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Schwinger

Showing results (601-610 of 849) with videos related to

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Human Mutation|April 23, 2002
Characterization of breakpoint sequences of five rearrangements in L1CAM and ABCD1 (ALD) genesKerstin Kutsche, Bernadette Ressler, Heide-Gertrude Katzera, et al.
Pflege|August 23, 2022
[Social participation in nursing homes with Covid-19 protection measures in the second pandemic wave? Linkage of prescriptions and survey]Annabell Gangnus, Christian Hering, Raphael Kohl, et al.
Urologia Internationalis|April 2, 2026
Perioperative Complications After URS, PNL, and ECIRS in Patients Receiving SGLT2 Inhibitor TherapyVincent Scheper, Clemens Meseck, Charis Kalogirou, et al.
The Annals of Thoracic Surgery|April 28, 2005
Daily assessment of organ dysfunction and survival in intensive care unit cardiac surgical patientsKhosro Hekmat, Axel Kroener, Hartmut Stuetzer, et al.
Clinical Genetics|March 1, 1987
Roberts syndrome and SC phocomelia. A single genetic entityC Römke, U Froster-Iskenius, K Heyne, et al.
Circulation|April 12, 2000
Myofilament calcium regulation in human myocardiumR J Hajjar, R H Schwinger, U Schmidt, et al.
Biological Psychiatry|April 3, 1999
Smooth pursuit performance in families with multiple occurrence of schizophrenia and nonpsychotic familiesR Lencer, C P Malchow, K Krecker, et al.
Journal of Medical Genetics|February 1, 1996
Five novel mutations in the L1CAM gene in families with X linked hydrocephalusS M Gu, U Orth, A Veske, et al.
Journal of Clinical Microbiology|April 9, 2005
Fusarium verticillioides abscess of the nasal septum in an immunosuppressed child: case report and identification of the morphologically atypical fungal strainHans Jürgen Dornbusch, Walter Buzina, Richard C Summerbell, et al.
European Journal of Haematology|November 22, 2007
Partial splenic embolization in children with hereditary spherocytosisBarbara Pratl, Martin Benesch, Herwig Lackner, et al.
Pageof 85

Showing results (601-610 of 849) with videos related to

Sort By:
Pageof 85
Human Mutation|April 23, 2002
Characterization of breakpoint sequences of five rearrangements in L1CAM and ABCD1 (ALD) genesKerstin Kutsche, Bernadette Ressler, Heide-Gertrude Katzera, et al.
Pflege|August 23, 2022
[Social participation in nursing homes with Covid-19 protection measures in the second pandemic wave? Linkage of prescriptions and survey]Annabell Gangnus, Christian Hering, Raphael Kohl, et al.
Urologia Internationalis|April 2, 2026
Perioperative Complications After URS, PNL, and ECIRS in Patients Receiving SGLT2 Inhibitor TherapyVincent Scheper, Clemens Meseck, Charis Kalogirou, et al.
The Annals of Thoracic Surgery|April 28, 2005
Daily assessment of organ dysfunction and survival in intensive care unit cardiac surgical patientsKhosro Hekmat, Axel Kroener, Hartmut Stuetzer, et al.
Clinical Genetics|March 1, 1987
Roberts syndrome and SC phocomelia. A single genetic entityC Römke, U Froster-Iskenius, K Heyne, et al.
Circulation|April 12, 2000
Myofilament calcium regulation in human myocardiumR J Hajjar, R H Schwinger, U Schmidt, et al.
Biological Psychiatry|April 3, 1999
Smooth pursuit performance in families with multiple occurrence of schizophrenia and nonpsychotic familiesR Lencer, C P Malchow, K Krecker, et al.
Journal of Medical Genetics|February 1, 1996
Five novel mutations in the L1CAM gene in families with X linked hydrocephalusS M Gu, U Orth, A Veske, et al.
Journal of Clinical Microbiology|April 9, 2005
Fusarium verticillioides abscess of the nasal septum in an immunosuppressed child: case report and identification of the morphologically atypical fungal strainHans Jürgen Dornbusch, Walter Buzina, Richard C Summerbell, et al.
European Journal of Haematology|November 22, 2007
Partial splenic embolization in children with hereditary spherocytosisBarbara Pratl, Martin Benesch, Herwig Lackner, et al.
Pageof 85