Results 21 to 30 of about 208,319 (209)

Intranasal glial heterotopia in an infant boy

open access: yesPediatric Investigation, 2021
Introduction Nasal glial heterotopia is a rare congenital developmental disorder characterized by meningeal epithelium and/or glial components. Case presentation A 2‐month‐old boy presented for treatment of a congenital mass in the right nasal cavity ...
Wei Zhang, Lixing Tang, Wentong Ge
doaj   +1 more source

Central Nervous System Tumors in Xeroderma Pigmentosum: Five Cases and Review of the Literature. [PDF]

open access: yesMov Disord
Abstract Background Xeroderma pigmentosum (XP) is a rare autosomal recessive DNA‐repair disorder characterized by extreme ultraviolet radiation (UVR) sensitivity, markedly increased cutaneous malignancy risk, and progressive neurological disease in approximately one‐third of patients.
Bakr FS   +4 more
europepmc   +2 more sources

Focused Ultrasound-Enhanced Delivery of Intranasally Administered Anti-Programmed Cell Death-Ligand 1 Antibody to an Intracranial Murine Glioma Model

open access: yesPharmaceutics, 2021
Immune checkpoint inhibitors have great potential for the treatment of gliomas; however, their therapeutic efficacy has been partially limited by their inability to efficiently cross the blood–brain barrier (BBB).
Dezhuang Ye   +4 more
doaj   +1 more source

Nasal lysine aspirin challenge in the diagnosis of aspirin - exacerbated respiratory disease [PDF]

open access: yes, 2013
Background Aspirin-exacerbated respiratory disease is under-diagnosed and therefore effective and inexpensive therapy with aspirin desensitization is rarely performed.
J. Larco   +13 more
core   +1 more source

Temozolomide hexadecyl ester targeted plga nanoparticles for drug-resistant glioblastoma therapy via intranasal administration

open access: yesFrontiers in Pharmacology, 2022
Introduction: Temozolomide (TMZ) is the first-line drug for glioblastoma (GBM), but it is limited in clinical use due to the drug resistance, poor brain targeting, and side effects.
Siqi Wang   +12 more
doaj   +1 more source

A Case Report of Nasal Glial Heterotopia

open access: yesB-ENT, 2023
Nasal glial heterotopia (NGH), also known as nasal glioma, is a rare congenital malformation in which a mature glial cell mass is found in a location other than the central nervous system.
Annelien Huygen   +4 more
doaj   +2 more sources

Clinical and Therapeutic Approaches to Nasal Glial Heterotopia in Children. [PDF]

open access: yesBatna Journal of Medical Sciences
Nasal heterotopias or gliomas are rare congenital malformations characterized by a nasal mass composed of heterotopic neuroglial tissue. They fall within the nosological spectrum of midline dysraphias, presenting a complex diagnostic and therapeutic ...
Fadila GHARSALLAH, Haroun BOUMAZA
doaj   +1 more source

Receptors for hyaluronic acid and poliovirus: a combinatorial role in glioma invasion? [PDF]

open access: yes, 2012
BACKGROUND: CD44 has long been associated with glioma invasion while, more recently, CD155 has been implicated in playing a similar role. Notably, these two receptors have been shown closely positioned on monocytes.
James R Smith   +11 more
core   +2 more sources

Nasal Glioma

open access: yesInternational Journal of Dermatology, 1982
ABSTRACT:Light and electron microscopic studies in a case of nasal Glioma revealed a tumor composed nearly entirely of astrocytes. No ganglion cells or neurons were present and the mass was not surrounded by a capsule reminiscent for meningeal tissue. The vasculature resembled dermal patterns rather than typical central nervous system.
W, Gebhart   +3 more
openaire   +4 more sources

Nasal glial heterotopia with cleft palate

open access: yesJournal of Indian Association of Pediatric Surgeons, 2018
Congenital midline nasal masses are rare anomalies of which nasal glial heterotopia represents an even rarer subset. We report a case of a 25-day-old male child with nasal glial heterotopia along with cleft palate suggesting embryonic fusion anomaly ...
Sudhir Chandna   +2 more
doaj   +1 more source

Home - About - Disclaimer - Privacy