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Peter Lohse

Showing results (41-50 of 121) with videos related to

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Transplantation|September 24, 2004
Impact of thrombophilic gene mutations and graft-versus-host disease on thromboembolic complications after allogeneic hematopoietic stem-cell transplantationMarkus Pihusch, Peter Lohse, Jill Reitberger, et al.
Orphanet Journal of Rare Diseases|December 17, 2009
Incidence and classification of pediatric diffuse parenchymal lung diseases in GermanyMatthias Griese, Melanie Haug, Frank Brasch, et al.
Rheumatology (Oxford, England)|June 23, 2009
Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristicsElke Lainka, Ulrich Neudorf, Peter Lohse, et al.
Inflammatory Bowel Diseases|November 21, 2007
Linking genetic susceptibility to Crohn's disease with Th17 cell function: IL-22 serum levels are increased in Crohn's disease and correlate with disease activity and IL23R genotype statusSilke Schmechel, Astrid Konrad, Julia Diegelmann, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|June 30, 2010
Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasisBarbara Kleinlein, Matthias Griese, Gerhard Liebisch, et al.
Blood|November 23, 2011
Immunohistochemistry in the classification of systemic forms of amyloidosis: a systematic investigation of 117 patientsStefan O Schönland, Ute Hegenbart, Tilmann Bochtler, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|January 24, 2008
Systemic changes in haemostatic balance are not associated with increased levels of circulating microparticles in women with recurrent spontaneous abortionBettina Toth, Rienk Nieuwland, Meike Kern, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Identification of a novel mevalonate kinase gene mutation in combination with the common MVK V377I substitution and the low-penetrance TNFRSF1A R92Q mutationFlorian Hoffmann, Peter Lohse, Silvia Stojanov, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|December 19, 2008
Potential cell sources for tissue engineering of heart valves in comparison with human pulmonary valve cellsPhilipp K Schaefermeier, Natalia Cabeza, Jaya C Besser, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|November 8, 2014
Risk factors for AA amyloidosis in GermanyNorbert Blank, Ute Hegenbart, Peter Lohse, et al.
Pageof 13

Showing results (41-50 of 121) with videos related to

Sort By:
Pageof 13
Transplantation|September 24, 2004
Impact of thrombophilic gene mutations and graft-versus-host disease on thromboembolic complications after allogeneic hematopoietic stem-cell transplantationMarkus Pihusch, Peter Lohse, Jill Reitberger, et al.
Orphanet Journal of Rare Diseases|December 17, 2009
Incidence and classification of pediatric diffuse parenchymal lung diseases in GermanyMatthias Griese, Melanie Haug, Frank Brasch, et al.
Rheumatology (Oxford, England)|June 23, 2009
Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristicsElke Lainka, Ulrich Neudorf, Peter Lohse, et al.
Inflammatory Bowel Diseases|November 21, 2007
Linking genetic susceptibility to Crohn's disease with Th17 cell function: IL-22 serum levels are increased in Crohn's disease and correlate with disease activity and IL23R genotype statusSilke Schmechel, Astrid Konrad, Julia Diegelmann, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|June 30, 2010
Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasisBarbara Kleinlein, Matthias Griese, Gerhard Liebisch, et al.
Blood|November 23, 2011
Immunohistochemistry in the classification of systemic forms of amyloidosis: a systematic investigation of 117 patientsStefan O Schönland, Ute Hegenbart, Tilmann Bochtler, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|January 24, 2008
Systemic changes in haemostatic balance are not associated with increased levels of circulating microparticles in women with recurrent spontaneous abortionBettina Toth, Rienk Nieuwland, Meike Kern, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Identification of a novel mevalonate kinase gene mutation in combination with the common MVK V377I substitution and the low-penetrance TNFRSF1A R92Q mutationFlorian Hoffmann, Peter Lohse, Silvia Stojanov, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|December 19, 2008
Potential cell sources for tissue engineering of heart valves in comparison with human pulmonary valve cellsPhilipp K Schaefermeier, Natalia Cabeza, Jaya C Besser, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|November 8, 2014
Risk factors for AA amyloidosis in GermanyNorbert Blank, Ute Hegenbart, Peter Lohse, et al.
Pageof 13