Goldfarb LG - Search Results

1

Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.

Goldfarb LG, Vasconcelos O, Platonov FA, Lunkes A, Kipnis V, Kononova S, Chabrashvili T, Vladimirtsev VA, Alexeev VP, Gajdusek DC. Goldfarb LG, et al. Ann Neurol. 1996 Apr;39(4):500-6. doi: 10.1002/ana.410390412. Ann Neurol. 1996. PMID: 8619528

2

Olivopontocerebellar atrophy in a large Iakut kinship in eastern Siberia.

Goldfarb LG, Chumakov MP, Petrov PA, Fedorova NI, Gajdusek DC. Goldfarb LG, et al. Neurology. 1989 Nov;39(11):1527-30. doi: 10.1212/wnl.39.11.1527. Neurology. 1989. PMID: 2812335

3

Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locus.

Lunkes A, Goldfarb LG, Platonov FA, Alexeev VP, Duenas-Barajas E, Gajdusek DC, Auburger G. Lunkes A, et al. Among authors: goldfarb lg. Exp Neurol. 1994 Apr;126(2):310-2. doi: 10.1006/exnr.1994.1070. Exp Neurol. 1994. PMID: 7925830

4

Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease.

Higgins JJ, Nee LE, Vasconcelos O, Ide SE, Lavedan C, Goldfarb LG, Polymeropoulos MH. Higgins JJ, et al. Among authors: goldfarb lg. Neurology. 1996 Jan;46(1):208-13. doi: 10.1212/wnl.46.1.208. Neurology. 1996. PMID: 8559377

5

Viliuisk encephalomyelitis in the Iakut people of Siberia.

Goldfarb LG, Gajdusek DC. Goldfarb LG, et al. Brain. 1992 Aug;115 ( Pt 4):961-78. doi: 10.1093/brain/115.4.961. Brain. 1992. PMID: 1393513

6

Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2.

Sambuughin N, Goldfarb LG, Sivtseva TM, Davydova TK, Vladimirtsev VA, Osakovskiy VL, Danilova AP, Nikitina RS, Ylakhova AN, Diachkovskaya MP, Sundborger AC, Renwick NM, Platonov FA, Hinshaw JE, Toro C. Sambuughin N, et al. Among authors: goldfarb lg. BMC Neurol. 2015 Oct 30;15:223. doi: 10.1186/s12883-015-0481-3. BMC Neurol. 2015. PMID: 26517984 Free PMC article.

7

Genetic fitness and selection intensity in a population affected with high-incidence spinocerebellar ataxia type 1.

Platonov FA, Tyryshkin K, Tikhonov DG, Neustroyeva TS, Sivtseva TM, Yakovleva NV, Nikolaev VP, Sidorova OG, Kononova SK, Goldfarb LG, Renwick NM. Platonov FA, et al. Among authors: goldfarb lg. Neurogenetics. 2016 Jul;17(3):179-85. doi: 10.1007/s10048-016-0481-5. Epub 2016 Apr 22. Neurogenetics. 2016. PMID: 27106293 Free PMC article.

8

Epidemiology of Viliuisk encephalomyelitis in Eastern Siberia.

Lee HS, Zhdanova SN, Vladimirtsev VA, Platonov FA, Osakovskiy VL, Subbotina EL, Broytman O, Danilova AP, Nikitina RS, Chepurnov AA, Krivoshapkin VG, Gajdusek DC, Savilov YD, Garruto RM, Goldfarb LG. Lee HS, et al. Among authors: goldfarb lg. Epidemiology. 2010 Jan;21(1):24-30. doi: 10.1097/EDE.0b013e3181c30fd2. Epidemiology. 2010. PMID: 20010208 Free PMC article.

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. Neurology. 1996 May;46(5):1337-42. doi: 10.1212/wnl.46.5.1337. Neurology. 1996. PMID: 8628478

10

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

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