Auburger G - 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. Among authors: auburger g. Exp Neurol. 1994 Apr;126(2):310-2. doi: 10.1006/exnr.1994.1070. Exp Neurol. 1994. PMID: 7925830

2

Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba.

Orozco Diaz G, Nodarse Fleites A, Cordovés Sagaz R, Auburger G. Orozco Diaz G, et al. Among authors: auburger g. Neurology. 1990 Sep;40(9):1369-75. doi: 10.1212/wnl.40.9.1369. Neurology. 1990. PMID: 2392220

3

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. Among authors: auburger g. Am J Hum Genet. 1995 Oct;57(4):968-70. Am J Hum Genet. 1995. PMID: 7573062 Free PMC article. No abstract available.

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: auburger g. Genomics. 1995 Jan 20;25(2):433-5. doi: 10.1016/0888-7543(95)80043-l. Genomics. 1995. PMID: 7789976

5

Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.

Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, Orozco G, Kreuz F, Weissenbach J, Auburger G. Gispert S, et al. Among authors: auburger g. Am J Hum Genet. 1995 Jan;56(1):183-7. Am J Hum Genet. 1995. PMID: 7825576 Free PMC article.

6

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus.

Belal S, Cancel G, Stevanin G, Hentati F, Khati C, Ben Hamida C, Auburger G, Agid Y, Ben Hamida M, Brice A. Belal S, et al. Among authors: auburger g. Neurology. 1994 Aug;44(8):1423-6. doi: 10.1212/wnl.44.8.1423. Neurology. 1994. PMID: 8058142

7

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. Among authors: auburger g. Hum Genet. 1993 May;91(4):362-6. doi: 10.1007/BF00217357. Hum Genet. 1993. PMID: 8099059

8

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. Genomics. 1996 Jan 1;31(1):90-4. doi: 10.1006/geno.1996.0013. Genomics. 1996. PMID: 8808284

9

Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution.

Leube B, Rudnicki D, Ratzlaff T, Kessler KR, Benecke R, Auburger G. Leube B, et al. Among authors: auburger g. Hum Mol Genet. 1996 Oct;5(10):1673-7. doi: 10.1093/hmg/5.10.1673. Hum Mol Genet. 1996. PMID: 8894706

10

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: auburger g. Nat Genet. 1996 Nov;14(3):269-76. doi: 10.1038/ng1196-269. Nat Genet. 1996. PMID: 8896555

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