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Allan Meldgaard Lund

Showing results (21-30 of 50) with videos related to

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Journal of Inherited Metabolic Disease|January 13, 2010
Clinical and biochemical monitoring of patients with fatty acid oxidation disordersAllan Meldgaard Lund, Flemming Skovby, Helle Vestergaard, et al.
Ugeskrift for Laeger|March 28, 2008
[Two cases of Richner-Hanhart syndrome (oculocutaneous tyrosinemia)]Anette Bygum, Flemming Brandrup, Else Fredsted Gade, et al.
Ugeskrift for Laeger|August 19, 2011
[Improved prognosis of cystinosis achieved by treatment with cysteamine and by kidney transplantation]Anna Ewa Oczachowska-Kulik, Allan Meldgaard Lund, Flemming Skovby, et al.
JIMD Reports|March 6, 2023
Relationship between <i>MAN2B1</i> genotype/subcellular localization subgroups, antidrug antibody detection, and long-term velmanase alfa treatment outcomes in patients with alpha-mannosidosisLine Gutte Borgwardt, Ferdinando Ceravolo, Giulia Zardi, et al.
Ugeskrift for Laeger|October 9, 2003
[Metabolic disease or shaken baby syndrome?]Lisbeth Samsø Schmidt, Jens Erik Klint Nielsen, Susanne Stilling Blichfeldt, et al.
Ugeskrift for Laeger|January 16, 2007
[Oesteogenesis imperfecta--genetics, diagnosis and medical treatment]Kim T Brixen, Niels O Illum, Birgitte Hansen, et al.
Journal of Inherited Metabolic Disease|February 27, 2023
The impact of phenylalanine levels during pregnancy on birth weight and later development in children born to women with phenylketonuriaMaja Risager Nielsen, Christine Jørgensen, Kirsten Ahring, et al.
JIMD Reports|March 4, 2015
Is L-Carnitine Supplementation Beneficial in 3-Methylcrotonyl-CoA Carboxylase Deficiency?Jákup Andreas Thomsen, Allan Meldgaard Lund, Jess Have Olesen, et al.
Ugeskrift for Laeger|February 1, 2011
[Clinical aspects of Marfan syndrome]Tina Zimmermann Belsing, Allan Meldgaard Lund, Lars Søndergaard, et al.
Ugeskrift for Laeger|April 2, 2011
[Increased nuchal translucency in osteogenesis imperfecta]Bitten Schönewolf-Greulich, Lillian Skibsted, Lisa Leth Maroun, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Journal of Inherited Metabolic Disease|January 13, 2010
Clinical and biochemical monitoring of patients with fatty acid oxidation disordersAllan Meldgaard Lund, Flemming Skovby, Helle Vestergaard, et al.
Ugeskrift for Laeger|March 28, 2008
[Two cases of Richner-Hanhart syndrome (oculocutaneous tyrosinemia)]Anette Bygum, Flemming Brandrup, Else Fredsted Gade, et al.
Ugeskrift for Laeger|August 19, 2011
[Improved prognosis of cystinosis achieved by treatment with cysteamine and by kidney transplantation]Anna Ewa Oczachowska-Kulik, Allan Meldgaard Lund, Flemming Skovby, et al.
JIMD Reports|March 6, 2023
Relationship between <i>MAN2B1</i> genotype/subcellular localization subgroups, antidrug antibody detection, and long-term velmanase alfa treatment outcomes in patients with alpha-mannosidosisLine Gutte Borgwardt, Ferdinando Ceravolo, Giulia Zardi, et al.
Ugeskrift for Laeger|October 9, 2003
[Metabolic disease or shaken baby syndrome?]Lisbeth Samsø Schmidt, Jens Erik Klint Nielsen, Susanne Stilling Blichfeldt, et al.
Ugeskrift for Laeger|January 16, 2007
[Oesteogenesis imperfecta--genetics, diagnosis and medical treatment]Kim T Brixen, Niels O Illum, Birgitte Hansen, et al.
Journal of Inherited Metabolic Disease|February 27, 2023
The impact of phenylalanine levels during pregnancy on birth weight and later development in children born to women with phenylketonuriaMaja Risager Nielsen, Christine Jørgensen, Kirsten Ahring, et al.
JIMD Reports|March 4, 2015
Is L-Carnitine Supplementation Beneficial in 3-Methylcrotonyl-CoA Carboxylase Deficiency?Jákup Andreas Thomsen, Allan Meldgaard Lund, Jess Have Olesen, et al.
Ugeskrift for Laeger|February 1, 2011
[Clinical aspects of Marfan syndrome]Tina Zimmermann Belsing, Allan Meldgaard Lund, Lars Søndergaard, et al.
Ugeskrift for Laeger|April 2, 2011
[Increased nuchal translucency in osteogenesis imperfecta]Bitten Schönewolf-Greulich, Lillian Skibsted, Lisa Leth Maroun, et al.
Pageof 5