Zobrazeno 1 - 10
of 132
pro vyhledávání: '"agyria"'
Akademický článek
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Autor:
Tomoe Yanagishita, Kaoru Eto, Keiko Yamamoto-Shimojima, Taichi Imaizumi, Satoru Nagata, Toshiyuki Yamamoto
Publikováno v:
Tokyo Women's Medical University Journal, Vol 4, Iss 0, Pp 85-89 (2020)
Lissencephaly is a severe brain malformation associated with abnormal formation of cerebral sulci. Until now, many genes related to lissencephaly have been identified. Among them, classical lissencephaly has been often related to the platelet activat
Externí odkaz:
https://doaj.org/article/28b4aad2e88d4302ab0ca84325d82c11
Autor:
Diego Noé Rodríguez-Sánchez, Giovana Boff Araujo Pinto, Edval Fernando Thomé, Vânia Maria de Vasconcelos Machado, Rogério Martins Amorim
Publikováno v:
Acta Veterinaria Scandinavica, Vol 62, Iss 1, Pp 1-9 (2020)
Abstract Background Lissencephaly is a brain malformation characterized by smooth and thickened cerebral surface, which may result in structural epilepsy. Lissencephaly is not common in veterinary medicine. Here, we characterize the first cases of li
Externí odkaz:
https://doaj.org/article/981fe60195cb44e58c2b3d3ca142d87d
Publikováno v:
Revista Mexicana de Neurociencia, Vol 22, Iss 4 (2021)
Background: The spectrum of lissencephaly (LIS) corresponds to a group of serious brain malformations in the cortex caused by a failure in neuronal migration. The spectrum includes agyria, pachygyria and subcortical band heterotopia (SBH). It has gen
Externí odkaz:
https://doaj.org/article/679b37ca96aa4e0eb2cbd9e24a0a028e
Akademický článek
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Publikováno v:
Gynecology Obstetrics & Reproductive Medicine, Vol 20, Iss 1 (2016)
We present the abnormal sonographic findings in the brain of a 26-week fetus, which increased the suspicion of isolated lissencephaly. The woman had a history of prednisolone use in early pregnancy, and conceived with copper containing intra uterine
Externí odkaz:
https://doaj.org/article/137fc7e331bb457ea0cb6c212349d0ca
Akademický článek
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Autor:
Sangmoon Lee, Ehsan Ghayoor Karimiani, Lauren Brick, Mariya Kozenko, Ghayda Mirzaa, Rachel Schot, M. Chiara Manzini, Kiely N. James, Henry Houlden, Grazia M.S. Mancini, Umut Altunoglu, Yalda Jamshidi, Dillon Y. Chen, Mehran Beiraghi Toosi, William B. Dobyns, Valentina Stanley, Reza Maroofian, Dalia Abdin, Tugba Kalayci, Heba Morsy, Jennifer McEvoy-Venneri, Nataliya Di Donato, Maha S. Zaki, Joseph G. Gleeson
Publikováno v:
American Journal of Human Genetics, 105(4), 844-853. Cell Press
American journal of human genetics, vol 105, iss 4
American journal of human genetics, vol 105, iss 4
Lissencephaly is a severe brain malformation in which failure of neuronal migration results in agyria or pachygyria and in which the brain surface appears unusually smooth. It is often associated with microcephaly, profound intellectual disability, e
Autor:
Edval Fernando Thomé, Rogério Martins Amorim, Giovana Boff Araujo Pinto, Diego Noé Rodríguez-Sánchez, Vânia Maria de Vasconcelos Machado
Publikováno v:
Acta Veterinaria Scandinavica
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Acta Veterinaria Scandinavica, Vol 62, Iss 1, Pp 1-9 (2020)
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Acta Veterinaria Scandinavica, Vol 62, Iss 1, Pp 1-9 (2020)
Made available in DSpace on 2020-12-12T02:11:50Z (GMT). No. of bitstreams: 0 Previous issue date: 2020-06-20 Background: Lissencephaly is a brain malformation characterized by smooth and thickened cerebral surface, which may result in structural epil