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The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial

PloS one, 2022-03, Vol.17 (3), p.e0264278-e0264278

2022

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Correction: Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience

PloS one, 2023-06, Vol.18 (6), p.e0287268-e0287268

2023

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Splenomegaly - Diagnostic validity, work-up, and underlying causes

PloS one, 2017-11, Vol.12 (11), p.e0186674-e0186674

2017

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The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model

PloS one, 2022-01, Vol.17 (1), p.e0261150-e0261150

2022

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Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease

Orphanet journal of rare diseases, 2011-11, Vol.6 (1), p.72-72, Article 72

2011

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The SPARKLE registry: protocol for an international prospective cohort study in patients with alpha-mannosidosis

Orphanet journal of rare diseases, 2020-09, Vol.15 (1), p.271-271, Article 271

2020

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Primary carnitine deficiency and pivalic acid exposure causing encephalopathy and fatal cardiac events

Journal of inherited metabolic disease, 2013-01, Vol.36 (1), p.35-41

2013

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Including Classical Galactosaemia in the Expanded Newborn Screening Panel Using Tandem Mass Spectrometry for Galactose-1-Phosphate

International journal of neonatal screening, 2019-05, Vol.5 (2), p.19-19

2019

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Variant non-ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5

Brain (London, England : 1878), 2014-02, Vol.137 (Pt 2), p.366-379

2014

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The impact of consanguinity on the frequency of inborn errors of metabolism

Molecular genetics and metabolism reports, 2018-06, Vol.15, p.6-10

2018

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Use of the Bruininks-Oseretsky test of motor proficiency (BOT-2) to assess efficacy of velmanase alfa as enzyme therapy for alpha-mannosidosis

Molecular genetics and metabolism reports, 2020-06, Vol.23, p.100586-100586, Article 100586

2020

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Glycogen Storage Disease Type IV: A Case With Histopathologic Findings in First-Trimester Placental Tissue

International journal of gynecological pathology, 2016-01, Vol.35 (1), p.38-40

2016

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Neonatal Screening for Primary Carnitine Deficiency: Lessons Learned from the Faroe Islands

International journal of neonatal screening, 2017-03, Vol.3 (1), p.1

2017

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Use of Molecular Genetic Analyses in Danish Routine Newborn Screening

International journal of neonatal screening, 2021-07, Vol.7 (3), p.50

2021

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Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency

Molecular genetics and metabolism reports, 2014-01, Vol.1 (C), p.241-248

2014

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Health Related Quality of Life, Disability, and Pain in Alpha Mannosidosis

Journal of inborn errors of metabolism and screening, 2018-09, Vol.6

2018

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Cardiac function and incidence of unexplained myocardial scarring in patients with primary carnitine deficiency - a cardiac magnetic resonance study

Scientific reports, 2019-09, Vol.9 (1), p.13909-7, Article 13909

2019

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Alpha-mannosidosis: Correlation between phenotype, genotype and mutant MAN2B1 subcellular localisation Inherited metabolic diseases

Orphanet journal of rare diseases, 2015-06

2015

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Health Related Quality of Life, Disability, and Pain in Alpha Mannosidosis: Long-Term Data of Enzyme Replacement Therapy With Velmanase Alfa (Human Recombinant Alpha Mannosidase)

Journal of inborn errors of metabolism and screening, 2018-09, Vol.6, p.232640981879685

2018

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Zur "Agrarverfassung" der Germanen (Tac. Germ. Kap. 26)

Symbolae Osloenses, 1985, Vol.60

Lund, Allan A

1985

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Zur ≫Agrarverfassung≪ Der Germanen (Tac. Germ. Kap. 26)

Symbolae Osloenses, 1985-01, Vol.60 (1), p.121-127

Lund, Allan A.

1985

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Neues zu Tac.Germ.46.2

Symbolae Osloenses, 1983, Vol.58

Lund, Allan A

1983

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Pariendum oder pereundum? (Tac. Germ. 18, 4)

Symbolae Osloenses, 1979-01, Vol.54 (1), p.119-123

Lund, Allan A.

1979

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Response to Roldan et al

The American journal of gastroenterology, 2021-07, Vol.116 (7), p.1552-1552

2021

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The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial

Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience

Correction: Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience

Splenomegaly - Diagnostic validity, work-up, and underlying causes

The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model

Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease

The SPARKLE registry: protocol for an international prospective cohort study in patients with alpha-mannosidosis

Primary carnitine deficiency and pivalic acid exposure causing encephalopathy and fatal cardiac events

Including Classical Galactosaemia in the Expanded Newborn Screening Panel Using Tandem Mass Spectrometry for Galactose-1-Phosphate

Variant non-ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5

The impact of consanguinity on the frequency of inborn errors of metabolism

Use of the Bruininks-Oseretsky test of motor proficiency (BOT-2) to assess efficacy of velmanase alfa as enzyme therapy for alpha-mannosidosis

Glycogen Storage Disease Type IV: A Case With Histopathologic Findings in First-Trimester Placental Tissue

Neonatal Screening for Primary Carnitine Deficiency: Lessons Learned from the Faroe Islands

Use of Molecular Genetic Analyses in Danish Routine Newborn Screening

Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency

Health Related Quality of Life, Disability, and Pain in Alpha Mannosidosis

Cardiac function and incidence of unexplained myocardial scarring in patients with primary carnitine deficiency - a cardiac magnetic resonance study

Alpha-mannosidosis: Correlation between phenotype, genotype and mutant MAN2B1 subcellular localisation Inherited metabolic diseases

Health Related Quality of Life, Disability, and Pain in Alpha Mannosidosis: Long-Term Data of Enzyme Replacement Therapy With Velmanase Alfa (Human Recombinant Alpha Mannosidase)

Zur "Agrarverfassung" der Germanen (Tac. Germ. Kap. 26)

Zur ≫Agrarverfassung≪ Der Germanen (Tac. Germ. Kap. 26)

Neues zu Tac.Germ.46.2

Pariendum oder pereundum? (Tac. Germ. 18, 4)

Response to Roldan et al

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