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K Momma

Showing results (181-190 of 196) with videos related to

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Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 19, 2000
Evidence for the expression of neonatal skeletal myosin heavy chain in primary myocardium and cardiac conduction tissue in the developing chick heartS Machida, R Matsuoka, S Noda, et al.
Journal of Bioscience and Bioengineering|October 20, 2005
Enzymatic and genetic bases on assimilation, depolymerization, and transport of heteropolysaccharides in bacteriaW Hashimoto, K Momma, H Miki, et al.
Nihon Geka Gakkai Zasshi|September 1, 1984
[External conduit repair for congenital heart diseases]Y Takanashi, Y Imai, H Kurosawa, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|March 24, 2009
Endocytoscopic observation for esophageal squamous cell carcinoma: can biopsy histology be omitted?Y Kumagai, K Kawada, S Yamazaki, et al.
Heart and Vessels|January 1, 1986
Detection of the drainage site in anomalous pulmonary venous connection by two-dimensional Doppler color flow-mapping echocardiographyG Satomi, A Takao, K Momma, et al.
Journal of Gastroenterology|February 1, 1997
Relationship between progression of gastric mucosal atrophy and Helicobacter pylori infection: retrospective long-term endoscopic follow-up studyN Sakaki, T Arakawa, H Katou, et al.
American Journal of Medical Genetics|November 15, 1994
Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2R Matsuoka, A Takao, M Kimura, et al.
Journal of Cardiology|July 17, 1998
[Catheter intervention for adult congenital heart diseases]T Nakanishi, T Tsuji, C Kondoh, et al.
Catheterization and Cardiovascular Diagnosis|February 24, 1998
Hemolysis complicating coil occlusion of patent ductus arteriosusH Tomita, S Fuse, T Akagi, et al.
Human Mutation|April 13, 1999
A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT sydrome. Mutations in brief no. 140. OnlineH Yamagishi, M Furutani, M Kamisago, et al.
Pageof 20

Showing results (181-190 of 196) with videos related to

Sort By:
Pageof 20
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 19, 2000
Evidence for the expression of neonatal skeletal myosin heavy chain in primary myocardium and cardiac conduction tissue in the developing chick heartS Machida, R Matsuoka, S Noda, et al.
Journal of Bioscience and Bioengineering|October 20, 2005
Enzymatic and genetic bases on assimilation, depolymerization, and transport of heteropolysaccharides in bacteriaW Hashimoto, K Momma, H Miki, et al.
Nihon Geka Gakkai Zasshi|September 1, 1984
[External conduit repair for congenital heart diseases]Y Takanashi, Y Imai, H Kurosawa, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|March 24, 2009
Endocytoscopic observation for esophageal squamous cell carcinoma: can biopsy histology be omitted?Y Kumagai, K Kawada, S Yamazaki, et al.
Heart and Vessels|January 1, 1986
Detection of the drainage site in anomalous pulmonary venous connection by two-dimensional Doppler color flow-mapping echocardiographyG Satomi, A Takao, K Momma, et al.
Journal of Gastroenterology|February 1, 1997
Relationship between progression of gastric mucosal atrophy and Helicobacter pylori infection: retrospective long-term endoscopic follow-up studyN Sakaki, T Arakawa, H Katou, et al.
American Journal of Medical Genetics|November 15, 1994
Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2R Matsuoka, A Takao, M Kimura, et al.
Journal of Cardiology|July 17, 1998
[Catheter intervention for adult congenital heart diseases]T Nakanishi, T Tsuji, C Kondoh, et al.
Catheterization and Cardiovascular Diagnosis|February 24, 1998
Hemolysis complicating coil occlusion of patent ductus arteriosusH Tomita, S Fuse, T Akagi, et al.
Human Mutation|April 13, 1999
A de novo missense mutation (R1623Q) of the SCN5A gene in a Japanese girl with sporadic long QT sydrome. Mutations in brief no. 140. OnlineH Yamagishi, M Furutani, M Kamisago, et al.
Pageof 20