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Flemming Skovby

Showing results (1-10 of 50) with videos related to

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Ugeskrift for Laeger|January 14, 2003
[Treatment of inborn metabolic disorders]Allan Meldgaard Lund, Flemming Skovby
Ugeskrift for Laeger|April 28, 2006
[Optimising treatment for people with rare diseases]Allan Meldgaard Lund, Flemming Skovby
Ugeskrift for Laeger|February 7, 2007
[Molecular diagnosis of CHARGE syndrom]Anne-Marie Bisgaard Pedersen, Flemming Skovby
Molecular Genetics and Metabolism|October 13, 2009
A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiencyFlemming Skovby, Mette Gaustadnes, S Harvey Mudd
Ugeskrift for Laeger|October 27, 2009
[Severe vitamin B12 deficiency in infants breastfed by vegans]Casper Roed, Flemming Skovby, Allan Meldgaard Lund
Ugeskrift for Laeger|January 14, 2003
[Diagnosis and acute treatment of inborn metabolic diseases in infants]Allan Meldgaard Lund, Ernst Christensen, Flemming Skovby
Molecular Genetics and Metabolism Reports|February 2, 2018
The impact of consanguinity on the frequency of inborn errors of metabolismRaja Majid Afzal, Allan Meldgaard Lund, Flemming Skovby
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
Ugeskrift for Laeger|November 18, 2025
Tanja Todberg, Jeanette Kaae, Flemming Skovby, 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.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Ugeskrift for Laeger|January 14, 2003
[Treatment of inborn metabolic disorders]Allan Meldgaard Lund, Flemming Skovby
Ugeskrift for Laeger|April 28, 2006
[Optimising treatment for people with rare diseases]Allan Meldgaard Lund, Flemming Skovby
Ugeskrift for Laeger|February 7, 2007
[Molecular diagnosis of CHARGE syndrom]Anne-Marie Bisgaard Pedersen, Flemming Skovby
Molecular Genetics and Metabolism|October 13, 2009
A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiencyFlemming Skovby, Mette Gaustadnes, S Harvey Mudd
Ugeskrift for Laeger|October 27, 2009
[Severe vitamin B12 deficiency in infants breastfed by vegans]Casper Roed, Flemming Skovby, Allan Meldgaard Lund
Ugeskrift for Laeger|January 14, 2003
[Diagnosis and acute treatment of inborn metabolic diseases in infants]Allan Meldgaard Lund, Ernst Christensen, Flemming Skovby
Molecular Genetics and Metabolism Reports|February 2, 2018
The impact of consanguinity on the frequency of inborn errors of metabolismRaja Majid Afzal, Allan Meldgaard Lund, Flemming Skovby
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
Ugeskrift for Laeger|November 18, 2025
Tanja Todberg, Jeanette Kaae, Flemming Skovby, 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.
Pageof 5