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H H-J Schmidt

Showing results (1-10 of 13) with videos related to

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European Journal of Medical Research|July 8, 2003
Lack of mutations in LMNA, its promoter region, and the cellular retinoic acid binding protein II (CRABP II) in HIV associated lipodystrophyG M N Behrens, J Genschel, R E Schmidt, et al.
Liver|September 11, 2002
Emerging indications for MARS dialysisG Schachschal, S Morgera, S Küpferling, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|October 26, 2005
Long-term treatment experience in a subject with Dunnigan-type familial partial lipodystrophy: efficacy of rosiglitazoneA Lüdtke, K Heck, J Genschel, et al.
Scandinavian Journal of Gastroenterology|October 30, 2004
Covered transjugular intrahepatic portosystemic stents maintain lower portal pressure and require fewer reinterventions than uncovered stentsJ Ockenga, T J Kroencke, T Schuetz, et al.
Clinical Genetics|November 15, 2005
Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's diseaseG Gromadzka, H H-J Schmidt, J Genschel, et al.
Journal of Mass Spectrometry : JMS|September 16, 2009
Laser secondary neutral mass spectrometry for copper detection in micro-scale biopsiesC Kriegeskotte, T Cantz, J Haberland, et al.
Gut|July 8, 2005
Genetic basis for increased intestinal permeability in families with Crohn's disease: role of CARD15 3020insC mutation?S Buhner, C Buning, J Genschel, et al.
Laboratory Animals|March 8, 2013
Gender and strain-specific differences in the development of steatosis in ratsS Stöppeler, D Palmes, M Fehr, et al.
Deutsche Medizinische Wochenschrift (1946)|July 13, 2006
[Interdisciplinary guidelines on diagnosis and treatment for extracerebral amyloidoses--published by the German Society of Amyloid Diseases (www.amyloid.de)]C Röcken, J Ernst, E Hund, et al.
Alimentary Pharmacology & Therapeutics|May 15, 2004
Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperationC Büning, J Genschel, S Bühner, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
European Journal of Medical Research|July 8, 2003
Lack of mutations in LMNA, its promoter region, and the cellular retinoic acid binding protein II (CRABP II) in HIV associated lipodystrophyG M N Behrens, J Genschel, R E Schmidt, et al.
Liver|September 11, 2002
Emerging indications for MARS dialysisG Schachschal, S Morgera, S Küpferling, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|October 26, 2005
Long-term treatment experience in a subject with Dunnigan-type familial partial lipodystrophy: efficacy of rosiglitazoneA Lüdtke, K Heck, J Genschel, et al.
Scandinavian Journal of Gastroenterology|October 30, 2004
Covered transjugular intrahepatic portosystemic stents maintain lower portal pressure and require fewer reinterventions than uncovered stentsJ Ockenga, T J Kroencke, T Schuetz, et al.
Clinical Genetics|November 15, 2005
Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's diseaseG Gromadzka, H H-J Schmidt, J Genschel, et al.
Journal of Mass Spectrometry : JMS|September 16, 2009
Laser secondary neutral mass spectrometry for copper detection in micro-scale biopsiesC Kriegeskotte, T Cantz, J Haberland, et al.
Gut|July 8, 2005
Genetic basis for increased intestinal permeability in families with Crohn's disease: role of CARD15 3020insC mutation?S Buhner, C Buning, J Genschel, et al.
Laboratory Animals|March 8, 2013
Gender and strain-specific differences in the development of steatosis in ratsS Stöppeler, D Palmes, M Fehr, et al.
Deutsche Medizinische Wochenschrift (1946)|July 13, 2006
[Interdisciplinary guidelines on diagnosis and treatment for extracerebral amyloidoses--published by the German Society of Amyloid Diseases (www.amyloid.de)]C Röcken, J Ernst, E Hund, et al.
Alimentary Pharmacology & Therapeutics|May 15, 2004
Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperationC Büning, J Genschel, S Bühner, et al.
Pageof 2