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BMJ Case Reports|May 13, 2016
Pseudohypoparathyroidism type 1B caused by methylation changes at the GNAS complex locusSabrina Poradosu, Bert Bravenboer, Rieko Takatani, et al.
Human Genome Variation|October 31, 2018
A novel <i>CUL7</i> mutation in a Japanese patient with 3M syndromeTomozumi Takatani, Tadashi Shiohama, Rieko Takatani, et al.
Molecular and Cellular Endocrinology|April 20, 2011
AMP-activated protein kinase attenuates Wnt/β-catenin signaling in human osteoblastic Saos-2 cellsTomozumi Takatani, Masanori Minagawa, Rieko Takatani, et al.
Frontiers in Endocrinology|November 14, 2024
Case report: Pediatric hepatopulmonary syndrome despite strict weight control after craniopharyngioma surgerySatoko Yoshikawa, Tomozumi Takatani, Rieko Takatani, et al.
European Journal of Medical Genetics|August 11, 2022
Two infants with mild, atypical clinical features of Kagami-Ogata syndrome caused by epimutationHiroyuki Higashiyama, Yoshiteru Ohsone, Rieko Takatani, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 30, 2010
A novel missense mutation in the AVPR2 gene of a Japanese infant with nephrogenic diabetes insipidusTomozumi Takatani, Kaoru Matsuo, Kaori Kinoshita, et al.
Frontiers in Neuroscience|September 13, 2024
Brain morphometric changes in children born as small for gestational age without catch up growthTomozumi Takatani, Tadashi Shiohama, Rieko Takatani, et al.
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