Lee HS - Search Results

1

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: lee hs. Ann Neurol. 2002 Sep;52(3):355-9. doi: 10.1002/ana.10267. Ann Neurol. 2002. PMID: 12205650

2

Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23.

Shatunov A, Sambuughin N, Jankovic J, Elble R, Lee HS, Singleton AB, Dagvadorj A, Ji J, Zhang Y, Kimonis VE, Hardy J, Hallett M, Goldfarb LG. Shatunov A, et al. Among authors: lee hs. Brain. 2006 Sep;129(Pt 9):2318-31. doi: 10.1093/brain/awl120. Epub 2006 May 15. Brain. 2006. PMID: 16702189 Free article.

3

APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathies.

Chapman J, Cervenáková L, Petersen RB, Lee HS, Estupinan J, Richardson S, Vnencak-Jones CL, Gajdusek DC, Korczyn AD, Brown P, Goldfarb LG. Chapman J, et al. Among authors: lee hs. Neurology. 1998 Aug;51(2):548-53. doi: 10.1212/wnl.51.2.548. Neurology. 1998. PMID: 9710033

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. Among authors: lee hs. 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

Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.

Lee HS, Sambuughin N, Cervenakova L, Chapman J, Pocchiari M, Litvak S, Qi HY, Budka H, del Ser T, Furukawa H, Brown P, Gajdusek DC, Long JC, Korczyn AD, Goldfarb LG. Lee HS, et al. Am J Hum Genet. 1999 Apr;64(4):1063-70. doi: 10.1086/302340. Am J Hum Genet. 1999. PMID: 10090891 Free PMC article.

6

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. Among authors: lee hs. 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

7

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

8

Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype.

Lee HS, Brown P, Cervenáková L, Garruto RM, Alpers MP, Gajdusek DC, Goldfarb LG. Lee HS, et al. J Infect Dis. 2001 Jan 15;183(2):192-196. doi: 10.1086/317935. Epub 2000 Dec 21. J Infect Dis. 2001. PMID: 11120925

9

In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy.

Shatunov A, Olivé M, Odgerel Z, Stadelmann-Nessler C, Irlbacher K, van Landeghem F, Bayarsaikhan M, Lee HS, Goudeau B, Chinnery PF, Straub V, Hilton-Jones D, Damian MS, Kaminska A, Vicart P, Bushby K, Dalakas MC, Sambuughin N, Ferrer I, Goebel HH, Goldfarb LG. Shatunov A, et al. Among authors: lee hs. Eur J Hum Genet. 2009 May;17(5):656-63. doi: 10.1038/ejhg.2008.226. Epub 2008 Dec 3. Eur J Hum Genet. 2009. PMID: 19050726 Free PMC article.

10

Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation.

Odgerel Z, Sarkozy A, Lee HS, McKenna C, Rankin J, Straub V, Lochmüller H, Paola F, D'Amico A, Bertini E, Bushby K, Goldfarb LG. Odgerel Z, et al. Among authors: lee hs. Neuromuscul Disord. 2010 Jul;20(7):438-42. doi: 10.1016/j.nmd.2010.05.004. Epub 2010 Jun 3. Neuromuscul Disord. 2010. PMID: 20605452 Free PMC 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

9,488 results

Search Page

Filters