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F Hoffmann

Showing results (541-550 of 1,255) with videos related to

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Der Nervenarzt|August 1, 1983
[Therapy of generalized epilepsies with long-term EEG guided single dose administration of sodium valproate]H Stefan, F Hoffmann, H Fichsel, et al.
Plos One|December 17, 2013
Polymorphic cytochrome P450 enzymes (CYPs) and their role in personalized therapySarah C Preissner, Michael F Hoffmann, Robert Preissner, et al.
Journal of Orthopaedic Surgery and Research|November 28, 2013
Clinical outcomes of locked plating of distal femoral fractures in a retrospective cohortMartin F Hoffmann, Clifford B Jones, Debra L Sietsema, et al.
Nucleic Acids Research|December 17, 2013
The Transformer database: biotransformation of xenobioticsMichael F Hoffmann, Sarah C Preissner, Janette Nickel, et al.
Journal of Inherited Metabolic Disease|September 14, 2017
Critical appraisal of genotype assessment in molybdenum cofactor deficiencyKatrin Hinderhofer, Konstantin Mechler, Georg F Hoffmann, et al.
Journal of Inherited Metabolic Disease|September 13, 2023
The challenge of understanding and predicting phenotypic diversity in urea cycle disordersRoland Posset, Matthias Zielonka, Florian Gleich, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|September 1, 1988
Malignant nerve sheath tumors of the head and neckD F Hoffmann, E C Everts, J D Smith, et al.
Circulation|January 12, 2011
Determinants of blood pressure in preschool children: the role of parental smokingGiacomo D Simonetti, Rainer Schwertz, Martin Klett, et al.
Biochemistry|April 1, 1980
Ovalbumin messenger ribonucleic acid accumulation in the chick oviduct during secondary stimulation: influence of combinations of steroid hormones and circannual rhythmsS S Seaver, D C Van Eys-Fuchs, J F Hoffmann, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Neonatal screening for glutaryl-CoA dehydrogenase deficiencyM Lindner, S Kölker, A Schulze, et al.
Pageof 126

Showing results (541-550 of 1,255) with videos related to

Sort By:
Pageof 126
Der Nervenarzt|August 1, 1983
[Therapy of generalized epilepsies with long-term EEG guided single dose administration of sodium valproate]H Stefan, F Hoffmann, H Fichsel, et al.
Plos One|December 17, 2013
Polymorphic cytochrome P450 enzymes (CYPs) and their role in personalized therapySarah C Preissner, Michael F Hoffmann, Robert Preissner, et al.
Journal of Orthopaedic Surgery and Research|November 28, 2013
Clinical outcomes of locked plating of distal femoral fractures in a retrospective cohortMartin F Hoffmann, Clifford B Jones, Debra L Sietsema, et al.
Nucleic Acids Research|December 17, 2013
The Transformer database: biotransformation of xenobioticsMichael F Hoffmann, Sarah C Preissner, Janette Nickel, et al.
Journal of Inherited Metabolic Disease|September 14, 2017
Critical appraisal of genotype assessment in molybdenum cofactor deficiencyKatrin Hinderhofer, Konstantin Mechler, Georg F Hoffmann, et al.
Journal of Inherited Metabolic Disease|September 13, 2023
The challenge of understanding and predicting phenotypic diversity in urea cycle disordersRoland Posset, Matthias Zielonka, Florian Gleich, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|September 1, 1988
Malignant nerve sheath tumors of the head and neckD F Hoffmann, E C Everts, J D Smith, et al.
Circulation|January 12, 2011
Determinants of blood pressure in preschool children: the role of parental smokingGiacomo D Simonetti, Rainer Schwertz, Martin Klett, et al.
Biochemistry|April 1, 1980
Ovalbumin messenger ribonucleic acid accumulation in the chick oviduct during secondary stimulation: influence of combinations of steroid hormones and circannual rhythmsS S Seaver, D C Van Eys-Fuchs, J F Hoffmann, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Neonatal screening for glutaryl-CoA dehydrogenase deficiencyM Lindner, S Kölker, A Schulze, et al.
Pageof 126