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Journal of Thrombosis and Haemostasis : JTH
|
October 3, 2003
Identification of a novel point mutation in platelet glycoprotein Ibalpha, Gly to Ser at residue 233, in a Japanese family with platelet-type von Willebrand disease
Y Matsubara, M Murata, K Sugita, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
January 8, 2000
A fluorogenic allele-specific amplification method for DNA-based screening for inherited metabolic disorders
Y Matsubara, K Fujii, P Rinaldo, et al.
Lancet (London, England)
|
December 12, 1992
Novel phenylketonuria mutation detected by analysis of ectopically transcribed phenylalanine hydroxylase mRNA from lymphoblast
K Takahashi, S Kure, Y Matsubara, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
January 1, 1976
[Determination of factors V,VII and X]
K Fukutake, Y Matsubara, H Tamura, et al.
Jikken Dobutsu. Experimental Animals
|
January 1, 1981
[Maternal and fetal response to hemorrhagic anemia during organogenesis in rats]
Y Matsubara, A Shirakabe, Y Suzuki, et al.
Nihon Geka Gakkai Zasshi
|
September 1, 1992
[Management of patients with impaired glucose tolerance following esophagectomy in carcinoma of the esophagus]
N Sato, Y Matsubara, O Tanaka, et al.
Enzyme
|
January 1, 1987
Molecular basis of isovaleric acidemia and medium-chain acyl-CoA dehydrogenase deficiency
K Tanaka, Y Ikeda, Y Matsubara, et al.
The Tohoku Journal of Experimental Medicine
|
October 20, 1999
Determining factors of mortality in the elderly with hip fractures
Y Koike, H Imaizumi, E Takahashi, et al.
Rinsho Kyobu Geka = Japanese Annals of Thoracic Surgery
|
September 1, 1983
[Design of a box (Portpot) used in valve drainage]
M Kuwahara, M Kosaba, Y Matsubara, et al.
Rinsho Kyobu Geka = Japanese Annals of Thoracic Surgery
|
November 1, 1984
[Reconstruction of the trachea and carina with prosthesis and related problems]
Y Matsubara, M Aoki, O Ike, et al.
Page
of 37
Search research articles
Search
Showing results (71-80 of 367) with videos related to
Sort By:
Page
of 37
Journal of Thrombosis and Haemostasis : JTH
|
October 3, 2003
Identification of a novel point mutation in platelet glycoprotein Ibalpha, Gly to Ser at residue 233, in a Japanese family with platelet-type von Willebrand disease
Y Matsubara, M Murata, K Sugita, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
January 8, 2000
A fluorogenic allele-specific amplification method for DNA-based screening for inherited metabolic disorders
Y Matsubara, K Fujii, P Rinaldo, et al.
Lancet (London, England)
|
December 12, 1992
Novel phenylketonuria mutation detected by analysis of ectopically transcribed phenylalanine hydroxylase mRNA from lymphoblast
K Takahashi, S Kure, Y Matsubara, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
January 1, 1976
[Determination of factors V,VII and X]
K Fukutake, Y Matsubara, H Tamura, et al.
Jikken Dobutsu. Experimental Animals
|
January 1, 1981
[Maternal and fetal response to hemorrhagic anemia during organogenesis in rats]
Y Matsubara, A Shirakabe, Y Suzuki, et al.
Nihon Geka Gakkai Zasshi
|
September 1, 1992
[Management of patients with impaired glucose tolerance following esophagectomy in carcinoma of the esophagus]
N Sato, Y Matsubara, O Tanaka, et al.
Enzyme
|
January 1, 1987
Molecular basis of isovaleric acidemia and medium-chain acyl-CoA dehydrogenase deficiency
K Tanaka, Y Ikeda, Y Matsubara, et al.
The Tohoku Journal of Experimental Medicine
|
October 20, 1999
Determining factors of mortality in the elderly with hip fractures
Y Koike, H Imaizumi, E Takahashi, et al.
Rinsho Kyobu Geka = Japanese Annals of Thoracic Surgery
|
September 1, 1983
[Design of a box (Portpot) used in valve drainage]
M Kuwahara, M Kosaba, Y Matsubara, et al.
Rinsho Kyobu Geka = Japanese Annals of Thoracic Surgery
|
November 1, 1984
[Reconstruction of the trachea and carina with prosthesis and related problems]
Y Matsubara, M Aoki, O Ike, et al.
Page
of 37