Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Juliana Parizotto"'
Autor:
Emília Katiane Embiruçu Leão, Marcília Martyn Lima, Otacílio de Oliveira Maia Júnior, Juliana Parizotto, Fernando Kok
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 68, Iss 2, Pp 273-276 (2010)
Joubert syndrome (JS) is an autosomal recessive inherited disorder characterized by hypotonia, cerebellar vermis hypoplasia, ocular abnormalities (e.g, pigmentary retinopathy, oculomotor apraxia and nystagmus), renal cysts and hepatic fibrosis. Respi
Externí odkaz:
https://doaj.org/article/723fcb2d9ecf47ffa6cdb6653b444014
Autor:
Emília Katiane Embiruçu de Araújo Leão, Juliana Parizotto, Fernando Kok, Otacílio de Oliveira Maia, Marcília Martyn Lima
Publikováno v:
Arquivos de Neuro-Psiquiatria v.68 n.2 2010
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Joubert syndrome (JS) is an autosomal recessive inherited disorder characterized by hypotonia, cerebellar vermis hypoplasia, ocular abnormalities (e.g, pigmentary retinopathy, oculomotor apraxia and nystagmus), renal cysts and hepatic fibrosis. Respi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a291136383800c0fa3f56ea920b30c59
https://pubmed.ncbi.nlm.nih.gov/20464299
https://pubmed.ncbi.nlm.nih.gov/20464299