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Journal of the Neurological Sciences
|
August 18, 1999
Positron emission tomography in juvenile Alexander disease
Y Sawaishi, J Hatazawa, N Ochi, et al.
The Tohoku Journal of Experimental Medicine
|
December 1, 1993
Two siblings with partial trisomy 15 and monosomy 21 associated with central nervous system anomalies
A Ishida, Y Sawaishi, A Goto, et al.
Biochemical and Biophysical Research Communications
|
June 9, 2001
A new locus for a dominant form of multinodular goiter on 3q26.1-q26.3
T Takahashi, J Nozaki, M Komatsu, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Transient 5-oxoprolinuria in a very low-birthweight infant
A Goto, A Ishida, R Goto, et al.
No to Hattatsu = Brain and Development
|
January 1, 1988
[Positron emission tomographic study in patients with MELAS]
Y Watahiki, M Tomiyama, K Nagata, et al.
Clinical Genetics
|
February 16, 2002
Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome
T Takahashi, I Takahashi, M Komatsu, et al.
Biochemistry and Molecular Biology International
|
August 1, 1994
A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
W Sato, K Hayasaka, Y Shoji, et al.
Journal of Computer Assisted Tomography
|
June 2, 1998
Transient neurotoxicity associated with FK506: MR findings
N Tomura, R Kurosawa, K Kato, et al.
Biochemical and Biophysical Research Communications
|
July 31, 1992
Isolation and sequence determination of cDNA encoding PMP-22 (PAS-II/SR13/Gas-3) of human peripheral myelin
K Hayasaka, M Himoro, K Nanao, et al.
Genomics
|
January 1, 1994
Structure and chromosomal localization of the aminomethyltransferase gene (AMT)
K Nanao, G Takada, E Takahashi, et al.
Page
of 21
Search research articles
Search
Showing results (161-170 of 201) with videos related to
Sort By:
Page
of 21
Journal of the Neurological Sciences
|
August 18, 1999
Positron emission tomography in juvenile Alexander disease
Y Sawaishi, J Hatazawa, N Ochi, et al.
The Tohoku Journal of Experimental Medicine
|
December 1, 1993
Two siblings with partial trisomy 15 and monosomy 21 associated with central nervous system anomalies
A Ishida, Y Sawaishi, A Goto, et al.
Biochemical and Biophysical Research Communications
|
June 9, 2001
A new locus for a dominant form of multinodular goiter on 3q26.1-q26.3
T Takahashi, J Nozaki, M Komatsu, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Transient 5-oxoprolinuria in a very low-birthweight infant
A Goto, A Ishida, R Goto, et al.
No to Hattatsu = Brain and Development
|
January 1, 1988
[Positron emission tomographic study in patients with MELAS]
Y Watahiki, M Tomiyama, K Nagata, et al.
Clinical Genetics
|
February 16, 2002
Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome
T Takahashi, I Takahashi, M Komatsu, et al.
Biochemistry and Molecular Biology International
|
August 1, 1994
A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
W Sato, K Hayasaka, Y Shoji, et al.
Journal of Computer Assisted Tomography
|
June 2, 1998
Transient neurotoxicity associated with FK506: MR findings
N Tomura, R Kurosawa, K Kato, et al.
Biochemical and Biophysical Research Communications
|
July 31, 1992
Isolation and sequence determination of cDNA encoding PMP-22 (PAS-II/SR13/Gas-3) of human peripheral myelin
K Hayasaka, M Himoro, K Nanao, et al.
Genomics
|
January 1, 1994
Structure and chromosomal localization of the aminomethyltransferase gene (AMT)
K Nanao, G Takada, E Takahashi, et al.
Page
of 21