Results 21 to 30 of about 331,329 (292)
Orbital myeloid sarcoma (chloroma): Report of 2 cases and literature review
American Journal of Ophthalmology Case Reports, 2020 Purpose: Myeloid sarcoma (MS) of the orbit is an uncommon condition in occurring in children, generally coupled to myeloproliferative neoplasms. Observations: We describe two rare cases of orbital MS in young boys with aggressive local symptoms but ...
Mohammad A. AlSemari +11 more
doaj +1 more source
Epigenetic Activation of SOX11 in Lymphoid Neoplasms by Histone Modifications [PDF]
, 2011 Recent studies have shown aberrant expression of SOX11 in various types of aggressive B-cell neoplasms. To elucidate the molecular mechanisms leading to such deregulation, we performed a comprehensive SOX11 gene expression and epigenetic study in stem ...
Amador Virginia +107 more
core +1 more source
A Rare Case of Intraconal Orbital Schwannoma
Archives of Medicine and Health SciencesSchwannoma is a benign, slow-growing peripheral nerve sheath tumor that originates from Schwann cells. Orbital schwannoma is relatively rare, accounting for only 1% of all orbital neoplasms. Intraconal orbital schwannoma (within the muscle cone) is rarer
Savithri Ravindra +2 more
doaj +1 more source
Congenital orbital teratoma: a case report with preservation of the globe and 18 years of follow-up
BMC Ophthalmology, 2021 Background Congenital orbital teratomas are extremely rare, usually benign neoplasms, comprised of cells originating from all three germ cell layers. Clinically the tumor appears solid, most of the times is intraconal and presents as a rapidly growing ...
Panagiotis A. Tsoutsanis +1 more
doaj +1 more source
The Orbital Hemangiopericytoma: The Number of Reported Cases and a Possible Risk Factor [PDF]
Journal of Advanced Biomedical Sciences, 2016 I read, with interest, the article entitled “The Orbital and Sinonasal Hemangiopericytoma, 2 Case Reports” by Maryam Maghbol et al. published in this journal.
Mohammad Reza Sasani
doaj +2 more sources
Molecular Oncology, EarlyView.Drug resistance limits treatment success in a subset of lung cancers driven by ROS1 gene alterations. Using patient‐derived cells and computer simulations, we studied three key mutations and how they affect five targeted drugs. The mutations reduced drug effectiveness in different ways by altering protein structure and behavior.
Farhan Ul Haq +8 more
wiley +1 more source
Protein‐Nanoarchitectures for Low‐Field Intracellular Electro‐Immunomodulation
Advanced Functional Materials, EarlyView.DHQ‐SDH‐mediated binding of AuNPs drives the formation of interconnected, chain‐like nanoarchitectures with enhanced electrical conductivity. These conductive assemblies undergo macrophage uptake and enable low‐field electrical stimulation, promoting M1‐to‐M2 phenotypic switching with decreased iNOS and increased CD206 expression. Such protein‐mediated
Viktoriya Pakharenko +7 more
wiley +1 more source
Advanced Healthcare Materials, EarlyView.Engineered red blood cell‐derived extracellular vesicles (eRBCEVs) are synthesized via controlled microfluidic assembly from native RBC lipids, enabling tunable encapsulation of proteins, nucleic acids, nanoparticles, and viral vectors. The platform demonstrates reproducible nanoscale architecture, preserved membrane composition, and functional cargo ...
Chiranth K. Nagaraj +23 more
wiley +1 more source
Cystic orbital schwannoma: A surgeon’s surprise
Indian Journal of Ophthalmology. Case ReportsSchwannomas, also known as neurilemmomas, are benign, encapsulated tumors arising from Schwann cells. Solitary orbital schwannomas are rare, comprising only 1% of orbital neoplasms.
Miriam Ankita Clement +5 more
doaj +1 more source
BMC Surgery, 2021 Background Orbital solitary fibrous tumors (SFTs) are rare neoplasms. Recurrent, hypervascular, malignant variations of orbital SFTs have recently been noted and can present a surgical challenge.
Xiawei Wang +7 more
doaj +1 more source