Mendell JR - Search Results

1

Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reaction.

Sciacco M, Gasparo-Rippa P, Vu TH, Tanji K, Shanske S, Mendell JR, Schon EA, DiMauro S, Bonilla E. Sciacco M, et al. Among authors: mendell jr. Muscle Nerve. 1998 Nov;21(11):1374-81. doi: 10.1002/(sici)1097-4598(199811)21:11<1374::aid-mus3>3.0.co;2-6. Muscle Nerve. 1998. PMID: 9771659

2

Clinical manifestations of mitochondrial DNA depletion.

Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728

3

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.

Santorelli FM, Sciacco M, Tanji K, Shanske S, Vu TH, Golzi V, Griggs RC, Mendell JR, Hays AP, Bertorini TE, Pestronk A, Bonilla E, DiMauro S. Santorelli FM, et al. Among authors: mendell jr. Ann Neurol. 1996 Jun;39(6):789-95. doi: 10.1002/ana.410390615. Ann Neurol. 1996. PMID: 8651651

4

Infantile encephalopathy associated with the MELAS A3243G mutation.

Sue CM, Bruno C, Andreu AL, Cargan A, Mendell JR, Tsao CY, Luquette M, Paolicchi J, Shanske S, DiMauro S, De Vivo DC. Sue CM, et al. Among authors: mendell jr. J Pediatr. 1999 Jun;134(6):696-700. doi: 10.1016/s0022-3476(99)70283-0. J Pediatr. 1999. PMID: 10356136 Free article.

5

Familial cerebellar ataxia with muscle coenzyme Q10 deficiency.

Musumeci O, Naini A, Slonim AE, Skavin N, Hadjigeorgiou GL, Krawiecki N, Weissman BM, Tsao CY, Mendell JR, Shanske S, De Vivo DC, Hirano M, DiMauro S. Musumeci O, et al. Among authors: mendell jr. Neurology. 2001 Apr 10;56(7):849-55. doi: 10.1212/wnl.56.7.849. Neurology. 2001. PMID: 11294920

6

Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular genetics.

Lombes A, Mendell JR, Nakase H, Barohn RJ, Bonilla E, Zeviani M, Yates AJ, Omerza J, Gales TL, Nakahara K, et al. Lombes A, et al. Among authors: mendell jr. Ann Neurol. 1989 Jul;26(1):20-33. doi: 10.1002/ana.410260104. Ann Neurol. 1989. PMID: 2549843

7

Three new mutations in patients with myophosphorylase deficiency (McArdle disease).

Tsujino S, Shanske S, Nonaka I, Eto Y, Mendell JR, Fenichel GM, DiMauro S. Tsujino S, et al. Among authors: mendell jr. Am J Hum Genet. 1994 Jan;54(1):44-52. Am J Hum Genet. 1994. PMID: 8279469 Free PMC article.

8

Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency.

DiMauro S, Mendell JR, Sahenk Z, Bachman D, Scarpa A, Scofield RM, Reiner C. DiMauro S, et al. Among authors: mendell jr. Neurology. 1980 Aug;30(8):795-804. doi: 10.1212/wnl.30.8.795. Neurology. 1980. PMID: 6251406

9

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: mendell jr. Ann Neurol. 1995 Nov;38(5):705-13. doi: 10.1002/ana.410380504. Ann Neurol. 1995. PMID: 7486861 Review. No abstract available.

10

Amyloidosis causing a progressive myopathy.

Nadkarni N, Freimer M, Mendell JR. Nadkarni N, et al. Among authors: mendell jr. Muscle Nerve. 1995 Sep;18(9):1016-8. doi: 10.1002/mus.880180914. Muscle Nerve. 1995. PMID: 7643863

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