Dalakas MC - Search Results

1

Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.

Fananapazir L, Dalakas MC, Cyran F, Cohn G, Epstein ND. Fananapazir L, et al. Among authors: dalakas mc. Proc Natl Acad Sci U S A. 1993 May 1;90(9):3993-7. doi: 10.1073/pnas.90.9.3993. Proc Natl Acad Sci U S A. 1993. PMID: 8483915 Free PMC article.

2

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle.

Poetter K, Jiang H, Hassanzadeh S, Master SR, Chang A, Dalakas MC, Rayment I, Sellers JR, Fananapazir L, Epstein ND. Poetter K, et al. Among authors: dalakas mc. Nat Genet. 1996 May;13(1):63-9. doi: 10.1038/ng0596-63. Nat Genet. 1996. PMID: 8673105

3

Nonsense mutation in the phosphofructokinase muscle subunit gene associated with retention of intron 10 in one of the isolated transcripts in Ashkenazi Jewish patients with Tarui disease.

Vasconcelos O, Sivakumar K, Dalakas MC, Quezado M, Nagle J, Leon-Monzon M, Dubnick M, Gajdusek DC, Goldfarb LG. Vasconcelos O, et al. Among authors: dalakas mc. Proc Natl Acad Sci U S A. 1995 Oct 24;92(22):10322-6. doi: 10.1073/pnas.92.22.10322. Proc Natl Acad Sci U S A. 1995. PMID: 7479776 Free PMC article.

4

Missense mutations in desmin associated with familial cardiac and skeletal myopathy.

Goldfarb LG, Park KY, Cervenáková L, Gorokhova S, Lee HS, Vasconcelos O, Nagle JW, Semino-Mora C, Sivakumar K, Dalakas MC. Goldfarb LG, et al. Among authors: dalakas mc. Nat Genet. 1998 Aug;19(4):402-3. doi: 10.1038/1300. Nat Genet. 1998. PMID: 9697706

5

Detection of poliovirus antibodies and poliovirus genome in patients with the post-polio syndrome.

Leon-Monzon ME, Dalakas MC. Leon-Monzon ME, et al. Among authors: dalakas mc. Ann N Y Acad Sci. 1995 May 25;753:208-18. doi: 10.1111/j.1749-6632.1995.tb27547.x. Ann N Y Acad Sci. 1995. PMID: 7611630

6

GNE mutations in an American family with quadriceps-sparing IBM and lack of mutations in s-IBM.

Vasconcelos OM, Raju R, Dalakas MC. Vasconcelos OM, et al. Among authors: dalakas mc. Neurology. 2002 Dec 10;59(11):1776-9. doi: 10.1212/01.wnl.0000039780.13681.ad. Neurology. 2002. PMID: 12473769

7

Exons 16 and 17 of the amyloid precursor protein gene in familial inclusion body myopathy.

Sivakumar K, Cervenáková L, Dalakas MC, Leon-Monzon M, Isaacson SH, Nagle JW, Vasconcelos O, Goldfarb LG. Sivakumar K, et al. Among authors: dalakas mc. Ann Neurol. 1995 Aug;38(2):267-9. doi: 10.1002/ana.410380222. Ann Neurol. 1995. PMID: 7654077

8

The alpha beta T-cell receptor repertoire in inclusion body myositis: diverse patterns of gene expression by muscle-infiltrating lymphocytes.

O'Hanlon TP, Dalakas MC, Plotz PH, Miller FW. O'Hanlon TP, et al. Among authors: dalakas mc. J Autoimmun. 1994 Jun;7(3):321-33. doi: 10.1006/jaut.1994.1023. J Autoimmun. 1994. PMID: 7916906

9

Late-onset muscle weakness in partial phosphofructokinase deficiency: a unique myopathy with vacuoles, abnormal mitochondria, and absence of the common exon 5/intron 5 junction point mutation.

Sivakumar K, Vasconcelos O, Goldfarb L, Dalakas MC. Sivakumar K, et al. Among authors: dalakas mc. Neurology. 1996 May;46(5):1337-42. doi: 10.1212/wnl.46.5.1337. Neurology. 1996. PMID: 8628478

10

Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.

Dalakas MC, Park KY, Semino-Mora C, Lee HS, Sivakumar K, Goldfarb LG. Dalakas MC, et al. N Engl J Med. 2000 Mar 16;342(11):770-80. doi: 10.1056/NEJM200003163421104. N Engl J Med. 2000. PMID: 10717012 Free article.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

519 results

Search Page

Filters