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S Andresen

Showing results (41-50 of 249) with videos related to

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The Laryngoscope|July 4, 2019
Hospital volume and failure to rescue after vestibular schwannoma resectionNicholas S Andresen, Christine G Gourin, C Matthew Stewart, et al.
Biochemical Society Transactions|July 26, 2000
Mutations of human medium-chian acyl-CoA dehydrogenaseS Udvari, P Bross, B S Andresen, et al.
Molecular Genetics and Metabolism|May 12, 2010
The phenylalanine hydroxylase c.30C>G synonymous variation (p.G10G) creates a common exonic splicing silencerSteven F Dobrowolski, Henriette S Andersen, Thomas K Doktor, et al.
Cellular and Molecular Life Sciences : CMLS|June 6, 2022
Essential role of CK2α for the interaction and stability of replication fork factors during DNA synthesis and activation of the S-phase checkpointBarbara Guerra, Thomas K Doktor, Sabrina B Frederiksen, et al.
Plos One|January 25, 2024
Study protocol for RUFUS-A randomized mixed methods pilot clinical trial investigating the relevance and feasibility of rumination-focused cognitive behavioral therapy in the treatment of patients with emergent psychosis spectrum disordersLars Clemmensen, Christin Nymann Lund, Birgitte S Andresen, et al.
Bone Marrow Transplantation|October 6, 1997
Platelet transfusion requirements during autologous peripheral blood progenitor cell transplantation correlate with the pretransplant platelet countB J Bolwell, M Goormastic, S Andresen, et al.
The Review of Scientific Instruments|May 30, 2023
Calibrated transmission and reflection from a multi-qubit microwave packageS Simbierowicz, V Y Monarkha, M von Soosten, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disordersN Gregersen, P Bross, M M Jørgensen, et al.
Molecular Genetics and Metabolism Reports|January 6, 2017
Long-term outcome of isobutyryl-CoA dehydrogenase deficiency diagnosed following an episode of ketotic hypoglycaemiaS Santra, A Macdonald, M A Preece, et al.
Plos Genetics|April 24, 2018
Intronic PAH gene mutations cause a splicing defect by a novel mechanism involving U1snRNP binding downstream of the 5' splice siteAinhoa Martínez-Pizarro, Maja Dembic, Belén Pérez, et al.
Pageof 25

Showing results (41-50 of 249) with videos related to

Sort By:
Pageof 25
The Laryngoscope|July 4, 2019
Hospital volume and failure to rescue after vestibular schwannoma resectionNicholas S Andresen, Christine G Gourin, C Matthew Stewart, et al.
Biochemical Society Transactions|July 26, 2000
Mutations of human medium-chian acyl-CoA dehydrogenaseS Udvari, P Bross, B S Andresen, et al.
Molecular Genetics and Metabolism|May 12, 2010
The phenylalanine hydroxylase c.30C>G synonymous variation (p.G10G) creates a common exonic splicing silencerSteven F Dobrowolski, Henriette S Andersen, Thomas K Doktor, et al.
Cellular and Molecular Life Sciences : CMLS|June 6, 2022
Essential role of CK2α for the interaction and stability of replication fork factors during DNA synthesis and activation of the S-phase checkpointBarbara Guerra, Thomas K Doktor, Sabrina B Frederiksen, et al.
Plos One|January 25, 2024
Study protocol for RUFUS-A randomized mixed methods pilot clinical trial investigating the relevance and feasibility of rumination-focused cognitive behavioral therapy in the treatment of patients with emergent psychosis spectrum disordersLars Clemmensen, Christin Nymann Lund, Birgitte S Andresen, et al.
Bone Marrow Transplantation|October 6, 1997
Platelet transfusion requirements during autologous peripheral blood progenitor cell transplantation correlate with the pretransplant platelet countB J Bolwell, M Goormastic, S Andresen, et al.
The Review of Scientific Instruments|May 30, 2023
Calibrated transmission and reflection from a multi-qubit microwave packageS Simbierowicz, V Y Monarkha, M von Soosten, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disordersN Gregersen, P Bross, M M Jørgensen, et al.
Molecular Genetics and Metabolism Reports|January 6, 2017
Long-term outcome of isobutyryl-CoA dehydrogenase deficiency diagnosed following an episode of ketotic hypoglycaemiaS Santra, A Macdonald, M A Preece, et al.
Plos Genetics|April 24, 2018
Intronic PAH gene mutations cause a splicing defect by a novel mechanism involving U1snRNP binding downstream of the 5' splice siteAinhoa Martínez-Pizarro, Maja Dembic, Belén Pérez, et al.
Pageof 25