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Results: 1 to 20 of 109

1.

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Gillingham MB, Connor WE, Matern D, Rinaldo P, Burlingame T, Meeuws K, Harding CO.

Mol Genet Metab. 2003 Jun;79(2):114-23.

PMID:
12809642
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency.

Gillingham MB, Scott B, Elliott D, Harding CO.

Mol Genet Metab. 2006 Sep-Oct;89(1-2):58-63. Epub 2006 Jul 27.

PMID:
16876451
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency.

Gillingham MB, Purnell JQ, Jordan J, Stadler D, Haqq AM, Harding CO.

Mol Genet Metab. 2007 Jan;90(1):64-9. Epub 2006 Sep 22.

PMID:
16996288
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency.

Gillingham MB, Weleber RG, Neuringer M, Connor WE, Mills M, van Calcar S, Ver Hoeve J, Wolff J, Harding CO.

Mol Genet Metab. 2005 Sep-Oct;86(1-2):124-33. Epub 2005 Jul 22.

PMID:
16040264
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey.

Gillingham M, Van Calcar S, Ney D, Wolff J, Harding C.

J Inherit Metab Dis. 1999 Apr;22(2):123-31.

PMID:
10234607
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Choice of oils for essential fat supplements can enhance production of abnormal metabolites in fat oxidation disorders.

Roe CR, Roe DS, Wallace M, Garritson B.

Mol Genet Metab. 2007 Dec;92(4):346-50. Epub 2007 Sep 6.

PMID:
17825594
[PubMed - indexed for MEDLINE]
8.

Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts.

Roe DS, Yang BZ, Vianey-Saban C, Struys E, Sweetman L, Roe CR.

Mol Genet Metab. 2006 Jan;87(1):40-7. Epub 2005 Nov 16.

PMID:
16297647
[PubMed - indexed for MEDLINE]
9.

Variability in the clinical management of fatty acid oxidation disorders: results of a survey of Canadian metabolic physicians.

Potter BK, Little J, Chakraborty P, Kronick JB, Evans J, Frei J, Sutherland SC, Wilson K, Wilson BJ.

J Inherit Metab Dis. 2012 Jan;35(1):115-23. doi: 10.1007/s10545-011-9352-2. Epub 2011 Jun 1.

PMID:
21630065
[PubMed - indexed for MEDLINE]
10.

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

Lund AM, Dixon MA, Vreken P, Leonard JV, Morris AA.

J Inherit Metab Dis. 2003;26(4):353-60.

PMID:
12971423
[PubMed - indexed for MEDLINE]
11.

Long-chain fatty acid oxidation during early human development.

Oey NA, den Boer ME, Wijburg FA, Vekemans M, Augé J, Steiner C, Wanders RJ, Waterham HR, Ruiter JP, Attié-Bitach T.

Pediatr Res. 2005 Jun;57(6):755-9. Epub 2005 Apr 21.

PMID:
15845636
[PubMed - indexed for MEDLINE]
12.

Elevated hydroxyacylcarnitines in a carrier of LCHAD deficiency during acute liver disease of pregnancy - a common feature of the pregnancy complication?

Eskelin PM, Laitinen KA, Tyni TA.

Mol Genet Metab. 2010 Jun;100(2):204-6. doi: 10.1016/j.ymgme.2010.03.006. Epub 2010 Mar 16.

PMID:
20363656
[PubMed - indexed for MEDLINE]
13.

Medium-chain acyl-CoA dehydrogenase deficiency: metabolic effects and therapeutic efficacy of long-term L-carnitine supplementation.

Treem WR, Stanley CA, Goodman SI.

J Inherit Metab Dis. 1989;12(2):112-9.

PMID:
2502671
[PubMed - indexed for MEDLINE]
14.

Mitochondrial fatty acid beta-oxidation in the human eye and brain: implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Tyni T, Paetau A, Strauss AW, Middleton B, Kivelä T.

Pediatr Res. 2004 Nov;56(5):744-50. Epub 2004 Sep 3.

PMID:
15347768
[PubMed - indexed for MEDLINE]
15.

Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders.

Shen JJ, Matern D, Millington DS, Hillman S, Feezor MD, Bennett MJ, Qumsiyeh M, Kahler SG, Chen YT, Van Hove JL.

J Inherit Metab Dis. 2000 Feb;23(1):27-44.

PMID:
10682306
[PubMed - indexed for MEDLINE]
17.

Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome?

Holub M, Bodamer OA, Item C, Mühl A, Pollak A, Stöckler-Ipsiroglu S.

Acta Paediatr. 2005 Jan;94(1):48-52.

PMID:
15858960
[PubMed - indexed for MEDLINE]
18.

The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy.

Sims HF, Brackett JC, Powell CK, Treem WR, Hale DE, Bennett MJ, Gibson B, Shapiro S, Strauss AW.

Proc Natl Acad Sci U S A. 1995 Jan 31;92(3):841-5.

PMID:
7846063
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Multiple acyl-CoA-dehydrogenase deficiency (MADD): use of acylcarnitines and fatty acids to monitor the response to dietary treatment.

Abdenur JE, Chamoles NA, Schenone AB, Jorge L, Guinle A, Bernard C, Levandovskiy V, Fusta M, Lavorgna S.

Pediatr Res. 2001 Jul;50(1):61-6.

PMID:
11420420
[PubMed - indexed for MEDLINE]
20.

Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening.

Sykut-Cegielska J, Gradowska W, Piekutowska-Abramczuk D, Andresen BS, Olsen RK, Ołtarzewski M, Pronicki M, Pajdowska M, Bogdańska A, Jabłońska E, Radomyska B, Kuśmierska K, Krajewska-Walasek M, Gregersen N, Pronicka E.

J Inherit Metab Dis. 2011 Feb;34(1):185-95. doi: 10.1007/s10545-010-9244-x. Epub 2010 Nov 20.

PMID:
21103935
[PubMed - indexed for MEDLINE]
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