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Scandinavian Journal of Gastroenterology
|
March 4, 2005
CARD15 frameshift mutation in patients with CROHN disease is associated with immune dysregulation
L Halme, U Turunen, P Paavola-Sakki, et al.
Gut
|
October 1, 1981
Endotoxin and liver diseases. High titres of enterobacterial common antigen antibodies in patients with alcoholic cirrhosis
U Turunen, M Malkamäki, V V Valtonen, et al.
Scandinavian Journal of Gastroenterology
|
July 20, 2002
Familial and sporadic inflammatory bowel disease: comparison of clinical features and serological markers in a genetically homogeneous population
L Halme, U Turunen, T Heliö, et al.
Gut
|
March 13, 2003
CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease
T Heliö, L Halme, M Lappalainen, et al.
Scandinavian Journal of Rheumatology
|
February 22, 2013
Normal inflammasome activation and low production of IL-23 by monocyte-derived macrophages from subjects with a history of reactive arthritis
E Välimäki, S Aittomäki, L Karenko, et al.
Journal of Medical Microbiology
|
February 1, 1983
Occurrence of antibodies to teichoic acid in patients with diseases other than staphylococcal infection
U Larinkari, M Leirisalo, P J Pentikäinen, et al.
Scandinavian Journal of Immunology
|
November 22, 2007
A novel modification of a flow cytometric assay of phosphorylated STAT1 in whole blood monocytes for immunomonitoring of patients on IFN alpha regimen
J Vakkila, U Nieminen, S Siitonen, et al.
Diabetes Care
|
July 1, 1993
Seven years of remission in a type I diabetic patient
V A Koivisto, M Leirisalo-Repo, P Ebeling, et al.
Alimentary Pharmacology & Therapeutics
|
December 1, 1994
Budesonide enema in active haemorrhagic proctitis--a controlled trial against hydrocortisone foam enema
S Tarpila, U Turunen, K Seppälä, et al.
European Journal of Human Genetics : EJHG
|
May 30, 2001
Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21
P Paavola, T Heliö, M Kiuru, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Scandinavian Journal of Gastroenterology
|
March 4, 2005
CARD15 frameshift mutation in patients with CROHN disease is associated with immune dysregulation
L Halme, U Turunen, P Paavola-Sakki, et al.
Gut
|
October 1, 1981
Endotoxin and liver diseases. High titres of enterobacterial common antigen antibodies in patients with alcoholic cirrhosis
U Turunen, M Malkamäki, V V Valtonen, et al.
Scandinavian Journal of Gastroenterology
|
July 20, 2002
Familial and sporadic inflammatory bowel disease: comparison of clinical features and serological markers in a genetically homogeneous population
L Halme, U Turunen, T Heliö, et al.
Gut
|
March 13, 2003
CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease
T Heliö, L Halme, M Lappalainen, et al.
Scandinavian Journal of Rheumatology
|
February 22, 2013
Normal inflammasome activation and low production of IL-23 by monocyte-derived macrophages from subjects with a history of reactive arthritis
E Välimäki, S Aittomäki, L Karenko, et al.
Journal of Medical Microbiology
|
February 1, 1983
Occurrence of antibodies to teichoic acid in patients with diseases other than staphylococcal infection
U Larinkari, M Leirisalo, P J Pentikäinen, et al.
Scandinavian Journal of Immunology
|
November 22, 2007
A novel modification of a flow cytometric assay of phosphorylated STAT1 in whole blood monocytes for immunomonitoring of patients on IFN alpha regimen
J Vakkila, U Nieminen, S Siitonen, et al.
Diabetes Care
|
July 1, 1993
Seven years of remission in a type I diabetic patient
V A Koivisto, M Leirisalo-Repo, P Ebeling, et al.
Alimentary Pharmacology & Therapeutics
|
December 1, 1994
Budesonide enema in active haemorrhagic proctitis--a controlled trial against hydrocortisone foam enema
S Tarpila, U Turunen, K Seppälä, et al.
European Journal of Human Genetics : EJHG
|
May 30, 2001
Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21
P Paavola, T Heliö, M Kiuru, et al.
Page
of 3