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Journal of Medical Virology|September 13, 2002
Detection of cytomegalovirus DNA in human placentaKaori Kumazaki, Keiichi Ozono, Takeshi Yahara, et al.
The Journal of Clinical Endocrinology and Metabolism|October 2, 2013
Identification of AP2S1 mutation and effects of low calcium formula in an infant with hypercalcemia and hypercalciuriaYasuko Fujisawa, Rie Yamaguchi, Eiichirou Satake, et al.
World Journal of Clinical Pediatrics|March 24, 2021
Neonatal cholestasis can be the first symptom of McCune-Albright syndrome: A case reportYoshinori Satomura, Kazuhiko Bessho, Taichi Kitaoka, et al.
Journal of Molecular Endocrinology|January 24, 2007
Growth hormone stimulates adipogenesis of 3T3-L1 cells through activation of the Stat5A/5B-PPARgamma pathwayMasanobu Kawai, Noriyuki Namba, Sotaro Mushiake, et al.
Journal of Human Genetics|April 5, 2018
Unfolded protein response is activated in Krabbe disease in a manner dependent on the mutation typeKaori Irahara-Miyana, Takanobu Otomo, Hidehito Kondo, et al.
The Journal of Obstetrics and Gynaecology Research|June 21, 2007
Sonographic femur length to trunk cross area ratio: prediction of fetal outcome in 30 cases in which micromelia was suspectedHitomi Arahori, Arihiro Tamura, Kenshi Wasada, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 16, 2014
Efficacy of micafungin in pediatric immunocompromised patients with invasive fungal infectionYoshiko Hashii, Shigenori Kusuki, Sachiko Takizawa, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Hormonal and genetical assessment of a Japanese girl with weaver syndromeYoko Miyoshi, Masako Taniike, Ikuko Mohri, et al.
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