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Robert Escher

Showing results (11-20 of 35) with videos related to

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BMC Pediatrics|June 8, 2019
Thrombophlebitis hiding under a KILT - case report on 40 years long-term follow-up of neonatal renal vein thrombosisStefan Lauener, Anne Bütikofer, Sandra Eigenheer, et al.
Journal of Bone and Joint Infection|February 8, 2021
Septic arthritis of the knee due to <i>Pantoea</i> <i>agglomerans</i>: look for the thornTobias Koester, Taro Kusano, Henk Eijer, et al.
Praxis|July 6, 2017
Barbara Birner, Theodor Glauser, Florian Balmer, et al.
Haematologica|September 2, 2004
Two clonal occurrences of tetrasomy 21 in an atypical chronic myeloid leukemia with wild-type RUNX1 alleles. Additional support for a gene dosage effect of chromosome 21 or RUNX1 in leukemiaRobert Escher, Dominique Mühlematter, Hamish S Scott, et al.
BMJ Open|June 11, 2018
Accuracy, reproducibility and costs of different laboratory assays for the monitoring of unfractionated heparin in clinical practice: a prospective evaluation study and survey among Swiss institutionsSusanne Bürki, Béatrice Brand, Robert Escher, et al.
Cureus|July 21, 2023
Fever of Unknown Origin, a Vascular Event, and Immunosuppression in Tick-Endemic Areas: Think About NeoehrlichiosisCristina Margini, Rafaela Maldonado, Peter Keller, et al.
Hepatology (Baltimore, Md.)|February 24, 2018
Favorable response to mammalian target of rapamycin inhibition in a young patient with unresectable fibrolamellar carcinoma of the liverRuben Bill, Matteo Montani, Benedikt Blum, et al.
BMC Infectious Diseases|May 15, 2016
Clinical and epidemiological analysis of Campylobacter fetus subsp. fetus infections in humans and comparative genetic analysis with strains isolated from cattleRobert Escher, Colette Brunner, Niklaus von Steiger, et al.
The American Journal of Medicine|February 3, 2009
A 40-day siegeRobert Escher, Ralph Kickuth, Niklaus von Steiger, et al.
Genes, Chromosomes & Cancer|August 31, 2004
Chromosome band 16q22-linked familial AML: exclusion of candidate genes, and possible disease risk modification by NQO1 polymorphismsRobert Escher, Antonia Jones, Fitsum Hagos, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
BMC Pediatrics|June 8, 2019
Thrombophlebitis hiding under a KILT - case report on 40 years long-term follow-up of neonatal renal vein thrombosisStefan Lauener, Anne Bütikofer, Sandra Eigenheer, et al.
Journal of Bone and Joint Infection|February 8, 2021
Septic arthritis of the knee due to <i>Pantoea</i> <i>agglomerans</i>: look for the thornTobias Koester, Taro Kusano, Henk Eijer, et al.
Praxis|July 6, 2017
Barbara Birner, Theodor Glauser, Florian Balmer, et al.
Haematologica|September 2, 2004
Two clonal occurrences of tetrasomy 21 in an atypical chronic myeloid leukemia with wild-type RUNX1 alleles. Additional support for a gene dosage effect of chromosome 21 or RUNX1 in leukemiaRobert Escher, Dominique Mühlematter, Hamish S Scott, et al.
BMJ Open|June 11, 2018
Accuracy, reproducibility and costs of different laboratory assays for the monitoring of unfractionated heparin in clinical practice: a prospective evaluation study and survey among Swiss institutionsSusanne Bürki, Béatrice Brand, Robert Escher, et al.
Cureus|July 21, 2023
Fever of Unknown Origin, a Vascular Event, and Immunosuppression in Tick-Endemic Areas: Think About NeoehrlichiosisCristina Margini, Rafaela Maldonado, Peter Keller, et al.
Hepatology (Baltimore, Md.)|February 24, 2018
Favorable response to mammalian target of rapamycin inhibition in a young patient with unresectable fibrolamellar carcinoma of the liverRuben Bill, Matteo Montani, Benedikt Blum, et al.
BMC Infectious Diseases|May 15, 2016
Clinical and epidemiological analysis of Campylobacter fetus subsp. fetus infections in humans and comparative genetic analysis with strains isolated from cattleRobert Escher, Colette Brunner, Niklaus von Steiger, et al.
The American Journal of Medicine|February 3, 2009
A 40-day siegeRobert Escher, Ralph Kickuth, Niklaus von Steiger, et al.
Genes, Chromosomes & Cancer|August 31, 2004
Chromosome band 16q22-linked familial AML: exclusion of candidate genes, and possible disease risk modification by NQO1 polymorphismsRobert Escher, Antonia Jones, Fitsum Hagos, et al.
Pageof 4