Sadeh M - Search Results

1

Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1.

Argov Z, Tiram E, Eisenberg I, Sadeh M, Seidman CE, Seidman JG, Karpati G, Mitrani-Rosenbaum S. Argov Z, et al. Among authors: sadeh m. Ann Neurol. 1997 Apr;41(4):548-51. doi: 10.1002/ana.410410419. Ann Neurol. 1997. PMID: 9124813

2

Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps.

Eisenberg I, Grabov-Nardini G, Hochner H, Korner M, Sadeh M, Bertorini T, Bushby K, Castellan C, Felice K, Mendell J, Merlini L, Shilling C, Wirguin I, Argov Z, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: sadeh m. Hum Mutat. 2003 Jan;21(1):99. doi: 10.1002/humu.9100. Hum Mutat. 2003. PMID: 12497639

3

Facial weakness in hereditary inclusion body myopathies.

Argov Z, Sadeh M, Eisenberg I, Karpati G, Mitrani-Rosenbaum S. Argov Z, et al. Among authors: sadeh m. Neurology. 1998 Jun;50(6):1925-6. doi: 10.1212/wnl.50.6.1925. Neurology. 1998. PMID: 9633772 No abstract available.

4

Fine-structure mapping of the hereditary inclusion body myopathy locus.

Eisenberg I, Thiel C, Levi T, Tiram E, Argov Z, Sadeh M, Jackson CL, Thierfelder L, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: sadeh m. Genomics. 1999 Jan 1;55(1):43-8. doi: 10.1006/geno.1998.5630. Genomics. 1999. PMID: 9888997

5

Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13.

Eisenberg I, Hochner H, Shemesh M, Levi T, Potikha T, Sadeh M, Argov Z, Jackson CL, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: sadeh m. Eur J Hum Genet. 2001 Jul;9(7):501-9. doi: 10.1038/sj.ejhg.5200665. Eur J Hum Genet. 2001. PMID: 11464241

6

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.

Eisenberg I, Avidan N, Potikha T, Hochner H, Chen M, Olender T, Barash M, Shemesh M, Sadeh M, Grabov-Nardini G, Shmilevich I, Friedmann A, Karpati G, Bradley WG, Baumbach L, Lancet D, Asher EB, Beckmann JS, Argov Z, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: sadeh m. Nat Genet. 2001 Sep;29(1):83-7. doi: 10.1038/ng718. Nat Genet. 2001. PMID: 11528398

7

Hereditary inclusion body myopathy: the Middle Eastern genetic cluster.

Argov Z, Eisenberg I, Grabov-Nardini G, Sadeh M, Wirguin I, Soffer D, Mitrani-Rosenbaum S. Argov Z, et al. Among authors: sadeh m. Neurology. 2003 May 13;60(9):1519-23. doi: 10.1212/01.wnl.0000061617.71839.42. Neurology. 2003. PMID: 12743242

8

The proteomic profile of hereditary inclusion body myopathy.

Sela I, Milman Krentsis I, Shlomai Z, Sadeh M, Dabby R, Argov Z, Ben-Bassat H, Mitrani-Rosenbaum S. Sela I, et al. Among authors: sadeh m. PLoS One. 2011 Jan 31;6(1):e16334. doi: 10.1371/journal.pone.0016334. PLoS One. 2011. PMID: 21305017 Free PMC article.

9

No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation.

Salama I, Hinderlich S, Shlomai Z, Eisenberg I, Krause S, Yarema K, Argov Z, Lochmuller H, Reutter W, Dabby R, Sadeh M, Ben-Bassat H, Mitrani-Rosenbaum S. Salama I, et al. Among authors: sadeh m. Biochem Biophys Res Commun. 2005 Mar 4;328(1):221-6. doi: 10.1016/j.bbrc.2004.12.157. Biochem Biophys Res Commun. 2005. PMID: 15670773

10

Mitochondrial processes are impaired in hereditary inclusion body myopathy.

Eisenberg I, Novershtern N, Itzhaki Z, Becker-Cohen M, Sadeh M, Willems PH, Friedman N, Koopman WJ, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: sadeh m. Hum Mol Genet. 2008 Dec 1;17(23):3663-74. doi: 10.1093/hmg/ddn261. Epub 2008 Aug 23. Hum Mol Genet. 2008. PMID: 18723858

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