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Allan Meldgaard Lund

Showing results (11-20 of 50) with videos related to

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Danish Medical Journal|October 2, 2018
The impact of consanguinity on the frequency of inborn errors of metabolismRaja Majid Afzal, Allan Meldgaard Lund, Flemming Skovby
Pediatric Endocrinology Reviews : PER|October 28, 2014
Alpha-mannosidosis - a review of genetic, clinical findings and options of treatmentLine Borgwardt, Allan Meldgaard Lund, Christine I Dali
Ugeskrift for Laeger|September 17, 2015
[Splenomegaly and failure to thrive as a result of Gaucher disease]Grith Lærkholm Hansen, Allan Meldgaard Lund, Malene Landbo Børresen
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|December 2, 2017
Simultaneous quantification of succinylacetone and nitisinone for therapeutic drug monitoring in the treatment of Tyrosinemia type 1Jonas Sundberg, Flemming Wibrand, Allan Meldgaard Lund, et al.
Ugeskrift for Laeger|November 25, 2010
[Fish odour--could be a sign of trimethylaminuria]Line Klingen Haugaard, Allan Meldgaard Lund, Poula Patursson, et al.
Ugeskrift for Laeger|September 3, 2008
[Congenital methaemoglobinaemia: an infrequent cause of neonatal cyanosis]Birgitte Smith, Ole Axel Pryds, Ernst Christensen, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 20, 2006
Case 2: Suspected non-accidental injuryKlaus Juul, Jesper Andersen, Veronica Basile Cvitanich, et al.
European Journal of Medical Genetics|January 17, 2023
Adult patient diagnosed with NADSYN1 associated congenital NAD deficiency and analysis of NAD levels to be published in: European Journal of Medical GeneticsEmilie Erbs, Claus Lohman Brasen, Allan Meldgaard Lund, et al.
Ugeskrift for Laeger|May 2, 2012
[Carnitine transporter deficiency is a hereditary disease with a high incidence in the Faroe Islands]Sissal Djurhuus Poulsen, Allan Meldgaard Lund, Ernst Christensen, et al.
Molecular Genetics and Metabolism|June 23, 2024
Hematopoietic stem cell transplantation or enzyme replacement therapy in Gaucher disease type 3Astrid Høj, Mette Cathrine Ørngreen, Marie Mostue Naume, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Danish Medical Journal|October 2, 2018
The impact of consanguinity on the frequency of inborn errors of metabolismRaja Majid Afzal, Allan Meldgaard Lund, Flemming Skovby
Pediatric Endocrinology Reviews : PER|October 28, 2014
Alpha-mannosidosis - a review of genetic, clinical findings and options of treatmentLine Borgwardt, Allan Meldgaard Lund, Christine I Dali
Ugeskrift for Laeger|September 17, 2015
[Splenomegaly and failure to thrive as a result of Gaucher disease]Grith Lærkholm Hansen, Allan Meldgaard Lund, Malene Landbo Børresen
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|December 2, 2017
Simultaneous quantification of succinylacetone and nitisinone for therapeutic drug monitoring in the treatment of Tyrosinemia type 1Jonas Sundberg, Flemming Wibrand, Allan Meldgaard Lund, et al.
Ugeskrift for Laeger|November 25, 2010
[Fish odour--could be a sign of trimethylaminuria]Line Klingen Haugaard, Allan Meldgaard Lund, Poula Patursson, et al.
Ugeskrift for Laeger|September 3, 2008
[Congenital methaemoglobinaemia: an infrequent cause of neonatal cyanosis]Birgitte Smith, Ole Axel Pryds, Ernst Christensen, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 20, 2006
Case 2: Suspected non-accidental injuryKlaus Juul, Jesper Andersen, Veronica Basile Cvitanich, et al.
European Journal of Medical Genetics|January 17, 2023
Adult patient diagnosed with NADSYN1 associated congenital NAD deficiency and analysis of NAD levels to be published in: European Journal of Medical GeneticsEmilie Erbs, Claus Lohman Brasen, Allan Meldgaard Lund, et al.
Ugeskrift for Laeger|May 2, 2012
[Carnitine transporter deficiency is a hereditary disease with a high incidence in the Faroe Islands]Sissal Djurhuus Poulsen, Allan Meldgaard Lund, Ernst Christensen, et al.
Molecular Genetics and Metabolism|June 23, 2024
Hematopoietic stem cell transplantation or enzyme replacement therapy in Gaucher disease type 3Astrid Høj, Mette Cathrine Ørngreen, Marie Mostue Naume, et al.
Pageof 5