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F HOFFMANN

Showing results (521-530 of 1,073) with videos related to

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World Journal of Pediatrics : WJP|June 28, 2018
High incidence of maternal vitamin B<sub>12</sub> deficiency detected by newborn screening: first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panelGwendolyn Gramer, Junmin Fang-Hoffmann, Patrik Feyh, et al.
The Journal of Biological Chemistry|October 23, 1997
Identification of an active site alanine in mevalonate kinase through characterization of a novel mutation in mevalonate kinase deficiencyD D Hinson, K L Chambliss, G F Hoffmann, et al.
The International Journal of Neuropsychopharmacology|October 9, 2002
Sleep microarchitecture as a predictor of recurrence in children and adolescents with depressionRoseanne Armitage, Robert F Hoffmann, Graham J Emslie, et al.
Chemical Communications (Cambridge, England)|August 12, 2022
Air-stable aryl derivatives of pentafluoroorthotellurateDaniel Wegener, Kurt F Hoffmann, Alberto Pérez-Bitrián, et al.
Neurology|August 23, 2006
Presymptomatic treatment of neonatal guanidinoacetate methyltransferase deficiencyA Schulze, G F Hoffmann, P Bachert, et al.
Chronobiology International|January 6, 2012
Dim light melatonin onset in alcohol-dependent men and women compared with healthy controlsDeirdre A Conroy, Ilana S Hairston, J Todd Arnedt, et al.
Pediatric Transplantation|September 3, 2011
High urgency liver transplantation in ornithine transcarbamylase deficiency presenting with acute liver failureUlrike Teufel, Jürgen Weitz, Christa Flechtenmacher, et al.
European Journal of Pediatrics|January 1, 1994
Neurological manifestations of organic acid disordersG F Hoffmann, K M Gibson, F K Trefz, et al.
Scientific Reports|October 28, 2016
CRISPR RNA-guided FokI nucleases repair a PAH variant in a phenylketonuria modelYi Pan, Nan Shen, Sabine Jung-Klawitter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2019
Clinical characteristics of 248 patients with Krabbe disease: quantitative natural history modeling based on published casesShoko Komatsuzaki, Matthias Zielonka, William K Mountford, et al.
Pageof 108

Showing results (521-530 of 1,073) with videos related to

Sort By:
Pageof 108
World Journal of Pediatrics : WJP|June 28, 2018
High incidence of maternal vitamin B<sub>12</sub> deficiency detected by newborn screening: first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panelGwendolyn Gramer, Junmin Fang-Hoffmann, Patrik Feyh, et al.
The Journal of Biological Chemistry|October 23, 1997
Identification of an active site alanine in mevalonate kinase through characterization of a novel mutation in mevalonate kinase deficiencyD D Hinson, K L Chambliss, G F Hoffmann, et al.
The International Journal of Neuropsychopharmacology|October 9, 2002
Sleep microarchitecture as a predictor of recurrence in children and adolescents with depressionRoseanne Armitage, Robert F Hoffmann, Graham J Emslie, et al.
Chemical Communications (Cambridge, England)|August 12, 2022
Air-stable aryl derivatives of pentafluoroorthotellurateDaniel Wegener, Kurt F Hoffmann, Alberto Pérez-Bitrián, et al.
Neurology|August 23, 2006
Presymptomatic treatment of neonatal guanidinoacetate methyltransferase deficiencyA Schulze, G F Hoffmann, P Bachert, et al.
Chronobiology International|January 6, 2012
Dim light melatonin onset in alcohol-dependent men and women compared with healthy controlsDeirdre A Conroy, Ilana S Hairston, J Todd Arnedt, et al.
Pediatric Transplantation|September 3, 2011
High urgency liver transplantation in ornithine transcarbamylase deficiency presenting with acute liver failureUlrike Teufel, Jürgen Weitz, Christa Flechtenmacher, et al.
European Journal of Pediatrics|January 1, 1994
Neurological manifestations of organic acid disordersG F Hoffmann, K M Gibson, F K Trefz, et al.
Scientific Reports|October 28, 2016
CRISPR RNA-guided FokI nucleases repair a PAH variant in a phenylketonuria modelYi Pan, Nan Shen, Sabine Jung-Klawitter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2019
Clinical characteristics of 248 patients with Krabbe disease: quantitative natural history modeling based on published casesShoko Komatsuzaki, Matthias Zielonka, William K Mountford, et al.
Pageof 108