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J Ockenga

Showing results (51-60 of 70) with videos related to

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Zeitschrift Fur Gastroenterologie|August 24, 1999
Diagnosis of Chilaiditi's syndrome with abdominal ultrasoundA Widjaja, B Walter, J S Bleck, et al.
Hepato-Gastroenterology|October 2, 1998
Perihepatic lymphadenopathy: a marker of response to interferon alpha in chronic hepatitis CH Wedemeyer, J Ockenga, H Frank, et al.
Scandinavian Journal of Gastroenterology|May 5, 2001
Hepatitis C and the leptin system: bound leptin levels are elevated in patients with hepatitis C and decrease during antiviral therapyA Widjaja, H Wedemeyer, H L Tillmann, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|July 14, 2004
Keratin 8 Y54H and G62C mutations are not associated with inflammatory bowel diseaseC Büning, J Halangk, A Dignass, et al.
Scandinavian Journal of Gastroenterology|June 11, 2003
The C/C(-13910) and G/G(-22018) genotypes for adult-type hypolactasia are not associated with inflammatory bowel diseaseC Büning, J Ockenga, S Krüger, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|February 24, 1999
[3D and color Doppler ultrasound evaluation of cystic space-occupying lesion near the head of the pancreas]B Boozari, M Gebel, J S Bleck, et al.
Scandinavian Journal of Gastroenterology|April 27, 2017
The C/C_₁₃₉₁₀ and G/G_₂₂₀₁₈ Genotypes for Adult-type Hypolactasia are not Associated with Inflammatory Bowel DiseaseC Büning, J Ockenga, S Krüger, 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.
The Journal of Infectious Diseases|June 2, 1998
GB virus C/hepatitis G virus infection: a favorable prognostic factor in human immunodeficiency virus-infected patients?S Heringlake, J Ockenga, H L Tillmann, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2001
Dyslipemia in familial partial lipodystrophy caused by an R482W mutation in the LMNA geneH H Schmidt, J Genschel, P Baier, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Zeitschrift Fur Gastroenterologie|August 24, 1999
Diagnosis of Chilaiditi's syndrome with abdominal ultrasoundA Widjaja, B Walter, J S Bleck, et al.
Hepato-Gastroenterology|October 2, 1998
Perihepatic lymphadenopathy: a marker of response to interferon alpha in chronic hepatitis CH Wedemeyer, J Ockenga, H Frank, et al.
Scandinavian Journal of Gastroenterology|May 5, 2001
Hepatitis C and the leptin system: bound leptin levels are elevated in patients with hepatitis C and decrease during antiviral therapyA Widjaja, H Wedemeyer, H L Tillmann, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|July 14, 2004
Keratin 8 Y54H and G62C mutations are not associated with inflammatory bowel diseaseC Büning, J Halangk, A Dignass, et al.
Scandinavian Journal of Gastroenterology|June 11, 2003
The C/C(-13910) and G/G(-22018) genotypes for adult-type hypolactasia are not associated with inflammatory bowel diseaseC Büning, J Ockenga, S Krüger, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|February 24, 1999
[3D and color Doppler ultrasound evaluation of cystic space-occupying lesion near the head of the pancreas]B Boozari, M Gebel, J S Bleck, et al.
Scandinavian Journal of Gastroenterology|April 27, 2017
The C/C_₁₃₉₁₀ and G/G_₂₂₀₁₈ Genotypes for Adult-type Hypolactasia are not Associated with Inflammatory Bowel DiseaseC Büning, J Ockenga, S Krüger, 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.
The Journal of Infectious Diseases|June 2, 1998
GB virus C/hepatitis G virus infection: a favorable prognostic factor in human immunodeficiency virus-infected patients?S Heringlake, J Ockenga, H L Tillmann, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2001
Dyslipemia in familial partial lipodystrophy caused by an R482W mutation in the LMNA geneH H Schmidt, J Genschel, P Baier, et al.
Pageof 7