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Gastro Hep Advances
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January 16, 2026
Gas-forming Pyogenic Liver Abscess Mimicking Gastric Perforation in a Patient With Diabetic Ketoacidosis and Subsequent Rupture: A Case Report
Tairyu 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 Report
Tairyu 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 morphogenesis
Joanna 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.
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of 5
Search research articles
Search
Showing results (41-50 of 45) with videos related to
Sort By:
Page
of 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 Report
Tairyu 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 Report
Tairyu 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 morphogenesis
Joanna 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.
Page
of 5