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Koki Yamada

Showing results (41-50 of 45) with videos related to

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Gastro Hep Advances|January 16, 2026
Gas-forming Pyogenic Liver Abscess Mimicking Gastric Perforation in a Patient With Diabetic Ketoacidosis and Subsequent Rupture: A Case ReportTairyu Sato, Koki Yamada, Akira Nishio, et al.
Gastro Hep Advances|January 26, 2026
Contrast-Enhanced Ultrasound and Somatostatin Receptor Scintigraphy Unveil an Occult Neuroendocrine Tumor With Carcinoid Syndrome and Presumed Small Intestinal Origin - A Case ReportTairyu Sato, Akira Nishio, Tadashi Kegasawa, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)Koki Yamada, Wai-Man Chan, Caroline Andrews, et al.
Science (New York, N.Y.)|April 24, 2004
Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesisJoanna C Jen, Wai-Man Chan, Thomas M Bosley, et al.
Nature Genetics|November 5, 2003
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)Koki Yamada, Caroline Andrews, Wai-Man Chan, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Gastro Hep Advances|January 16, 2026
Gas-forming Pyogenic Liver Abscess Mimicking Gastric Perforation in a Patient With Diabetic Ketoacidosis and Subsequent Rupture: A Case ReportTairyu Sato, Koki Yamada, Akira Nishio, et al.
Gastro Hep Advances|January 26, 2026
Contrast-Enhanced Ultrasound and Somatostatin Receptor Scintigraphy Unveil an Occult Neuroendocrine Tumor With Carcinoid Syndrome and Presumed Small Intestinal Origin - A Case ReportTairyu Sato, Akira Nishio, Tadashi Kegasawa, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3)Koki Yamada, Wai-Man Chan, Caroline Andrews, et al.
Science (New York, N.Y.)|April 24, 2004
Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesisJoanna C Jen, Wai-Man Chan, Thomas M Bosley, et al.
Nature Genetics|November 5, 2003
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)Koki Yamada, Caroline Andrews, Wai-Man Chan, et al.
Pageof 5