Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Donald L. Rucknagel"'
Autor:
Donald L. Rucknagel
Publikováno v:
Handbook of Hematologic Pathology ISBN: 9780429115721
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c47ab714c13c170ee08c5184bd72882
https://doi.org/10.1201/9780429115721-17
https://doi.org/10.1201/9780429115721-17
Autor:
Donald L. Rucknagel, Mary B. Palascak, Peter Ciraolo, Robert S. Franco, Zahida Yasin, Clinton H. Joiner
Publikováno v:
Blood. 108:1073-1076
The determinants of sickle red blood cell (RBC) life span have not been well-defined but may include both intrinsic factors (eg, the tendency to sickle) and extrinsic factors (eg, the capacity of the reticuloendothelial system to remove defective RBC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a37f839a68c618509cdec1afd1e5557a
https://doi.org/10.1182/blood-2005-09-008318
https://doi.org/10.1182/blood-2005-09-008318
Autor:
Donald L. Rucknagel
Publikováno v:
Pediatric Pathology & Molecular Medicine. 20:137-154
The acute chest syndrome is a generic term for pulmonary complications of sickle cell diseases with heterogeneous etiologies that include pneumonia, vaso-occlusion of pulmonary arterioles, rib infarction, and fat embolism syndrome. My review summariz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50391ec7041ec85e8d81d0ec8192bfee
https://doi.org/10.1080/15513810109168607
https://doi.org/10.1080/15513810109168607
Autor:
Robert S. Franco, Clinton H. Joiner, Murray Weiner, Joni M. Lohmann, Zahida Yasin, Therese A. Nemeth, Mary B. Palascak, Donald L. Rucknagel
Publikováno v:
Blood. 96:3610-3617
Sickle red blood cells (RBCs) become depleted of potassium, leading to dehydration and abnormally elevated cellular density. The increased sickling that results is important for both hemolysis and vasocclusion. In this study, sickle cells were subjec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4257c919da2c8097b7eb72d2c7aebab
https://doi.org/10.1182/blood.v96.10.3610.h8003610_3610_3617
https://doi.org/10.1182/blood.v96.10.3610.h8003610_3610_3617
Autor:
Clinton H. Joiner, Donald L. Rucknagel, G Mayfield-Pratt, Robert S. Franco, Mary B. Palascak, Murray Weiner, T A Nemeth, E B Silberstein, J Lohmann
Publikováno v:
Journal of Clinical Investigation. 101:2730-2740
Sickle red blood cells (RBC) are subject to a number of important cellular changes and selection pressures. In this study, we validated a biotin RBC label by comparison to the standard 51Cr label, and used it to study changes that occur in sickle cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e0c204eb9fbf2fd448c01a47a30d863
https://doi.org/10.1172/jci2484
https://doi.org/10.1172/jci2484
Publikováno v:
Blood. 88:4359-4365
The K+ efflux that mediates sickle-cell dehydration may occur through several pathways, including two with a high capacity for mediating rapid K+ loss, KCl cotransport and the Ca(2+)-dependent K+ channel [K(Ca2+)]. The rate and pathway of red blood c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18fdacd9416c0f8c38ab4d836d54cb28
https://doi.org/10.1182/blood.v88.11.4359.4359
https://doi.org/10.1182/blood.v88.11.4359.4359
Autor:
Karen Kalinyak, M. Douglas Ris, Robert B. Noll, William S. Ball, Robert J. Wells, Donald L. Rucknagel
Publikováno v:
Archives of Clinical Neuropsychology. 11:481-490
The case of a patient with sickle cell disease is presented in which neuropsychological and magnetic resonance imaging studies were completed prior to and after a right hemispheric stroke. The contribution of a new MR perfusion technique in understan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67d8af8eaf85511516949079d9fe808c
https://doi.org/10.1016/0887-6177(95)00035-6
https://doi.org/10.1016/0887-6177(95)00035-6
Publikováno v:
American Journal of Hematology. 49:43-47
A term infant presented with mild cyanosis without evidence of hypoxia. Cardiopulmonary disease, polycythemia, and methemoglobinemia were excluded. Standard hemoglobin electrophoresis, including isoelectric focusing, were normal. However, by reverse-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea9c4265649b873d7e5521cefa0394b6
https://doi.org/10.1002/ajh.2830490108
https://doi.org/10.1002/ajh.2830490108
Publikováno v:
Blood. 84:3915-3924
In 1945, Thomas Cooley described the first cases of X-linked sideroblastic anemia (XLSA) in two brothers from a large family in which the inheritance of the disease was documented through six generations. Almost 40 years later the enzymatic defect in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b291f853d52e0125e1f9a1dd587e0268
https://doi.org/10.1182/blood.v84.11.3915.bloodjournal84113915
https://doi.org/10.1182/blood.v84.11.3915.bloodjournal84113915
Fetal hemoglobin and potassium in isolated transferrin receptor- positive dense sickle reticulocytes
Autor:
SM Williams, R Barker-Gear, Donald L. Rucknagel, Mary Ann Miller, Robert S. Franco, Clinton H. Joiner
Publikováno v:
Blood. 84:2013-2020
A subset of sickle cells have an increased density at the reticulocyte stage of development, indicating that they are either abnormally dense upon release from the bone marrow or become dense quickly in the circulation. These cells are of interest be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad9b2a74c51573a9574df7b00e3e3106
https://doi.org/10.1182/blood.v84.6.2013.2013
https://doi.org/10.1182/blood.v84.6.2013.2013