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Y S Hong

Showing results (51-60 of 127) with videos related to

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The British Journal of Radiology|July 28, 2011
Transthoracic needle biopsy using a C-arm cone-beam CT system: diagnostic accuracy and safetyM J Choi, Y Kim, Y S Hong, et al.
Gene|July 4, 1995
Structure and function of the HOX A1 human homeobox gene cDNAY S Hong, S Y Kim, A Bhattacharya, et al.
Japanese Journal of Clinical Oncology|January 8, 1999
Quality of life (QOL) assessment of MIP (mitomycin, ifosfamide and cisplatin) chemotherapy in advanced non-small cell lung cancers (NSCLC)J Y Han, H K Kim, B G Choi, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Deficiency of dihydrolipoamide dehydrogenase due to two mutant alleles (E340K and G101del). Analysis of a family and prenatal testingY S Hong, D S Kerr, T C Liu, et al.
Phytotherapy Research : PTR|October 31, 2008
Appetite suppressive effects of yeast hydrolysate on nitric oxide synthase (NOS) expression and vasoactive intestinal peptide (VIP) immunoreactivity in hypothalamusE Y Jung, H J Suh, S Y Kim, et al.
Scandinavian Journal of Rheumatology|October 30, 2014
The predictors of development of new syndesmophytes in female patients with ankylosing spondylitisK Y Kang, S-K Kwok, J H Ju, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 11, 1999
INAF, a protein required for transient receptor potential Ca(2+) channel functionC Li, C Geng, H T Leung, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|August 5, 1999
High glucose solution and spent dialysate stimulate the synthesis of transforming growth factor-beta1 of human peritoneal mesothelial cells: effect of cytokine costimulationD H Kang, Y S Hong, H J Lim, et al.
Emergency Medicine Journal : EMJ|April 22, 2006
Diagnostic radiopacity and hepatotoxicity following chloroform ingestion: a case reportS H Choi, S W Lee, Y S Hong, et al.
Human Molecular Genetics|December 1, 1996
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.
Pageof 13

Showing results (51-60 of 127) with videos related to

Sort By:
Pageof 13
The British Journal of Radiology|July 28, 2011
Transthoracic needle biopsy using a C-arm cone-beam CT system: diagnostic accuracy and safetyM J Choi, Y Kim, Y S Hong, et al.
Gene|July 4, 1995
Structure and function of the HOX A1 human homeobox gene cDNAY S Hong, S Y Kim, A Bhattacharya, et al.
Japanese Journal of Clinical Oncology|January 8, 1999
Quality of life (QOL) assessment of MIP (mitomycin, ifosfamide and cisplatin) chemotherapy in advanced non-small cell lung cancers (NSCLC)J Y Han, H K Kim, B G Choi, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Deficiency of dihydrolipoamide dehydrogenase due to two mutant alleles (E340K and G101del). Analysis of a family and prenatal testingY S Hong, D S Kerr, T C Liu, et al.
Phytotherapy Research : PTR|October 31, 2008
Appetite suppressive effects of yeast hydrolysate on nitric oxide synthase (NOS) expression and vasoactive intestinal peptide (VIP) immunoreactivity in hypothalamusE Y Jung, H J Suh, S Y Kim, et al.
Scandinavian Journal of Rheumatology|October 30, 2014
The predictors of development of new syndesmophytes in female patients with ankylosing spondylitisK Y Kang, S-K Kwok, J H Ju, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 11, 1999
INAF, a protein required for transient receptor potential Ca(2+) channel functionC Li, C Geng, H T Leung, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|August 5, 1999
High glucose solution and spent dialysate stimulate the synthesis of transforming growth factor-beta1 of human peritoneal mesothelial cells: effect of cytokine costimulationD H Kang, Y S Hong, H J Lim, et al.
Emergency Medicine Journal : EMJ|April 22, 2006
Diagnostic radiopacity and hepatotoxicity following chloroform ingestion: a case reportS H Choi, S W Lee, Y S Hong, et al.
Human Molecular Genetics|December 1, 1996
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.
Pageof 13