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Articles, 2 registres trobats
Articles 2 registres trobats  
1.
10 p, 1.8 MB Density, heterogeneity and deformability of red cells as markers of clinical severity in hereditary spherocytosis / Huisjes, R. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Makhro, A. (Red Blood Cell Research Group. Institute of Veterinary Physiology. Vetsuisse Faculty. Zurich Center for Integrative Human Physiology (ZIHP). University of Zurich) ; Llaudet-Planas, Esther (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Hertz, L. (Theoretical Medicine and Biosciences. Medical Faculty. Saarland University) ; Petkova-Kirova, P. (Theoretical Medicine and Biosciences. Medical Faculty. Saarland University) ; Verhagen, L. P. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Pignatelli, S. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Rab, M. A. E. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Schiffelers, Raymond M. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Seiler, E. (Red Blood Cell Research Group. Institute of Veterinary Physiology. Vetsuisse Faculty. Zurich Center for Integrative Human Physiology (ZIHP). University of Zurich) ; Van Solinge, W. W. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Vives Corrons, Juan Luís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Kaestner, L. (Experimental Physics. Saarland University) ; Mañú Pereira, María del Mar (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Bogdanov, A. (Red Blood Cell Research Group. Institute of Veterinary Physiology. Vetsuisse Faculty. Zurich Center for Integrative Human Physiology (ZIHP). University of Zurich) ; Van Wijk, R. (Department of Clinical Chemistry and Hematology. University Medical Center Utrecht. Utrecht University) ; Universitat Autònoma de Barcelona
Hereditary spherocytosis (HS) originates from defective anchoring of the cytoskeletal network to the transmembrane protein complexes of the red blood cell (RBC). Red cells in HS are characterized by membrane instability and reduced deformability and there is marked heterogeneity in disease severity among patients. [...]
2020 - 10.3324/haematol.2018.188151
Haematologica, Vol. 105 Núm. 2 (31 2020) , p. 338-347  
2.
17 p, 1.8 MB Red blood cell membrane conductance in hereditary haemolytic anaemias / Petkova-Kirova, P. (Institute of Molecular Cell Biology. Saarland University) ; Hertz, L. (Experimental Physics. Saarland University) ; Danielczok, J. (Theoretical Medicine and Biosciences. Saarland University) ; Huisjes, R. (Department of Clinical Chemistry and Haematology. University Medical Center Utrecht) ; Makhro, A. (Red Blood Cell Research Group. Institute of Veterinary Physiology. Vetsuisse Faculty. Zurich Center for Integrative Human Physiology (ZIHP). University of Zürich) ; Bogdanova, A. (Red Blood Cell Research Group. Institute of Veterinary Physiology. Vetsuisse Faculty. Zurich Center for Integrative Human Physiology (ZIHP). University of Zürich) ; Mañú Pereira, María del Mar (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Vives Corrons, Juan Luís (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Van Wijk, R. (Department of Clinical Chemistry and Haematology. University Medical Center Utrecht) ; Kaestner, L. (Experimental Physics. Saarland University) ; Universitat Autònoma de Barcelona
Congenital haemolytic anaemias are inherited disorders caused by red blood cell membrane and cytoskeletal protein defects, deviant hemoglobin synthesis and metabolic enzyme deficiencies. In many cases, although the causing mutation might be known, the pathophysiology and the connection between the particular mutation and the symptoms of the disease are not completely understood. [...]
2019 - 10.3389/fphys.2019.00386
Frontiers in physiology, Vol. 10 Núm. MAR (2019) , p. 386  

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