Noise Suppression Using Symmetric Exchange Gates in Spin Qubits von Martins, Frederico, Malinowski, Filip K, Nissen, Peter D, Barnes, Edwin, Fallahi, Saeed, Gardner, Geoffrey C, Manfra, Michael J, Marcus, Charles M, Kuemmeth, Ferdinand

Volltext

Spectrum of the Nuclear Environment for GaAs Spin Qubits von Malinowski, Filip K, Martins, Frederico, Cywiński, Łukasz, Rudner, Mark S, Nissen, Peter D, Fallahi, Saeed, Gardner, Geoffrey C, Manfra, Michael J, Marcus, Charles M, Kuemmeth, Ferdinand

Volltext

Notch filtering the nuclear environment of a spin qubit von Malinowski, Filip K., Martins, Frederico, Nissen, Peter D., Barnes, Edwin, Cywiński, Łukasz, Rudner, Mark S., Fallahi, Saeed, Gardner, Geoffrey C., Manfra, Michael J., Marcus, Charles M., Kuemmeth, Ferdinand

Volltext

Genetic determinants of on-aspirin platelet reactivity: focus on the influence of PEAR1 von Würtz, Morten, Nissen, Peter H, Grove, Erik Lerkevang, Kristensen, Steen Dalby, Hvas, Anne-Mette

Volltext

Short-term biological variation of plasma uracil in a Caucasian healthy population von Winther-Larsen, Anne, Madsen, Anne Tranberg, Nissen, Peter H., Hoffmann-Lücke, Elke, Greibe, Eva

Volltext

Negative Spin Exchange in a Multielectron Quantum Dot von Martins, Frederico, Malinowski, Filip K, Nissen, Peter D, Fallahi, Saeed, Gardner, Geoffrey C, Manfra, Michael J, Marcus, Charles M, Kuemmeth, Ferdinand

Volltext

Expanding the spectrum of genetic variants in the calcium‐sensing receptor (CASR) gene in hypercalcemic individuals von Nissen, Peter H., Rejnmark, Lars

Volltext

Fast spin exchange across a multielectron mediator von Malinowski, Filip K., Martins, Frederico, Smith, Thomas B., Bartlett, Stephen D., Doherty, Andrew C., Nissen, Peter D., Fallahi, Saeed, Gardner, Geoffrey C., Manfra, Michael J., Marcus, Charles M., Kuemmeth, Ferdinand

Volltext

Pro-FHH: A Risk Equation to Facilitate the Diagnosis of Parathyroid-Related Hypercalcemia von Bertocchio, Jean-Philippe, Tafflet, Muriel, Koumakis, Eugénie, Maruani, Gérard, Vargas-Poussou, Rosa, Silve, Caroline, Nissen, Peter H, Baron, Stéphanie, Prot-Bertoye, Caroline, Courbebaisse, Marie, Souberbielle, Jean-Claude, Rejnmark, Lars, Cormier, Catherine, Houillier, Pascal

Volltext

Vita Radbodi: Het Leven van Radboud

Volltext bestellen

Immature platelets and platelet reactivity in patients with acute ST-segment Elevation Myocardial Infarction using whole blood flow cytometry with SYTO-13 staining von Pedersen, Oliver Buchhave, Hvas, Anne-Mette, Nissen, Peter H., Pasalic, Leonardo, Kristensen, Steen Dalby, Grove, Erik Lerkevang

Volltext

The effect of induced hyperammonaemia on sleep and melanopsin-mediated pupillary light response in patients with liver cirrhosis: A single-blinded randomized crossover trial von Kann, Anna Emilie, Ba-Ali, Shakoor, Seidelin, Jakob B, Larsen, Fin Stolze, Hamann, Steffen, Bjerring, Peter Nissen

Volltext

Spin of a Multielectron Quantum Dot and Its Interaction with a Neighboring Electron von Malinowski, Filip K., Martins, Frederico, Smith, Thomas B., Bartlett, Stephen D., Doherty, Andrew C., Nissen, Peter D., Fallahi, Saeed, Gardner, Geoffrey C., Manfra, Michael J., Marcus, Charles M., Kuemmeth, Ferdinand

Volltext

Discriminative power of three indices of renal calcium excretion for the distinction between familial hypocalciuric hypercalcaemia and primary hyperparathyroidism: a follow-up stud... von Christensen, Signe Engkjær, Nissen, Peter H., Vestergaard, Peter, Heickendorff, Lene, Brixen, Kim, Mosekilde, Leif

Volltext

Familial hypocalciuric hypercalcaemia: a review von Christensen, Signe E., Nissen, Peter H., Vestergaard, Peter, Mosekilde, Leif

Volltext

Association of whole blood microRNA expression with platelet function and turnover in patients with coronary artery disease von Pedersen, Oliver Buchhave, Hvas, Anne-Mette, Grove, Erik Lerkevang, Larsen, Sanne Bøjet, Pasalic, Leonardo, Kristensen, Steen Dalby, Nissen, Peter H.

Volltext

AP2S1 and GNA11 mutations – not a common cause of familial hypocalciuric hypercalcemia von Hovden, Silje, Rejnmark, Lars, Ladefoged, Søren A, Nissen, Peter H

Volltext

Long-term Outcome of 4 Patients With Transcobalamin Deficiency Caused by 2 Novel TCN2 Mutations von Nashabat, Marwan, Maegawa, Gustavo, Nissen, Peter H, Nexo, Ebba, Al-Shamrani, Hussain, Al-Owain, Mohammed, Alfadhel, Majid

Volltext

A calcium-sensing receptor mutation causing hypocalcemia disrupts a transmembrane salt bridge to activate β-arrestin-biased signaling von Gorvin, Caroline M, Babinsky, Valerie N, Malinauskas, Tomas, Nissen, Peter H, Schou, Anders J, Hanyaloglu, Aylin C, Siebold, Christian, Jones, E Yvonne, Hannan, Fadil M, Thakker, Rajesh V

Volltext

Lactase persistence genotyping on whole blood by loop-mediated isothermal amplification and melting curve analysis von Abildgaard, Anders, Tovbjerg, Sara K., Giltay, Axel, Detemmerman, Liselot, Nissen, Peter H.

Volltext