Search Results - "Detterich, Jon"

Exercise Performance: A Fontan Phenotype Predictive of Long-Term Survival by Detterich, Jon A.

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Myocardial fibrosis: the heart of diastole? by Detterich, Jon A.

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Nitric oxide, vasodilation and the red blood cell by Simmonds, Michael J, Detterich, Jon A, Connes, Philippe

“…Since the identification of the elusive endothelium-derived relaxing factor as nitric oxide (NO), much attention has been devoted to understanding its…”
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Blood Rheology and Hemodynamics: Still Illuminating after 20 Years by Simmonds, Michael J, Meiselman, Herbert J, Detterich, Jon A

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Simple chronic transfusion therapy, a crucial therapeutic option for sickle cell disease, improves but does not normalize blood rheology: What should be our goals for transfusion therapy? by Detterich, Jon A

“…Sickle cell anemia is characterized by a mutation resulting in the formation of an abnormal beta-hemoglobin called hemoglobin S. Hemoglobin S polymerizes upon…”
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Biophysical markers of the peripheral vasoconstriction response to pain in sickle cell disease by Chalacheva, Patjanaporn, Khaleel, Maha, Sunwoo, John, Shah, Payal, Detterich, Jon A, Kato, Roberta M, Thuptimdang, Wanwara, Meiselman, Herbert J, Sposto, Richard, Tsao, Jennie, Wood, John C, Zeltzer, Lonnie, Coates, Thomas D, Khoo, Michael C K

“…Painful vaso-occlusive crisis (VOC), a complication of sickle cell disease (SCD), occurs when sickled red blood cells obstruct flow in the microvasculature. We…”
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Red blood cell mechanical sensitivity improves in patients with sickle cell disease undergoing chronic transfusion after prolonged, subhemolytic shear exposure by Simmonds, Michael J., Suriany, Silvie, Ponce, Derek, Detterich, Jon A.

“…Background Sickle cell disease (SCD) is a genetically inherited hemoglobinopathy in which deoxygenated hemoglobin S polymerizes, leading to stiff red blood…”
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Chronic transfusion therapy improves but does not normalize systemic and pulmonary vasculopathy in sickle cell disease by Detterich, Jon A., Kato, Roberta M., Rabai, Miklos, Meiselman, Herbert J., Coates, Thomas D., Wood, John C.

“…Tricuspid regurgitant (TR) jet velocity and its relationship to pulmonary hypertension has been controversial in sickle cell disease (SCD). Plasma free…”
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Procedural, pregnancy, and short‐term outcomes after fetal aortic valvuloplasty by Patel, Neil D., Nageotte, Stephen, Ing, Frank F., Armstrong, Aimee K., Chmait, Ramen, Detterich, Jon A., Galindo, Alberto, Gardiner, Helena, Grinenco, Sofia, Herberg, Ulrike, Jaeggi, Edgar, Morris, Shaine A., Oepkes, Dick, Simpson, John M., Moon‐Grady, Anita, Pruetz, Jay D.

“…Objectives We aimed to evaluate the effect of technical aspects of fetal aortic valvuloplasty (FAV) on procedural risks and pregnancy outcomes. Background FAV…”
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Kidney iron deposition by R2 is associated with haemolysis and urinary iron by Denton, Christopher C., Detterich, Jon A., Coates, Thomas D., Wood, John C.

“…Summary Kidney iron deposition measured by R2* (magnetic resonance imaging) MRI is posited to result from tubular reabsorption of filtered haemoglobin due to…”
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Decreased erythrocyte aggregation in Glenn and Fontan: univentricular circulation as a rheologic disease model by Suriany, Silvie, Liu, Honglei, Cheng, Andrew L., Wenby, Rosalinda, Patel, Neil, Badran, Sarah, Meiselman, Herbert J., Denton, Christopher, Coates, Thomas D., Wood, John C., Detterich, Jon A.

“…Background In the Fontan palliation for single ventricle heart disease (SVHD), pulmonary blood flow is non-pulsatile/passive, low velocity, and low shear,…”
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Physical Properties of Blood and their Relationship to Clinical Conditions by Alexy, Tamas, Detterich, Jon, Connes, Philippe, Toth, Kalman, Nader, Elie, Kenyeres, Peter, Arriola-Montenegro, Jose, Ulker, Pinar, Simmonds, Michael J.

“…It has been long known that blood health heavily influences optimal physiological function. Abnormalities affecting the physical properties of blood have been…”
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Mental stress causes vasoconstriction in subjects with sickle cell disease and in normal controls by Shah, Payal, Khaleel, Maha, Thuptimdang, Wanwara, Sunwoo, John, Veluswamy, Saranya, Chalacheva, Patjanaporn, Kato, Roberta M, Detterich, Jon, Wood, John C, Zeltzer, Lonnie, Sposto, Richard, Khoo, Michael C K, Coates, Thomas D

“…Vaso-occlusive crisis (VOC) is a hallmark of sickle cell disease (SCD) and occurs when deoxygenated sickled red blood cells occlude the microvasculature. Any…”
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Fetal Cardiac 3D Cine Imaging at 0.55T - Whole Heart Slice-to-volume Reconstruction from Real-time Spiral MRI by Amerom, Joshua van, Tian, Ye, Goolaub, Datta, Wood, John, Detterich, Jon, Nayak, Krishna, Macgowan, Christopher

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Multiresolution Comparison of Fetal CINE MRI at 0.55T by Goolaub, Datta Singh, Tian, Ye, Amerom, Joshua van, Wood, John, Detterich, Jon, Nayak, Krishna, Macgowan, Christopher

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Longitudinal Follow-Up of Children With HLHS and Association Between Norwood Shunt Type and Long-Term Outcomes: The SVR III Study by Goldberg, Caren S, Trachtenberg, Felicia, William Gaynor, J, Mahle, William T, Ravishankar, Chitra, Schwartz, Steven M, Cnota, James F, Ohye, Richard G, Gongwer, Russell, Taylor, Michael, Paridon, Stephen, Frommelt, Peter C, Afton, Katherine, Atz, Andrew M, Burns, Kristin M, Detterich, Jon A, Hill, Kevin D, Cabrera, Antonio G, Lewis, Alan B, Pizarro, Christian, Shah, Amee, Sharma, Binu, Newburger, Jane W

“…In the SVR trial (Single Ventricle Reconstruction), newborns with hypoplastic left heart syndrome were randomly assigned to receive a modified…”
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Mediastinal infantile hemangioma with spinal canal extension and extensive gastrointestinal involvement complicated by respiratory failure by Cohen‐Cutler, Sally, Detterich, Jon A., Miller, Joseph M., Anselmo, Dean M., Luu, Minnelly, Mascarenhas, Leo

“…Infantile hemangioma is the most common soft tissue tumor of infancy. Extensive organ involvement is rare. This report describes an infant with biopsy…”
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Individual red blood cell nitric oxide production in sickle cell anemia: Nitric oxide production is increased and sickle shaped cells have unique morphologic change compared to discoid cells by Suriany, Silvie, Xu, Iris, Liu, Honglei, Ulker, Pinar, Fernandez, G. Esteban, Sposto, Richard, Borzage, Matthew, Wenby, Rosalinda, Meiselman, Herbert J., Forman, Henry Jay, Coates, Thomas D., Detterich, Jon A.

“…Sickle cell anemia (SCA) is characterized by decreased red blood cell (RBC) deformability due to polymerization of deoxygenated hemoglobin, leading to abnormal…”
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Accuracy of a Novel Handheld Wireless Platform for Detection of Cardiac Dysfunction in Anthracycline-Exposed Survivors of Childhood Cancer by Armenian, Saro H, Rinderknecht, Derek, Au, Kaylene, Lindenfeld, Lanie, Mills, George, Siyahian, Aida, Herrera, Claudia, Wilson, Karla, Venkataraman, Kalyanasundaram, Mascarenhas, Kristen, Tavallali, Peyman, Razavi, Marianne, Pahlevan, Niema, Detterich, Jon, Bhatia, Smita, Gharib, Morteza

“…Childhood cancer survivors are at risk for anthracycline-related cardiac dysfunction, often developing at a time when they are least engaged in long-term…”
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Loss of alpha‐globin genes in human subjects is associated with improved nitric oxide‐mediated vascular perfusion by Denton, Christopher C., Shah, Payal, Suriany, Silvie, Liu, Honglei, Thuptimdang, Wanwara, Sunwoo, John, Chalacheva, Patjanaporn, Veluswamy, Saranya, Kato, Roberta, Wood, John C., Detterich, Jon A., Khoo, Michael C. K., Coates, Thomas D.

“…Alpha thalassemia is a hemoglobinopathy due to decreased production of the α‐globin protein from loss of up to four α‐globin genes, with one or two missing in…”
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