Results 81 to 90 of about 3,674 (207)

Scientific and Educational Value of Case Reports [PDF]

, 2017
info:eu-repo/semantics ...
Donato, H
core  

Thalamic intracerebral schwannoma: case report [PDF]

, 2002
The intracranial schwannomas cover about 8% of all the brain tumors, although, those localized inside the encephalic parenchyma are rare only 55 cases being reported in the literature.
Andrade, Guilherme Cabral De, Braga, Fernando Menezes, Paiva Neto, Manoel Antonio de   +2 more
core   +2 more sources

Gonadal and gonadosomatic mosaicism in NF1: report of two families

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 3, Page 426-428, March 2024.
Magdalena Seidl‐Philipp, Nathalie Veyt, Simon Schnaiter, Anne Krogsdam, Simon Schwendinger, Ophélia Maertens, Christine Fauth, Matthias Schmuth, Eric Legius, Katharina Wimmer, Hilde Brems   +10 more
wiley   +1 more source

Gonadales und gonadosomatisches Neurofibromatose‐Typ‐1‐Mosaik: ein Bericht über zwei Familien

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 3, Page 426-429, March 2024.
Magdalena Seidl‐Philipp, Nathalie Veyt, Simon Schnaiter, Anne Krogsdam, Simon Schwendinger, Ophélia Maertens, Christine Fauth, Matthias Schmuth, Eric Legius, Katharina Wimmer, Hilde Brems   +10 more
wiley   +1 more source

Neurofibrossarcoma associado a neurofibromatose

Revista do Colégio Brasileiro de Cirurgiões
The clinical and pathological aspects of neurofibromatosis are summarized and an updated pathogeny of the tumor is made. The malignancy of the NFS senns to be linled to the NF - 1 gene mutations, with loss of the suppressor gene in the chromosone 17 pl ...
Alcino Lázaro da Silva, Venício do Amaral Quirino   +1 more
doaj   +1 more source

Neurofibromatose e doença arterial oclusiva intracraniana extensa (doença de Moya-Moya): registro de um caso

Arquivos de Neuro-Psiquiatria, 1986
O caso de urna paciente de 33 anos com neurofibromatose e lesões vasculares intracranianas do tipo Moya-Moya é discutido com relação a aspectos clínicos e angiográficos.
C. M. Gracia, P. C. T. Bittencourt, S. Mazer, P. R. M. Bittencourt   +3 more
doaj   +1 more source

Maladie de Von Recklinghausen compliquée de Neurofibromes plexiformes cervico-faciaux

The Pan African Medical Journal, 2015
La neurofibromatose de type 1 (NF1), appelée également maladie de Von Recklinghausen, est une affection autosomique dominante caractérisée par son polymorphisme clinique.
Madiha Mahfoudhi, Khamassi Khaled
doaj   +1 more source

Jejunal stromal tumor and neurofibromatosis

Journal of Coloproctology, 2019
Gastrointestinal stromal tumors, although rare, are the most common primary mesenchymal neoplasms of the gastrointestinal tract and originate from the interstitial cells of Cajal.
Daniela Fonseca Lisboa Kayser, Lígia Nascimento Figueiredo Amaral, Livia Paulucci Cavalcanti Andrade, Fernando Augusto Santos Vasconcelos, Luiz Felipe de Campos-Lobato, Juliano Alves Figueiredo   +5 more
doaj   +1 more source

La neurofibromatose 1 [PDF]

médecine/sciences, 2001
La neurofibromatose 1 (NF1) est une maladie autosomique dominante qui atteint environ 1 individu sur 4 000. Le gene NF1 situe sur le chromosome 17 en q11.2 est constitue d’un domaine d’environ 335 kilobases et code pour une proteine de 2 818 acides amines, la neurofibromine. C’est un gene suppresseur de tumeur.
openaire   +1 more source

Doença de Moyamoya: relato de três pacientes brasileiros [PDF]

, 1999
Moyamoya disease (MMD) is a chronic occlusive cerebrovascular disease of unknown etiology reported mainly in the Japanese. Most cases occur in children. The disease is rare in non-Oriental adults manifesting itself mostly as intracerebral hemorrhages. We
Franco, Clélia Maria Ribeiro, Fukujima, Marcia Maiumi, Gabbai, Alberto Alain, Oliveira, Roberto de Magalhães Carneiro de   +3 more
core   +3 more sources