Hays AP - Search Results

1

Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.

Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, Collin H, Dovico SA, Stolle CA, Fardeau M, Tomé FM, Campbell KP. Crosbie RH, et al. Among authors: hays ap. Hum Mol Genet. 2000 Aug 12;9(13):2019-27. doi: 10.1093/hmg/9.13.2019. Hum Mol Genet. 2000. PMID: 10942431

2

X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.

Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, Grewal RP, Kattah A, Camaño P, Otaegui D, Kunimatsu T, Blake DM, Wilhelmsen KC, Rowland LP, Hays AP, Bonilla E, Hirano M. Quinzii CM, et al. Among authors: hays ap. Am J Hum Genet. 2008 Jan;82(1):208-13. doi: 10.1016/j.ajhg.2007.09.013. Am J Hum Genet. 2008. PMID: 18179901 Free PMC article.

3

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder.

Hirano M, Silvestri G, Blake DM, Lombes A, Minetti C, Bonilla E, Hays AP, Lovelace RE, Butler I, Bertorini TE, et al. Hirano M, et al. Among authors: hays ap. Neurology. 1994 Apr;44(4):721-7. doi: 10.1212/wnl.44.4.721. Neurology. 1994. PMID: 8164833

4

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation.

Santorelli FM, Tanji K, Manta P, Casali C, Krishna S, Hays AP, Mancini DM, DiMauro S, Hirano M. Santorelli FM, et al. Among authors: hays ap. Am J Hum Genet. 1999 Jan;64(1):295-300. doi: 10.1086/302188. Am J Hum Genet. 1999. PMID: 9915970 Free PMC article. No abstract available.

5

Does increased superoxide dismutase activity really cause muscular dystrophy?

Almer G, Rosoklija G, Hirano M, Hays AP, Przedborski S. Almer G, et al. Among authors: hays ap. Ann Neurol. 1999 Jul;46(1):135. doi: 10.1002/1531-8249(199907)46:1<135::aid-ana23>3.0.co;2-t. Ann Neurol. 1999. PMID: 10401794 No abstract available.

6

Ubiquitin expression in acute steroid myopathy with loss of myosin thick filaments.

Minetti C, Hirano M, Morreale G, Pedemonte M, Cordone G, Hays AP, Bonilla E. Minetti C, et al. Among authors: hays ap. Muscle Nerve. 1996 Jan;19(1):94-6. doi: 10.1002/(SICI)1097-4598(199601)19:1<94::AID-MUS14>3.0.CO;2-3. Muscle Nerve. 1996. PMID: 8538677 No abstract available.

7

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. Among authors: hays ap. Rev Neurol (Paris). 1991;147(6-7):467-73. Rev Neurol (Paris). 1991. PMID: 1962052

8

Senataxin mutations and amyotrophic lateral sclerosis.

Hirano M, Quinzii CM, Mitsumoto H, Hays AP, Roberts JK, Richard P, Rowland LP. Hirano M, et al. Among authors: hays ap. Amyotroph Lateral Scler. 2011 May;12(3):223-7. doi: 10.3109/17482968.2010.545952. Epub 2010 Dec 29. Amyotroph Lateral Scler. 2011. PMID: 21190393 Free PMC article.

9

Multifocal motor neuropathy with conduction block: is it a distinct clinical entity?

Lange DJ, Trojaborg W, Latov N, Hays AP, Younger DS, Uncini A, Blake DM, Hirano M, Burns SM, Lovelace RE, et al. Lange DJ, et al. Among authors: hays ap. Neurology. 1992 Mar;42(3 Pt 1):497-505. doi: 10.1212/wnl.42.3.497. Neurology. 1992. PMID: 1549208

10

Amyotrophic lateral sclerosis with ragged-red fibers.

Hirano M, Angelini C, Montagna P, Hays AP, Tanji K, Mitsumoto H, Gordon PH, Naini AB, DiMauro S, Rowland LP. Hirano M, et al. Among authors: hays ap. Arch Neurol. 2008 Mar;65(3):403-6. doi: 10.1001/archneurol.2007.65. Arch Neurol. 2008. PMID: 18332255 Review.

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