Schimke immuno-osseous dysplasia, two new cases with peculiar EEG pattern-Reference-Cited by-同舟云学术

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Schimke immuno-osseous dysplasia, two new cases with peculiar EEG pattern

Published:2020-05 Issue:5 Volume:42 Page:408-413
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Prato Giulia,De Grandis Elisa,Mancardi Maria Margherita,Cordani Ramona,Giacomini Thea,Pisciotta Livia,Uccella Sara,Severino Mariasavina,Tortora Domenico,Pavanello Marco,Bertamino Marta,Verrina Enrico,Caridi Gianluca,Di Rocco Maja,Nobili Lino

Funder

Compagnia San Paolo/Italy

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. SMARCAL1 catalyzes fork regression and Holliday junction migration to maintain genome stability during DNA replication;Betous;Genes Dev,2012

2. Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia;Boerkoel;Nat Genet,2002

3. Insights into the renal pathogenesis in Schimke immuno-osseous dysplasia;Sarin;J Histochem Cytochem,2015

4. Schimke immunoosseous dysplasia;Morimoto;GeneReviews,1993

5. Neurologic phenotype of schimke immuno-osseous dysplasia and neurodevelopmental expression of SMARCAL1;Deguchi;J Neuropathol Exp Neurol,2008

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. T-cell receptor signaling in Schimke immuno-osseous dysplasia is SMARCAL1-independent;Frontiers in Immunology;2022-10-18

2. Ciclosporin/tacrolimus;Reactions Weekly;2020-05

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