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Brain & Development|July 13, 2013
Nationwide survey of Arima syndrome: revised diagnostic criteria from epidemiological analysisMasayuki Itoh, Yuji Iwasaki, Kohsaku Ohno, et al.
Molecular Genetics & Genomic Medicine|December 10, 2019
MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndromeRyo Takeguchi, Satoru Takahashi, Mami Kuroda, et al.
Molecular and Clinical Oncology|June 23, 2016
Successful desensitization therapy involving fluoroquinolone for the treatment of a solitary tuberculoma: A case report and literature reviewHidehiro Watanabe, Tomonori Uruma, Ikuo Seita, et al.
Neurology. Genetics|September 30, 2022
Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous <i>CPLANE1</i> VariantKento Matoba, Norio Chihara, Wataru Satake, et al.
Microbes and Environments|May 12, 2011
Denitrification activity and relevant bacteria revealed by nitrite reductase gene fragments in soil of temperate mixed forestChie Katsuyama, Naho Kondo, Yuichi Suwa, et al.
Biochemical and Biophysical Research Communications|June 27, 2002
An extra human chromosome 21 reduces mlc-2a expression in chimeric mice and Down syndromeRyuichi Nishigaki, Tokuyuki Shinohara, Tosifusa Toda, et al.
Epilepsia|February 8, 2007
Altered distribution of KCC2 in cortical dysplasia in patients with intractable epilepsyMitsutoshi Munakata, Mika Watanabe, Taisuke Otsuki, et al.
American Journal of Medical Genetics. Part A|October 4, 2011
Progressive leukoencephalopathy with intracranial calcification, congenital deafness, and developmental deteriorationIchiro Kuki, Hisashi Kawawaki, Shin Okazaki, et al.
Differentiation; Research in Biological Diversity|June 12, 2010
Partial loss of pancreas endocrine and exocrine cells of human ARX-null mutation: consideration of pancreas differentiationMasayuki Itoh, Yuji Takizawa, Sae Hanai, et al.
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