Results 131 to 140 of about 200,342 (292)

Lash Impaction in Meibomian Gland Orifice

open access: yesClinical Ophthalmology, 2020
Ahmad M Mansour,1,2 Khalil M El Jawhari3 1Department of Ophthalmology, American University of Beirut, Beirut, Lebanon; 2Department of Ophthalmology, Rafic Hariri University Hospital, Beirut, Lebanon; 3Medical University of Lodz, Lodz ...
Mansour AM, El Jawhari KM
doaj  

An overview of virtual city modelling : emerging organisational issues [PDF]

open access: yes, 2007
This paper presents a recent overview of the increasing use of Virtual Reality (VR) technologies for the simulation of urban environments. It builds on previous research conducted on the identification of three-dimensional (3D) city models and offers an ...
Horne, Margaret   +2 more
core  

Non‐T‐Depleted Haploidentical Transplantation Compared to Allogeneic Transplantation From Matched Siblings or Unrelated Donors in Patients With Secondary AML in First Complete Remission: A Study From the ALWP/EBMT

open access: yesAmerican Journal of Hematology, Volume 101, Issue 2, Page 281-290, February 2026.
ABSTRACT Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative option for secondary acute myeloid leukemia (sAML). This study compared haploidentical donor (Haplo), matched sibling donor (MSD), and matched unrelated donor (MUD) HSCT in patients with sAML in first complete remission (CR1).
Arnon Nagler   +20 more
wiley   +1 more source

A Unique Complex Variation Profile in a Patient with Familial Mediterranean Fever (FMF): Triple Homozygous E148Q-P369S-R408Q – “Case Report”

open access: yesThe Application of Clinical Genetics
Nour Abi Chakra,1,* Nadine Yazbeck,2,* Mohammad Omar Fattah,3 Rima Hanna-Wakim2,4,5 1American University of Beirut, Beirut, Lebanon; 2Department of Pediatrics and Adolescent Medicine, American University of Beirut, Beirut, Lebanon ...
Abi Chakra N   +3 more
doaj  

Rare DMD Gene Duplication in a Lebanese Child With Duchene Muscular Dystrophy

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT A five‐year‐old boy with clinical features of Duchenne muscular dystrophy was found to have a rare de novo DMD exon 2–9 duplication. Reporting such atypical duplications improves genotype–phenotype interpretation and highlights the need for multidisciplinary care, particularly in resource‐limited settings.
Nada Assaf   +4 more
wiley   +1 more source

Epstein–Barr Virus and Hepatitis E Virus in an Immunocompetent Adult: A Rare Case Report

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Epstein–Barr virus (EBV) and Hepatitis E virus (HEV) are two distinct viral pathogens known to affect the liver. While EBV commonly causes mild, self‐limited hepatitis, and HEV is the leading cause of acute viral hepatitis globally, co‐infection with both viruses is exceedingly rare.
Philippe Attieh   +4 more
wiley   +1 more source

Slater to Mott crossover in the metal to insulator transition of Nd2Ir2O7

open access: yes, 2016
We present an angle-resolved photoemission study of the electronic structure of the three-dimensional pyrochlore iridate Nd2Ir2O7 through its magnetic metal-insulator transition.
Balents, L.   +18 more
core   +1 more source

Minimal residual disease in solid tumors: Clinical applications and future directions

open access: yesCancer, Volume 132, Issue 3, 1 February 2026.
Abstract Minimal residual disease (MRD) refers to the presence of residual cancer cells or tumor‐derived fragments that persist after treatment and remain undetectable by conventional imaging or protein‐based assays. Circulating tumor DNA (ctDNA) has emerged as a dynamic biomarker for MRD detection.
Theresa Abdo   +8 more
wiley   +1 more source

Subtitling Arabic profanities into English and that aggro: the case of West Beirut

open access: yesHeliyon, 2022
Mohammad Ahmad Thawabteh   +2 more
semanticscholar   +1 more source

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