Results 81 to 90 of about 20,018 (209)
Solitary neurofibroma of the inferior orbit: A rare occurrence
Muller Journal of Medical Sciences and Research, 2015 Solitary neurofibroma in the absence of neurofibromatosis is of rare occurrence and very few have been reported in the literature till now especially in the inferior orbit. A case of solitary neurofibroma of the inferior orbit is presented here.
V Sowmya +3 more
doaj +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
Occlusal traits in children with neurofibromatosis type 1 [PDF]
, 2015 Literature is poor of data about the occlusion in children affected by neurofibromatosis type 1 (NF1).
Amadori, F +7 more
core +1 more source
Brain and Behavior, Volume 16, Issue 1, January 2026.6/7 patients achieved CMI by the third follow‐up, sustained to the fourth follow‐up, and 4/6 reached MSE by the fifth follow‐up. First real‐world evidence of adding telitacicept efficacy in refractory ocular MG symptoms Abstract Introduction Refractory ocular myasthenia gravis (MG) represents a significant therapeutic challenge, as conventional ...
Jing Lin +4 more
wiley +1 more source
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
Clinical Case Reports, Volume 14, Issue 1, January 2026.ABSTRACT This case report highlights a rare malignant transformation of a cervical intranodal schwannoma in a 46‐year‐old man. The patient first came in with a slow‐growing, painless nodule in the right neck. Surgical excision was performed and histopathological examinations revealed a benign intranodal cellular schwannoma.
Shahab Hussain +5 more
wiley +1 more source
Schwannoma of the nasal septum-a case report [PDF]
, 2012 Schwannomas of the nasal cavity and paranasal sinuses are very rare. We report the case of a50-year-old woman with a schwannoma arising from the nasal septum.
Felix, Vinod +2 more
core +1 more source
CPT: Pharmacometrics &Systems Pharmacology, Volume 15, Issue 1, January 2026.ABSTRACT A twice‐daily administration of oral selumetinib (SLT) in the fasted state is the only approved pharmaceutical option for treating inoperable neurofibromatosis type I (NF‐1) and plexiform neurofibromas (PN). In children, exposure to SLT is highly variable, and fasting presents a substantial burden.
Zoltán Köllő +7 more
wiley +1 more source
Chemokine receptor CCR3 is important for migration of mast cells in neurofibroma
Dermatologica Sinica, 2010 Background: Neurofibroma consists of abundant extracellular matrix and many types of cells, including Schwann cells (SCs), mast cells (MCs), fibroblasts and endothelial cells.
Wei-Chun Tai +4 more
doaj +1 more source
Intramuscular (infiltrating) Lipoma [PDF]
, 2011 Intraoral lipomas are benign and relatively rare tumors, although they occur with higher frequencies in other areas, most especially the back, abdomen and shoulders of adults.
Kashyap, Bina +2 more
core +1 more source