A Nordenstrom
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Explore the profile of A Nordenstrom including associated specialties, affiliations and a list of published articles.
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24
Citations
326
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Recent Articles
11.
Haglind C, Nordenstrom A, Ask S, von Dobeln U, Gustafsson J, Stenlid M
J Inherit Metab Dis
. 2014 Aug;
38(2):315-22.
PMID: 25141826
Children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHAD) have a defect in the degradation of long-chain fatty acids and are at risk of hypoketotic hypoglycemia and insufficient energy production as well...
12.
Strandqvist A, Falhammar H, Lichtenstein P, Hirschberg A, Wedell A, Norrby C, et al.
J Clin Endocrinol Metab
. 2014 Jan;
99(4):1425-32.
PMID: 24476073
Context: Congenital adrenal hyperplasia (CAH), CYP21A2 deficiency, results in cortisol and aldosterone deficiency and increased production of androgens, with a good genotype phenotype correlation. Objective: The objective of the investigation...
13.
Haglind C, Stenlid M, Ask S, Alm J, Nemeth A, Dobeln U, et al.
JIMD Rep
. 2013 Feb;
8:81-90.
PMID: 23430524
Unlabelled: Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is an inborn error of fatty acid metabolism that affects the degradation of long chain fatty acids and causes insufficient energy production and accumulation...
14.
Barbaro M, Wedell A, Nordenstrom A
Semin Fetal Neonatal Med
. 2011 Feb;
16(2):119-27.
PMID: 21303737
Infants born with ambiguous genitalia represent a complex clinical challenge. A systematic clinical investigation aims at determining the hormone production and which anatomical structures are present in order to understand...
15.
A trial with N-carbamylglutamate may not detect all patients with NAGS deficiency and neonatal onset
Nordenstrom A, Halldin M, Hallberg B, Alm J
J Inherit Metab Dis
. 2007 May;
30(3):400.
PMID: 17510757
N-acetylglutamate synthase (NAGS) deficiency is a rare urea cycle disorder. An effective treatment, N-carbamoyl-L-glutamic acid (NCGA), is now available, increasing the importance of identifying and treating these patients early. We...
16.
Nordenstrom A, Ahmed S, Jones J, Coleman M, Price D, Clayton P, et al.
Horm Res
. 2005 Jan;
63(1):22-8.
PMID: 15627780
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase (CYP21) deficiency causes symptoms ranging from life-threatening neonatal adrenal crises to minimal virilization in adulthood. The relationship between CYP21 genotype and phenotypic markers...
17.
Nordenstrom A, Wedell A, Hagenfeldt L, Marcus C, Larsson A
Pediatrics
. 2001 Oct;
108(4):E68.
PMID: 11581476
Objective: Neonatal screening for congenital adrenal hyperplasia (CAH) among preterm infants is complicated by the fact that healthy preterm infants have higher levels of 17-hydroxyprogesterone (17-OHP) than term infants, resulting...
18.
Nordenstrom A, Thilen A, Hagenfeldt L, Larsson A, Wedell A
J Clin Endocrinol Metab
. 1999 May;
84(5):1505-9.
PMID: 10323369
To evaluate genotyping as a diagnostic complement to neonatal screening for congenital adrenal hyperplasia, 91 children who had been diagnosed with this condition between 1986 and 1997 were analyzed for...
19.
Nordenstrom A, Marcus C, Axelson M, Wedell A, Ritzen E
J Clin Endocrinol Metab
. 1999 Apr;
84(4):1210-3.
PMID: 10199755
Congenital adrenal hyperplasia in children is often treated with cortisone acetate and fludrocortisone. It is known that certain patients with congenital adrenal hyperplasia require very high substitution doses of cortisone...
20.
Thilen A, Nordenstrom A, Hagenfeldt L, von Dobeln U, Guthenberg C, Larsson A
Pediatrics
. 1998 Apr;
101(4):E11.
PMID: 9521977
Objectives: The aim of this study was to evaluate the benefits of neonatal screening for congenital adrenal hyperplasia (CAH). Methods: All children with CAH born in Sweden from January 1989...