Literature DB >> 5386840

[Developmental anomalies of the retina and vitreous body (dysplasia retinae, plica retinae congenita, corpus vitreum hyperplasticum persistens)].

S Mondelski, K Pecoldowa, M Müllauerowa.   

Abstract

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Mesh：

Year:  1969        PMID： 5386840

Source DB:  PubMed          Journal:  Klin Oczna        ISSN： 0023-2157


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  5 in total

1.  Epilepsy in NF1: a systematic review of the literature.

Authors:  Pia Bernardo; Giuseppe Cinalli; Claudia Santoro
Journal:  Childs Nerv Syst       Date:  2020-07-01       Impact factor: 1.475

2.  Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders.

Authors:  Michal Gafner; Marina Michelson; Emanuela Argilli; Keren Yosovich; Elliott H Sherr; Kendall C Parks; Eleina M England; Ronen Hady-Cohen; Zvi Leibovitz; Dorit Lev; Yael Michaeli-Yosef; Tally Lerman-Sagie; Lubov Blumkin
Journal:  J Hum Genet       Date:  2021-08-16       Impact factor: 3.755

3.  Mild phenotype in a patient with developmental and epileptic encephalopathy carrying a novel de novo KCNB1 variant.

Authors:  Jin-Mei Lu; Jian-Fang Zhang; Cai-Hong Ji; Jing Hu; Kang Wang
Journal:  Neurol Sci       Date:  2021-06-26       Impact factor: 3.307

4.  Functional Genomics of Epileptogenesis in Animal Models and Humans.

Authors:  Diego A Forero
Journal:  Cell Mol Neurobiol       Date:  2020-07-28       Impact factor: 5.046

Review 5.  Headache in people with epilepsy.

Authors:  Prisca R Bauer; Else A Tolner; Mark R Keezer; Michel D Ferrari; Josemir W Sander
Journal:  Nat Rev Neurol       Date:  2021-07-26       Impact factor: 42.937
  5 in total

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