Results 131 to 140 of about 62,771 (244)

Macrocephaly in neurofibromatosis type 1: a sign post for optic pathway gliomas? [PDF]

, 2018
Purpose: Optic pathway gliomas, which occur in 15-20% of paediatric patients with neurofibromatosis type 1, are the most common central nervous system tumour associated with this neurocutaneous disorder.
Diepold, Miriam, Fleischhauer, Johannes, Goeggel Simonetti, Barbara, Nauer, Claude, Schindera, Christina, Steinlin, Maja, Wingeier, Kevin   +6 more
core  

Neurofibromatosis tipos 1 y 2

Revista del Hospital Italiano de Buenos Aires
La neurofibromatosis (NF) comprende un grupo de enfermedades genéticas de herencia autosómica dominante, que se clasifican de la siguiente manera: neurofibromatosis tipo 1 (NF1), neurofibromatosis tipo 2 (NF2) y schwannomatosis (también conocida como ...
María Florencia Correa, Natalia Inés Pasik   +1 more
doaj  

Neurofibromatosis: chronological history and current issues Neurofibromatose: histórico cronológico e aspectos atuais

Anais Brasileiros de Dermatologia, 2013
Neurofibromatosis, which was first described in 1882 by Von Recklinghausen, is a genetic disease characterized by a neuroectodermal abnormality and by clinical manifestations of systemic and progressive involvement which mainly affect the skin, nervous ...
João Roberto Antônio, Eny Maria Goloni-Bertollo, Lívia Arroyo Trídico   +2 more
doaj  

Pathology in Practice [PDF]

, 2017
Lofts, R, Priestnall, S L, Summers, B A, Terry, R   +3 more
core   +1 more source

Fatal Tension Hemothorax Combined with Exanguination: A Rare Complication of Neurofibromatosis [PDF]

, 2019
Neurofibromatosis (NF) is a common autosomal dominant disorder that can be subdivided into type 1, type 2, and schwannomatosis. Patients with NF1 typically develop café-au-lait spots, scoliosis, and benign neurofibromas.
Bidad, Roz, Blohm, Eike, Hall, Caroline
core  

Giant gluteal and vesical plexiform neurofibromas in a patient with neurofibromatosis type 1: a case report

Journal of Medical Case Reports
Background Neurofibromatosis type 1 is a neurocutaneous genetic disorder caused by mutations in the NF1 gene, resulting in the formation of benign tumors called neurofibromas.
Imen Sassi, Mohamed Amine Bouida, Anis Hasnaoui, Ines Zemni, Tarek Ben Dhieb   +4 more
doaj   +1 more source

Plexiform neurofibroma

Journal of the European Academy of Dermatology and Venereology, Volume 40, Issue 4, Page 693-694, April 2026.
Francisco Martins, Ana Carolina Figueiredo   +1 more
wiley   +1 more source

"Cornflake nevoid" lesions, mimicking choroidal lesions of neurofibromatosis 1, in the absence of neurofibromatosis 1: An imaging-based hypothesis. [PDF]

Saudi J Ophthalmol, 2023
Papasavvas I, Herbort CP.
europepmc   +1 more source

Neurofibromatosis tipo 1 y embarazo: consideraciones sobre un caso clínico Neurofibromatosis type 1 and pregnancy: considerations on a clinical case

Revista Médica Electrónica, 2012
Se presenta el caso de gestante de 27 años de edad, afecta de neurofibromatosis tipo 1, diagnosticada preconcepcionalmente, la cual fue atendida en el consultorio del médico de familia no.
Pedro Lorenzo Rodríguez Domínguez, Damarys Hernández Suárez   +1 more
doaj  

Meningioma (ECR 2014 Case of the Day) [PDF]

, 2014
De Belder, F, Eyselbergs, M, Gielen, J, Lammens, M, Parizel, PM, Salgado, R, Somville, J, Van Dyck, P, Vanhoenacker, Filip   +8 more
core   +2 more sources