Giese A - Search Results

1

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.

Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar H. Parchi P, et al. Among authors: giese a. Ann Neurol. 1999 Aug;46(2):224-33. Ann Neurol. 1999. PMID: 10443888

2

Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.

Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, Ruf V, Windl O, Capellari S, Parchi P. Baiardi S, et al. Among authors: giese a. Acta Neuropathol. 2021 Oct;142(4):707-728. doi: 10.1007/s00401-021-02350-y. Epub 2021 Jul 29. Acta Neuropathol. 2021. PMID: 34324063 Free PMC article.

3

Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease.

Schulz-Schaeffer WJ, Giese A, Windl O, Kretzschmar HA. Schulz-Schaeffer WJ, et al. Among authors: giese a. Clin Neuropathol. 1996 Nov-Dec;15(6):353-7. Clin Neuropathol. 1996. PMID: 8937783

4

Phenotypic variability in fatal familial insomnia (D178N-129M) genotype.

Zerr I, Giese A, Windl O, Kropp S, Schulz-Schaeffer W, Riedemann C, Skworc K, Bodemer M, Kretzschmar HA, Poser S. Zerr I, et al. Among authors: giese a. Neurology. 1998 Nov;51(5):1398-405. doi: 10.1212/wnl.51.5.1398. Neurology. 1998. PMID: 9818868

5

Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene.

Skworc KH, Windl O, Schulz-Schaeffer WJ, Giese A, Bergk J, Nägele A, Vieregge P, Zerr I, Poser S, Kretzschmar HA. Skworc KH, et al. Among authors: giese a. Ann Neurol. 1999 Nov;46(5):693-700. Ann Neurol. 1999. PMID: 10970246

6

Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variants.

Zerr I, Schulz-Schaeffer WJ, Giese A, Bodemer M, Schröter A, Henkel K, Tschampa HJ, Windl O, Pfahlberg A, Steinhoff BJ, Gefeller O, Kretzschmar HA, Poser S. Zerr I, et al. Among authors: giese a. Ann Neurol. 2000 Sep;48(3):323-9. Ann Neurol. 2000. PMID: 10976638

7

Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.

Notari S, Capellari S, Giese A, Westner I, Baruzzi A, Ghetti B, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. Among authors: giese a. J Biol Chem. 2004 Apr 16;279(16):16797-804. doi: 10.1074/jbc.M313220200. Epub 2004 Jan 29. J Biol Chem. 2004. PMID: 14754888 Free article.

8

A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule.

Notari S, Capellari S, Langeveld J, Giese A, Strammiello R, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. Among authors: giese a. Lab Invest. 2007 Nov;87(11):1103-12. doi: 10.1038/labinvest.3700676. Epub 2007 Sep 24. Lab Invest. 2007. PMID: 17893675 Free article.

9

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. Among authors: giese a. 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.

10

Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification.

Parchi P, Strammiello R, Notari S, Giese A, Langeveld JP, Ladogana A, Zerr I, Roncaroli F, Cras P, Ghetti B, Pocchiari M, Kretzschmar H, Capellari S. Parchi P, et al. Among authors: giese a. Acta Neuropathol. 2009 Nov;118(5):659-71. doi: 10.1007/s00401-009-0585-1. Epub 2009 Aug 29. Acta Neuropathol. 2009. PMID: 19718500 Free PMC article.

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