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F Hoffmann

Showing results (801-810 of 1,255) with videos related to

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Cell Death and Differentiation|April 28, 2007
Delayed neuronal death after brain trauma involves p53-dependent inhibition of NF-kappaB transcriptional activityN Plesnila, L von Baumgarten, M Retiounskaia, et al.
Journal of Inherited Metabolic Disease|July 13, 2004
Sedation with 4-hydroxybutyric acid: a potential pitfall in the diagnosis of SSADH deficiencyN I Wolf, D Haas, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Maintenance treatment of glutaryl-CoA dehydrogenase deficiencyC Mühlhausen, G F Hoffmann, K A Strauss, et al.
Molecular and Biochemical Parasitology|April 7, 2005
An oligonucleotide microarray for transcriptome analysis of Schistosoma mansoni and its application/use to investigate gender-associated gene expressionJennifer M Fitzpatrick, David A Johnston, Gary W Williams, et al.
Journal of Inherited Metabolic Disease|August 18, 2010
Initial evaluation of a biochemical cystic fibrosis newborn screening by sequential analysis of immunoreactive trypsinogen and pancreatitis-associated protein (IRT/PAP) as a strategy that does not involve DNA testing in a Northern European populationOlaf Sommerburg, Martin Lindner, Martina Muckenthaler, et al.
American Journal of Medical Genetics|August 26, 1998
Hematological abnormalities and cholestatic liver disease in two patients with mevalonate kinase deficiencyD D Hinson, Z R Rogers, G F Hoffmann, et al.
Clinical Endocrinology|July 9, 2024
Resource use and costs of transitioning from paediatric to adult care for patients with chronic endocrine diseaseDaniela Choukair, Janna Mittnacht, Dorothea Treiber, et al.
Pediatrics|May 1, 1993
Clinical and biochemical phenotype in 11 patients with mevalonic aciduriaG F Hoffmann, C Charpentier, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.
BMC Genomics|December 31, 2008
Biomphalaria glabrata transcriptome: cDNA microarray profiling identifies resistant- and susceptible-specific gene expression in haemocytes from snail strains exposed to Schistosoma mansoniAnne E Lockyer, Jenny Spinks, Richard A Kane, et al.
Pageof 126

Showing results (801-810 of 1,255) with videos related to

Sort By:
Pageof 126
Cell Death and Differentiation|April 28, 2007
Delayed neuronal death after brain trauma involves p53-dependent inhibition of NF-kappaB transcriptional activityN Plesnila, L von Baumgarten, M Retiounskaia, et al.
Journal of Inherited Metabolic Disease|July 13, 2004
Sedation with 4-hydroxybutyric acid: a potential pitfall in the diagnosis of SSADH deficiencyN I Wolf, D Haas, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Maintenance treatment of glutaryl-CoA dehydrogenase deficiencyC Mühlhausen, G F Hoffmann, K A Strauss, et al.
Molecular and Biochemical Parasitology|April 7, 2005
An oligonucleotide microarray for transcriptome analysis of Schistosoma mansoni and its application/use to investigate gender-associated gene expressionJennifer M Fitzpatrick, David A Johnston, Gary W Williams, et al.
Journal of Inherited Metabolic Disease|August 18, 2010
Initial evaluation of a biochemical cystic fibrosis newborn screening by sequential analysis of immunoreactive trypsinogen and pancreatitis-associated protein (IRT/PAP) as a strategy that does not involve DNA testing in a Northern European populationOlaf Sommerburg, Martin Lindner, Martina Muckenthaler, et al.
American Journal of Medical Genetics|August 26, 1998
Hematological abnormalities and cholestatic liver disease in two patients with mevalonate kinase deficiencyD D Hinson, Z R Rogers, G F Hoffmann, et al.
Clinical Endocrinology|July 9, 2024
Resource use and costs of transitioning from paediatric to adult care for patients with chronic endocrine diseaseDaniela Choukair, Janna Mittnacht, Dorothea Treiber, et al.
Pediatrics|May 1, 1993
Clinical and biochemical phenotype in 11 patients with mevalonic aciduriaG F Hoffmann, C Charpentier, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.
BMC Genomics|December 31, 2008
Biomphalaria glabrata transcriptome: cDNA microarray profiling identifies resistant- and susceptible-specific gene expression in haemocytes from snail strains exposed to Schistosoma mansoniAnne E Lockyer, Jenny Spinks, Richard A Kane, et al.
Pageof 126