Cervenáková L - Search Results

1

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

2

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

3

Novel PRNP sequence variant associated with familial encephalopathy.

Cervenáková L, Buetefisch C, Lee HS, Taller I, Stone G, Gibbs CJ Jr, Brown P, Hallett M, Goldfarb LG. Cervenáková L, et al. Am J Med Genet. 1999 Dec 15;88(6):653-6. doi: 10.1002/(sici)1096-8628(19991215)88:6<653::aid-ajmg14>3.0.co;2-e. Am J Med Genet. 1999. PMID: 10581485

4

Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease.

Cervenáková L, Goldfarb LG, Garruto R, Lee HS, Gajdusek DC, Brown P. Cervenáková L, et al. Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):13239-41. doi: 10.1073/pnas.95.22.13239. Proc Natl Acad Sci U S A. 1998. PMID: 9789072 Free PMC article.

5

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

6

Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS).

Cervenakova L, Protas II, Hirano A, Votiakov VI, Nedzved MK, Kolomiets ND, Taller I, Park KY, Sambuughin N, Gajdusek DC, Brown P, Goldfarb LG. Cervenakova L, et al. J Neurol Sci. 2000 Aug 15;177(2):124-30. doi: 10.1016/s0022-510x(00)00350-6. J Neurol Sci. 2000. PMID: 10980308 Clinical Trial.

7

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

8

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

9

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.

10

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.

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