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Items: 1 to 20 of 76

1.

Defects of beta-oxidation including carnitine deficiency.

Bartlett K, Pourfarzam M.

Int Rev Neurobiol. 2002;53:469-516. Review. No abstract available.

PMID:
12512350
2.

[Therapy of metabolic myopathies].

Reichmann H.

Nervenarzt. 1993 Oct;64(10):627-32. Review. German.

PMID:
8232675
3.

[Mitochondrial beta-oxidation defects].

Woldseth B, Rootwelt T.

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

4.

Carnitine deficiency.

Gilbert EF.

Pathology. 1985 Apr;17(2):161-71. Review.

PMID:
3900894
5.

[Lipidic myopathies].

Muñoz-Blanco JL.

Rev Neurol. 1998 Apr;26 Suppl 1:S72-80. Review. Spanish.

PMID:
9810593
6.

Mitochondrial myopathies.

DiMauro S, Bonilla E, Zeviani M, Servidei S, DeVivo DC, Schon EA.

J Inherit Metab Dis. 1987;10 Suppl 1:113-28. Review.

PMID:
2824920
7.

Mitochondrial myopathies.

DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC.

Ann Neurol. 1985 Jun;17(6):521-38. Review.

PMID:
3927817
8.
9.

Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of beta-oxidation.

Angelini C, Vergani L, Martinuzzi A.

Crit Rev Clin Lab Sci. 1992;29(3-4):217-42. Review.

PMID:
1489518
10.

Inherited disorders of mitochondrial fatty acid oxidation.

Coates PM, Stanley CA.

Prog Liver Dis. 1992;10:123-38. Review. No abstract available.

PMID:
1296227
11.

[New approaches for the treatment of metabolic myopathies].

Laforêt P, Nicolino M, Eymard B.

Rev Neurol (Paris). 2007 Oct;163(10):930-5. Review. French.

PMID:
18033029
12.

Primary and secondary alterations of neonatal carnitine metabolism.

Scaglia F, Longo N.

Semin Perinatol. 1999 Apr;23(2):152-61. Review.

PMID:
10331466
14.

Carnitine metabolism and human carnitine deficiency.

Tanphaichitr V, Leelahagul P.

Nutrition. 1993 May-Jun;9(3):246-54. Review.

PMID:
8353366
15.

[Hereditary metabolic muscular diseases caused by demonstrable enzyme defect].

Kuhn E.

Dtsch Med Wochenschr. 1980 Oct 17;105(42):1469-73. Review. German. No abstract available.

PMID:
6450673
16.

Genetic disorders of carnitine metabolism and their nutritional management.

Kerner J, Hoppel C.

Annu Rev Nutr. 1998;18:179-206. Review.

PMID:
9706223
17.

[Treatment of mitochondrial diseases in childhood and adolescence].

Castro-Gago M, Novo-Rodríguez MI, Eirís-Puñal J.

Rev Neurol. 1998 Apr;26 Suppl 1:S92-8. Review. Spanish.

PMID:
9810596
18.

[Carnitine palmitoyltransferase I(CPT1) deficiency].

Yorifuji S.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):401-2. Review. Japanese. No abstract available.

PMID:
9590082
19.

[Carnitine transporter defect].

Yorifuji S.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):398-400. Review. Japanese. No abstract available.

PMID:
9590081
20.

[Changes in carnitine metabolism. A case report about probable partial deficiency of muscle carnitine palmitoyltransferase].

De Prà M, Oberti F, De Benedittis A.

Pediatr Med Chir. 1990 Jul-Aug;12(4):397-403. Review. Italian.

PMID:
2075107

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