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Bone Marrow Transplantation
|
December 1, 1989
Fractionated total body irradiation plus high-dose VP-16 prior to allogeneic bone marrow transplantation in children with poor risk acute leukaemias
M Suttorp, N Schmitz, S Leuschner, et al.
Biology of the Neonate
|
January 1, 1980
Lysosomal enzyme activities of human fetal organs during development
Y S Shin-Buehring, M Dallinger, M Osang, et al.
Nature Genetics
|
November 14, 1997
Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome
R Santer, R Schneppenheim, A Dombrowski, et al.
European Journal of Pediatrics
|
October 1, 1993
Comparison of umbilical arterial versus umbilical venous blood pH correlated with arterio-venous glucose difference and cardiotocographic score
W Nikischin, E Lehmann-Willenbrock, D Weisner, et al.
Pediatric Research
|
October 1, 1977
The activity of galactose-1-phosphate uridyltransferase and galactokinase in human fetal organs
Y S Shin-Buehring, T Beier, A Tan, et al.
Bone Marrow Transplantation
|
January 1, 1991
Successful stimulation of autologous bone marrow recovery by GM-CSF and IL-3 after an unrelated donor BMT for juvenile CML complicated by graft failure
M Suttorp, N Schmitz, E Prange, et al.
Acta Paediatrica Scandinavica
|
February 1, 1991
Iron availability from an infant formula supplemented with bovine lactoferrin
G Schulz-Lell, K Dörner, H D Oldigs, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1987
Agarose gel isoelectrofocusing of UDP-galactose pyrophosphorylase and galactose-1-phosphate uridyltransferase. Developmental aspect of UDP-galactose pyrophosphorylase
Y S Shin, H P Niedermeier, W Endres, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Fanconi-Bickel syndrome--a congenital defect of the liver-type facilitative glucose transporter. SSIEM Award. Society for the Study of Inborn Errors of Metabolism
R Santer, R Schneppenheim, A Dombrowski, et al.
Helvetica Paediatrica Acta
|
January 1, 1982
Atypical phenylketonuria due to biopterin deficiency. Early treatment with tetrahydrobiopterin and neurotransmitter precursors, trials of monotherapy
W Endres, A Niederwieser, H C Curtius, et al.
Page
of 19
Search research articles
Search
Showing results (101-110 of 190) with videos related to
Sort By:
Page
of 19
Bone Marrow Transplantation
|
December 1, 1989
Fractionated total body irradiation plus high-dose VP-16 prior to allogeneic bone marrow transplantation in children with poor risk acute leukaemias
M Suttorp, N Schmitz, S Leuschner, et al.
Biology of the Neonate
|
January 1, 1980
Lysosomal enzyme activities of human fetal organs during development
Y S Shin-Buehring, M Dallinger, M Osang, et al.
Nature Genetics
|
November 14, 1997
Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome
R Santer, R Schneppenheim, A Dombrowski, et al.
European Journal of Pediatrics
|
October 1, 1993
Comparison of umbilical arterial versus umbilical venous blood pH correlated with arterio-venous glucose difference and cardiotocographic score
W Nikischin, E Lehmann-Willenbrock, D Weisner, et al.
Pediatric Research
|
October 1, 1977
The activity of galactose-1-phosphate uridyltransferase and galactokinase in human fetal organs
Y S Shin-Buehring, T Beier, A Tan, et al.
Bone Marrow Transplantation
|
January 1, 1991
Successful stimulation of autologous bone marrow recovery by GM-CSF and IL-3 after an unrelated donor BMT for juvenile CML complicated by graft failure
M Suttorp, N Schmitz, E Prange, et al.
Acta Paediatrica Scandinavica
|
February 1, 1991
Iron availability from an infant formula supplemented with bovine lactoferrin
G Schulz-Lell, K Dörner, H D Oldigs, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1987
Agarose gel isoelectrofocusing of UDP-galactose pyrophosphorylase and galactose-1-phosphate uridyltransferase. Developmental aspect of UDP-galactose pyrophosphorylase
Y S Shin, H P Niedermeier, W Endres, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Fanconi-Bickel syndrome--a congenital defect of the liver-type facilitative glucose transporter. SSIEM Award. Society for the Study of Inborn Errors of Metabolism
R Santer, R Schneppenheim, A Dombrowski, et al.
Helvetica Paediatrica Acta
|
January 1, 1982
Atypical phenylketonuria due to biopterin deficiency. Early treatment with tetrahydrobiopterin and neurotransmitter precursors, trials of monotherapy
W Endres, A Niederwieser, H C Curtius, et al.
Page
of 19