Flanigan KM - Search Results

1

Clinical and genetic characterization of manifesting carriers of DMD mutations.

Soltanzadeh P, Friez MJ, Dunn D, von Niederhausern A, Gurvich OL, Swoboda KJ, Sampson JB, Pestronk A, Connolly AM, Florence JM, Finkel RS, Bönnemann CG, Medne L, Mendell JR, Mathews KD, Wong BL, Sussman MD, Zonana J, Kovak K, Gospe SM Jr, Gappmaier E, Taylor LE, Howard MT, Weiss RB, Flanigan KM. Soltanzadeh P, et al. Among authors: flanigan km. Neuromuscul Disord. 2010 Aug;20(8):499-504. doi: 10.1016/j.nmd.2010.05.010. Epub 2010 Jul 13. Neuromuscul Disord. 2010. PMID: 20630757 Free PMC article.

2

Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophy.

Howard MT, Shirts BH, Petros LM, Flanigan KM, Gesteland RF, Atkins JF. Howard MT, et al. Among authors: flanigan km. Ann Neurol. 2000 Aug;48(2):164-9. Ann Neurol. 2000. PMID: 10939566

3

Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy.

Flanigan KM, Coffeen CM, Sexton L, Stauffer D, Brunner S, Leppert MF. Flanigan KM, et al. Neuromuscul Disord. 2001 Sep;11(6-7):525-9. doi: 10.1016/s0960-8966(01)00201-2. Neuromuscul Disord. 2001. PMID: 11525880

4

Rapid direct sequence analysis of the dystrophin gene.

Flanigan KM, von Niederhausern A, Dunn DM, Alder J, Mendell JR, Weiss RB. Flanigan KM, et al. Am J Hum Genet. 2003 Apr;72(4):931-9. doi: 10.1086/374176. Epub 2003 Mar 11. Am J Hum Genet. 2003. PMID: 12632325 Free PMC article.

5

Readthrough of dystrophin stop codon mutations induced by aminoglycosides.

Howard MT, Anderson CB, Fass U, Khatri S, Gesteland RF, Atkins JF, Flanigan KM. Howard MT, et al. Among authors: flanigan km. Ann Neurol. 2004 Mar;55(3):422-6. doi: 10.1002/ana.20052. Ann Neurol. 2004. PMID: 14991821

6

Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy.

Lampe AK, Dunn DM, von Niederhausern AC, Hamil C, Aoyagi A, Laval SH, Marie SK, Chu ML, Swoboda K, Muntoni F, Bonnemann CG, Flanigan KM, Bushby KM, Weiss RB. Lampe AK, et al. Among authors: flanigan km. J Med Genet. 2005 Feb;42(2):108-20. doi: 10.1136/jmg.2004.023754. J Med Genet. 2005. PMID: 15689448 Free PMC article.

7

Improved molecular diagnosis of dystrophinopathies in an unselected clinical cohort.

Dent KM, Dunn DM, von Niederhausern AC, Aoyagi AT, Kerr L, Bromberg MB, Hart KJ, Tuohy T, White S, den Dunnen JT, Weiss RB, Flanigan KM. Dent KM, et al. Among authors: flanigan km. Am J Med Genet A. 2005 Apr 30;134(3):295-8. doi: 10.1002/ajmg.a.30617. Am J Med Genet A. 2005. PMID: 15723292

8

Recoding elements located adjacent to a subset of eukaryal selenocysteine-specifying UGA codons.

Howard MT, Aggarwal G, Anderson CB, Khatri S, Flanigan KM, Atkins JF. Howard MT, et al. Among authors: flanigan km. EMBO J. 2005 Apr 20;24(8):1596-607. doi: 10.1038/sj.emboj.7600642. Epub 2005 Mar 24. EMBO J. 2005. PMID: 15791204 Free PMC article.

9

Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathy.

Mercuri E, Lampe A, Allsop J, Knight R, Pane M, Kinali M, Bonnemann C, Flanigan K, Lapini I, Bushby K, Pepe G, Muntoni F. Mercuri E, et al. Neuromuscul Disord. 2005 Apr;15(4):303-10. doi: 10.1016/j.nmd.2005.01.004. Neuromuscul Disord. 2005. PMID: 15792870

10

An unusual pathologic feature associated with dermatomyositis.

Sampson JB, Chin SS, Clayton FC, Pestronk A, Swoboda KJ, Flanigan KM. Sampson JB, et al. Among authors: flanigan km. Neuromuscul Disord. 2006 Jun;16(6):391-3. doi: 10.1016/j.nmd.2006.03.013. Epub 2006 May 11. Neuromuscul Disord. 2006. PMID: 16697198

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

189 results

Search Page