A. Lund

发表

Highly variable clinical phenotype of carbamylphosphate synthetase 1 deficiency in one family: an effect of allelic variation in gene expression?

E. Christensen, J. Häberle, V. Klaus, 2009, Clinical genetics.

Phospholipid molecular species with eicosapentaenoic acid (20:5(n-3)) are less stable than species with arachidonic acid (20:4(n-6)) in isolated rat liver cells.

A. Lund, B. Woldseth, B. Christophersen, 1995, Scandinavian journal of clinical and laboratory investigation.

Four novel mutations identified in Norwegian patients result in intermittent maple syrup urine disease when combined with the R301C mutation.

H. Rootwelt, M. Bjørås, A. Lund, 2010, Molecular genetics and metabolism.

COVID-19 Vaccination Might Induce Reversible Cerebral Vasoconstriction Syndrome Attacks: A Case Report

A. Lund, Mohammad Al-Mahdi Al-Karagholi, 2022, Vaccines.

X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome

N. de Leeuw, J. Tolmie, Z. Tümer, 2013, Human Genetics.

What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?

P. Vreken, J. Leonard, A. Lund, 2003, Journal of Inherited Metabolic Disease.

Cataract in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD)

J. Leonard, A. Lund, A. Morris, 2003, Ophthalmic genetics.

Feeding difficulties in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

J. Leonard, A. Lund, 2001, Archives of disease in childhood.

Feeding diYculties in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

J. Leonard, A. Lund, 2001 .

Metabolism of some radiolabeled essential fatty acids in isolated rat hepatocytes is affected by dietary ethanol.

A. Lund, K. Retterstøl, S. Tverdal, 2000, Alcohol.

X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome

J. Tolmie, Z. Tümer, R. Møller, 2014, Human Genetics.

Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family

M. Rocco, A. Lund, A. Lund, 2006, Journal of Medical Genetics.

Localization of the neuropeptides pituitary adenylate cyclase-activating polypeptide, vasoactive intestinal peptide, and their receptors in the basal brain blood vessels and trigeminal ganglion of the mouse CNS; an immunohistochemical study

J. Hannibal, A. Lund, 2022, Frontiers in Neuroanatomy.

Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy

M. Schwartz, E. Christensen, M. Kirchhoff, 2009, Clinical genetics.

Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

P. Vreken, J. Leonard, A. Lund, 2003, Journal of Inherited Metabolic Disease.