Results 91 to 100 of about 19,908 (210)
Telomere erosion in NF1 tumorigenesis [PDF]
, 2017 Neurofibromatosis type 1 (NF1; MIM# 162200) is a familial cancer syndrome that affects 1 in 3,500 individuals worldwide and is inherited in an autosomal dominant fashion.
Baird, Duncan +4 more
core +2 more sources
Brain Pathology, Volume 36, Issue 2, March 2026.Mesenchymal stromal cell‐and fibroblast‐expressing Linx paralogue (Meflin) is expressed in embryonic meninges and contributes to meningeal homeostasis. In meningiomas, elevated Meflin correlates with higher grade and recurrence. Single‐cell RNA sequencing revealed a Meflin‐high tumor cell subset marked by reduced proliferation, WNT6 expression, and ...
Yukihiro Shiraki +13 more
wiley +1 more source
Neurofibroma mediastínico [PDF]
, 2014 Varón de 3 añios y 9 meses de edad, remitido por su Pediatra, por hallazgo casual de masa torácica tras práctica de radiografía de tórax, con motivo de una infección respiratoria intercurrente...
Jorba, J. +5 more
core
Oral manifestations of Type I Neurofibromatosis in a family [PDF]
, 2011 Neurofibroma is a benign peripheral nerve sheath tumor. It is one of the most frequent tumors of neural origin and its presence is one of the clinical criteria for the diagnosis of neurofibromatosis type I (NF-I).
Khan, Mubeen, Ohri, Neera
core +1 more source
Endobronchial neurofibroma [PDF]
QJM, 2015 N, Srivali, J M, Boland, J H, Ryu
openaire +2 more sources
Solitary eyelid neurofibroma presenting as tarsal cyst: Report of a case and review of literature
American Journal of Ophthalmology Case Reports, 2018 Purpose: To report a rare case of solitary eyelid neurofiboma presenting as tarsal cyst. Observation: A 64 year old male, presented with a painless, non progressive swelling in the right upper eye lid.
Nisar Sonam Poonam +3 more
doaj +1 more source
Anais Brasileiros de Dermatologia, 2011 Neurofibroma é uma proliferação hamartomatosa de origem neuromesenquimal. Pode ser encontrado associado à neurofibromatose ou como tumor solitário, sendo sua apresentação subungueal solitária bastante rara.
Dionne de Almeida Stolarczuk +4 more
doaj +1 more source
Monozygotic twins with Neurofibromatosis type 1, concordant phenotype and synchronous development of MPNST and metastasis [PDF]
, 2010 Background Neurofibromatosis type 1 is a common autosomal dominant disorder with full penetrance and variable expression. The condition predisposes individuals to the development of malignant nervous system tumours, most frequently Malignant ...
German Melean +5 more
core +1 more source
Gorlin syndrome in a patient with skin type VI [PDF]
, 2019 Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare autosomal dominant disorder that is characterized by multiple basal cell carcinomas developing at a young age, keratocystic odontogenic tumors of the jaw, palmar or plantar ...
Anderson, Kathryn L +3 more
core
Canadian Journal of Anesthesia/Journal canadien d'anesthésie, 2015 Kamath, Sriganesh +3 more
openaire +2 more sources