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Items: 1 to 20 of 33

1.

Anle138b: a novel oligomer modulator for disease-modifying therapy of neurodegenerative diseases such as prion and Parkinson's disease.

Wagner J, Ryazanov S, Leonov A, Levin J, Shi S, Schmidt F, Prix C, Pan-Montojo F, Bertsch U, Mitteregger-Kretzschmar G, Geissen M, Eiden M, Leidel F, Hirschberger T, Deeg AA, Krauth JJ, Zinth W, Tavan P, Pilger J, Zweckstetter M, Frank T, Bähr M, Weishaupt JH, Uhr M, Urlaub H, Teichmann U, Samwer M, Bötzel K, Groschup M, Kretzschmar H, Griesinger C, Giese A.

Acta Neuropathol. 2013 Jun;125(6):795-813. doi: 10.1007/s00401-013-1114-9. Epub 2013 Apr 19.

2.

Ethical and policy issues in genetic testing and screening of children.

COMMITTEE ON BIOETHICS; COMMITTEE ON GENETICS, AND; AMERICAN COLLEGE OF MEDICAL GENETICS AND; GENOMICS SOCIAL; ETHICAL; LEGAL ISSUES COMMITTEE.

Pediatrics. 2013 Mar;131(3):620-2. doi: 10.1542/peds.2012-3680. Epub 2013 Feb 21.

3.

Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study.

Coulthart MB, Jansen GH, Olsen E, Godal DL, Connolly T, Choi BC, Wang Z, Cashman NR.

BMC Neurol. 2011 Oct 27;11:133. doi: 10.1186/1471-2377-11-133.

4.

D178N, 129Val and N171S, 129Val genotype in a family with Creutzfeldt-Jakob disease.

Appleby BS, Appleby KK, Hall RC, Wallin MT.

Dement Geriatr Cogn Disord. 2010;30(5):424-31. doi: 10.1159/000321472. Epub 2010 Nov 12.

PMID:
21071944
5.

Atypical prion protein conformation in familial prion disease with PRNP P105T mutation.

Polymenidou M, Prokop S, Jung HH, Hewer E, Peretz D, Moos R, Tolnay M, Aguzzi A.

Brain Pathol. 2011 Mar;21(2):209-14. doi: 10.1111/j.1750-3639.2010.00439.x. Epub 2010 Sep 28.

PMID:
20875062
6.

A novel human disease with abnormal prion protein sensitive to protease.

Gambetti P, Dong Z, Yuan J, Xiao X, Zheng M, Alshekhlee A, Castellani R, Cohen M, Barria MA, Gonzalez-Romero D, Belay ED, Schonberger LB, Marder K, Harris C, Burke JR, Montine T, Wisniewski T, Dickson DW, Soto C, Hulette CM, Mastrianni JA, Kong Q, Zou WQ.

Ann Neurol. 2008 Jun;63(6):697-708. doi: 10.1002/ana.21420.

7.

Washington statewide pathology surveillance for prion disease.

Allen CT, Sonnen J, Leslie MJ, Kidoguchi L, Harris C, Gambetti P, Montine TJ.

Ann Neurol. 2007 Apr;61(4):371-2.

PMID:
17358023
8.

CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.

Sanchez-Juan P, Green A, Ladogana A, Cuadrado-Corrales N, Sáanchez-Valle R, Mitrováa E, Stoeck K, Sklaviadis T, Kulczycki J, Hess K, Bodemer M, Slivarichová D, Saiz A, Calero M, Ingrosso L, Knight R, Janssens AC, van Duijn CM, Zerr I.

Neurology. 2006 Aug 22;67(4):637-43.

PMID:
16924018
9.

Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

Mead S, Poulter M, Beck J, Webb TE, Campbell TA, Linehan JM, Desbruslais M, Joiner S, Wadsworth JD, King A, Lantos P, Collinge J.

Brain. 2006 Sep;129(Pt 9):2297-317.

PMID:
16923955
10.

Childhood onset in familial prion disease with a novel mutation in the PRNP gene.

Rogaeva E, Zadikoff C, Ponesse J, Schmitt-Ulms G, Kawarai T, Sato C, Salehi-Rad S, St George-Hyslop P, Lang AE.

Arch Neurol. 2006 Jul;63(7):1016-21.

PMID:
16831973
11.

Genetic prion disease: the EUROCJD experience.

Kovács GG, Puopolo M, Ladogana A, Pocchiari M, Budka H, van Duijn C, Collins SJ, Boyd A, Giulivi A, Coulthart M, Delasnerie-Laupretre N, Brandel JP, Zerr I, Kretzschmar HA, de Pedro-Cuesta J, Calero-Lara M, Glatzel M, Aguzzi A, Bishop M, Knight R, Belay G, Will R, Mitrova E; EUROCJD.

Hum Genet. 2005 Nov;118(2):166-74. Epub 2005 Nov 15.

PMID:
16187142
12.

High incidence of genetic human transmissible spongiform encephalopathies in Italy.

Ladogana A, Puopolo M, Poleggi A, Almonti S, Mellina V, Equestre M, Pocchiari M.

Neurology. 2005 May 10;64(9):1592-7.

PMID:
15883322
13.

PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia.

Hall DA, Leehey MA, Filley CM, Steinbart E, Montine T, Schellenberg GD, Bosque P, Nixon R, Bird T.

Neurology. 2005 Apr 12;64(7):1304-6.

PMID:
15824374
14.

Ultrastructural pathology of prion diseases revisited: brain biopsy studies.

Liberski PP, Streichenberger N, Giraud P, Soutrenon M, Meyronnet D, Sikorska B, Kopp N.

Neuropathol Appl Neurobiol. 2005 Feb;31(1):88-96.

PMID:
15634235
15.

14-3-3 {gamma}-isoform detection distinguishes sporadic Creutzfeldt-Jakob disease from other dementias.

Van Everbroeck BR, Boons J, Cras P.

J Neurol Neurosurg Psychiatry. 2005 Jan;76(1):100-2.

16.

Human prion diseases: cause, clinical and diagnostic aspects.

Knight R, Brazier M, Collins SJ.

Contrib Microbiol. 2004;11:72-97. Review. No abstract available.

PMID:
15077404
17.

Prion diseases.

Knight RS, Will RG.

J Neurol Neurosurg Psychiatry. 2004 Mar;75 Suppl 1:i36-42. Review. No abstract available.

18.

When sporadic disease is not sporadic: the potential for genetic etiology.

Goldman JS, Miller BL, Safar J, de Tourreil S, Martindale JL, Prusiner SB, Geschwind MD.

Arch Neurol. 2004 Feb;61(2):213-6.

PMID:
14967768
19.

14-3-3 protein in the CSF of patients with rapidly progressive dementia.

Huang N, Marie SK, Livramento JA, Chammas R, Nitrini R.

Neurology. 2003 Aug 12;61(3):354-7.

PMID:
12913197
20.

Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.

Gambetti P, Parchi P, Chen SG.

Clin Lab Med. 2003 Mar;23(1):43-64. Review.

PMID:
12733424

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