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Epilepsy Research|September 29, 2024
Serum matrix metallopeptidase-9 levels in infantile epileptic spasms syndrome of unknown etiologyRyuki Matsuura, Shin-Ichiro Hamano, Reiko Koichihara, et al.
Journal of Human Genetics|May 20, 2020
Incomplete cryptic splicing by an intronic mutation of OCRL in patients with partial phenotypes of Lowe syndromeEiji Nakano, Amine Yoshida, Yudai Miyama, et al.
Journal of Pediatric Nursing|November 21, 2017
A Qualitative Assessment of Adolescent Girls' Perception of Living with Congenital Heart Disease: Focusing on Future Pregnancies and ChildbirthMayumi Nakamura, Sachiko Kita, Ryota Kikuchi, et al.
Genome Biology and Evolution|March 5, 2014
Divergence of East Asians and Europeans estimated using male- and female-specific genetic markersYoshio Tateno, Tomoyoshi Komiyama, Toru Katoh, et al.
Developmental Medicine and Child Neurology|January 7, 2012
Progressive conduction defects and cardiac death in late infantile neuronal ceroid lipofuscinosisShinobu Fukumura, Yoshiaki Saito, Takashi Saito, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 13, 2013
Alu-mediated nonallelic homologous and nonhomologous recombination in the BMPR2 gene in heritable pulmonary arterial hypertensionMasaharu Kataoka, Yuki Aimi, Ryoji Yanagisawa, et al.
The Journal of Dermatology|August 8, 2014
HLA-C*12:02 is a susceptibility factor in late-onset type of psoriasis in JapaneseTomotaka Mabuchi, Tami Ota, Yasuaki Manabe, et al.
Human Genome Variation|April 16, 2016
MLC1 mutations in Japanese patients with megalencephalic leukoencephalopathy with subcortical cystsShino Shimada, Keiko Shimojima, Teruaki Masuda, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|March 14, 2025
Three-year hearing outcomes in infants with congenital cytomegalovirus disease treated with oral valganciclovir: Interim results of a six-year follow-up study in JapanIchiro Morioka, Yasumasa Kakei, Takumi Imai, et al.
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