Access the latest scientific research and medical evidence related to Lissencephaly treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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29673 Abstracts
Research
Sociodemographic patterns in spina bifida birth prevalence trends--North Carolina, 1995-1999.
Meyer Robert E, Siega-Riz Anna-Maria
MMWR. Recommendations and reports : Morbidity and mortality weekly rep... Vol 51(RR-13)
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Date 13 Sep 2002
Research
Infant mortality statistics from the 1997 period linked birth/infant death data set.
MacDorman M F, Atkinson J O
National vital statistics reports : from the Centers for Disease Contr... Vol 47(23)
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Date 30 Jul 1999
Research
Births: final data for 2001.
Martin Joyce A, Hamilton Brady E, Ventura Stephanie J, Menacker Fay, Park Melissa M ...
National vital statistics reports : from the Centers for Disease Contr... Vol 51(2)
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Date 18 Dec 2002
Research
Infant mortality statistics from the 1998 period linked birth/infant death data set.
Mathews T J, Curtin S C, MacDorman M F
National vital statistics reports : from the Centers for Disease Contr... Vol 48(12)
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Date 20 Jul 2000
Research
Human ADAR1 Prevents Endogenous RNA from Triggering Translational Shutdown.
Chung Hachung, Calis Jorg J A, Wu Xianfang, Sun Tony, Yu Yingpu ...
Cell Vol 172(4)
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Date 08 Feb 2018
Research
Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in Mice.
Zhou Haibo, Su Jinlin, Hu Xinde, Zhou Changyang, Li He ...
Cell Vol 181(3)
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Date 30 Apr 2020
Research
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.
des Portes V, Pinard J M, Billuart P, Vinet M C, Koulakoff A ...
Cell Vol 92(1)
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Date 09 Jan 1998
Research
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.
Gleeson J G, Allen K M, Fox J W, Lamperti E D, Berkovic S ...
Cell Vol 92(1)
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Date 09 Jan 1998
Research
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.
Keays David A, Tian Guoling, Poirier Karine, Huang Guo-Jen, Siebold Christian ...
Cell Vol 128(1)
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Date 12 Jan 2007
Research
Single-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain.
Evrony Gilad D, Cai Xuyu, Lee Eunjung, Hills L Benjamin, Elhosary Princess C ...
Cell Vol 151(3)
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Date 26 Oct 2012
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