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F Hoffmann

Showing results (781-790 of 1,255) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1997
Association of extracolonic manifestations of familial adenomatous polyposis with acetylation phenotype in a large FAP kindredR J Scott, W Taeschner, K Heinimann, et al.
Pediatric Research|March 22, 2006
Phenylalanine reduces synaptic density in mixed cortical cultures from miceFriederike Hörster, Marina A Schwab, Sven W Sauer, et al.
Orphanet Journal of Rare Diseases|June 17, 2017
Incidence, disease onset and short-term outcome in urea cycle disorders -cross-border surveillance in Germany, Austria and SwitzerlandSusanne Nettesheim, Stefan Kölker, Daniela Karall, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiencyS Kölker, D M Koeller, S Sauer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 1, 2007
Qualitative and quantitative analysis of antibody response against IFNbeta in patients with multiple sclerosisF Gilli, F Hoffmann, A Sala, et al.
International Journal of Neonatal Screening|March 27, 2024
New Cases of Maleylacetoacetate Isomerase Deficiency with Detection by Newborn Screening and Natural History over 32 Years: Experience from a German Newborn Screening CenterGwendolyn Gramer, Saskia B Wortmann, Junmin Fang-Hoffmann, et al.
European Journal of Pediatrics|August 1, 1997
Assessment of energy expenditure in metabolic disordersO A Bodamer, G F Hoffmann, G H Visser, et al.
Journal of Orthopaedic Trauma|August 14, 2015
Fate of Patients With a "Surprise" Positive Culture After Nonunion SurgeryDana Olszewski, Philipp N Streubel, Charlton Stucken, et al.
The Journal of Pediatrics|June 20, 2002
The diagnosis of mitochondrial HMG-CoA synthase deficiencyJohannes Zschocke, Johannes M Penzien, Rainer Bielen, et al.
Plos Neglected Tropical Diseases|November 4, 2009
Anti-schistosomal intervention targets identified by lifecycle transcriptomic analysesJennifer M Fitzpatrick, Emily Peak, Samirah Perally, et al.
Pageof 126

Showing results (781-790 of 1,255) with videos related to

Sort By:
Pageof 126
European Journal of Human Genetics : EJHG|January 1, 1997
Association of extracolonic manifestations of familial adenomatous polyposis with acetylation phenotype in a large FAP kindredR J Scott, W Taeschner, K Heinimann, et al.
Pediatric Research|March 22, 2006
Phenylalanine reduces synaptic density in mixed cortical cultures from miceFriederike Hörster, Marina A Schwab, Sven W Sauer, et al.
Orphanet Journal of Rare Diseases|June 17, 2017
Incidence, disease onset and short-term outcome in urea cycle disorders -cross-border surveillance in Germany, Austria and SwitzerlandSusanne Nettesheim, Stefan Kölker, Daniela Karall, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiencyS Kölker, D M Koeller, S Sauer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 1, 2007
Qualitative and quantitative analysis of antibody response against IFNbeta in patients with multiple sclerosisF Gilli, F Hoffmann, A Sala, et al.
International Journal of Neonatal Screening|March 27, 2024
New Cases of Maleylacetoacetate Isomerase Deficiency with Detection by Newborn Screening and Natural History over 32 Years: Experience from a German Newborn Screening CenterGwendolyn Gramer, Saskia B Wortmann, Junmin Fang-Hoffmann, et al.
European Journal of Pediatrics|August 1, 1997
Assessment of energy expenditure in metabolic disordersO A Bodamer, G F Hoffmann, G H Visser, et al.
Journal of Orthopaedic Trauma|August 14, 2015
Fate of Patients With a "Surprise" Positive Culture After Nonunion SurgeryDana Olszewski, Philipp N Streubel, Charlton Stucken, et al.
The Journal of Pediatrics|June 20, 2002
The diagnosis of mitochondrial HMG-CoA synthase deficiencyJohannes Zschocke, Johannes M Penzien, Rainer Bielen, et al.
Plos Neglected Tropical Diseases|November 4, 2009
Anti-schistosomal intervention targets identified by lifecycle transcriptomic analysesJennifer M Fitzpatrick, Emily Peak, Samirah Perally, et al.
Pageof 126