Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Peter Lohse

Showing results (71-80 of 121) with videos related to

Pageof 13
Sort By:
Inflammatory Bowel Diseases|April 3, 2008
NOD2/CARD15 genotype influences MDP-induced cytokine release and basal IL-12p40 levels in primary isolated peripheral blood monocytesVanessa Beynon, Sebastian Cotofana, Stephan Brand, et al.
Pediatric Rheumatology Online Journal|November 5, 2015
Early detection of sensorineural hearing loss in Muckle-Wells-syndromeJasmin B Kuemmerle-Deschner, Assen Koitschev, Pascal N Tyrrell, et al.
The American Journal of Surgical Pathology|October 3, 2008
Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloidMagdalena Eriksson, Janine Büttner, Theodor Todorov, et al.
Journal of Pediatric Surgery|August 18, 2010
NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's diseaseMartin Lacher, Johanna Helmbrecht, Sebastian Schroepf, et al.
Plos One|July 7, 2015
The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 MutationsFabian Schnitzler, Matthias Friedrich, Christiane Wolf, et al.
Plos One|July 28, 2020
Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resulting in ileal stenosis requiring surgeryFabian Schnitzler, Matthias Friedrich, Marianne Angelberger, et al.
Inflammatory Bowel Diseases|June 24, 2005
The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's diseaseStephan Brand, Tanja Staudinger, Fabian Schnitzler, et al.
Scandinavian Journal of Gastroenterology|November 15, 2006
Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosisJulia Seiderer, Fabian Schnitzler, Stephan Brand, et al.
Arthritis and Rheumatism|March 2, 2011
Efficacy and safety of anakinra therapy in pediatric and adult patients with the autoinflammatory Muckle-Wells syndromeJasmin B Kuemmerle-Deschner, Pascal N Tyrrell, Ina Koetter, et al.
Annals of the Rheumatic Diseases|September 13, 2011
MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromesHelmut Wittkowski, Jasmin B Kuemmerle-Deschner, Judith Austermann, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Inflammatory Bowel Diseases|April 3, 2008
NOD2/CARD15 genotype influences MDP-induced cytokine release and basal IL-12p40 levels in primary isolated peripheral blood monocytesVanessa Beynon, Sebastian Cotofana, Stephan Brand, et al.
Pediatric Rheumatology Online Journal|November 5, 2015
Early detection of sensorineural hearing loss in Muckle-Wells-syndromeJasmin B Kuemmerle-Deschner, Assen Koitschev, Pascal N Tyrrell, et al.
The American Journal of Surgical Pathology|October 3, 2008
Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloidMagdalena Eriksson, Janine Büttner, Theodor Todorov, et al.
Journal of Pediatric Surgery|August 18, 2010
NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's diseaseMartin Lacher, Johanna Helmbrecht, Sebastian Schroepf, et al.
Plos One|July 7, 2015
The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 MutationsFabian Schnitzler, Matthias Friedrich, Christiane Wolf, et al.
Plos One|July 28, 2020
Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resulting in ileal stenosis requiring surgeryFabian Schnitzler, Matthias Friedrich, Marianne Angelberger, et al.
Inflammatory Bowel Diseases|June 24, 2005
The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's diseaseStephan Brand, Tanja Staudinger, Fabian Schnitzler, et al.
Scandinavian Journal of Gastroenterology|November 15, 2006
Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosisJulia Seiderer, Fabian Schnitzler, Stephan Brand, et al.
Arthritis and Rheumatism|March 2, 2011
Efficacy and safety of anakinra therapy in pediatric and adult patients with the autoinflammatory Muckle-Wells syndromeJasmin B Kuemmerle-Deschner, Pascal N Tyrrell, Ina Koetter, et al.
Annals of the Rheumatic Diseases|September 13, 2011
MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromesHelmut Wittkowski, Jasmin B Kuemmerle-Deschner, Judith Austermann, et al.
Pageof 13