Mendell JR - Search Results

1

Diagnosis of Duchenne dystrophy by enhanced detection of small mutations.

Mendell JR, Buzin CH, Feng J, Yan J, Serrano C, Sangani DS, Wall C, Prior TW, Sommer SS. Mendell JR, et al. Neurology. 2001 Aug 28;57(4):645-50. doi: 10.1212/wnl.57.4.645. Neurology. 2001. PMID: 11524473

2

Three-tiered noninvasive diagnosis in 96% of patients with Duchenne muscular dystrophy (DMD).

Yan J, Feng J, Buzin CH, Scaringe W, Liu Q, Mendell JR, Dunnen JD, Sommer SS. Yan J, et al. Among authors: mendell jr. Hum Mutat. 2004 Feb;23(2):203-204. doi: 10.1002/humu.10307. Hum Mutat. 2004. PMID: 14722924 No abstract available.

3

The childhood muscular dystrophies: diseases sharing a common pathogenesis of membrane instability.

Mendell JR, Sahenk Z, Prior TW. Mendell JR, et al. J Child Neurol. 1995 Mar;10(2):150-9. doi: 10.1177/088307389501000219. J Child Neurol. 1995. PMID: 7782608 Review.

4

The impact of molecular genetics on the care of patients with muscle disease.

Nadkarni N, Prior TW, Mendell JR. Nadkarni N, et al. Among authors: mendell jr. Curr Opin Neurol. 1994 Oct;7(5):435-47. doi: 10.1097/00019052-199410000-00012. Curr Opin Neurol. 1994. PMID: 7804465 Review.

5

Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production.

Winnard AV, Mendell JR, Prior TW, Florence J, Burghes AH. Winnard AV, et al. Among authors: mendell jr. Am J Hum Genet. 1995 Jan;56(1):158-66. Am J Hum Genet. 1995. PMID: 7825572 Free PMC article.

6

Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor gene.

Amato AA, Prior TW, Barohn RJ, Snyder P, Papp A, Mendell JR. Amato AA, et al. Among authors: mendell jr. Neurology. 1993 Apr;43(4):791-4. doi: 10.1212/wnl.43.4.791. Neurology. 1993. PMID: 8469342

7

Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletion.

Prior TW, Bartolo C, Papp AC, Snyder PJ, Sedra MS, Burghes AH, Kissel JT, Luquette MH, Tsao CY, Mendell JR. Prior TW, et al. Among authors: mendell jr. Neurology. 1997 Feb;48(2):486-8. doi: 10.1212/wnl.48.2.486. Neurology. 1997. PMID: 9040743

8

Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.

Prior TW, Papp AC, Snyder PJ, Mendell JR. Prior TW, et al. Among authors: mendell jr. Muscle Nerve. 1992 Aug;15(8):960-3. doi: 10.1002/mus.880150815. Muscle Nerve. 1992. PMID: 1353862

9

Fidelity of gamma-glutamyl transferase (GGT) in differentiating skeletal muscle from liver damage.

Rosales XQ, Chu ML, Shilling C, Wall C, Pastores GM, Mendell JR. Rosales XQ, et al. Among authors: mendell jr. J Child Neurol. 2008 Jul;23(7):748-51. doi: 10.1177/0883073808314365. Epub 2008 Mar 19. J Child Neurol. 2008. PMID: 18354148

10

Gentamicin-induced readthrough of stop codons in Duchenne muscular dystrophy.

Malik V, Rodino-Klapac LR, Viollet L, Wall C, King W, Al-Dahhak R, Lewis S, Shilling CJ, Kota J, Serrano-Munuera C, Hayes J, Mahan JD, Campbell KJ, Banwell B, Dasouki M, Watts V, Sivakumar K, Bien-Willner R, Flanigan KM, Sahenk Z, Barohn RJ, Walker CM, Mendell JR. Malik V, et al. Among authors: mendell jr. Ann Neurol. 2010 Jun;67(6):771-80. doi: 10.1002/ana.22024. Ann Neurol. 2010. PMID: 20517938 Clinical Trial.

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