Cervenáková L - Search Results

1

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: cervenakova l. Ann Neurol. 1995 Aug;38(2):267-9. doi: 10.1002/ana.410380222. Ann Neurol. 1995. PMID: 7654077

2

Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy.

Dagvadorj A, Petersen RB, Lee HS, Cervenakova L, Shatunov A, Budka H, Brown P, Gambetti P, Goldfarb LG. Dagvadorj A, et al. Among authors: cervenakova l. Ann Neurol. 2002 Sep;52(3):355-9. doi: 10.1002/ana.10267. Ann Neurol. 2002. PMID: 12205650

3

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: cervenakova l. Nat Genet. 1998 Aug;19(4):402-3. doi: 10.1038/1300. Nat Genet. 1998. PMID: 9697706

4

Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study.

Bütefisch CM, Gambetti P, Cervenakova L, Park KY, Hallett M, Goldfarb LG. Bütefisch CM, et al. Among authors: cervenakova l. Neurology. 2000 Aug 22;55(4):517-22. doi: 10.1212/wnl.55.4.517. Neurology. 2000. PMID: 10953183

5

Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin.

Goldfarb LG, Brown P, Haltia M, Cathala F, McCombie WR, Kovanen J, Cervenáková L, Goldin L, Nieto A, Godec MS, et al. Goldfarb LG, et al. Among authors: cervenakova l. Ann Neurol. 1992 Mar;31(3):274-81. doi: 10.1002/ana.410310308. Ann Neurol. 1992. PMID: 1353341

6

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.

Goldfarb LG, Brown P, McCombie WR, Goldgaber D, Swergold GD, Wills PR, Cervenakova L, Baron H, Gibbs CJ Jr, Gajdusek DC. Goldfarb LG, et al. Among authors: cervenakova l. Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10926-30. doi: 10.1073/pnas.88.23.10926. Proc Natl Acad Sci U S A. 1991. PMID: 1683708 Free PMC article.

7

Infectious amyloid precursor gene sequences in primates used for experimental transmission of human spongiform encephalopathy.

Cervenáková L, Brown P, Goldfarb LG, Nagle J, Pettrone K, Rubenstein R, Dubnick M, Gibbs CJ Jr, Gajdusek DC. Cervenáková L, et al. Proc Natl Acad Sci U S A. 1994 Dec 6;91(25):12159-62. doi: 10.1073/pnas.91.25.12159. Proc Natl Acad Sci U S A. 1994. PMID: 7991600 Free PMC article.

8

Molecular genetic studies of Creutzfeldt-Jakob disease.

Goldfarb LG, Brown P, Cervenakova L, Gajdusek DC. Goldfarb LG, et al. Among authors: cervenakova l. Mol Neurobiol. 1994 Apr-Jun;8(2-3):89-97. doi: 10.1007/BF02780658. Mol Neurobiol. 1994. PMID: 7999318 Review.

9

Genetic analysis of Creutzfeldt-Jakob disease and related disorders.

Goldfarb LG, Brown P, Cervenakova L, Gajdusek DC. Goldfarb LG, et al. Among authors: cervenakova l. Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):379-84. doi: 10.1098/rstb.1994.0032. Philos Trans R Soc Lond B Biol Sci. 1994. PMID: 8041803 Review.

10

A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob disease.

Goldfarb LG, Brown P, Little BW, Cervenáková L, Kenney K, Gibbs CJ Jr, Gajdusek DC. Goldfarb LG, et al. Among authors: cervenakova l. Neurology. 1993 Nov;43(11):2392-4. doi: 10.1212/wnl.43.11.2392. Neurology. 1993. PMID: 8232966

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