Publications by authors named "Lifang Dai"

14Publications

Increasing vaccination coverage: The school entry vaccination record check program in Guizhou Province China, 2003-2018.

Vaccine 2020 Oct 3;38(46):7379-7383. Epub 2020 Sep 3.

Office of the WHO Western Pacific Region, Manila, Philippines.

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http://dx.doi.org/10.1016/j.vaccine.2020.08.055DOI Listing
October 2020

Two Chinese siblings with two novel KCTD7 mutations have dystonia or seizures and epileptic discharge on electroencephalograms.

Seizure 2019 Aug 15;70:27-29. Epub 2019 Jun 15.

Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center For Children's Health, Nanlishi Road No 56, Xi District, Beijing, 100045, China. Electronic address:

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http://dx.doi.org/10.1016/j.seizure.2019.06.007DOI Listing
August 2019

An inherited KMT2B duplication variant in a Chinese family with dystonia and/or development delay.

Parkinsonism Relat Disord 2019 06 31;63:227-228. Epub 2018 Aug 31.

Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center For Children's Health, China, Nanlishi Road No 56, Xi Strict, Beijing, 100045, China. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2018.08.021DOI Listing
June 2019

A novel DDC gene deletion mutation in two Chinese mainland siblings with aromatic l-amino acid decarboxylase deficiency.

Brain Dev 2019 Feb 23;41(2):205-209. Epub 2018 Aug 23.

Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center For Children's Health, 100045, China. Electronic address:

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http://dx.doi.org/10.1016/j.braindev.2018.08.003DOI Listing
February 2019

Similarities and differences between infantile and early childhood onset vanishing white matter disease.

J Neurol 2018 Jun 16;265(6):1410-1418. Epub 2018 Apr 16.

Department of Pediatrics, Peking University First Hospital, Beijing, 100034, China.

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http://dx.doi.org/10.1007/s00415-018-8851-6DOI Listing
June 2018

WITHDRAWN: Clinical and molecular analysis of six novel GALC mutations identified in 7 Chinese children with Krabbe disease.

Brain Dev 2017 May 25. Epub 2017 May 25.

Department of Neurology, Beijing Children's Hospital, Capital Medical University, Beijing 100045, China. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S03877604173014
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http://dx.doi.org/10.1016/j.braindev.2017.05.005DOI Listing
May 2017

Endoplasmic reticulum stress intolerance in EIF2B3 mutant oligodendrocytes is modulated by depressed autophagy.

Brain Dev 2016 May 25;38(5):507-15. Epub 2015 Nov 25.

Department of Pediatrics, Peking University First Hospital, Beijing 100034, China. Electronic address:

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http://dx.doi.org/10.1016/j.braindev.2015.11.002DOI Listing
May 2016