Kretzschmar H - Search Results

1

Atypical prion diseases in humans and animals.

Tranulis MA, Benestad SL, Baron T, Kretzschmar H. Tranulis MA, et al. Among authors: kretzschmar h. Top Curr Chem. 2011;305:23-50. doi: 10.1007/128_2011_161. Top Curr Chem. 2011. PMID: 21598097 Review.

2

Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases.

Lorenz H, Windl O, Kretzschmar HA. Lorenz H, et al. Among authors: kretzschmar ha. J Biol Chem. 2002 Mar 8;277(10):8508-16. doi: 10.1074/jbc.M110197200. Epub 2001 Dec 27. J Biol Chem. 2002. PMID: 11756421 Free article.

3

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.

Mead S, Uphill J, Beck J, Poulter M, Campbell T, Lowe J, Adamson G, Hummerich H, Klopp N, Rückert IM, Wichmann HE, Azazi D, Plagnol V, Pako WH, Whitfield J, Alpers MP, Whittaker J, Balding DJ, Zerr I, Kretzschmar H, Collinge J. Mead S, et al. Among authors: kretzschmar h. Hum Mol Genet. 2012 Apr 15;21(8):1897-906. doi: 10.1093/hmg/ddr607. Epub 2011 Dec 30. Hum Mol Genet. 2012. PMID: 22210626 Free PMC article.

4

Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.

Notari S, Strammiello R, Capellari S, Giese A, Cescatti M, Grassi J, Ghetti B, Langeveld JP, Zou WQ, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. J Biol Chem. 2008 Nov 7;283(45):30557-65. doi: 10.1074/jbc.M801877200. Epub 2008 Aug 27. J Biol Chem. 2008. PMID: 18753138 Free PMC article.

5

Report about four novel mutations in the prion protein gene.

Schelzke G, Stoeck K, Eigenbrod S, Grasbon-Frodl E, Raddatz LM, Ponto C, Kretzschmar HA, Zerr I. Schelzke G, et al. Dement Geriatr Cogn Disord. 2013;35(3-4):229-37. doi: 10.1159/000345991. Epub 2013 Mar 5. Dement Geriatr Cogn Disord. 2013. PMID: 23467330 Free article.

6

[Interesting not only as differential Alzheimer dementia diagnosis. Bovine spongiform encephalopathy and other prion diseases].

Kretzschmar H. Kretzschmar H. MMW Fortschr Med. 2000 Sep 28;142(39):34-8. MMW Fortschr Med. 2000. PMID: 11072695 Review. German.

7

Prion disease: a tale of folds and strains.

Kretzschmar H, Tatzelt J. Kretzschmar H, et al. Brain Pathol. 2013 May;23(3):321-32. doi: 10.1111/bpa.12045. Brain Pathol. 2013. PMID: 23587138 Free PMC article. Review.

8

Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions.

Saverioni D, Notari S, Capellari S, Poggiolini I, Giese A, Kretzschmar HA, Parchi P. Saverioni D, et al. J Biol Chem. 2013 Sep 27;288(39):27972-85. doi: 10.1074/jbc.M113.477547. Epub 2013 Jul 29. J Biol Chem. 2013. PMID: 23897825 Free PMC article.

9

Molecular subtype-specific clinical diagnosis of prion diseases.

Heinemann U, Krasnianski A, Meissner B, Gloeckner SF, Kretzschmar HA, Zerr I. Heinemann U, et al. Vet Microbiol. 2007 Aug 31;123(4):328-35. doi: 10.1016/j.vetmic.2007.04.002. Epub 2007 Apr 7. Vet Microbiol. 2007. PMID: 17513070

10

Genetic prion disease with codon 196 PRNP mutation: clinical and pathological findings.

Schelzke G, Eigenbrod S, Romero C, Varges D, Breithaupt M, Taratuto AL, Kretzschmar HA, Zerr I. Schelzke G, et al. Neurobiol Aging. 2011 Apr;32(4):756.e1-9. doi: 10.1016/j.neurobiolaging.2010.11.023. Epub 2011 Jan 12. Neurobiol Aging. 2011. PMID: 21232818

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