Zobrazeno 1 - 10
of 414
pro vyhledávání: '"neurofibromatose"'
Autor:
Vanessa Luisa Destro Fidêncio, Ingrid Moura de Jesus Pereira, Victoria Maia Rodrigues, Francisca Samara Freitas Oliveira, Maria Renata José
Publikováno v:
Audiology: Communication Research, Vol 27 (2022)
RESUMO Objetivo mapear as evidências atuais em relação à percepção auditiva da fala e desenvolvimento de linguagem oral em usuários de implante auditivo de tronco encefálico (auditory brainstem implant - ABI), para responder à seguinte quest
Externí odkaz:
https://doaj.org/article/2d80373e9267437facfc4b583265d042
Publikováno v:
Revista Educar +, Vol 6 (2022)
Este artigo é um relato de experiência de caso clínico de intervenção psicopedagógica por mediação lúdica com criança acometida de neurofibromatose tipo 1. Seu objetivo é relatar um excerto do caso, em que foi usada a intervenção psicope
Externí odkaz:
https://doaj.org/article/d984c160b076440fb5bf4dbac3ae95eb
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 41, Iss 6, Pp 511.e1-511.e5 (2022)
Neurofibromatosis type 1 (NF1) is a common autosomal dominant genetic disorder that affects multiple organ systems and has a wide range of clinical manifestations. Pulmonary hypertension (PH) associated with NF1 (PH-NF1) is rarely seen, but confers a
Externí odkaz:
https://doaj.org/article/07ed86ab0f204dffba1fd2f1d423b663
Autor:
Luciane Prado Silva Tavares, Osterno Potenciano, Yasmin Pugliesi, Raissa Lelitscewa da Bela Cruz Faria, Nathalia Lelitscewa da Bela Cruz Potenciano, Lara Silva Paixão
Publikováno v:
Surgical & Cosmetic Dermatology, Vol 11, Iss 1, Pp 72-75 (2019)
A neurofibromatose tipo 1 apresenta lesões cutâneas múltiplas e limitadas opções terapêuticas. O laser de CO2 é ferramenta útil na remoção de neurofibromas, a principal fonte de desfiguração cosmética nesses pacientes. Apresentamos o tra
Externí odkaz:
https://doaj.org/article/30492510d1074a41812564ae50e64a05
Autor:
Younes Barbach, Fatima Zahra Mernissi
Publikováno v:
The Pan African Medical Journal, Vol 38, Iss 256 (2021)
La neurofibromatose type I est une maladie génétique fréquente. Les patients qui en sont atteints ont 4 fois plus de risque de développer une pathologie tumorale. La majorité des tumeurs sont bénignes (neurofibromes), même si les complications
Externí odkaz:
https://doaj.org/article/b5c81bd6bca54fea826a2eb8fea1ed96
Publikováno v:
Acta Médica Portuguesa, Vol 33, Iss 2 (2020)
N/a.
Externí odkaz:
https://doaj.org/article/e6ddad06c11a4d8c953be2abd8aa1dca
Autor:
Kawtar Hessaki
Publikováno v:
PAMJ Clinical Medicine, Vol 1, Iss 61 (2019)
La maladie de Von Recklinghausen est une maladie systémique génétique et hétérogène. L´atteinte oculaire au cous de cette phacomatose est rare mais pathognomonique. Il s´agit d´une jeune femme de 35 ans suivie dans notre formation pour la ma
Externí odkaz:
https://doaj.org/article/2aceb27134414180ab87c06330311c48
Autor:
Fatima-Zahra Agharbi
Publikováno v:
The Pan African Medical Journal, Vol 33, Iss 190 (2019)
Lentigines sont des macules hyperpigmentées, de petite taille (1 à 3mm), qui se distinguent des éphélides: par leur teinte plus foncée (brune ou noire) et par leur absence de modification après exposition solaire. Généralement régionales, el
Externí odkaz:
https://doaj.org/article/eb3ceacde2264194b6eda55f87a839b0
Autor:
Pollyanna Barros Batista, Eny Maria Goloni Bertollo, Danielle de Souza Costa, Lucas Eliam, Karin Soares Gonçalves Cunha, José Renan Cunha-Melo, Luiz Guilherme Darrigo Junior, Mauro Geller, Ingrid Faria Gianordoli-Nascimento, Luciana Gonçalves Madeira, Hérika Martins Mendes, Débora Marques de Miranda, Nikolas Andre Mata-Machado, Eric Grossi Morato, Érika Cristina Pavarino, Luciana Baptista Pereira, Nilton Alves de Rezende, Luíza de Oliveira Rodrigues, Jorge Bezerra Cavalcanti Sette, Carla Menezes da Silva, Juliana Ferreira de Souza, Márcio Leandro Ribeiro de Souza, Aline Stangherlin Martins, Eugênia Ribeiro Valadares, Paula Vieira Teixeira Vidigal, Vanessa Waisberg, Yehuda Waisberg, Luiz Oswaldo Carneiro Rodrigues
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 73, Iss 6, Pp 531-543 (2015)
Part 1 of this guideline addressed the differential diagnosis of the neurofibromatoses (NF): neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2) and schwannomatosis (SCH). NF shares some features such as the genetic origin of the neural tu
Externí odkaz:
https://doaj.org/article/0818ac13f908496e8fc2d555dde570e6
Autor:
Fonseca, Igor Oliveira da, Luvizutto, Gustavo José, Souza, Isaac Pantaleão, Trindade, André Petean, Freitas, Carlos Clayton Macedo de, Bazan, Rodrigo, Modolo, Gabriel Pinheiro
Publikováno v:
Jornal Vascular Brasileiro, Volume: 22, Article number: e20220118, Published: 26 MAY 2023
Neurofibromatosis Type 1 (NF1) is a rare cause of ischemic stroke (IS) in the general population. We report a case of a young patient with NF1 in whom IS was caused by fibromuscular dysplasia. An angiographic study demonstrated occlusion in the right
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::415a9ac91d7830d457c5510a40f55d84
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-54492023000100605&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-54492023000100605&lng=en&tlng=en
