Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Margaret Fadojutimi-Akinsiku"'
Autor:
Leah Passmore, Helen Harrison, James C. Barton, David M. Reboussin, Charles A. Rivers, Margaret Fadojutimi-Akinsiku, Sharmin Diaz, Mark Speechley, Emily L. Harris, Lari Wenzel
Publikováno v:
Genetic Testing and Molecular Biomarkers. 13:721-728
Background: Little is known about the factors affecting participation in clinical assessments after HEmochromatosis and IRon Overload Screening. Methods: Initial screening of 101,168 primary care patients in the HEmochromatosis and IRon Overload Scre
Autor:
Catherine Nwokolo, Sharmin Diaz, Victor R. Gordeuk, Margaret Fadojutimi-Akinsiku, Georgia Willie-Carnegie, Newton Andrews, Shahla G. Naoman, Mehdi Nouraie, Oswaldo Castro
Publikováno v:
Annals of Hematology. 89:61-66
Pulmonary hypertension is a complication of sickle cell disease that is associated with increased mortality. Whether this complication is associated with hemolysis has been questioned. Systolic pulmonary artery blood pressure can be estimated from ec
Autor:
Helen Harrison, Margaret Fadojutimi-Akinsiku, Beverly M. Snively, Shana L. Palla, Diane C. Tucker, Ometha Lewis-Jack, Mark Speechley, Jacob A. Reiss, John H. Eckfeldt, Elizabeth J. Thomson, Charles A. Rivers, Lari Wenzel, Christine E. McLaren, Ebony Bookman, Roger T. Anderson
Publikováno v:
Genetics in Medicine. 9:705-712
The HEIRS Study screened 101,168 primary care participants for iron overload with serum transferrin saturation (TS), serum ferritin (SF), and C282Y and H63D mutations of the HFE gene. The objective of this study was to evaluate the impact of screenin
Autor:
P. Kamineni, Fitzroy W. Dawkins, Margaret Fadojutimi-Akinsiku, T.N. Johnson-Largent, Onyinye Onyekwere, Victor R. Gordeuk
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 405(1-2)
Background Increased serum ferritin (SF) in combination with increased total iron binding capacity saturation (TS) in the upper reference internal was evaluated to identify African Americans with increased iron stores. Methods Among 16,856 primary ca
Autor:
Charles A. Rivers, Margaret Fadojutimi-Akinsiku, Paul C. Adams, Mark A. Hall, Kurt Lohman, Barbara Harrison, Helen Harrison, Shellie D. Ellis, Jacob A. Reiss, Ronald T. Acton, Ann P. Walker, Joan Holup, Thomas C. Bent
Publikováno v:
Genetic testing. 12(4)
The purpose of this study was to assess the level of satisfaction and understanding of test results, by a sample of non-C282Y homozygous participants in the hemochromatosis and iron overload screening (HEIRS) study, who received serum ferritin (SF),
Autor:
Barbara Harrison, Ann P. Walker, Elizabeth J. Thomson, Diane C. Tucker, Helen Harrison, Andrea Ruggiero, Roger T. Anderson, Nancy Press, Lari Wenzel, Margaret Fadojutimi-Akinsiku, Ronald T. Acton, Jennifer A. Crabb, Jacob A. Reiss, Paul C. Adams
Publikováno v:
Genetic testing. 10(1)
We queried 101,951 white, Hispanic, black, Asian, American Indian (i.e., American Indian or Alaska Native in the United States and North American Indian, Metis, or Inuit in Canada) and Pacific Islander (including Native Hawaiian) adults who agreed to
Autor:
Fitzroy W. Dawkins, Margaret Fadojutimi-Akinsiku, Victor R. Gordeuk, Tiffany N. Johnson, Onyinye Onyekwere
Publikováno v:
Blood. 106:3729-3729
Non-HFE primary iron overload exists in African Americans and other ethnic groups, but the prevalence and spectrum of clinical manifestations are not known. In the HEIRS (Hereditary Hemochromatosis and Iron Overload Screening) Study, participants wer
Autor:
Helen F. Harrison, Barbara W. Harrison, Ann P. Walker, Kurt Lohman, Shellie D. Ellis, Mark A. Hall, Jacob Reiss, Paul C. Adams, Joan Holup, Ronald T. Acton, Thomas Bent, Charles Rivers, Margaret Fadojutimi-Akinsiku
Publikováno v:
Genetic Testing; Dec2008, Vol. 12 Issue 4, p491-500, 10p
Autor:
Diane C. Tucker, Ronald T. Acton, Nancy Press, Andrea Ruggiero, Jacob A. Reiss, Ann P. Walker, Lari Wenzel, Barbara Harrison, Margaret Fadojutimi-Akinsiku, Helen Harrison, Paul Adams, Jennifer A. Crabb, Roger Anderson, Elizabeth Thomson
Publikováno v:
Genetic Testing; Spring2006, Vol. 10 Issue 1, p50-59, 10p