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Items: 20

1.

Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträussler syndrome.

Nochlin D, Sumi SM, Bird TD, Snow AD, Leventhal CM, Beyreuther K, Masters CL.

Neurology. 1989 Jul;39(7):910-8.

PMID:
2500619
2.
3.

Upregulation of micro RNA-146a (miRNA-146a), a marker for inflammatory neurodegeneration, in sporadic Creutzfeldt-Jakob disease (sCJD) and Gerstmann-Straussler-Scheinker (GSS) syndrome.

Lukiw WJ, Dua P, Pogue AI, Eicken C, Hill JM.

J Toxicol Environ Health A. 2011;74(22-24):1460-8. doi: 10.1080/15287394.2011.618973.

4.

Gerstmann-Sträussler-Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt-Jakob disease: a case report and review of the literature.

Rusina R, Fiala J, Holada K, Matějčková M, Nováková J, Ampapa R, Koukolík F, Matěj R.

Neurocase. 2013;19(1):41-53. doi: 10.1080/13554794.2011.654215. Epub 2012 Apr 12.

PMID:
22494260
5.

Gerstmann meets Geschwind: a crossing (or kissing) variant of a subcortical disconnection syndrome?

Kleinschmidt A, Rusconi E.

Neuroscientist. 2011 Dec;17(6):633-44. doi: 10.1177/1073858411402093. Epub 2011 Jun 13. Review.

PMID:
21670425
6.

A disconnection account of Gerstmann syndrome: functional neuroanatomy evidence.

Rusconi E, Pinel P, Eger E, LeBihan D, Thirion B, Dehaene S, Kleinschmidt A.

Ann Neurol. 2009 Nov;66(5):654-62. doi: 10.1002/ana.21776. Erratum in: Ann Neurol. 2009 Dec;66(6):869.

PMID:
19938150
7.

A pure case of Gerstmann syndrome with a subangular lesion.

Mayer E, Martory MD, Pegna AJ, Landis T, Delavelle J, Annoni JM.

Brain. 1999 Jun;122 ( Pt 6):1107-20.

PMID:
10356063
8.

[Acquired and developmental Gerstmann syndrome. Illustration from a patient with multiple sclerosis].

Ehrlé N, Maarouf A, Chaunu MP, Sabbagh-Peignot S, Bakchine S.

Rev Neurol (Paris). 2012 Nov;168(11):852-60. doi: 10.1016/j.neurol.2011.11.006. Epub 2012 May 5. Review. French.

PMID:
22560518
9.

Writing, calculating, and finger recognition in the region of the angular gyrus: a cortical stimulation study of Gerstmann syndrome.

Roux FE, Boetto S, Sacko O, Chollet F, Trémoulet M.

J Neurosurg. 2003 Oct;99(4):716-27.

PMID:
14567608
10.

[A 68 year-old man presenting ideomotor apraxia and incomplete Gerstmann syndrome with multiple cystic lesions in the left hemisphere].

Miyaji Y, Miyasaki H, Ning Z, Watanabe D, Suzuki Y, Kuroiwa Y.

Rinsho Shinkeigaku. 2012;52(9):681-4. Japanese.

PMID:
22989905
11.

Early clinical signs and imaging findings in Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu).

Arata H, Takashima H, Hirano R, Tomimitsu H, Machigashira K, Izumi K, Kikuno M, Ng AR, Umehara F, Arisato T, Ohkubo R, Nakabeppu Y, Nakajo M, Osame M, Arimura K.

Neurology. 2006 Jun 13;66(11):1672-8.

PMID:
16769939
12.
13.

A New Transgenic Mouse Model of Gerstmann-Straussler-Scheinker Syndrome Caused by the A117V Mutation of PRNP.

Yang W, Cook J, Rassbach B, Lemus A, DeArmond SJ, Mastrianni JA.

J Neurosci. 2009 Aug 12;29(32):10072-80. doi: 10.1523/JNEUROSCI.2542-09.2009.

14.

Gerstmann-Sträussler-Scheinker syndrome masquerading as multiple sclerosis.

Karmon Y, Kurzweil A, Lindzen E, Holmlund T, Weinstock-Guttman B.

J Neurol Sci. 2011 Oct 15;309(1-2):55-7. doi: 10.1016/j.jns.2011.07.028. Epub 2011 Aug 11.

PMID:
21839476
15.

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome.

Hsiao K, Baker HF, Crow TJ, Poulter M, Owen F, Terwilliger JD, Westaway D, Ott J, Prusiner SB.

Nature. 1989 Mar 23;338(6213):342-5.

PMID:
2564168
16.

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome.

Goldgaber D, Goldfarb LG, Brown P, Asher DM, Brown WT, Lin S, Teener JW, Feinstone SM, Rubenstein R, Kascsak RJ, et al.

Exp Neurol. 1989 Nov;106(2):204-6.

PMID:
2572450
17.

[Incomplete Gerstmann syndrome with a cerebral infarct in the left middle frontal gyrus].

Ando Y, Sawada M, Morita M, Kawamura M, Nakano I.

Rinsho Shinkeigaku. 2009 Sep;49(9):560-5. Japanese.

PMID:
19928685
18.

Findings in the Gerstmann-Sträussler-Scheinker syndrome in an 18F-FDG PET-CT study.

Achury C, Camacho V, Fernández A, Gómez-Ansón B, Jaller R, Carrió I.

Rev Esp Med Nucl Imagen Mol. 2012 Nov-Dec;31(6):352-3. doi: 10.1016/j.remn.2012.04.002. Epub 2012 May 31. English, Spanish. No abstract available.

19.

Loss of anti-Bax function in Gerstmann-Sträussler-Scheinker syndrome-associated prion protein mutants.

Jodoin J, Misiewicz M, Makhijani P, Giannopoulos PN, Hammond J, Goodyer CG, LeBlanc AC.

PLoS One. 2009 Aug 14;4(8):e6647. doi: 10.1371/journal.pone.0006647.

20.

A distinct phenotype of leg hyperreflexia in a Japanese family with Gerstmann-Sträussler-Scheinker syndrome (P102L).

Takazawa T, Ikeda K, Ito H, Aoyagi J, Nakamura Y, Miura K, Iwamoto K, Kano O, Kawabe K, Iwasaki Y.

Intern Med. 2010;49(4):339-42. Epub 2010 Feb 15.

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