F Hoffmann|K Jessen - JoVE Visualize

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Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1986

Ultrastructure of the rabbit corneal stroma after experimental keratomileusisN Bornfeld, F Hoffmann, K B Mellin, et al.

Angewandte Chemie (International Ed. in English)|December 29, 2020

Fluorescent and Water Dispersible Single-Chain Nanoparticles: Core-Shell Structured CompartmentationJustus F Hoffmann, Andreas H Roos, Franz-Josef Schmitt, et al.

Endocrinology|May 15, 2003

Vitamin D and dexamethasone inversely regulate parathyroid hormone-induced regulator of G protein signaling-2 expression in osteoblast-like cellsM Hömme, C P Schmitt, R Himmele, et al.

Pediatric Neurology|September 6, 2002

L-alanine supplementation in late infantile glycogen storage disease type IIOlaf A Bodamer, Dorothea Haas, Monique M Hermans, et al.

Molecular Genetics and Metabolism|February 19, 2020

Cardiac phenotype in propionic acidemia - Results of an observational monocentric studyA Kovacevic, S F Garbade, G F Hoffmann, et al.

European Journal of Pediatrics|August 1, 1997

Protein turnover in critically ill childrenO A Bodamer, J V Leonard, R C Tasker, et al.

Molecular Genetics and Metabolism|July 25, 2018

Relationship between genotype, phenylalanine hydroxylase expression and in vitro activity and metabolic phenotype in phenylketonuriaNastassja Himmelreich, Nan Shen, Jürgen G Okun, et al.

Der Unfallchirurg|March 31, 1999

[Replacement of the anterior cruciate ligament. Biomechanical studies for patellar and semitendinosus tendon fixation with a poly(D,L-lactide) interference screw]A Weiler, R F Hoffmann, N P Südkamp, et al.

American Journal of Medical Genetics|October 21, 1999

Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: further evidence for a contiguous gene syndrome in 17q11.2B Streubel, E Latta, H Kehrer-Sawatzki, et al.

Journal of Inherited Metabolic Disease|March 19, 2011

Diagnosis of tetrahydrobiopterin deficiency using filter paper blood spots: further development of the method and 5 years experienceThomas Opladen, Bettina Abu Seda, Anahita Rassi, et al.

Pageof 114

Showing results (451-460 of 1,133) with videos related to

Sort By:

Pageof 114

Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1986

Ultrastructure of the rabbit corneal stroma after experimental keratomileusisN Bornfeld, F Hoffmann, K B Mellin, et al.

Angewandte Chemie (International Ed. in English)|December 29, 2020

Fluorescent and Water Dispersible Single-Chain Nanoparticles: Core-Shell Structured CompartmentationJustus F Hoffmann, Andreas H Roos, Franz-Josef Schmitt, et al.

Endocrinology|May 15, 2003

Vitamin D and dexamethasone inversely regulate parathyroid hormone-induced regulator of G protein signaling-2 expression in osteoblast-like cellsM Hömme, C P Schmitt, R Himmele, et al.

Pediatric Neurology|September 6, 2002

L-alanine supplementation in late infantile glycogen storage disease type IIOlaf A Bodamer, Dorothea Haas, Monique M Hermans, et al.

Molecular Genetics and Metabolism|February 19, 2020

Cardiac phenotype in propionic acidemia - Results of an observational monocentric studyA Kovacevic, S F Garbade, G F Hoffmann, et al.

European Journal of Pediatrics|August 1, 1997

Protein turnover in critically ill childrenO A Bodamer, J V Leonard, R C Tasker, et al.

Molecular Genetics and Metabolism|July 25, 2018

Relationship between genotype, phenylalanine hydroxylase expression and in vitro activity and metabolic phenotype in phenylketonuriaNastassja Himmelreich, Nan Shen, Jürgen G Okun, et al.

Der Unfallchirurg|March 31, 1999

[Replacement of the anterior cruciate ligament. Biomechanical studies for patellar and semitendinosus tendon fixation with a poly(D,L-lactide) interference screw]A Weiler, R F Hoffmann, N P Südkamp, et al.

American Journal of Medical Genetics|October 21, 1999

Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: further evidence for a contiguous gene syndrome in 17q11.2B Streubel, E Latta, H Kehrer-Sawatzki, et al.

Journal of Inherited Metabolic Disease|March 19, 2011

Diagnosis of tetrahydrobiopterin deficiency using filter paper blood spots: further development of the method and 5 years experienceThomas Opladen, Bettina Abu Seda, Anahita Rassi, et al.

Pageof 114