DiMauro S - Search Results

1

Carnitine palmityl transferase deficiency: myoglobinuria and respiratory failure.

Bertorini T, Yeh YY, Trevisan C, Stadlan E, Sabesin S, DiMauro S. Bertorini T, et al. Among authors: dimauro s. Neurology. 1980 Mar;30(3):263-71. doi: 10.1212/wnl.30.3.263. Neurology. 1980. PMID: 7189025

2

Familial systemic carnitine deficiency.

Cruse RP, Di Mauro S, Towfighi J, Trevisan C. Cruse RP, et al. Arch Neurol. 1984 Mar;41(3):301-5. doi: 10.1001/archneur.1984.04050150079021. Arch Neurol. 1984. PMID: 6696649

3

Disorders of lipid metabolism in muscle.

Di Mauro S, Trevisan C, Hays A. Di Mauro S, et al. Muscle Nerve. 1980 Sep-Oct;3(5):369-88. doi: 10.1002/mus.880030502. Muscle Nerve. 1980. PMID: 7421873

4

Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency.

Trevisan CP, Reichmann H, DeVivo DC, DiMauro S. Trevisan CP, et al. Among authors: dimauro s. Muscle Nerve. 1985 Oct;8(8):672-5. doi: 10.1002/mus.880080809. Muscle Nerve. 1985. PMID: 2932640

5

Corticosteroid-responsive skeletal muscle disease associated with partial carnitine deficiency: studies of liver and metabolic alterations.

Whitaker JN, Dimauro S, Solomon SS, Sabesin S, Duckworth WC, Mendell JR. Whitaker JN, et al. Among authors: dimauro s. Am J Med. 1977 Nov;63(5):805-15. doi: 10.1016/0002-9343(77)90167-x. Am J Med. 1977. PMID: 201171

6

Activation of free fatty acids in subcellular fractions of human skeletal muscle.

Trevisan C, DiMauro S. Trevisan C, et al. Among authors: dimauro s. Neurochem Res. 1983 May;8(5):551-61. doi: 10.1007/BF00964696. Neurochem Res. 1983. PMID: 6225030

7

Muscle carnitine deficiency and fatal cardiomyopathy.

Hart ZH, Chang CH, Di Mauro S, Farooki Q, Ayyar R. Hart ZH, et al. Neurology. 1978 Feb;28(2):147-51. doi: 10.1212/wnl.28.2.147. Neurology. 1978. PMID: 563997

8

Tissue carnitine in Reye syndrome.

Willner JH, Chutorian AM, DiMauro S. Willner JH, et al. Among authors: dimauro s. Ann Neurol. 1978 Nov;4(5):468-9. doi: 10.1002/ana.410040514. Ann Neurol. 1978. PMID: 736529

9

Metabolic causes of myoglobinuria.

Tonin P, Lewis P, Servidei S, DiMauro S. Tonin P, et al. Among authors: dimauro s. Ann Neurol. 1990 Feb;27(2):181-5. doi: 10.1002/ana.410270214. Ann Neurol. 1990. PMID: 2156480

10

Hereditary carnitine deficiency of muscle.

VanDyke DH, Griggs RC, Markesbery W, Dimauro S. VanDyke DH, et al. Among authors: dimauro s. Neurology. 1975 Feb;25(2):154-9. doi: 10.1212/wnl.25.2.154. Neurology. 1975. PMID: 123043

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