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F HOFFMANN

Showing results (511-520 of 1,073) with videos related to

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Pediatric Research|December 5, 2000
Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolismJ Zschocke, J P Ruiter, J Brand, et al.
Infection and Immunity|October 13, 2001
Patterns of chemokine expression in models of Schistosoma mansoni inflammation and infection reveal relationships between type 1 and type 2 responses and chemokines in vivoM K Park, K F Hoffmann, A W Cheever, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|January 27, 2015
[Linkage of statutory health insurance data with those of a hospital information system: feasible, but also "useful"?]C Ohlmeier, F Hoffmann, K Giersiepen, et al.
Early Human Development|April 22, 2024
Characteristics and special challenges of neonatal emergency transportsS Schumacher, B Mitzlaff, C Mohrmann, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 27, 2026
Simple Access to a Series of Higher Substituted Pentafluoroorthotellurate-Based SilanesFriederike Oesten, Lukas Fischer, Kurt F Hoffmann, et al.
The Pediatric Infectious Disease Journal|July 9, 1998
Comparison of two antiretroviral triple combinations including the protease inhibitor indinavir in children infected with human immunodeficiency virusU Wintergerst, F Hoffmann, B Sölder, et al.
AIDS (London, England)|June 17, 2004
Long-term pharmacokinetics of amprenavir in combination with delavirdine in HIV-infected childrenC Engelhorn, F Hoffmann, M Kurowski, et al.
Orphanet Journal of Rare Diseases|April 10, 2019
High blood pressure, a red flag for the neonatal manifestation of urea cycle disordersUlrike Teufel, Peter Burgard, Jochen Meyburg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 21, 2020
Cross-sectional quantitative analysis of the natural history of TUBA1A and TUBB2B tubulinopathiesJulian Schröter, Jan H Döring, Sven F Garbade, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Knowledge base and mini-expert platform for the diagnosis of inborn errors of metabolismJessica J Y Lee, Wyeth W Wasserman, Georg F Hoffmann, et al.
Pageof 108

Showing results (511-520 of 1,073) with videos related to

Sort By:
Pageof 108
Pediatric Research|December 5, 2000
Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolismJ Zschocke, J P Ruiter, J Brand, et al.
Infection and Immunity|October 13, 2001
Patterns of chemokine expression in models of Schistosoma mansoni inflammation and infection reveal relationships between type 1 and type 2 responses and chemokines in vivoM K Park, K F Hoffmann, A W Cheever, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|January 27, 2015
[Linkage of statutory health insurance data with those of a hospital information system: feasible, but also "useful"?]C Ohlmeier, F Hoffmann, K Giersiepen, et al.
Early Human Development|April 22, 2024
Characteristics and special challenges of neonatal emergency transportsS Schumacher, B Mitzlaff, C Mohrmann, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 27, 2026
Simple Access to a Series of Higher Substituted Pentafluoroorthotellurate-Based SilanesFriederike Oesten, Lukas Fischer, Kurt F Hoffmann, et al.
The Pediatric Infectious Disease Journal|July 9, 1998
Comparison of two antiretroviral triple combinations including the protease inhibitor indinavir in children infected with human immunodeficiency virusU Wintergerst, F Hoffmann, B Sölder, et al.
AIDS (London, England)|June 17, 2004
Long-term pharmacokinetics of amprenavir in combination with delavirdine in HIV-infected childrenC Engelhorn, F Hoffmann, M Kurowski, et al.
Orphanet Journal of Rare Diseases|April 10, 2019
High blood pressure, a red flag for the neonatal manifestation of urea cycle disordersUlrike Teufel, Peter Burgard, Jochen Meyburg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 21, 2020
Cross-sectional quantitative analysis of the natural history of TUBA1A and TUBB2B tubulinopathiesJulian Schröter, Jan H Döring, Sven F Garbade, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Knowledge base and mini-expert platform for the diagnosis of inborn errors of metabolismJessica J Y Lee, Wyeth W Wasserman, Georg F Hoffmann, et al.
Pageof 108