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F Hoffmann

Showing results (681-690 of 1,255) with videos related to

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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.
Biological Chemistry|October 1, 2003
Kinin-B1 receptors in ischaemia-induced pancreatitis: functional importance and cellular localisationJoachim F Kuebler, Elisabeth Schremmer-Danninger, Kanti D Bhoola, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 1, 1994
Leflunomide therapy following penetrating keratoplasty in the ratS E Coupland, S Klebe, A C Karow, et al.
Electrophoresis|August 19, 2000
An alternative approach to deal with geometric uncertainties in computer analysis of two-dimensional electrophoresis gelsK Kriegel, I Seefeldt, F Hoffmann, et al.
The International Journal of Neuropsychopharmacology|July 24, 2001
Sleep polysomnography as a predictor of recurrence in children and adolescents with major depressive disorderG J Emslie, R Armitage, W A Weinberg, et al.
Pediatrics|November 29, 2002
Incidence and short-term outcome of children with symptomatic presentation of organic acid and fatty acid oxidation disorders in GermanyDaniela A Klose, Stefan Kölker, Beate Heinrich, et al.
European Journal of Pediatrics|May 1, 1996
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?E Mayatepek, G F Hoffmann, R Baumgartner, et al.
Journal of Inherited Metabolic Disease|November 24, 2016
Analysis of the functional muscle-bone unit of the forearm in patients with phenylketonuria by peripheral quantitative computed tomographyDaniela Choukair, Carolin Kneppo, Reinhard Feneberg, et al.
Pageof 126

Showing results (681-690 of 1,255) with videos related to

Sort By:
Pageof 126
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.
Biological Chemistry|October 1, 2003
Kinin-B1 receptors in ischaemia-induced pancreatitis: functional importance and cellular localisationJoachim F Kuebler, Elisabeth Schremmer-Danninger, Kanti D Bhoola, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 1, 1994
Leflunomide therapy following penetrating keratoplasty in the ratS E Coupland, S Klebe, A C Karow, et al.
Electrophoresis|August 19, 2000
An alternative approach to deal with geometric uncertainties in computer analysis of two-dimensional electrophoresis gelsK Kriegel, I Seefeldt, F Hoffmann, et al.
The International Journal of Neuropsychopharmacology|July 24, 2001
Sleep polysomnography as a predictor of recurrence in children and adolescents with major depressive disorderG J Emslie, R Armitage, W A Weinberg, et al.
Pediatrics|November 29, 2002
Incidence and short-term outcome of children with symptomatic presentation of organic acid and fatty acid oxidation disorders in GermanyDaniela A Klose, Stefan Kölker, Beate Heinrich, et al.
European Journal of Pediatrics|May 1, 1996
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?E Mayatepek, G F Hoffmann, R Baumgartner, et al.
Journal of Inherited Metabolic Disease|November 24, 2016
Analysis of the functional muscle-bone unit of the forearm in patients with phenylketonuria by peripheral quantitative computed tomographyDaniela Choukair, Carolin Kneppo, Reinhard Feneberg, et al.
Pageof 126