Showing 1 - 19 results of 19 for search 'S. Stoltze', query time: 0.06s
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Diffuse Dermal Angiomatosis Manifestation of Underlying Severe Peripheral Vascular Disease by Abu Baker Sheikh, Nismat Javed, Karl Stoltze
Published 2020-06-01
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Germline whole genome sequencing in pediatric oncology in Denmark—Practitioner perspectives by Anna Byrjalsen, Ulrik K. Stoltze, Anders Castor, Ayo Wahlberg
Published 2020-08-01
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Restricting child-directed ads is effective, but adding a time-based ban is better: evaluating a multi-phase regulation to protect children from unhealthy food marketing on televis... by Francesca R. Dillman Carpentier, Fernanda Mediano Stoltze, Marcela Reyes, Lindsey Smith Taillie, Camila Corvalán, Teresa Correa
Published 2023-05-01
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Beverage industry TV advertising shifts after a stepwise mandatory food marketing restriction: achievements and challenges with regulating the food marketing environment by Fernanda Mediano Stoltze, Teresa Correa, Camila Luz Corvalán Aguilar, Lindsey Smith Taillie, Marcela Reyes, Francesca Renee Dillman Carpentier
Published 2024-01-01
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Clinical characteristics and registry-validated extended pedigrees of germline TP53 mutation carriers in Denmark. by Ulrik Stoltze, Anne-Bine Skytte, Henriette Roed, Henrik Hasle, Bent Ejlertsen, Thomas van Overeem Hansen, Kjeld Schmiegelow, Anne-Marie Gerdes, Karin Wadt
Published 2018-01-01
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Early Stages of Obesity-related Heart Failure Are Associated with Natriuretic Peptide Deficiency and an Overall Lack of Neurohormonal Activation: The Copenhagen Heart Failure Risk... by Freja Stoltze Gaborit, Caroline Kistorp, Thomas Kümler, Christian Hassager, Niels Tønder, Kasper Iversen, Pia R. Kamstrup, Jens Faber, Lars Køber, Morten Schou
Published 2020-03-01
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Prevalence of early stages of heart failure in an elderly risk population: the Copenhagen Heart Failure Risk Study by Lars Køber, Morten Schou, Kasper Karmark Iversen, Freja Stoltze Gaborit, Caroline Kistorp, Thomas Kümler, Christian Hassager, Niels Tønder, Pernille Mørk Hansen, Pia Rørbæk Kamstrup, Jens Faber
Published 2019-05-01
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The effect of a single SMARCA4 exon deletion on RNA splicing: Implications for variant classification by Anna Byrjalsen, Ulrik Stoltze, Mana Mehrjouy, Jane Hübertz Frederiksen, Mads Bak, Ulf Birkedal, Henrik Hasle, Anne‐Marie Gerdes, Kjeld Schmiegelow, Karin Wadt, Thomas van Overeem Hansen
Published 2023-10-01
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Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants by Ulrik Kristoffer Stoltze, Christian Munch Hagen, Thomas van Overeem Hansen, Anna Byrjalsen, Anne-Marie Gerdes, Victor Yakimov, Simon Rasmussen, Marie Bækvad-Hansen, David Michael Hougaard, Kjeld Schmiegelow, Henrik Hjalgrim, Karin Wadt, Jonas Bybjerg-Grauholm
Published 2023-03-01
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Population-based whole-genome sequencing with constrained gene analysis identifies predisposing germline variants in children with central nervous system tumors by J. Foss-Skiftesvik, U. Stoltze, T. van Overeem Hansen, A. Byrjalsen, A. Sehested, D. Scheie, T. Stamm Mikkelsen, S. Rasmussen, M. Bak, H. Okkels, M.T. Callesen, J. Skjøth-Rasmussen, A.-M. Gerdes, K. Schmiegelow, R. Mathiasen, K. Wadt
Published 2022-01-01
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Redefining germline predisposition in children with molecularly characterized ependymoma: a population-based 20-year cohort by Jon Foss-Skiftesvik, Ulrik Kristoffer Stoltze, Thomas van Overeem Hansen, Lise Barlebo Ahlborn, Erik Sørensen, Sisse Rye Ostrowski, Solvej Margrete Aldringer Kullegaard, Adrian Otamendi Laspiur, Linea Cecilie Melchior, David Scheie, Bjarne Winther Kristensen, Jane Skjøth-Rasmussen, Kjeld Schmiegelow, Karin Wadt, René Mathiasen
Published 2022-08-01
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Direct observation of E0 transitions in 188Pb through in-beam spectroscopy by P. Papadakis, J. Pakarinen, A.D. Briscoe, D.M. Cox, R. Julin, K. Auranen, T. Grahn, P.T. Greenlees, K. Hadyńska-Klek, A. Herzáň, R.-D. Herzberg, U. Jakobsson, S. Juutinen, J. Konki, M. Leino, A. Mistry, D. O'Donnell, P. Peura, P. Rahkila, P. Ruotsalainen, M. Sandzelius, J. Sarén, C. Scholey, S. Stoltze, J. Sorri, J. Uusitalo, K. Wrzosek-Lipska
Published 2024-11-01
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Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes. by Anna Byrjalsen, Thomas V O Hansen, Ulrik K Stoltze, Mana M Mehrjouy, Nanna Moeller Barnkob, Lisa L Hjalgrim, René Mathiasen, Charlotte K Lautrup, Pernille A Gregersen, Henrik Hasle, Peder S Wehner, Ruta Tuckuviene, Peter Wad Sackett, Adrian O Laspiur, Maria Rossing, Rasmus L Marvig, Niels Tommerup, Tina Elisabeth Olsen, David Scheie, Ramneek Gupta, Anne-Marie Gerdes, Kjeld Schmiegelow, Karin Wadt
Published 2020-12-01
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