Search research articles
Contact Us
Filters
Showing results (511-520 of 1,073) with videos related to
Page
of 108
Sort By:
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 metabolism
J 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 vivo
M 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 transports
S 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 Silanes
Friederike 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 virus
U 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 children
C 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 disorders
Ulrike 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 tubulinopathies
Julian 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 metabolism
Jessica J Y Lee, Wyeth W Wasserman, Georg F Hoffmann, et al.
Page
of 108
Search research articles
Search
Showing results (511-520 of 1,073) with videos related to
Sort By:
Page
of 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 metabolism
J 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 vivo
M 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 transports
S 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 Silanes
Friederike 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 virus
U 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 children
C 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 disorders
Ulrike 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 tubulinopathies
Julian 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 metabolism
Jessica J Y Lee, Wyeth W Wasserman, Georg F Hoffmann, et al.
Page
of 108