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Clinical Pharmacology and Therapeutics
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June 13, 2006
Effect of age on functional P-glycoprotein in the blood-brain barrier measured by use of (R)-[(11)C]verapamil and positron emission tomography
Rolf Toornvliet, Bart N M van Berckel, Gert Luurtsema, et al.
Journal of Inherited Metabolic Disease
|
August 2, 2025
Effectiveness of Pyridoxal-5'-Phosphate in PNPO Deficiency: A Systematic Review
Nina N Stolwijk, Laura van Dussen, Niels D Reijnhout, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
March 23, 1999
Comparison of two aquaretic drugs (niravoline and OPC-31260) in cirrhotic rats with ascites and water retention
M Bosch-Marcé, J L Poo, W Jiménez, et al.
Gastroenterology
|
December 31, 1998
Chronic blockade of endothelin receptors in cirrhotic rats: hepatic and hemodynamic effects
J L Poo, W Jiménez, R María Muñoz, et al.
The Journal of Physical Chemistry Letters
|
April 28, 2017
Electrostatic Screening of Charged Defects in Monolayer MoS<sub>2</sub>
T L Atallah, J Wang, M Bosch, et al.
JIMD Reports
|
May 22, 2016
Establishing New Cut-Off Limits for Galactose 1-Phosphate-Uridyltransferase Deficiency for the Dutch Newborn Screening Programme
E A Kemper, A Boelen, A M Bosch, et al.
Cancer Chemotherapy and Pharmacology
|
September 22, 2006
Metabolism of trabectedin (ET-743, Yondelis) in patients with advanced cancer
Jan H Beumer, Jeany M Rademaker-Lakhai, Hilde Rosing, et al.
Orphanet Journal of Rare Diseases
|
November 27, 2014
Rare inborn errors of metabolism with movement disorders: a case study to evaluate the impact upon quality of life and adaptive functioning
Hendriekje Eggink, Anouk Kuiper, Kathryn J Peall, et al.
Orphanet Journal of Rare Diseases
|
January 30, 2016
The neonatal tetrahydrobiopterin loading test in phenylketonuria: what is the predictive value?
Karen Anjema, Floris C Hofstede, Annet M Bosch, et al.
Journal of Inherited Metabolic Disease
|
September 19, 2007
High incidence of hypermethioninaemia in a single neonatal intensive care unit detected by a newly introduced neonatal screening programme
A E ten Hoedt, A A van Kempen, A Boelen, et al.
Page
of 42
Search research articles
Search
Showing results (261-270 of 412) with videos related to
Sort By:
Page
of 42
Clinical Pharmacology and Therapeutics
|
June 13, 2006
Effect of age on functional P-glycoprotein in the blood-brain barrier measured by use of (R)-[(11)C]verapamil and positron emission tomography
Rolf Toornvliet, Bart N M van Berckel, Gert Luurtsema, et al.
Journal of Inherited Metabolic Disease
|
August 2, 2025
Effectiveness of Pyridoxal-5'-Phosphate in PNPO Deficiency: A Systematic Review
Nina N Stolwijk, Laura van Dussen, Niels D Reijnhout, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
March 23, 1999
Comparison of two aquaretic drugs (niravoline and OPC-31260) in cirrhotic rats with ascites and water retention
M Bosch-Marcé, J L Poo, W Jiménez, et al.
Gastroenterology
|
December 31, 1998
Chronic blockade of endothelin receptors in cirrhotic rats: hepatic and hemodynamic effects
J L Poo, W Jiménez, R María Muñoz, et al.
The Journal of Physical Chemistry Letters
|
April 28, 2017
Electrostatic Screening of Charged Defects in Monolayer MoS<sub>2</sub>
T L Atallah, J Wang, M Bosch, et al.
JIMD Reports
|
May 22, 2016
Establishing New Cut-Off Limits for Galactose 1-Phosphate-Uridyltransferase Deficiency for the Dutch Newborn Screening Programme
E A Kemper, A Boelen, A M Bosch, et al.
Cancer Chemotherapy and Pharmacology
|
September 22, 2006
Metabolism of trabectedin (ET-743, Yondelis) in patients with advanced cancer
Jan H Beumer, Jeany M Rademaker-Lakhai, Hilde Rosing, et al.
Orphanet Journal of Rare Diseases
|
November 27, 2014
Rare inborn errors of metabolism with movement disorders: a case study to evaluate the impact upon quality of life and adaptive functioning
Hendriekje Eggink, Anouk Kuiper, Kathryn J Peall, et al.
Orphanet Journal of Rare Diseases
|
January 30, 2016
The neonatal tetrahydrobiopterin loading test in phenylketonuria: what is the predictive value?
Karen Anjema, Floris C Hofstede, Annet M Bosch, et al.
Journal of Inherited Metabolic Disease
|
September 19, 2007
High incidence of hypermethioninaemia in a single neonatal intensive care unit detected by a newly introduced neonatal screening programme
A E ten Hoedt, A A van Kempen, A Boelen, et al.
Page
of 42