulcers (VLUs) are chronic wounds in the lower limbs that cause significant morbidity. The underlying biology underpinning non‐healing in VLUs is still poorly understood and differences in transcriptomic profiles may help elucidate biological pathways involved in wound chronicity.
Chien Lin Soh +3 more
wiley +1 more source
Safety evaluation of chloramine-T on ornamental zebra fish (Danio rerio) using LC50 calculation and organ pathology [PDF]
, 2017 The need of aquarists for proper and safe disinfection of fish with Chloramine-T (CL-T) necessitates toxico/pathologic examinations. This study assays toxicity level of CL-T and histopathologic changes of gills, liver, kidney and brain of treated ...
Alidadi Soleimani, T. +3 more
core
Unilateral Nevoid Telangiectasis: Report of Five Cases [PDF]
, 2010 Unilateral nevoid telangiectasia (UNT) is a rare cutaneous disorder characterized by superficial telangiectasias distributed unilaterally. UNT can be congenital or acquired.
Canan Aslan +4 more
core +1 more source
Novel Simplified Nasal Endoscopy Grading System for Hereditary Hemorrhagic Telangiectasia Patients
The Laryngoscope, Volume 136, Issue 2, Page 652-657, February 2026.We validated a novel, simplified nasal endoscopy grading system for patients with Hereditary Hemorrhagic Telangiectasia (HHT). Our grading (mild, moderate, severe) demonstrated strong correlation with Epistaxis Severity Score (ESS) and Quality of Life (QoL), and showed substantial inter‐rater reliability (ICC = 0.8).
Ethan Soudry +4 more
wiley +1 more source
Uncommon skeletal findings in systemic sclerosis (scleroderma)
South African Journal of Radiology, 2002 Scleroderma or progressive systemic sclerosis is a diffuse disease characterised by excessive deposition of collagen and small-vessel arteritis. Systemic sclerosis is divided into two groups. 1.
Betsie van der Walt +2 more
doaj +1 more source
European Journal of Neurology, Volume 33, Issue 2, February 2026.Hereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Matteo Palermo, Carmelo Lucio Sturiale
wiley +1 more source
Acta Dermato-VenereologicaTelangiectasia macularis multiplex acquisita is an acquired cutaneous telangiectasis of unknown aetiology, and it lacks both effective and cost-efficient treatment.
Tian Chen +6 more
doaj +1 more source
Endoscopic Vascular Grading Directs Stepwise Therapy in Hereditary Hemorrhagic Telangiectasia
Laryngoscope Investigative Otolaryngology, Volume 10, Issue 5, October 2025.This study introduces a novel endoscopic vascular grading system for HHT. The system is inspired by intergenerational family observations and correlates with epistaxis severity. It guides personalized therapy based on grade, offering simplicity and clinical utility.
Hong‐Gang Duan +5 more
wiley +1 more source