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Terri Gelbart

Showing results (21-30 of 41) with videos related to

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Mayo Clinic Proceedings|June 13, 2002
Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE geneJill Waalen, Vincent Felitti, Terri Gelbart, et al.
British Journal of Haematology|September 16, 2009
Suppression of the hepcidin-encoding gene Hamp permits iron overload in mice lacking both hemojuvelin and matriptase-2/TMPRSS6Jaroslav Truksa, Terri Gelbart, Hongfan Peng, et al.
Acta Haematologica|August 17, 2005
Relationship between molecular variants and clinical manifestions in twelve glucose-6-phosphate dehydrogenase-deficient patients in JordanNaif S Karadsheh, Terri Gelbart, Hans-Jurgen Schulten, et al.
The Journal of Pediatrics|March 28, 2009
Fatal kernicterus in a girl deficient in glucose-6-phosphate dehydrogenase: a paradigm of synergistic heterozygosityShmuel Zangen, Devorah Kidron, Terri Gelbart, et al.
Lancet (London, England)|January 29, 2002
Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USAErnest Beutler, Vincent J Felitti, James A Koziol, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's diseasePauline L Lee, Terri Gelbart, Carol West, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 19, 2013
RNA purification and expression analysis using microarrays and RNA deep sequencingSteven R Head, Tony Mondala, Terri Gelbart, et al.
Acta Haematologica|November 23, 2006
Soluble transferrin receptor-1 levels in mice do not affect iron absorptionJonathan M Flanagan, Hongfan Peng, Lei Wang, et al.
Blood Cells, Molecules & Diseases|November 26, 2003
Genotypic and phenotypic heterogeneity of African Americans with primary iron overloadJames C Barton, Ronald T Acton, Charles A Rivers, et al.
Blood|October 24, 2002
Disruption of a novel regulatory element in the erythroid-specific promoter of the human PKLR gene causes severe pyruvate kinase deficiencyRichard van Wijk, Wouter W van Solinge, Claus Nerlov, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Mayo Clinic Proceedings|June 13, 2002
Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE geneJill Waalen, Vincent Felitti, Terri Gelbart, et al.
British Journal of Haematology|September 16, 2009
Suppression of the hepcidin-encoding gene Hamp permits iron overload in mice lacking both hemojuvelin and matriptase-2/TMPRSS6Jaroslav Truksa, Terri Gelbart, Hongfan Peng, et al.
Acta Haematologica|August 17, 2005
Relationship between molecular variants and clinical manifestions in twelve glucose-6-phosphate dehydrogenase-deficient patients in JordanNaif S Karadsheh, Terri Gelbart, Hans-Jurgen Schulten, et al.
The Journal of Pediatrics|March 28, 2009
Fatal kernicterus in a girl deficient in glucose-6-phosphate dehydrogenase: a paradigm of synergistic heterozygosityShmuel Zangen, Devorah Kidron, Terri Gelbart, et al.
Lancet (London, England)|January 29, 2002
Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USAErnest Beutler, Vincent J Felitti, James A Koziol, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's diseasePauline L Lee, Terri Gelbart, Carol West, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 19, 2013
RNA purification and expression analysis using microarrays and RNA deep sequencingSteven R Head, Tony Mondala, Terri Gelbart, et al.
Acta Haematologica|November 23, 2006
Soluble transferrin receptor-1 levels in mice do not affect iron absorptionJonathan M Flanagan, Hongfan Peng, Lei Wang, et al.
Blood Cells, Molecules & Diseases|November 26, 2003
Genotypic and phenotypic heterogeneity of African Americans with primary iron overloadJames C Barton, Ronald T Acton, Charles A Rivers, et al.
Blood|October 24, 2002
Disruption of a novel regulatory element in the erythroid-specific promoter of the human PKLR gene causes severe pyruvate kinase deficiencyRichard van Wijk, Wouter W van Solinge, Claus Nerlov, et al.
Pageof 5