Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
6 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Plasticity and injury in the developing brain.
Brain Dev. 2009 Jan;31(1):1-10. doi: 10.1016/j.braindev.2008.03.014. Epub 2008 May 19.
Brain Dev. 2009.
PMID: 18490122
Free PMC article.
Review.
Protective effect of erythropoietin in neonatal hypoxic ischemia in mice.
Matsushita H, Johnston MV, Lange MS, Wilson MA.
Matsushita H, et al.
Neuroreport. 2003 Sep 15;14(13):1757-61. doi: 10.1097/00001756-200309150-00020.
Neuroreport. 2003.
PMID: 14512852
Item in Clipboard
PARP-1 gene disruption in mice preferentially protects males from perinatal brain injury.
Hagberg H, Wilson MA, Matsushita H, Zhu C, Lange M, Gustavsson M, Poitras MF, Dawson TM, Dawson VL, Northington F, Johnston MV.
Hagberg H, et al.
J Neurochem. 2004 Sep;90(5):1068-75. doi: 10.1111/j.1471-4159.2004.02547.x.
J Neurochem. 2004.
PMID: 15312162
Free article.
Item in Clipboard
Compound heterozygous ADAMTS9 variants in Joubert syndrome-related disorders without renal manifestation.
Matsushita HB, Hiraide T, Hayakawa K, Okano S, Nakashima M, Saitsu H, Kato M.
Matsushita HB, et al.
Brain Dev. 2022 Feb;44(2):161-165. doi: 10.1016/j.braindev.2021.10.004. Epub 2021 Nov 5.
Brain Dev. 2022.
PMID: 34750010
Item in Clipboard
Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies.
Miyamoto S, Kato M, Hiraide T, Shiohama T, Goto T, Hojo A, Ebata A, Suzuki M, Kobayashi K, Chong PF, Kira R, Matsushita HB, Ikeda H, Hoshino K, Matsufuji M, Moriyama N, Furuyama M, Yamamoto T, Nakashima M, Saitsu H.
Miyamoto S, et al. Among authors: matsushita hb.
J Hum Genet. 2021 Nov;66(11):1061-1068. doi: 10.1038/s10038-021-00932-y. Epub 2021 May 6.
J Hum Genet. 2021.
PMID: 33958710
Item in Clipboard
[A female patient with a hot spot mutation of PRRT2 gene suffering from several types of epileptic seizures in infancy].
Matsushita HB, Okano S, Ishii A, Hirose S.
Matsushita HB, et al.
No To Hattatsu. 2016 Sep;48(5):351-4.
No To Hattatsu. 2016.
PMID: 30010281
Japanese.
Item in Clipboard
Cite
Cite