Müller U - Search Results

1

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.

Cossée M, Dürr A, Schmitt M, Dahl N, Trouillas P, Allinson P, Kostrzewa M, Nivelon-Chevallier A, Gustavson KH, Kohlschütter A, Müller U, Mandel JL, Brice A, Koenig M, Cavalcanti F, Tammaro A, De Michele G, Filla A, Cocozza S, Labuda M, Montermini L, Poirier J, Pandolfo M. Cossée M, et al. Among authors: muller u. Ann Neurol. 1999 Feb;45(2):200-6. doi: 10.1002/1531-8249(199902)45:2<200::aid-ana10>3.0.co;2-u. Ann Neurol. 1999. PMID: 9989622

2

Locus heterogeneity in Friedreich ataxia.

Kostrzewa M, Klockgether T, Damian MS, Müller U. Kostrzewa M, et al. Among authors: muller u. Neurogenetics. 1997 May;1(1):43-7. doi: 10.1007/s100480050007. Neurogenetics. 1997. PMID: 10735274

3

Superoxide dismutase 1: identification of a novel mutation in a case of familial amyotrophic lateral sclerosis.

Kostrzewa M, Damian MS, Müller U. Kostrzewa M, et al. Among authors: muller u. Hum Genet. 1996 Jul;98(1):48-50. doi: 10.1007/s004390050157. Hum Genet. 1996. PMID: 8682505

4

Genomic structure and complete sequence of the human FGFR4 gene.

Kostrzewa M, Müller U. Kostrzewa M, et al. Among authors: muller u. Mamm Genome. 1998 Feb;9(2):131-5. doi: 10.1007/s003359900703. Mamm Genome. 1998. PMID: 9457674

5

Autosomal dominant amyotrophic lateral sclerosis: a novel mutation in the Cu/Zn superoxide dismutase-1 gene.

Kostrzewa M, Burck-Lehmann U, Müller U. Kostrzewa M, et al. Among authors: muller u. Hum Mol Genet. 1994 Dec;3(12):2261-2. doi: 10.1093/hmg/3.12.2261. Hum Mol Genet. 1994. PMID: 7881433 No abstract available.

6

AFX1 and p54nrb: fine mapping, genomic structure, and exclusion as candidate genes of X-linked dystonia parkinsonism.

Peters U, Haberhausen G, Kostrzewa M, Nolte D, Müller U. Peters U, et al. Among authors: muller u. Hum Genet. 1997 Oct;100(5-6):569-72. doi: 10.1007/s004390050553. Hum Genet. 1997. PMID: 9341872

7

Transcript map of the chromosome 2-linked autosomal dominant spastic paraplegia (SPG4) critical region and identification of a highly informative STRP.

Lau EL, Kostrzewa M, Müller U. Lau EL, et al. Among authors: muller u. Neurogenetics. 1998 Dec;2(1):75-6. doi: 10.1007/s100480050055. Neurogenetics. 1998. PMID: 9933304 No abstract available.

8

Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia.

Nolte D, Kang JS, Hofmann A, Schwaab E, Krämer HH, Müller U. Nolte D, et al. Among authors: muller u. J Neurol. 2021 Dec;268(12):4866-4873. doi: 10.1007/s00415-021-10607-5. Epub 2021 May 26. J Neurol. 2021. PMID: 34037856 Free PMC article.

9

High penetrance and pronounced variation in expressivity of GCH1 mutations in five families with dopa-responsive dystonia.

Steinberger D, Weber Y, Korinthenberg R, Deuschl G, Benecke R, Martinius J, Müller U. Steinberger D, et al. Among authors: muller u. Ann Neurol. 1998 May;43(5):634-9. doi: 10.1002/ana.410430512. Ann Neurol. 1998. PMID: 9585358

10

Integrated physical and transcript map of 5q31.3-qter.

Kostrzewa M, Krings BW, Dixon MJ, Eppelt K, Köhler A, Grady DL, Steinberger D, Fairweather ND, Moyzis RK, Monaco AP, Müller U. Kostrzewa M, et al. Among authors: muller u. Eur J Hum Genet. 1998 May-Jun;6(3):266-74. doi: 10.1038/sj.ejhg.5200188. Eur J Hum Genet. 1998. PMID: 9781031

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

2,063 results

Search Page

Filters