FAP expression as a marker of malignant transformation enabling in vivo characterization in peripheral nerve sheath tumors: a multimodal and translational study. [PDF]
Reitsam NG +15 more
europepmc +1 more source
Differentiation of MPNSTs from benign neurofibromas in neurofibromatosis patients using ADC and SUV biomarkers in children and young adults. [PDF]
Shokri Varniab Z +6 more
europepmc +1 more source
The Complexities of Periorbital Neurofibroma: Diagnostic Ambiguity and Therapeutic Dilemmas: A Case Report and Literature Review. [PDF]
Leketas M +5 more
europepmc +1 more source
Severe Necrotizing Pneumonia as an Unusual Initial Manifestation of Neurofibromatosis Type 1: A Case Presentation. [PDF]
Anyfanti P +14 more
europepmc +1 more source
Anomalous hemorrhage in myxopapillar ependymoma: illustrative case. [PDF]
Caelers IJMH, van Nie FA, Smeets AYJM.
europepmc +1 more source
Related searches:
FDA Approval Summary: Selumetinib for Plexiform Neurofibroma
Clinical Cancer Research, 2021On April 10, 2020, the FDA approved selumetinib (KOSELUGO, AstraZeneca) for the treatment of pediatric patients 2 years of age and older with neurofibromatosis type 1 who have symptomatic, inoperable plexiform neurofibromas.
Denise Casey +27 more
semanticscholar +1 more source
Although neurofibroma is a rare orbital tumor, ophthalmic nurses may have the first opportunity to observe patients with this tumor. These patients may first be seen with normal visual acuity, proptosis, or affected ocular motility. An interesting patient who was diagnosed with an orbital neurofibroma is presented.
C A, Servodidio +2 more
openaire +2 more sources
Collagens in Neurofibromas and Neurofibroma Cell Cultures
Annals of the New York Academy of Sciences, 1986Neurofibromas contain approximately 30-50% collagen of their lipid-free dry weight, which is about half of the value of skin but approximately twice that described for peripheral nerve endoneurium. Immunohistochemical stainings indicate that neurofibromas contain types I, III, IV, and V collagens and fibronectin. Most of the neurofibroma cells are type
J, Peltonen +3 more
openaire +2 more sources
Unless omitted and underreported, penile neurofibromas are rare. Between January 2, 1982 and December 31, 1997 through the USF Regional Genetics Program we evaluated 566 propositi with suspected or clinically diagnosed neurofibromatosis (NF1, NF2, segmental NF=NF5, NF/Noonan syndrome, familial café-au-lait macules, and solitary neurofibroma, NF). These
B G, Kousseff, D L, Hoover
openaire +2 more sources
Cholinesterases in Neurofibromas
Archives of Dermatology, 1962Cholinesterase is an enzyme associated with neural tissue. It has been demonstrated chemically and histochemically in sensory and motor tissue of the central nervous system, the myoneural junction, and the sensory end-organs. 1 Specific cholinesterase, which hydrolyzes acetylcholine and acetylbetamethylcholine (methacholine), is found in autonomic ...
R K, WINKELMANN, L A, JOHNSON
openaire +2 more sources

