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J Schaub

Showing results (111-120 of 190) with videos related to

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Human Genetics|April 17, 1979
Characteristics of galactokinase and galactose-1-phosphate uridyltransferase in cultivated fibroblasts and amniotic fluid cellsY Shin-Buehring, H Leitner, H Henseleit, et al.
European Journal of Pediatrics|June 1, 1995
The prevalence of the G985 allele of medium-chain acyl-CoA dehydrogenase deficiency among sudden infant death victims and healthy newborns in northern GermanyR Santer, N Gregersen, K Tanaka, et al.
American Journal of Medical Genetics|August 1, 1994
Natural history of body mass index in Williams-Beuren syndromeR Pankau, C J Partsch, A Neblung, et al.
Human Mutation|August 3, 2000
Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patientsR Santer, J Rischewski, G Block, et al.
Journal of Trace Elements and Electrolytes in Health and Disease|March 1, 1990
Selenium balances in young infants fed on breast milk and adapted cow's milk formulaK Dörner, K Schneider, E Sievers, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Association of malonyl-CoA decarboxylase deficiency and heterozygote state for haemoglobin C diseaseM B Krawinkel, H D Oldigs, R Santer, et al.
Leukemia|August 1, 1991
Remission of juvenile chronic myeloid leukemia following graft failure of an unrelated marrow transplant and autologous recovery of marrow function promoted by GM-CSF and IL-3M Suttorp, N Schmitz, E Prange, et al.
Helvetica Paediatrica Acta|February 1, 1978
In vivo studies of the phenylalanine-4-hydroxylase system in hyperphenylalaninemics and phenylketonuricsH C Curtius, M J Zagalak, K Baerlocher, et al.
Chemical Research in Toxicology|October 28, 2014
Reduced astrocyte viability at physiological temperatures from magnetically activated iron oxide nanoparticlesNicholas J Schaub, Deniz Rende, Yuan Yuan, et al.
European Journal of Pediatrics|April 1, 1986
Rett syndrome revisited: a patient with biotin dependencyC Bachmann, J Schaub, J P Colombo, et al.
Pageof 19

Showing results (111-120 of 190) with videos related to

Sort By:
Pageof 19
Human Genetics|April 17, 1979
Characteristics of galactokinase and galactose-1-phosphate uridyltransferase in cultivated fibroblasts and amniotic fluid cellsY Shin-Buehring, H Leitner, H Henseleit, et al.
European Journal of Pediatrics|June 1, 1995
The prevalence of the G985 allele of medium-chain acyl-CoA dehydrogenase deficiency among sudden infant death victims and healthy newborns in northern GermanyR Santer, N Gregersen, K Tanaka, et al.
American Journal of Medical Genetics|August 1, 1994
Natural history of body mass index in Williams-Beuren syndromeR Pankau, C J Partsch, A Neblung, et al.
Human Mutation|August 3, 2000
Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patientsR Santer, J Rischewski, G Block, et al.
Journal of Trace Elements and Electrolytes in Health and Disease|March 1, 1990
Selenium balances in young infants fed on breast milk and adapted cow's milk formulaK Dörner, K Schneider, E Sievers, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Association of malonyl-CoA decarboxylase deficiency and heterozygote state for haemoglobin C diseaseM B Krawinkel, H D Oldigs, R Santer, et al.
Leukemia|August 1, 1991
Remission of juvenile chronic myeloid leukemia following graft failure of an unrelated marrow transplant and autologous recovery of marrow function promoted by GM-CSF and IL-3M Suttorp, N Schmitz, E Prange, et al.
Helvetica Paediatrica Acta|February 1, 1978
In vivo studies of the phenylalanine-4-hydroxylase system in hyperphenylalaninemics and phenylketonuricsH C Curtius, M J Zagalak, K Baerlocher, et al.
Chemical Research in Toxicology|October 28, 2014
Reduced astrocyte viability at physiological temperatures from magnetically activated iron oxide nanoparticlesNicholas J Schaub, Deniz Rende, Yuan Yuan, et al.
European Journal of Pediatrics|April 1, 1986
Rett syndrome revisited: a patient with biotin dependencyC Bachmann, J Schaub, J P Colombo, et al.
Pageof 19