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International Journal of Neonatal Screening
|
October 19, 2020
Including Classical Galactosaemia in the Expanded Newborn Screening Panel Using Tandem Mass Spectrometry for Galactose-1-Phosphate
Arieh S Cohen, Marta Baurek, Allan M Lund, et al.
Pediatrics
|
May 29, 2024
Late-Onset Molybdenum Cofactor Deficiency Type A: A Treatable Cause of Developmental Delay
Allan M Lund, Siren Berland, Trine Tangeraas, et al.
JIMD Reports
|
June 27, 2019
Genotype and phenotype classification of 29 patients affected by Krabbe disease
Anna M H Madsen, Flemming Wibrand, Allan M Lund, et al.
Haematologica
|
April 24, 2025
Asparaginase-associated hyperammonemia
Raheel Altaf Raja, Bodil Als-Nielsen, Allan M Lund, et al.
JIMD Reports
|
January 21, 2017
Primary Carnitine Deficiency: Is Foetal Development Affected and Can Newborn Screening Be Improved?
Jan Rasmussen, David M Hougaard, Noreen Sandhu, et al.
Journal of Inherited Metabolic Disease
|
May 9, 2013
Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in the Faroe Islands
Jan Rasmussen, Olav W Nielsen, Nils Janzen, et al.
Molecular Genetics and Metabolism Reports
|
November 30, 2016
Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency
Jan Rasmussen, Allan M Lund, Lotte Risom, et al.
JIMD Reports
|
May 13, 2020
Impaired lipolysis in propionic acidemia: A new metabolic myopathy?
Jesper H Storgaard, Karen L Madsen, Nicoline Løkken, et al.
Plos One
|
March 14, 2022
The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial
Nina Kimer, Mads Meldgaard, Ole Hamberg, et al.
Pediatric Pulmonology
|
November 5, 2019
Cystic fibrosis newborn screening in Denmark: Experience from the first 2 years
Marianne Skov, Marie Baekvad-Hansen, David M Hougaard, et al.
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of 8
Search research articles
Search
Showing results (11-20 of 77) with videos related to
Sort By:
Page
of 8
International Journal of Neonatal Screening
|
October 19, 2020
Including Classical Galactosaemia in the Expanded Newborn Screening Panel Using Tandem Mass Spectrometry for Galactose-1-Phosphate
Arieh S Cohen, Marta Baurek, Allan M Lund, et al.
Pediatrics
|
May 29, 2024
Late-Onset Molybdenum Cofactor Deficiency Type A: A Treatable Cause of Developmental Delay
Allan M Lund, Siren Berland, Trine Tangeraas, et al.
JIMD Reports
|
June 27, 2019
Genotype and phenotype classification of 29 patients affected by Krabbe disease
Anna M H Madsen, Flemming Wibrand, Allan M Lund, et al.
Haematologica
|
April 24, 2025
Asparaginase-associated hyperammonemia
Raheel Altaf Raja, Bodil Als-Nielsen, Allan M Lund, et al.
JIMD Reports
|
January 21, 2017
Primary Carnitine Deficiency: Is Foetal Development Affected and Can Newborn Screening Be Improved?
Jan Rasmussen, David M Hougaard, Noreen Sandhu, et al.
Journal of Inherited Metabolic Disease
|
May 9, 2013
Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in the Faroe Islands
Jan Rasmussen, Olav W Nielsen, Nils Janzen, et al.
Molecular Genetics and Metabolism Reports
|
November 30, 2016
Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency
Jan Rasmussen, Allan M Lund, Lotte Risom, et al.
JIMD Reports
|
May 13, 2020
Impaired lipolysis in propionic acidemia: A new metabolic myopathy?
Jesper H Storgaard, Karen L Madsen, Nicoline Løkken, et al.
Plos One
|
March 14, 2022
The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial
Nina Kimer, Mads Meldgaard, Ole Hamberg, et al.
Pediatric Pulmonology
|
November 5, 2019
Cystic fibrosis newborn screening in Denmark: Experience from the first 2 years
Marianne Skov, Marie Baekvad-Hansen, David M Hougaard, et al.
Page
of 8