Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Unilateral polymicrogyria"'
Autor:
Pengxia Wu, Qingzhu Liu, Xianyu Liu, Yu Sun, Jie Zhang, Ruofan Wang, Taoyun Ji, Shuang Wang, Xiaoyan Liu, Yuwu Jiang, Lixin Cai, Ye Wu
Publikováno v:
Epilepsia Open, Vol 9, Iss 4, Pp 1480-1492 (2024)
Abstract Objective To provide evidence for choosing surgical or nonsurgical treatment for epilepsy in patients with unilateral multilobar and hemispheric polymicrogyria (PMG). Methods We searched published studies until September 2022 related to unil
Externí odkaz:
https://doaj.org/article/512f0d3951944d33ac93e5d1827aad38
Akademický článek
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Autor:
Andrea Righini, M. Di Maurizio, Fabio Triulzi, Paul D. Griffiths, Andrea Rossi, Mariasavina Severino, Elisa Scola, Cecilia Parazzini, I. D'Errico, Lorenzo Pinelli, Giovanni Palumbo, M. Scarabello
Publikováno v:
AJNR Am J Neuroradiol
BACKGROUND AND PURPOSE: The ganglionic eminences are transient fetal brain structures that produce a range of neuron types. Ganglionic eminence anomalies have been recognized on fetal MR imaging and anecdotally found in association with a number of n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::471cafb63edc12f262cb103bd4660dae
https://doi.org/10.3174/ajnr.a7062
https://doi.org/10.3174/ajnr.a7062
Autor:
Yumi Nakayama, Kou Matsui, Mitsuhiro Kato, Yu Kobayashi, Moemi Hojo, Takao Komatsubara, Akiko Hiraiwa, Shinichi Magara, Toshiyuki Yamamoto, Jun Tohyama
Publikováno v:
Brain and Development. 43:448-453
Background Pallister-Killian syndrome (PKS) is a rare disorder caused by the mosaic tetrasomy of chromosome 12p, and is characterized by facial dysmorphism, developmental delay, hypotonia and seizures. Results We report a patient with PKS showing uni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c58b39baab115642f1e0a5854082f50
https://doi.org/10.1016/j.braindev.2020.11.003
https://doi.org/10.1016/j.braindev.2020.11.003
Autor:
Shobhit Mathur, Timo Krings, Jesse M. Klostranec, Waleed Brinjikji, Emanuele Orru, Danielle M. Andrade
Publikováno v:
Clinical Neuroradiology. 30:389-394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c3bbc5ce7a3e9e32508e6b1bc757536
https://doi.org/10.1007/s00062-019-00824-x
https://doi.org/10.1007/s00062-019-00824-x
Autor:
Karl Rössler, Samir Jabari, Wim G.M. Spliet, Friedrich G. Woermann, Manfred Kudernatsch, Angelika Mühlebner, Hajo M. Hamer, Damian Stichel, Yanghao Hou, Ingmar Blümcke, Andrey Korshunov, Tom Pieper, Katja Kobow, Andreas von Deimling, Thilo Kalbhenn, Felix Sahm, Roland Coras, Martha Feucht, Tilman Polster
Publikováno v:
Acta neuropathologica, 140(6), 881-891. Springer Verlag
Acta Neuropathologica
Acta Neuropathologica
Polymicrogyria (PMG) is a developmental cortical malformation characterized by an excess of small and frustrane gyration and abnormal cortical lamination. PMG frequently associates with seizures. The molecular pathomechanisms underlying PMG developme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d874a9c6b734ca9b223c7b92cc59507
https://pure.amc.nl/en/publications/mosaic-trisomy-of-chromosome-1q-in-human-brain-tissue-associates-with-unilateral-polymicrogyria-very-earlyonset-focal-epilepsy-and-severe-developmental-delay(8b3fcd3d-cd91-43e1-91db-95833741a4ae).html
https://pure.amc.nl/en/publications/mosaic-trisomy-of-chromosome-1q-in-human-brain-tissue-associates-with-unilateral-polymicrogyria-very-earlyonset-focal-epilepsy-and-severe-developmental-delay(8b3fcd3d-cd91-43e1-91db-95833741a4ae).html
Publikováno v:
Acta Neurologica Belgica.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27d981be68e8ecad760af3627d591432
https://doi.org/10.1007/s13760-020-01537-6
https://doi.org/10.1007/s13760-020-01537-6
Autor:
Belen Ramos, Raffaele Falsaperla, Gabriela Reyes, Roberto Caraballo, Aliria Carpio Ruiz, Gabriela Peretti, Cecilia Aguilar Fernandez, Lucas Beltran
Publikováno v:
Seizure. 35:88-92
Objective We analyzed the electroclinical features, etiology, treatment, and outcome of 12 patients with West syndrome (WS) associated with focal hypsarrhythmia (FH). Methods Between February 2005 and July 2013, 12 patients met the electroclinical di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aea3af7b58bd186227d9ee3fb93fc79e
https://doi.org/10.1016/j.seizure.2016.01.012
https://doi.org/10.1016/j.seizure.2016.01.012
Autor:
Karl-Heinz Nenning, Tatjana Traub-Weidinger, Daniela Prayer, Christian Dorfer, O. Foesleitner, Thomas Czech, Gregor Kasprian, Martha Feucht, Silvia B. Bonelli
Publikováno v:
AJNR Am J Neuroradiol
BACKGROUND AND PURPOSE: Asymmetry of the corticospinal tract in congenital lesions is a good prognostic marker for preserved motor function after hemispherectomy. This study aimed to assess this marker and provide a clinically feasible approach in se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ed779d37ec32cf8abee48c957864a32
https://doi.org/10.3174/ajnr.a5715
https://doi.org/10.3174/ajnr.a5715
Publikováno v:
Neuropathology. 35:569-574
Polymicrogyria (PMG) is a complex malformation accompanied with abnormal cortical laminations (two-, four- or six-layered cortex), and horizontally oriented myelinated fiber layer is evident in four-layered PMG in older individuals. Here we report a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d23096dd20c002ddbfea981565e0b725
https://doi.org/10.1111/neup.12219
https://doi.org/10.1111/neup.12219