Lunkes A - Search Results

1

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. Exp Neurol. 1994 Apr;126(2):310-2. doi: 10.1006/exnr.1994.1070. Exp Neurol. 1994. PMID: 7925830

2

Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage.

Lunkes A, Gispert S, Enczmann J, Auburger G. Lunkes A, et al. Hum Genet. 1993 May;91(4):362-6. doi: 10.1007/BF00217357. Hum Genet. 1993. PMID: 8099059

3

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. Among authors: lunkes a. Ann Neurol. 1996 Apr;39(4):500-6. doi: 10.1002/ana.410390412. Ann Neurol. 1996. PMID: 8619528

4

Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1.

Hernández A, Magariño C, Gispert S, Santos N, Lunkes A, Orozco G, Heredero L, Beckmann J, Auburger G. Hernández A, et al. Among authors: lunkes a. Genomics. 1995 Jan 20;25(2):433-5. doi: 10.1016/0888-7543(95)80043-l. Genomics. 1995. PMID: 7789976

5

A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197.

Auburger G, Ratzlaff T, Lunkes A, Nelles HW, Leube B, Binkofski F, Kugel H, Heindel W, Seitz R, Benecke R, Witte OW, Voit T. Auburger G, et al. Among authors: lunkes a. Genomics. 1996 Jan 1;31(1):90-4. doi: 10.1006/geno.1996.0013. Genomics. 1996. PMID: 8808284

6

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, Pearlman S, Starkman S, Orozco-Diaz G, Lunkes A, DeJong P, Rouleau GA, Auburger G, Korenberg JR, Figueroa C, Sahba S. Pulst SM, et al. Among authors: lunkes a. Nat Genet. 1996 Nov;14(3):269-76. doi: 10.1038/ng1196-269. Nat Genet. 1996. PMID: 8896555

7

SCA2 trinucleotide expansion in German SCA patients.

Riess O, Laccone FA, Gispert S, Schöls L, Zühlke C, Vieira-Saecker AM, Herlt S, Wessel K, Epplen JT, Weber BH, Kreuz F, Chahrokh-Zadeh S, Meindl A, Lunkes A, Aguiar J, Macek M Jr, Krebsová A, Macek M Sr, Bürk K, Tinschert S, Schreyer I, Pulst SM, Auburger G. Riess O, et al. Among authors: lunkes a. Neurogenetics. 1997 May;1(1):59-64. doi: 10.1007/s100480050009. Neurogenetics. 1997. PMID: 10735276

8

Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type Kjer.

Lunkes A, Hartung U, Magariño C, Rodríguez M, Palmero A, Rodríguez L, Heredero L, Weissenbach J, Weber J, Auburger G. Lunkes A, et al. Am J Hum Genet. 1995 Oct;57(4):968-70. Am J Hum Genet. 1995. PMID: 7573062 Free PMC article. No abstract available.

9

Mutation detection in Machado-Joseph disease using repeat expansion detection.

Lindblad K, Lunkes A, Maciel P, Stevanin G, Zander C, Klockgether T, Ratzlaff T, Brice A, Rouleau GA, Hudson T, Auburger G, Schalling M. Lindblad K, et al. Among authors: lunkes a. Mol Med. 1996 Jan;2(1):77-85. Mol Med. 1996. PMID: 8900536 Free PMC article.

10

Machado-Joseph disease is genetically different from Holguin dominant ataxia (SCA2).

Silveira I, Manaia A, Melki J, Magariño C, Lunkes A, Hernandez A, Gispert S, Burlet P, Rozet JM, Coutinho P, et al. Silveira I, et al. Among authors: lunkes a. Genomics. 1993 Sep;17(3):556-9. doi: 10.1006/geno.1993.1371. Genomics. 1993. PMID: 7902323

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