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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 heart
S 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 bacteria
W 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 echocardiography
G 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 study
N 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 22q11.2
R 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 arteriosus
H 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. Online
H Yamagishi, M Furutani, M Kamisago, et al.
Page
of 20
Search research articles
Search
Showing results (181-190 of 196) with videos related to
Sort By:
Page
of 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 heart
S 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 bacteria
W 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 echocardiography
G 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 study
N 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 22q11.2
R 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 arteriosus
H 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. Online
H Yamagishi, M Furutani, M Kamisago, et al.
Page
of 20