Mastrianni J - Search Results

1

Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity.

Telling GC, Parchi P, DeArmond SJ, Cortelli P, Montagna P, Gabizon R, Mastrianni J, Lugaresi E, Gambetti P, Prusiner SB. Telling GC, et al. Among authors: mastrianni j. Science. 1996 Dec 20;274(5295):2079-82. doi: 10.1126/science.274.5295.2079. Science. 1996. PMID: 8953038

2

Prion disease (PrP-A117V) presenting with ataxia instead of dementia.

Mastrianni JA, Curtis MT, Oberholtzer JC, Da Costa MM, DeArmond S, Prusiner SB, Garbern JY. Mastrianni JA, et al. Neurology. 1995 Nov;45(11):2042-50. doi: 10.1212/wnl.45.11.2042. Neurology. 1995. PMID: 7501157

3

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein.

Telling GC, Scott M, Mastrianni J, Gabizon R, Torchia M, Cohen FE, DeArmond SJ, Prusiner SB. Telling GC, et al. Among authors: mastrianni j. Cell. 1995 Oct 6;83(1):79-90. doi: 10.1016/0092-8674(95)90236-8. Cell. 1995. PMID: 7553876 Free article.

4

Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein gene.

Spudich S, Mastrianni JA, Wrensch M, Gabizon R, Meiner Z, Kahana I, Rosenmann H, Kahana E, Prusiner SB. Spudich S, et al. Among authors: mastrianni ja. Mol Med. 1995 Sep;1(6):607-13. Mol Med. 1995. PMID: 8529127 Free PMC article.

5

Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease.

Mastrianni JA, Iannicola C, Myers RM, DeArmond S, Prusiner SB. Mastrianni JA, et al. Neurology. 1996 Nov;47(5):1305-12. doi: 10.1212/wnl.47.5.1305. Neurology. 1996. PMID: 8909447

6

Isolated myoclonic alien hand as the sole presentation of pathologically established Creutzfeldt-Jakob disease: a report of two patients.

MacGowan DJ, Delanty N, Petito F, Edgar M, Mastrianni J, DeArmond SJ. MacGowan DJ, et al. Among authors: mastrianni j. J Neurol Neurosurg Psychiatry. 1997 Sep;63(3):404-7. doi: 10.1136/jnnp.63.3.404. J Neurol Neurosurg Psychiatry. 1997. PMID: 9328266 Free PMC article.

7

A transmembrane form of the prion protein in neurodegenerative disease.

Hegde RS, Mastrianni JA, Scott MR, DeFea KA, Tremblay P, Torchia M, DeArmond SJ, Prusiner SB, Lingappa VR. Hegde RS, et al. Among authors: mastrianni ja. Science. 1998 Feb 6;279(5352):827-34. doi: 10.1126/science.279.5352.827. Science. 1998. PMID: 9452375

8

The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders.

Mastrianni JA. Mastrianni JA. J Geriatr Psychiatry Neurol. 1998 Summer;11(2):78-97. doi: 10.1177/089198879801100206. J Geriatr Psychiatry Neurol. 1998. PMID: 9877529 Review.

9

Prion protein conformation in a patient with sporadic fatal insomnia.

Mastrianni JA, Nixon R, Layzer R, Telling GC, Han D, DeArmond SJ, Prusiner SB. Mastrianni JA, et al. N Engl J Med. 1999 May 27;340(21):1630-8. doi: 10.1056/NEJM199905273402104. N Engl J Med. 1999. PMID: 10341275 Free article. No abstract available.

10

The prion diseases.

Mastrianni JA, Roos RP. Mastrianni JA, et al. Semin Neurol. 2000;20(3):337-52. doi: 10.1055/s-2000-9396. Semin Neurol. 2000. PMID: 11051298 Review.

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