Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Comprehensive Sickle Cell Centers"'
Autor:
A. Muma, Barry E. Eggleston, C. Johnson, Thomas J. Harrington, Comprehensive Sickle Cell Centers, C. Rutherford, Jeffrey I. Gold, Donald Armstrong, L. De Castro, L. McMahon, Karen Kalinyak, Lynne Neumayr, Elliott Vichinsky, Michael W. Weiner, Atif Mahmoud Hussein, Eugene P. Orringer, Randall R. Rule, D. Bessman, Susan Lieff
Publikováno v:
Blood. 110:428-428
Background. Brain dysfunction may be the most important and least studied problem afflicting the aging SCD population. 25% of neurologically intact pediatric SCD patients have NP dysfunction and silent CNS infarction. In children, age is associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2368ce273548d3954cabf0054f2adfbc
https://doi.org/10.1182/blood.v110.11.428.428
https://doi.org/10.1182/blood.v110.11.428.428
Autor:
Vichinsky, Elliott, Gold, J. *, Rule, R. *, Weiner, M. *, Eggleston, B. *, Muma, A. *, Neumayr, L. *, Lieff, S. *, Bessman, D. *, Kalinyak, K., De Castro, L., Harrington, T. *, Hussein, A., Johnson, C., McMahon, L. *, Orringer, E., Rutherford, C., Armstrong, D., Comprehensive Sickle Cell Centers *
Publikováno v:
In Blood 16 November 2007 110(11):428-428
Autor:
Felice, Alex, Ozdonmez, R., Headlee, M. E., Huisman, T. H. J., Annual Meeting of the Comprehensive Sickle Cell Centers and Sickle Cell Screening and Education Elinics
The proportion of some a chain variants in the peripheral blood of heterozygotes has been a most useful marker for the number and activity of the a chain genes of human hemoglobin. Among these, Hb G-Philadelphia(or α2 68Lys β2) has been found in as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3549::d02d9036c0bae2f200bed7d599528325
https://www.um.edu.mt/library/oar/handle/123456789/82293
https://www.um.edu.mt/library/oar/handle/123456789/82293
