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Photis Beris

Showing results (11-20 of 25) with videos related to

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European Journal of Haematology|February 28, 2003
Complete remission of pure white cell aplasia associated with thymoma, autoimmune thyroiditis and type 1 diabetesZina Fumeaux, Photis Beris, Bettina Borisch, et al.
European Journal of Haematology|July 22, 2006
Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletionThomas Matthes, Pierre Rustin, Hedwige Trachsel, et al.
British Journal of Haematology|November 28, 2008
Growth differentiation factor 15 production is necessary for normal erythroid differentiation and is increased in refractory anaemia with ring-sideroblastsJean-Marie Ramirez, Olivier Schaad, Stephane Durual, et al.
Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals|July 1, 2009
Growth-differentiation factor-15, endoglin and N-terminal pro-brain natriuretic peptide induction in athletes participating in an ultramarathon foot raceIsabelle Tchou, Alexandra Margeli, Maria Tsironi, et al.
Blood|June 17, 2004
Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5'-UTR of the HAMP geneThomas Matthes, Patricia Aguilar-Martinez, Loredana Pizzi-Bosman, et al.
European Journal of Haematology|June 9, 2011
Response of iron overload to deferasirox in rare transfusion-dependent anaemias: equivalent effects on serum ferritin and labile plasma iron for haemolytic or production anaemiasJohn B Porter, Kai-Hsin Lin, Photis Beris, et al.
Expert Review of Hematology|November 25, 2010
Nilotinib is superior to imatinib as first-line therapy of chronic myeloid leukemia: the ENESTnd studyFrancis J Giles, Gianantonio Rosti, Photis Beris, et al.
Blood|March 22, 2003
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndromeSamuel Deutsch, Alexandra Rideau, Marie-Luce Bochaton-Piallat, et al.
Analytical and Bioanalytical Chemistry|March 11, 2015
Identification of hemoglobin variants by top-down mass spectrometry using selected diagnostic product ionsDidia Coelho Graça, Ralf Hartmer, Wolfgang Jabs, et al.
Transfusion|November 8, 2002
Acquired and transient RBC CD55 deficiency (Inab phenotype) and anti-IFCThomas Matthes, Emanuelle Tullen, Joyce Poole, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
European Journal of Haematology|February 28, 2003
Complete remission of pure white cell aplasia associated with thymoma, autoimmune thyroiditis and type 1 diabetesZina Fumeaux, Photis Beris, Bettina Borisch, et al.
European Journal of Haematology|July 22, 2006
Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletionThomas Matthes, Pierre Rustin, Hedwige Trachsel, et al.
British Journal of Haematology|November 28, 2008
Growth differentiation factor 15 production is necessary for normal erythroid differentiation and is increased in refractory anaemia with ring-sideroblastsJean-Marie Ramirez, Olivier Schaad, Stephane Durual, et al.
Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals|July 1, 2009
Growth-differentiation factor-15, endoglin and N-terminal pro-brain natriuretic peptide induction in athletes participating in an ultramarathon foot raceIsabelle Tchou, Alexandra Margeli, Maria Tsironi, et al.
Blood|June 17, 2004
Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5'-UTR of the HAMP geneThomas Matthes, Patricia Aguilar-Martinez, Loredana Pizzi-Bosman, et al.
European Journal of Haematology|June 9, 2011
Response of iron overload to deferasirox in rare transfusion-dependent anaemias: equivalent effects on serum ferritin and labile plasma iron for haemolytic or production anaemiasJohn B Porter, Kai-Hsin Lin, Photis Beris, et al.
Expert Review of Hematology|November 25, 2010
Nilotinib is superior to imatinib as first-line therapy of chronic myeloid leukemia: the ENESTnd studyFrancis J Giles, Gianantonio Rosti, Photis Beris, et al.
Blood|March 22, 2003
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndromeSamuel Deutsch, Alexandra Rideau, Marie-Luce Bochaton-Piallat, et al.
Analytical and Bioanalytical Chemistry|March 11, 2015
Identification of hemoglobin variants by top-down mass spectrometry using selected diagnostic product ionsDidia Coelho Graça, Ralf Hartmer, Wolfgang Jabs, et al.
Transfusion|November 8, 2002
Acquired and transient RBC CD55 deficiency (Inab phenotype) and anti-IFCThomas Matthes, Emanuelle Tullen, Joyce Poole, et al.
Pageof 3