Results 101 to 110 of about 2,439 (246)

NF1 tumor suppressor in skin : Expression in response to tissue trauma and in cellular differentiation [PDF]

, 2002
Type 1 neurofibromatosis (NF1) syndrome is caused by a mutation of the NF1 gene. NF1 protein (neurofibromin) contains a domain which is related to the GTPase activating protein (GAP) and accelerates the switch of active Ras-GTP to inactive Ras-GDP.
Ylä-Outinen, Heli
core  

Schwannomas in the head and neck: retrospective analysis of 21 patients and review of the literature

São Paulo Medical Journal
CONTEXT AND OBJECTIVE: Schwannomas are benign neoplasms of the peripheral nerves originating in the Schwann cells. According to their cellularity, they can be subdivided into Antoni A or Antoni B types.
Erwin Langner, André Del Negro, Hugo Kenzo Akashi, Priscila Pereira Costa Araújo, Alfio José Tincani, Antonio Santos Martins   +5 more
doaj   +1 more source

Intussuscepção intestinal decorrente de tumor de estroma gastrointestinal (GIST) em paciente com neurofibromatose tipo 1 / Intestinal intusception arising from gastrointestinal stroma tumor (GIST) in patient with neurofibromatosis type 1

, 2020
Laila de Castro Tayer, Emanuely Sampaio Clemente dos Reis, Larissa de Castro Tayer, Larissa Morais Souza, Vanessa Tayer Nogueira, Flávia Gomes Fialho, Omar Tayer   +6 more
openalex   +1 more source

RECKLINGHAUSEN'S DISEASE IN А PREGNANT WOMAN: A CLINICAL CASE

Мать и дитя в Кузбассе
Recklinghausen's disease (neurofibromatosis) was first described in 1882. Neurofibromatosis (non-malignant) is classified as a phacomatosis according to the International Classification of Diseases X revision (Q85.0) and is included in the list of orphan
Владимир Кириллович Чайка, Ирина Тихоновна Говоруха, Виталина Васильевна Вустенко, Арина Александровна Земелько   +3 more
doaj  

Segmental neurofibromatosis: A report of 3 cases

Indian Journal of Dermatology, 2010
Neurofibromatosis is a genetic disorder of neural crest-derived cells that primarily affect growth of neural tissues. It is broadly divided into three categories: (a) von Recklinghausen′s neurofibromatosis or NF-1, (b) bilateral acoustic neuroma ...
Gabhane Sushma, Kotwal Mrunmayi, Bobhate Sudhakar   +2 more
doaj  

Neurofibromatose tipo 1: Ensaio para abertura de novos possíveis.

, 2020
Amália Neide Covic, Thomas Pontes Chequetto   +1 more
openalex   +1 more source

Neurofibromatoses

CA: A Cancer Journal for Clinicians, 1992
K L, Roos, D W, Dunn
openaire   +2 more sources

Neurofibromatose tipo 1: mais comum e grave do que se imagina [PDF]

, 2009
Juliana Ferreira de Souza, Luana Lopes de Toledo, Maria Clara Magni Ferreira, Luiz Oswaldo Carneiro Rodrigues, Nilton Alves de Rezende   +4 more
openalex   +1 more source

Neurofibromatose de von Recklinghausen.

Acta Médica Portuguesa, 1989
Neurofibromatosis is a multisystemic disease in which the multiple possible clinical manifestations may have important diagnostic and prognostic implications; if arterial hypertension coexists, many pathogenic mechanisms justify that the possible secondary etiology must be considered.
Ventura, A, Murinello, A, Ribeiro, J, Morgado, A, Castel-Branco Mota, J   +4 more
openaire   +2 more sources

The Roots of Neurofibromas in Neurofibromatosis 1 — A Question of Multipotency, Differentiation and Hiding [PDF]

, 2012
Neurofibromatosis type 1 (NF1) is an autosomal dominant cancer predisposition syndrome that affects about 1 in 3500 individuals worldwide. NF1 is caused by mutations in the NF1 gene that encodes the tumor suppressor protein neurofibromin, an ...
Jouhilahti, Eeva-Mari
core   +1 more source