Unverricht-Lundborg disease with cystatin B gene abnormalities-Reference-Cited by-同舟云学术

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Unverricht-Lundborg disease with cystatin B gene abnormalities

Published:2002-01 Issue:1 Volume:26 Page:55-60
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Kagitani-Shimono Kuriko,Imai Katsumi,Okamoto Nobuhiko,Ono Jiro,Okada Shintaro

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference15 articles.

1. “Baltic” myoclonus epilepsy;Eldridge;Lancet,1983

2. Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1);Pennacchio;Science,1996

3. Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy;Lalioti;Nature,1997

4. Progressive myoclonus epilepsy;Norio;Clin Genet,1979

5. Novel cystatin B mutation and diagnostic PCR assay in an Unverricht-Lundborg progressive myoclonus epilepsy patient;Bespalova;Am J Med Genet,1997

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1. The Roles of Cystatin B in the Brain and Pathophysiological Mechanisms of Progressive Myoclonic Epilepsy Type 1;Cells;2024-01-16

2. Molecular characterization, expression, and functional analysis of cystatin B in the big-belly seahorse (Hippocampus abdominalis);Fish & Shellfish Immunology;2022-05

3. Update on Pharmacological Treatment of Progressive Myoclonus Epilepsies;Current Pharmaceutical Design;2018-02-09

4. The ‘Photosensitivity Model’ is ( also) a model for focal (partial) seizures;Epilepsy Research;2017-07

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