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Journal of Pediatric Gastroenterology and Nutrition
|
January 1, 1990
Carnitine status and blood ammonium levels in low birth weight infants
T Nakamura, S Nakamura, Y Kondo, et al.
Neuropediatrics
|
May 31, 2003
Longitudinal study of auditory brainstem response in leigh syndrome
H Yoshinaga, T Ogino, F Endo, et al.
American Journal of Medical Genetics
|
August 23, 1996
Prenatal monitoring in a family at high risk for ornithine transcarbamylase (OTC) deficiency: a new mutation of an A-to-C transversion in position +4 of intron 1 of the OTC gene that is likely to abolish enzyme activity
R Hoshide, T Matsuura, Y Sagara, et al.
The Tohoku Journal of Experimental Medicine
|
January 1, 1981
The role of monocytes and prostaglandin E in the regulation of mitogen response
F Endo, T Sasaki, Y Sekiguchi, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
June 26, 2002
[A case of late-onset carbamoyl phosphate synthetase I deficiency, presenting periodic psychotic episodes coinciding with menstrual periods]
Y Wakutani, H Nakayasu, T Takeshima, et al.
Nephron
|
September 8, 1998
Alport syndrome with a peculiar pattern of distribution of the alpha3-alpha6 chains of type IV collagen in renal basement membrane
M Fujieda, F Endo, Y Morisawa, et al.
European Journal of Pediatrics
|
November 1, 1988
Plasma concentrations of vitamin K1 and PIVKA-II in bottle-fed and breast-fed infants with and without vitamin K prophylaxis at birth
J Widdershoven, W Lambert, K Motohara, et al.
Genomics
|
July 1, 1995
Assignment of the human carbamyl phosphate synthetase I gene (CPS1) to 2q35 by fluorescence in situ hybridization
R Hoshide, H Soejima, T Ohta, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
May 1, 1993
[Gene analysis of maple syrup urine disease (MSUD)]
H Mitsubuchi, Y Nobukuni, Y Hayashida, et al.
Biochemical and Biophysical Research Communications
|
December 15, 1992
Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency
K Ohta, Y Nobukuni, H Mitsubuchi, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 197) with videos related to
Sort By:
Page
of 20
Journal of Pediatric Gastroenterology and Nutrition
|
January 1, 1990
Carnitine status and blood ammonium levels in low birth weight infants
T Nakamura, S Nakamura, Y Kondo, et al.
Neuropediatrics
|
May 31, 2003
Longitudinal study of auditory brainstem response in leigh syndrome
H Yoshinaga, T Ogino, F Endo, et al.
American Journal of Medical Genetics
|
August 23, 1996
Prenatal monitoring in a family at high risk for ornithine transcarbamylase (OTC) deficiency: a new mutation of an A-to-C transversion in position +4 of intron 1 of the OTC gene that is likely to abolish enzyme activity
R Hoshide, T Matsuura, Y Sagara, et al.
The Tohoku Journal of Experimental Medicine
|
January 1, 1981
The role of monocytes and prostaglandin E in the regulation of mitogen response
F Endo, T Sasaki, Y Sekiguchi, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
June 26, 2002
[A case of late-onset carbamoyl phosphate synthetase I deficiency, presenting periodic psychotic episodes coinciding with menstrual periods]
Y Wakutani, H Nakayasu, T Takeshima, et al.
Nephron
|
September 8, 1998
Alport syndrome with a peculiar pattern of distribution of the alpha3-alpha6 chains of type IV collagen in renal basement membrane
M Fujieda, F Endo, Y Morisawa, et al.
European Journal of Pediatrics
|
November 1, 1988
Plasma concentrations of vitamin K1 and PIVKA-II in bottle-fed and breast-fed infants with and without vitamin K prophylaxis at birth
J Widdershoven, W Lambert, K Motohara, et al.
Genomics
|
July 1, 1995
Assignment of the human carbamyl phosphate synthetase I gene (CPS1) to 2q35 by fluorescence in situ hybridization
R Hoshide, H Soejima, T Ohta, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
May 1, 1993
[Gene analysis of maple syrup urine disease (MSUD)]
H Mitsubuchi, Y Nobukuni, Y Hayashida, et al.
Biochemical and Biophysical Research Communications
|
December 15, 1992
Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency
K Ohta, Y Nobukuni, H Mitsubuchi, et al.
Page
of 20