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American Journal of Medical Genetics. Part A|May 25, 2013
Clinical manifestations of Xq28 functional disomy involving MECP2 in one female and two male patientsShino Shimada, Nobuhiko Okamoto, Kyoko Hirasawa, et al.
Respiratory Investigation|April 17, 2019
Microdeletion in Xq28 with a polymorphic inversion in a patient with FLNA-associated progressive lung diseaseKeisuke Yoshii, Hideki Matsumoto, Kyoko Hirasawa, et al.
Epilepsia|January 6, 2011
STXBP1 mutations cause not only Ohtahara syndrome but also West syndrome--result of Japanese cohort studyMotoko Otsuka, Hirokazu Oguni, Jao-Shwann Liang, et al.
Antimicrobial Agents and Chemotherapy|January 28, 2005
Antimicrobial susceptibility survey of Streptococcus pyogenes isolated in Japan from patients with severe invasive group A streptococcal infectionsTadayoshi Ikebe, Kyoko Hirasawa, Rieko Suzuki, et al.
Japanese Journal of Infectious Diseases|June 21, 2006
Surveillance of group B streptococcal toxic shock-like syndrome in nonpregnant adults and characterization of the strains in JapanBin Chang, Tadayoshi Ikebe, Akihito Wada, et al.
American Journal of Medical Genetics. Part A|May 4, 2023
Craniofacial and dental characteristics of three Japanese individuals with genetically diagnosed SATB2-associated syndromeHiroshi Kurosaka, Sayuri Yamamoto, Kyoko Hirasawa, et al.
International Journal of Antimicrobial Agents|January 25, 2005
Molecular mechanisms of high level tetracycline-resistance in group A streptococcal isolates, T serotypes 4 and 11Masakado Matsumoto, Kenji Sakae, Michio Ohta, et al.
Epilepsia|July 21, 2011
CDKL5 alterations lead to early epileptic encephalopathy in both gendersJao-Shwann Liang, Keiko Shimojima, Rumiko Takayama, et al.
Microbiology and Immunology|October 21, 2005
Close correlation of streptococcal DNase B (sdaB) alleles with emm genotypes in Streptococcus pyogenesMasakado Matsumoto, Kenji Sakae, Shinnosuke Hashikawa, et al.
Brain & Development|August 31, 2014
Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complicationsShino Shimada, Keiko Shimojima, Nobuhiko Okamoto, et al.
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