Prenatal Diagnosis of Isolated Lissencephaly by Ultrasonography and Magnetic Resonance Imaging: A Case Report by Mehmet Serdar Kütük, Mehmet Dolanbay, Mahmut Tuncay Özgün, Hülya Akgün, Ali Yıkılmaz

Subjects: “…Lissencephaly…”
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Hippocampal and Congenital Brain Malformations by J Gordon Millichap

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GENOTYPE-PHENOTYPE CORRELATION IN CASES WITH LISSENCEPHALY SPECTRUM by Ayça Dilruba Aslanger, Zehra Oya Uyguner, Birsen Karaman, Seher Başaran, Hülya Kayserili Karabey

Subjects: “…lissencephaly…”
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Double Cortex Syndrome by J Gordon Millichap

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Characteristics of symptomatic epilepsy and other neurological disorders in children with lissencephaly by V. I. Guzeva, I. V. Ochrim, V. R. Kasumov, O. V. Guzeva, V. V. Guzeva, N. E. Maksimova

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TUBGCP2 variants cause lissencephaly spectrum disorders: a case report and literature review by Tao Yu, Miao Yu, Xueyan Liu, Hua Wang

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Clinical and genetic characteristics of type 3 lissencephaly caused by a mutation in the TUBA1A gene (OMIM: 611603) by D. M. Guseva, T. V. Markova, L. A. Bessonova, S. S. Nikitin, E. L. Dadali, O. A. Shchagina

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Walker-Warburg syndrome: report of two cases by VASCONCELOS MARCIO M., GUEDES CÁSSIA R., DOMINGUES ROMEU C., VIANNA RAUL N. G., SOTERO MARCIO, VIEIRA MÔNICA M.

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Prenatal diagnosis of lissencephaly: A case report by Cerovac Nataša, Terzić Milan, Borković Milan, Divac Nevena, Stojanović Radan, Prostran Milica

Subjects: “…lissencephaly…”
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Malformations of the cerebral cortex and epilepsy. Clinical lecture by A. S. Kotov, K. V. Firsov

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Lissencephaly Syndromes by J Gordon Millichap

Subjects: “…isolated lissencephaly sequence…”
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Lizensefali Tip 1'in eşlik ettiği dikkat eksikliği ve hiperaktivite bozukluğu by Dilcan Kotan, İsmet Kırpınar, Tülin Fidan

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Deep clinical and genetic analysis of 17p13.3 region: 38 pediatric patients diagnosed using next-generation sequencing and literature review by Xiaoshan Ji, Qiong Xu, Yulan Lu, Bo Liu, Feifan Xiao, Qi Ni, Suzhen Xu, Renchao Liu, Gang Li, Bingbing Wu, Shuizhen Zhou, Huijun Wang

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