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Peter Lohse

Showing results (61-70 of 121) with videos related to

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Blood|June 24, 2008
Successful treatment of progressive cutaneous mastocytosis with imatinib in a 2-year-old boy carrying a somatic KIT mutationKarl M Hoffmann, Andrea Moser, Peter Lohse, et al.
World Journal of Gastroenterology|March 9, 2005
Role of the intracellular receptor domain of gp130 (exon 17) in human inflammatory bowel diseaseChristoph-J Auernhammer, Kathrin Zitzmann, Fabian Schnitzler, et al.
Inflammatory Bowel Diseases|August 12, 2015
Lipocalin-2 Is a Disease Activity Marker in Inflammatory Bowel Disease Regulated by IL-17A, IL-22, and TNF-α and Modulated by IL23R Genotype StatusJohannes Stallhofer, Matthias Friedrich, Astrid Konrad-Zerna, et al.
Genes, Chromosomes & Cancer|December 2, 2005
D324N single-nucleotide polymorphism in the FLT3 gene is associated with higher risk of myeloid leukemiasSusanne Schnittger, Tobias M Kohl, Nina Leopold, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2013
Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndromeWalter Bonfig, Nabeel J M Salem, Katrin Heiliger, et al.
European Journal of Haematology|July 13, 2004
Periodic fever, mild arthralgias, and reversible moderate and severe organ inflammation associated with the V198M mutation in the CIAS1 gene in three German patients--expanding phenotype of CIAS1 related autoinflammatory syndromeGönke Pörksen, Peter Lohse, Angela Rösen-Wolff, et al.
The American Journal of Gastroenterology|January 13, 2006
Increased expression of the chemokine fractalkine in Crohn's disease and association of the fractalkine receptor T280M polymorphism with a fibrostenosing disease PhenotypeStephan Brand, Katrin Hofbauer, Julia Dambacher, et al.
Inflammatory Bowel Diseases|November 23, 2006
Predictive value of the CARD15 variant 1007fs for the diagnosis of intestinal stenoses and the need for surgery in Crohn's disease in clinical practice: results of a prospective studyJulia Seiderer, Stephan Brand, Karin A Herrmann, et al.
Arthritis Research & Therapy|December 8, 2011
NLRP3 E311K mutation in a large family with Muckle-Wells syndrome--description of a heterogeneous phenotype and response to treatmentJasmin B Kuemmerle-Deschner, Peter Lohse, Ina Koetter, et al.
Journal of Pediatric Surgery|September 21, 2010
Hirschsprung-associated enterocolitis develops independently of NOD2 variantsMartin Lacher, Guido Fitze, Johanna Helmbrecht, et al.
Pageof 13

Showing results (61-70 of 121) with videos related to

Sort By:
Pageof 13
Blood|June 24, 2008
Successful treatment of progressive cutaneous mastocytosis with imatinib in a 2-year-old boy carrying a somatic KIT mutationKarl M Hoffmann, Andrea Moser, Peter Lohse, et al.
World Journal of Gastroenterology|March 9, 2005
Role of the intracellular receptor domain of gp130 (exon 17) in human inflammatory bowel diseaseChristoph-J Auernhammer, Kathrin Zitzmann, Fabian Schnitzler, et al.
Inflammatory Bowel Diseases|August 12, 2015
Lipocalin-2 Is a Disease Activity Marker in Inflammatory Bowel Disease Regulated by IL-17A, IL-22, and TNF-α and Modulated by IL23R Genotype StatusJohannes Stallhofer, Matthias Friedrich, Astrid Konrad-Zerna, et al.
Genes, Chromosomes & Cancer|December 2, 2005
D324N single-nucleotide polymorphism in the FLT3 gene is associated with higher risk of myeloid leukemiasSusanne Schnittger, Tobias M Kohl, Nina Leopold, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2013
Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndromeWalter Bonfig, Nabeel J M Salem, Katrin Heiliger, et al.
European Journal of Haematology|July 13, 2004
Periodic fever, mild arthralgias, and reversible moderate and severe organ inflammation associated with the V198M mutation in the CIAS1 gene in three German patients--expanding phenotype of CIAS1 related autoinflammatory syndromeGönke Pörksen, Peter Lohse, Angela Rösen-Wolff, et al.
The American Journal of Gastroenterology|January 13, 2006
Increased expression of the chemokine fractalkine in Crohn's disease and association of the fractalkine receptor T280M polymorphism with a fibrostenosing disease PhenotypeStephan Brand, Katrin Hofbauer, Julia Dambacher, et al.
Inflammatory Bowel Diseases|November 23, 2006
Predictive value of the CARD15 variant 1007fs for the diagnosis of intestinal stenoses and the need for surgery in Crohn's disease in clinical practice: results of a prospective studyJulia Seiderer, Stephan Brand, Karin A Herrmann, et al.
Arthritis Research & Therapy|December 8, 2011
NLRP3 E311K mutation in a large family with Muckle-Wells syndrome--description of a heterogeneous phenotype and response to treatmentJasmin B Kuemmerle-Deschner, Peter Lohse, Ina Koetter, et al.
Journal of Pediatric Surgery|September 21, 2010
Hirschsprung-associated enterocolitis develops independently of NOD2 variantsMartin Lacher, Guido Fitze, Johanna Helmbrecht, et al.
Pageof 13