Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Vanessa, Waisberg"'
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:
Luciana Bastos-Rodrigues, Márcio Bittar Nehemy, Luiz Oswaldo Carneiro Rodrigues, Débora Marques de Miranda, Vanessa Waisberg
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 257:1453-1458
To evaluate ophthalmological and molecular findings in eight patients with a clinical diagnosis of neurofibromatosis type 2 (NF2). New pathological mutations are described and variability in the ophthalmic phenotype and NF2 allelic heterogeneity are
Autor:
Vanessa Waisberg
Publikováno v:
Repositório Institucional da UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
RESUMO Alterações Genéticas e Oftalmológicas na Neurofibromatose Tipo 2 Introdução: Neurofibromatose tipo 2 (NF2) é uma doença autossômica dominante caracterizada por schwannomas vestibulares bilaterais, múltiplos tumores do sistema nervoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::e188fb1d928605a8b85cb195310cc202
Autor:
Eric Grossi Morato, Hérika Martins Mendes, Nilton Alves de Rezende, Juliana Ferreira de Souza, Aline Stangherlin Martins, Eny Maria Goloni Bertollo, Pollyanna Barros Batista, Lucas Eliam, Vanessa Waisberg, Luciana Baptista Pereira, Eugênia Ribeiro Valadares, Yehuda Waisberg, Ingrid Faria Gianordoli-Nascimento, Luíza de Oliveira Rodrigues, Nikolas Andre Mata-Machado, Jorge Bezerra Cavalcanti Sette, Mauro Geller, Érika Cristina Pavarino, Luiz Oswaldo Carneiro Rodrigues, Luciana Gonçalves Madeira, Paula Vieira Teixeira Vidigal, Débora Marques de Miranda, Marcio Leandro Ribeiro de Souza, Karin Soares Gonçalves Cunha, Luiz Guilherme Darrigo Junior, Carla Menezes da Silva, José Renan Cunha-Melo, Danielle de Souza Costa
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 73, Iss 6, Pp 531-543 (2015)
Arquivos de Neuro-Psiquiatria, Volume: 73, Issue: 6, Pages: 531-543, Published: JUN 2015
Arquivos de Neuro-Psiquiatria, Volume: 73, Issue: 6, Pages: 531-543, Published: JUN 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
Autor:
Luiz Oswaldo Carneiro Rodrigues, Galton Carvalho Vasconcelos, Juliana Ferreira de Souza, Ana Rosa Pimentel de Figueiredo, Débora Marques de Miranda, Vanessa Waisberg
Publikováno v:
Arquivos Brasileiros de Oftalmologia, Vol 79, Iss 2, Pp 132-132 (2016)
Arquivos Brasileiros de Oftalmologia, Volume: 79, Issue: 2, Pages: 132-132, Published: APR 2016
Arquivos Brasileiros de Oftalmologia, Volume: 79, Issue: 2, Pages: 132-132, Published: APR 2016
Publikováno v:
Revista Médica de Minas Gerais. 24
Treacher-Collins syndrome is a rare, inherited malformation of the first and second brancheal arches and Down syndrome or trisomy 21 is the most common human chromosomal alteration. This study describes the co-occurrence of these two syndromes, and i
Publikováno v:
Arquivos Brasileiros de Oftalmologia. 72:394-396
A case of a local reaction related to a subtenonian deep injection of triamcinolone is reported. The patient was a 6 year old child, with intermediate uveitis. Intense edema and erythema of the eyelids appeared approximately 30 minutes after the inje
Publikováno v:
Arquivos Brasileiros de Oftalmologia, Vol 72, Iss 3, Pp 394-396 (2009)
Relata-se o caso de reação local após injeção subtenoniana profunda de1 ml de suspensão contendo 40 mg de triancinolona, realizada em uma criança de seis anos de idade, portadora de uveíte intermediária. Observou-se edema e eritema das pálp
Publikováno v:
Arquivos brasileiros de oftalmologia. 72(3)
A case of a local reaction related to a subtenonian deep injection of triamcinolone is reported. The patient was a 6 year old child, with intermediate uveitis. Intense edema and erythema of the eyelids appeared approximately 30 minutes after the inje