Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Meldgaard Lund, A"'
Autor:
Line Gutte Borgwardt, Ferdinando Ceravolo, Giulia Zardi, Andrea Ballabeni, Allan Meldgaard Lund
Publikováno v:
JIMD Reports, Vol 64, Iss 2, Pp 187-198 (2023)
Abstract Alpha‐mannosidosis (AM), an autosomal recessive disorder caused by pathogenic biallelic variants in the MAN2B1 gene, leads to lysosomal alpha‐mannosidase deficiency and accumulation of mannose‐rich oligosaccharides. Velmanase alfa (VA)
Externí odkaz:
https://doaj.org/article/70f1d07fdc024aabb477b895d1046324
Publikováno v:
Clinical and Translational Science, Vol 12, Iss 5, Pp 481-489 (2019)
This review characterizes clinical development that supported the label dose in 60 drug indications recently approved by the US Food and Drug Administration. With Lewis B. Sheiner's Learning vs. Confirming clinical drug development paradigm as a refe
Externí odkaz:
https://doaj.org/article/d316e312125c454daea3bc3bf94e500e
Autor:
Anders Deichmann Springborg, Elisabeth Kjær Jensen, Mads Kreilgaard, Morten Aagaard Petersen, Theodoros Papathanasiou, Trine Meldgaard Lund, Bradley Kenneth Taylor, Mads Utke Werner
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0242169 (2020)
Severe chronic postsurgical pain has a prevalence of 4-10% in the surgical population. The underlying nociceptive mechanisms have not been well characterized. Following the late resolution phase of an inflammatory injury, high-dose μ-opioid-receptor
Externí odkaz:
https://doaj.org/article/6f867c45c1aa4cf7bf084c748ea69262
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 15, Iss , Pp 6-10 (2018)
Inborn errors of metabolism (IEM) are a heterogeneous group of genetic disorders present in all ethnic groups. We investigated the frequency of consanguinity among parents of newborns with IEM diagnosed by neonatal screening.Data were obtained from 1
Externí odkaz:
https://doaj.org/article/f171be3b1a3046459428075c8e108ff5
Autor:
Line Gutte Borgwardt, Ferdinando Ceravolo, Giulia Zardi, Andrea Ballabeni, Allan Meldgaard Lund
Publikováno v:
JIMD Reports. 64:187-198
Autor:
Allan Meldgaard Lund, Flemming Wibrand, Kristin Skogstrand, Marie Bækvad-Hansen, Niels Gregersen, Brage Storstein Andresen, David M. Hougaard, Morten Dunø, Rikke Katrine Jentoft Olsen
Publikováno v:
International Journal of Neonatal Screening, Vol 7, Iss 3, p 50 (2021)
Historically, the analyses used for newborn screening (NBS) were biochemical, but increasingly, molecular genetic analyses are being introduced in the workflow. We describe the application of molecular genetic analyses in the Danish NBS programme and
Externí odkaz:
https://doaj.org/article/e2d3d02166b1482183928729f9ccf7df
Autor:
Morten Baltzer Houlind, Esben Iversen, Viktor Rotbain Curovic, Morten Buss Jørgensen, Aino Andersen, Finn Gustafsson, Lærke Marie Sidenius Nelson, Michael Perch, Morten Damgaard, Frederik Persson, Bo Feldt-Rasmussen, Ove Andersen, Trine Meldgaard Lund, Mads Hornum
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM).
Autor:
Maja Risager Nielsen, Christine Jørgensen, Kirsten Ahring, Allan Meldgaard Lund, Mette Cathrine Ørngreen
Publikováno v:
Journal of Inherited Metabolic Disease.
Publikováno v:
Soeorg, H, Sverrisdóttir, E, Andersen, M, Lund, T M & Sessa, M 2022, ' Artificial neural network vs pharmacometric model for population prediction of plasma concentration in real-world data : a case study on valproic acid ', Clinical Pharmacology and Therapeutics, vol. 111, no. 6, pp. 1278-1285 . https://doi.org/10.1002/cpt.2577
We compared the predictive performance of an artificial neural network to traditional pharmacometric modeling for population prediction of plasma concentrations of valproate in real-world data. We included individuals aged 65 years or older with epil
Autor:
Emelie Curovic Rotbain, Dennis Lund Hansen, Ove Schaffalitzky de Muckadell, Flemming Wibrand, Allan Meldgaard Lund, Henrik Frederiksen
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0186674 (2017)
Our aim was to assess the validity of the ICD-10 code for splenomegaly in the Danish National Registry of Patients (DNRP), as well as to investigate which underlying diseases explained the observed splenomegaly.Splenomegaly is a common finding in pat
Externí odkaz:
https://doaj.org/article/f6e6fceefc3744e6bc64a293f4114b42