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Biochemical and Biophysical Research Communications|October 30, 2008
Mutations in the gene encoding CADM1 are associated with autism spectrum disorderYu Zhiling, Eriko Fujita, Yuko Tanabe, et al.
Biochemical and Biophysical Research Communications|January 2, 2007
Intracellular distribution of a speech/language disorder associated FOXP2 mutantAkifumi Mizutani, Ayumi Matsuzaki, Mariko Y Momoi, et al.
Journal of Neurochemistry|October 12, 2011
Temporal expression and mitochondrial localization of a Foxp2 isoform lacking the forkhead domain in developing Purkinje cellsYuko Tanabe, Yuji Fujiwara, Ayumi Matsuzaki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 3, 2024
Platelet and white blood cell counts correlate with leptin and body mass index in Japanese adolescentsJunji Takaya, Yuko Tanabe, Naohiro Nomura, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 9, 2026
The serum oxytocin correlated with serum leptin and body mass index in Japanese adolescentsJunji Takaya, Yuko Tanabe, Naohiro Nomura, et al.
American Journal of Medical Genetics. Part A|September 24, 2021
Expanding the phenotypic spectrum of cardiospondylocarpofacial syndrome: From a detailed clinical and radiological observation of a boy with a novel missense variant in MAP3K7Mari Minatogawa, Noriko Miyake, Yoshinori Tsukahara, et al.
Journal of Pediatric Hematology/Oncology|April 27, 2013
A child with Epstein-Barr Virus-associated hemophagocytic lymphohistiocytosis complicated by coronary artery lesion mimicking Kawasaki diseaseShogo Kato, Ken Yoshimura, Yuko Tanabe, et al.
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