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Biochemical and Biophysical Research Communications
|
November 27, 1991
Isolation and sequence determination of cDNA encoding P2 protein of human peripheral myelin
K Hayasaka, K Nanao, M Tahara, et al.
The American Journal of Cardiology
|
September 1, 1995
Role of age on transmitral flow velocity patterns in assessing left ventricular diastolic function in normal infants and children
K Harada, T Suzuki, M Tamura, et al.
The American Journal of Cardiology
|
September 15, 1995
Effect of heart rate on left ventricular diastolic filling patterns assessed by Doppler echocardiography in normal infants
K Harada, Y Takahashi, T Shiota, et al.
The Tohoku Journal of Experimental Medicine
|
February 1, 1994
Left ventricular contractile state of early human neonates with patent ductus arteriosus
Y Takahashi, K Harada, T Shiota, et al.
Clinical Genetics
|
May 29, 2002
An SEDL gene mutation in a Japanese kindred of X-linked spondyloepiphyseal dysplasia tarda
T Takahashi, I Takahashi, S Tsuchida, et al.
Radiation Medicine
|
December 11, 1999
A case of moyamoya-like vessels combined with brain anomaly
K Kato, N Tomura, S Takahashi, et al.
Early Human Development
|
August 6, 1998
Abnormal left ventricular diastolic filling patterns in small-for-gestational-age infants
K Harada, T Suzuki, Y Takahashi, et al.
European Journal of Pediatrics
|
January 1, 1992
A case of tubulo-interstitial nephritis with exfoliative dermatitis and hepatitis due to phenobarbital hypersensitivity
Y Sawaishi, K Komatsu, O Takeda, et al.
The Tohoku Journal of Experimental Medicine
|
January 1, 1994
A preterm infant with secondary carnitine deficiency due to MCT formula--effective treatment of L-carnitine
A Ishida, A Goto, Y Takahashi, et al.
American Journal of Human Genetics
|
March 1, 1992
Genetic analysis of three pedigrees of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)
W Sato, K Hayasaka, K Komatsu, et al.
Page
of 21
Search research articles
Search
Showing results (141-150 of 201) with videos related to
Sort By:
Page
of 21
Biochemical and Biophysical Research Communications
|
November 27, 1991
Isolation and sequence determination of cDNA encoding P2 protein of human peripheral myelin
K Hayasaka, K Nanao, M Tahara, et al.
The American Journal of Cardiology
|
September 1, 1995
Role of age on transmitral flow velocity patterns in assessing left ventricular diastolic function in normal infants and children
K Harada, T Suzuki, M Tamura, et al.
The American Journal of Cardiology
|
September 15, 1995
Effect of heart rate on left ventricular diastolic filling patterns assessed by Doppler echocardiography in normal infants
K Harada, Y Takahashi, T Shiota, et al.
The Tohoku Journal of Experimental Medicine
|
February 1, 1994
Left ventricular contractile state of early human neonates with patent ductus arteriosus
Y Takahashi, K Harada, T Shiota, et al.
Clinical Genetics
|
May 29, 2002
An SEDL gene mutation in a Japanese kindred of X-linked spondyloepiphyseal dysplasia tarda
T Takahashi, I Takahashi, S Tsuchida, et al.
Radiation Medicine
|
December 11, 1999
A case of moyamoya-like vessels combined with brain anomaly
K Kato, N Tomura, S Takahashi, et al.
Early Human Development
|
August 6, 1998
Abnormal left ventricular diastolic filling patterns in small-for-gestational-age infants
K Harada, T Suzuki, Y Takahashi, et al.
European Journal of Pediatrics
|
January 1, 1992
A case of tubulo-interstitial nephritis with exfoliative dermatitis and hepatitis due to phenobarbital hypersensitivity
Y Sawaishi, K Komatsu, O Takeda, et al.
The Tohoku Journal of Experimental Medicine
|
January 1, 1994
A preterm infant with secondary carnitine deficiency due to MCT formula--effective treatment of L-carnitine
A Ishida, A Goto, Y Takahashi, et al.
American Journal of Human Genetics
|
March 1, 1992
Genetic analysis of three pedigrees of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)
W Sato, K Hayasaka, K Komatsu, et al.
Page
of 21