Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Sten Petersen"'
Autor:
Astrid Janssens, Danielle Drachmann, Kristy Barnes-Cullen, Austin Carrigg, Henrik Thybo Christesen, Becky Futers, Yvette Ollada Lavery, Tiffany Palms, Jacob Sten Petersen, Pratik Shah, Paul Thornton, Joseph Wolfsdorf
Publikováno v:
Research Involvement and Engagement, Vol 10, Iss 1, Pp 1-15 (2024)
Abstract Background In rare diseases, limited access to services and rare disease experts may force families to act as medical advocates for their child; they can volunteer to support clinician-initiated research or initiate and lead research themsel
Externí odkaz:
https://doaj.org/article/f8f4cef7cbb940a5b123b0b6e96f438d
Autor:
Danielle Drachmann, Austin Carrigg, David A. Weinstein, Jacob Sten Petersen, Henrik Thybo Christesen
Publikováno v:
JIMD Reports, Vol 62, Iss 1, Pp 70-73 (2021)
ABSTRACT Background Ketotic hypoglycemia (KH) without an identifiable underlying metabolic or hormonal disease is historically named idiopathic KH. The prevalence is unknown, but idiopathic KH is considered the most frequent cause of hypoglycemia bey
Externí odkaz:
https://doaj.org/article/598744c01ba84884a24612bc93e2281a
Autor:
Austin Carrigg, Danielle Drachmann, Henrik Thybo Christesen, David A. Weinstein, Jacob Sten Petersen
Publikováno v:
JIMD Reports, Vol 62, Iss 1, Pp 70-73 (2021)
Drachmann, D, Carrigg, A, Weinstein, D A, Petersen, J S & Christesen, H T 2021, ' Ketotic hypoglycemia in patients with Down syndrome ', JIMD Reports, vol. 62, no. 1, pp. 70-73 . https://doi.org/10.1002/jmd2.12241
JIMD Reports
Drachmann, D, Carrigg, A, Weinstein, D A, Petersen, J S & Christesen, H T 2021, ' Ketotic hypoglycemia in patients with Down syndrome ', JIMD Reports, vol. 62, no. 1, pp. 70-73 . https://doi.org/10.1002/jmd2.12241
JIMD Reports
Background: Ketotic hypoglycemia (KH) without an identifiable underlying metabolic or hormonal disease is historically named idiopathic KH. The prevalence is unknown, but idiopathic KH is considered the most frequent cause of hypoglycemia beyond the
Autor:
Jacob Sten Petersen, Gustaf Christoffersson, Mads Tang-Christensen, Allan E. Karlsen, Kevin L. Grove, Philippe P. Pagni, Matthias von Herrath
Publikováno v:
Cell Metabolism. 29:795-802
Recent articles have highlighted the lack of reproducibility of data from scientific publications. Here we would argue that a better way to describe and also tackle this matter is to use the term "lack of robustness," since it points toward potential
Autor:
Marie Louise Max Andersen, Morten Arendt Rasmussen, Sven Pörksen, Jannet Svensson, Jennifer Vikre-Jørgensen, Jane Thomsen, Niels Thomas Hertel, Jesper Johannesen, Flemming Pociot, Jacob Sten Petersen, Lars Hansen, Henrik Bindesbøl Mortensen, Lotte Brøndum Nielsen
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e64632 (2013)
The purpose of the present study is to explore the progression of type 1 diabetes (T1D) in Danish children 12 months after diagnosis using Latent Factor Modelling. We include three data blocks of dynamic paraclinical biomarkers, baseline clinical cha
Externí odkaz:
https://doaj.org/article/5df222310e0c47e0a594aa9df8c59778
Publikováno v:
Scandinavian Journal of Haematology. 25:5-11
22 newborn infants delivered by Caesarean section were investigated in order to ascertain the number and morphology of megakaryocytes in the umbilical artery and vein. Averages of 65.5 and 47 MK per ml blood were found, respectively. 25% of MK in the
Autor:
Sten Petersen, Ellen Taaning
Publikováno v:
European Journal of Haematology. 41:449-453
Platelet-associated Ig classes and IgG subclasses were studied by a semiquantitative platelet ELISA test in 17 children with immune thrombocytopenic purpura (ITP). An elevation of PAIg was found in 94% of the children. In nearly all cases increased a
Autor:
Sten Petersen, Lars P. Ryder, Gitte Olesen, Lars Vindeløv, Tania N. Masmas, Hans O. Madsen, Brian Kornblit, Ebbe Dickmeiss, Bodil K Jakobsen, Henrik Sengeløv, Carsten Heilmann, A. Svejgaard
Publikováno v:
Bone Marrow Transplantation. 41:851-859
We analysed the outcome and hospitalization requirements of the first 100 patients (Hodgkin's disease (HD), N=13; multiple myeloma (MM), N=14; CLL, N=12; non-Hodgkin's lymphoma (NHL), N=17; myelodysplastic syndrome (MDS), N=18; AML, N=24 and CML, N=2
Autor:
Ellen Taaning, Tommy Söderstrom, Tom Christensen, Lisbeth Tranebjærg, Hans Erik Nielsen, Bente Pilgaard, Sten Petersen
Publikováno v:
Acta Paediatrica. 80:1037-1043
In 35 children with Schonlein-Henoch Syndrome (SHS) serum IgG, IgM, and IgA concentrations were increased in 15%, 21%, and 44% of cases, respectively. Seven children with other vasculitic syndromes (VS) had normal serum Ig concentrations. Serum conce
Publikováno v:
Tissue Antigens. 70:151-156
High-mobility group box 1 protein (HMGB1) is a nuclear DNA-binding protein, which also functions as a pleiotropic cytokine, implicated in the pathology of several different immune-mediated diseases. The purpose of this study was to examine the HMGB1