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N Blau

Showing results (121-130 of 278) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1996
International database of tetrahydrobiopterin deficienciesN Blau, I Barnes, J L Dhondt
Catheterization and Cardiovascular Diagnosis|January 1, 1977
Coronary artery fistula: estimation of shunt using 99m Tc-albumin particlesN Blau, M H Adatepe, F R Begg
Clinical Chemistry|December 10, 1999
Single-step mutation scanning of the 6-pyruvoyltetrahydropterin synthase gene in patients with hyperphenylalaninemiaA Romstad, P Guldberg, N Blau, et al.
Circulation|October 27, 1998
Regulation of 6-pyruvoyltetrahydropterin synthase activity and messenger RNA abundance in human vascular endothelial cellsP Linscheid, A Schaffner, N Blau, et al.
European Journal of Pediatrics|June 5, 2001
Successful treatment of phenylketonuria with tetrahydrobiopterinF K Trefz, C Aulela-Scholz, N Blau
Lijecnicki Vjesnik|July 1, 1994
[Homocystinuria: case reports with a note on hyperhomocysteinemia as a risk factor for the early onset of vascular disease]I Barić, N Barisić, N Blau, et al.
Lancet (London, England)|October 4, 1986
Paroxysmal hemiglossal twistingA J Lees, J N Blau, F Schon
The Turkish Journal of Pediatrics|January 1, 1996
Tetrahydrobiopterin and inherited hyperphenylalaninemiasN Blau, B Thony, M Spada, et al.
Journal of Inherited Metabolic Disease|May 10, 2002
Tetrahydrobiopterin responsiveness in phenylketonuria. Two new cases and a review of molecular genetic findingsU Lässker, J Zschocke, N Blau, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Efficacy of oral citrate administration in primary hyperoxaluriaE Leumann, B Hoppe, T Neuhaus, et al.
Pageof 28

Showing results (121-130 of 278) with videos related to

Sort By:
Pageof 28
Journal of Inherited Metabolic Disease|January 1, 1996
International database of tetrahydrobiopterin deficienciesN Blau, I Barnes, J L Dhondt
Catheterization and Cardiovascular Diagnosis|January 1, 1977
Coronary artery fistula: estimation of shunt using 99m Tc-albumin particlesN Blau, M H Adatepe, F R Begg
Clinical Chemistry|December 10, 1999
Single-step mutation scanning of the 6-pyruvoyltetrahydropterin synthase gene in patients with hyperphenylalaninemiaA Romstad, P Guldberg, N Blau, et al.
Circulation|October 27, 1998
Regulation of 6-pyruvoyltetrahydropterin synthase activity and messenger RNA abundance in human vascular endothelial cellsP Linscheid, A Schaffner, N Blau, et al.
European Journal of Pediatrics|June 5, 2001
Successful treatment of phenylketonuria with tetrahydrobiopterinF K Trefz, C Aulela-Scholz, N Blau
Lijecnicki Vjesnik|July 1, 1994
[Homocystinuria: case reports with a note on hyperhomocysteinemia as a risk factor for the early onset of vascular disease]I Barić, N Barisić, N Blau, et al.
Lancet (London, England)|October 4, 1986
Paroxysmal hemiglossal twistingA J Lees, J N Blau, F Schon
The Turkish Journal of Pediatrics|January 1, 1996
Tetrahydrobiopterin and inherited hyperphenylalaninemiasN Blau, B Thony, M Spada, et al.
Journal of Inherited Metabolic Disease|May 10, 2002
Tetrahydrobiopterin responsiveness in phenylketonuria. Two new cases and a review of molecular genetic findingsU Lässker, J Zschocke, N Blau, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Efficacy of oral citrate administration in primary hyperoxaluriaE Leumann, B Hoppe, T Neuhaus, et al.
Pageof 28