Allan M. Lund

Copenhagen, Denmark

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 144 publications

Disease Outcomes in Boys with ABCD1 Variants Identified by Newborn Screening for X-ALD.

Disease Outcomes in Boys with ABCD1 Variants Identified by Newborn Screening for X-ALD.

Journal: medRxiv : the preprint server for health sciences

Published: July 10, 2026

Predictors of improved attentional control after Virtual Reality-based cognitive rehabilitation in chronic traumatic brain injury.

Predictors of improved attentional control after Virtual Reality-based cognitive rehabilitation in chronic traumatic brain injury.

Journal: Disability and rehabilitation

Published: April 29, 2026

Phase 3 Randomized Trial Results of DTX401 AAV Gene Therapy for the Treatment of GSDIa.

Phase 3 Randomized Trial Results of DTX401 AAV Gene Therapy for the Treatment of GSDIa.

Journal: Journal of inherited metabolic disease

Published: April 29, 2026

Pregnancies in Women With Long-Chain Fatty Acid Oxidation Disorders: Results of a European and North American Survey.

Pregnancies in Women With Long-Chain Fatty Acid Oxidation Disorders: Results of a European and North American Survey.

Journal: Journal of inherited metabolic disease

Published: October 24, 2025

Nationwide Study of the Epidemiology and Clinical Features of X-Linked Adrenoleukodystrophy in Denmark.

Nationwide Study of the Epidemiology and Clinical Features of X-Linked Adrenoleukodystrophy in Denmark.

Journal: Molecular genetics and metabolism

Published: September 03, 2025

Effect of long-term sepiapterin treatment on dietary phenylalanine tolerance in patients with phenylketonuria: Interim results from the phase 3 APHENITY Extension Study.

Effect of long-term sepiapterin treatment on dietary phenylalanine tolerance in patients with phenylketonuria: Interim results from the phase 3 APHENITY Extension Study.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 01, 2025

A diagnostic algorithm for inherited metabolic disorders using untargeted metabolomics.

A diagnostic algorithm for inherited metabolic disorders using untargeted metabolomics.

Journal: Metabolomics : Official journal of the Metabolomic Society

Published: March 21, 2025

Human D-Lactate Dehydrogenase Deficiency: A Case Report in a Young Boy.

Human D-Lactate Dehydrogenase Deficiency: A Case Report in a Young Boy.

Journal: JIMD reports

Published: March 12, 2025

Outcome of Haemopoietic Stem Cell Transplantation in 21 Patients With Alpha-Mannosidosis.

Outcome of Haemopoietic Stem Cell Transplantation in 21 Patients With Alpha-Mannosidosis.

Journal: Journal of inherited metabolic disease

Published: February 14, 2025

Clinical assessment of growth patterns, weight, and dietary management in children and adults with phenylketonuria - a retrospective study.

Clinical assessment of growth patterns, weight, and dietary management in children and adults with phenylketonuria - a retrospective study.

Journal: Orphanet journal of rare diseases

Published: February 02, 2025

Asparaginase-associated hyperammonemia.

Asparaginase-associated hyperammonemia.

Journal: Haematologica

Published: January 03, 2025

Evolution of mobility, pain/discomfort, self-care, and mental health in patients with alpha-mannosidosis: an international caregiver and patient survey.

Evolution of mobility, pain/discomfort, self-care, and mental health in patients with alpha-mannosidosis: an international caregiver and patient survey.

Journal: Orphanet journal of rare diseases

Published: December 18, 2024

Showing 1-12 of 144

Last Updated: 09/26/2026