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Results: 1 to 20 of 104

Similar articles for PubMed (Select 9007409)

1.

Fatty acid mitochondrial beta-oxidation and hypoglycaemia in children.

Taroni F, Uziel G.

Curr Opin Neurol. 1996 Dec;9(6):477-85. Review.

PMID:
9007409
2.
3.

[Hypoglycaemia without ketosis. A case report].

Ferraz C, Reis ME, Lopes MM, Cardoso ML, Barbosa CR.

Rev Neurol. 2005 Sep 16-30;41(6):349-53. Spanish.

4.

The enzymes of mitochondrial fatty acid oxidation.

Bennett MJ.

Clin Chim Acta. 1994 May;226(2):211-24. Review.

PMID:
7923814
5.

[Mitochondrial beta-oxidation defects].

Woldseth B, Rootwelt T.

Tidsskr Nor Laegeforen. 2006 Mar 9;126(6):756-9. Review. Norwegian.

6.

Disorders of lipid metabolism in skeletal muscle.

Cwik VA.

Neurol Clin. 2000 Feb;18(1):167-84. Review.

PMID:
10658173
7.

Mitochondrial fatty-acid oxidation disorders.

Kompare M, Rizzo WB.

Semin Pediatr Neurol. 2008 Sep;15(3):140-9. doi: 10.1016/j.spen.2008.05.008. Review.

PMID:
18708005
8.

The inborn errors of mitochondrial fatty acid oxidation.

Vianey-Liaud C, Divry P, Gregersen N, Mathieu M.

J Inherit Metab Dis. 1987;10 Suppl 1:159-200. Review.

PMID:
3119938
9.
10.

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.

11.

Mitochondrial trifunctional protein defects: molecular basis and novel therapeutic approaches.

Angdisen J, Moore VD, Cline JM, Payne RM, Ibdah JA.

Curr Drug Targets Immune Endocr Metabol Disord. 2005 Mar;5(1):27-40. Review.

PMID:
15777202
12.

Role of carnitine and fatty acid oxidation and its defects in infantile epilepsy.

Tein I.

J Child Neurol. 2002 Dec;17 Suppl 3:3S57-82; discussion 3S82-3. Review.

PMID:
12597056
13.
14.

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women.

Ibdah JA, Bennett MJ, Rinaldo P, Zhao Y, Gibson B, Sims HF, Strauss AW.

N Engl J Med. 1999 Jun 3;340(22):1723-31.

15.

A general introduction to the biochemistry of mitochondrial fatty acid β-oxidation.

Houten SM, Wanders RJ.

J Inherit Metab Dis. 2010 Oct;33(5):469-77. doi: 10.1007/s10545-010-9061-2. Epub 2010 Mar 2. Review.

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18.

Recognition and management of fatty acid oxidation defects: a series of 107 patients.

Saudubray JM, Martin D, de Lonlay P, Touati G, Poggi-Travert F, Bonnet D, Jouvet P, Boutron M, Slama A, Vianey-Saban C, Bonnefont JP, Rabier D, Kamoun P, Brivet M.

J Inherit Metab Dis. 1999 Jun;22(4):488-502. Review.

PMID:
10407781
19.

Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening.

Spiekerkoetter U.

J Inherit Metab Dis. 2010 Oct;33(5):527-32. doi: 10.1007/s10545-010-9090-x. Epub 2010 May 7. Review.

PMID:
20449660
20.

[Diagnostic approach and treatment of inherited mitochondrial fatty acid oxidation disorders].

Peña Quintana L, Sanjurjo Crespo P.

An Esp Pediatr. 2001 Dec;55(6):524-34. Review. Spanish.

PMID:
11730586
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