Dimauro S - Search Results

1

Cafferty MS, Lovelace RE, Hays AP, Servidei S, Dimauro S, Rowland LP. Cafferty MS, et al. Among authors: dimauro s. Muscle Nerve. 1991 Feb;14(2):102-7. doi: 10.1002/mus.880140203. Muscle Nerve. 1991. PMID: 1847989 Review.

2

High serum levels of creatine kinase: asymptomatic prelude to distal myopathy.

Galassi G, Rowland LP, Hays AP, Hopkins LC, DiMauro S. Galassi G, et al. Among authors: dimauro s. Muscle Nerve. 1987 May;10(4):346-50. doi: 10.1002/mus.880100411. Muscle Nerve. 1987. PMID: 3587269

3

Biochemistry and molecular genetics of human glycogenoses: an overview.

DiMauro S, Tsujino S, Shanske S, Rowland LP. DiMauro S, et al. Muscle Nerve Suppl. 1995;3:S10-7. doi: 10.1002/mus.880181405. Muscle Nerve Suppl. 1995. PMID: 7603508 Review. No abstract available.

4

Glycogen branching enzyme deficiency in adult polyglucosan body disease.

Bruno C, Servidei S, Shanske S, Karpati G, Carpenter S, McKee D, Barohn RJ, Hirano M, Rifai Z, DiMauro S. Bruno C, et al. Among authors: dimauro s. Ann Neurol. 1993 Jan;33(1):88-93. doi: 10.1002/ana.410330114. Ann Neurol. 1993. PMID: 8494336

5

Recurrent myoglobinuria and HIV seropositivity: incidental or pathogenic association?

Younger DS, Hays AP, Uncini A, Lange DJ, Lovelace RE, DiMauro S. Younger DS, et al. Among authors: dimauro s. Muscle Nerve. 1989 Oct;12(10):842-3. doi: 10.1002/mus.880121009. Muscle Nerve. 1989. PMID: 2608081

6

Benign course of glycogen storage disease type IIb in two brothers: nature or nurture?

Slonim AE, Bulone L, Minikes J, Hays AP, Shanske S, Tsujino S, DiMauro S. Slonim AE, et al. Among authors: dimauro s. Muscle Nerve. 2006 Apr;33(4):571-4. doi: 10.1002/mus.20473. Muscle Nerve. 2006. PMID: 16320310

7

Inclusion body myositis and myopathies.

Griggs RC, Askanas V, DiMauro S, Engel A, Karpati G, Mendell JR, Rowland LP. Griggs RC, et al. Among authors: dimauro s. Ann Neurol. 1995 Nov;38(5):705-13. doi: 10.1002/ana.410380504. Ann Neurol. 1995. PMID: 7486861 Review. No abstract available.

8

Clinical syndromes associated with ragged red fibers.

Rowland LP, Blake DM, Hirano M, Di Mauro S, Schon EA, Hays AP, Devivo DC. Rowland LP, et al. Rev Neurol (Paris). 1991;147(6-7):467-73. Rev Neurol (Paris). 1991. PMID: 1962052

9

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

10

Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease.

Salviati L, Sacconi S, Rasalan MM, Kronn DF, Braun A, Canoll P, Davidson M, Shanske S, Bonilla E, Hays AP, Schon EA, DiMauro S. Salviati L, et al. Among authors: dimauro s. Arch Neurol. 2002 May;59(5):862-5. doi: 10.1001/archneur.59.5.862. Arch Neurol. 2002. PMID: 12020273

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