Berger J - Search Results

1

Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophy.

Unterrainer G, Molzer B, Forss-Petter S, Berger J. Unterrainer G, et al. Among authors: berger j. Hum Mol Genet. 2000 Nov 1;9(18):2609-16. doi: 10.1093/hmg/9.18.2609. Hum Mol Genet. 2000. PMID: 11063720

2

Association of X-linked adrenoleukodystrophy with HLA DRB1 alleles.

Berger J, Bernheimer H, Faé I, Braun A, Roscher A, Molzer B, Fischer G. Berger J, et al. Biochem Biophys Res Commun. 1995 Nov 13;216(2):447-51. doi: 10.1006/bbrc.1995.2643. Biochem Biophys Res Commun. 1995. PMID: 7488132

3

X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes.

Berger J, Molzer B, Faé I, Bernheimer H. Berger J, et al. Biochem Biophys Res Commun. 1994 Dec 30;205(3):1638-43. doi: 10.1006/bbrc.1994.2855. Biochem Biophys Res Commun. 1994. PMID: 7811247

4

Simultaneous detection of the two most frequent metachromatic leukodystrophy mutations.

Berger J, Molzer B, Gieselmann V, Bernheimer H. Berger J, et al. Hum Genet. 1993 Oct;92(4):421-3. doi: 10.1007/BF01247349. Hum Genet. 1993. PMID: 7901143

5

A new polymorphism of arylsulfatase A within the coding region.

Berger J, Gmach M, Faé I, Molzer B, Bernheimer H. Berger J, et al. Hum Genet. 1996 Sep;98(3):348-50. doi: 10.1007/s004390050221. Hum Genet. 1996. PMID: 8707308

6

Late juvenile metachromatic leukodystrophy (MLD) in three patients with a similar clinical course and identical mutation on one allele.

Tylki-Szymanska A, Berger J, Löschl B, Lugowska A, Molzer B. Tylki-Szymanska A, et al. Among authors: berger j. Clin Genet. 1996 Nov;50(5):287-92. doi: 10.1111/j.1399-0004.1996.tb02376.x. Clin Genet. 1996. PMID: 9007312

7

Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophy.

Berger J, Löschl B, Bernheimer H, Lugowska A, Tylki-Szymanska A, Gieselmann V, Molzer B. Berger J, et al. Am J Med Genet. 1997 Mar 31;69(3):335-40. Am J Med Genet. 1997. PMID: 9096767

8

Elevated sulfatide excretion in compound heterozygotes of metachromatic leukodystrophy and ASA-pseudodeficiency allele.

Lugowska A, Tylki-Szymańska A, Berger J, Molzer B. Lugowska A, et al. Among authors: berger j. Clin Biochem. 1997 Jun;30(4):325-31. doi: 10.1016/s0009-9120(97)00033-7. Clin Biochem. 1997. PMID: 9209791 Clinical Trial.

9

False polymerase chain reaction-based diagnosis: is it avoidable?

Berger J, Bernheimer H, Forss-Petter S. Berger J, et al. Am J Med Genet. 1997 Oct 17;72(2):241. doi: 10.1002/(sici)1096-8628(19971017)72:2<241::aid-ajmg22>3.0.co;2-m. Am J Med Genet. 1997. PMID: 9382151 No abstract available.

10

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice.

Forss-Petter S, Werner H, Berger J, Lassmann H, Molzer B, Schwab MH, Bernheimer H, Zimmermann F, Nave KA. Forss-Petter S, et al. Among authors: berger j. J Neurosci Res. 1997 Dec 1;50(5):829-43. doi: 10.1002/(SICI)1097-4547(19971201)50:5<829::AID-JNR19>3.0.CO;2-W. J Neurosci Res. 1997. PMID: 9418970

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