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Nr.	Year OPEN	Title	rate good	rate bad	no link	Citation
1	1991	From simplicity to complexity (1950-1990): the case of peptic ulceration--II. Animal studies.	+	-	nl	Psychosom Med 53(5):491-516 (1991)
2	1991	From simplicity to complexity (1950-1990): the case of peptic ulceration--I. Human studies.	+	-	nl	Psychosom Med 53(5):467-90 (1991)
3	2002	First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological features.	+	-	nl	BMJ 324(7352):1479-82 (2002)
4	1974	Editorial: Slow virus infections.	+	-	nl	Br Med J 2(5915):343-4 (1974)
5	1997	Prion; the unconventional slow infectious agent.	+	-	nl	J Korean Med Sci 12(1):1-8 (1997)
6	2007	Molecular biology of prion protein and its first homologous protein.	+	-	nl	J Med Invest 54(3-4):211-23 (2007)
7	1998	Bovine spongiform encephalopathy and new variant Creutzfeldt-Jakob disease.	+	-	nl	Br Med Bull 54(3):749-59 (1998)
8	2005	Psychiatric manifestations of Creutzfeldt-Jakob disease: a 25-year analysis.	+	-	nl	J Neuropsychiatry Clin Neurosci 17(4):489-95 (2005)
9	2009	The transcellular spread of cytosolic amyloids, prions, and prionoids.	+	-	nl	Neuron 64(6):783-90 (2009)
10	2006	New insights into prion structure and toxicity.	+	-	nl	Neuron 50(3):353-7 (2006)
11	2007	Neurotoxic species in prion disease: a role for PrP isoforms?	+	-	nl	J Neurochem 103(5):1709-20 (2007)
12	2006	Prion diseases of humans and farm animals: epidemiology, genetics, and pathogenesis.	+	-	nl	J Neurochem 97(6):1726-39 (2006)
13	2005	Prion protein glycosylation.	+	-	nl	J Neurochem 93(4):793-801 (2005)
14	2004	PrPc on the road: trafficking of the cellular prion protein.	+	-	nl	J Neurochem 88(4):769-81 (2004)
15	2003	Cellular prion protein function in copper homeostasis and redox signalling at the synapse.	+	-	nl	J Neurochem 86(3):538-44 (2003)
16	2002	Mayhem of the multiple mechanisms: modelling neurodegeneration in prion disease.	+	-	nl	J Neurochem 82(2):209-15 (2002)
17	1999	Cellular biology of prion diseases.	+	-	nl	Clin Microbiol Rev 12(3):429-44 (1999)
18	2002	Current perspectives on bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease.	+	-	nl	Clin Microbiol Infect 8(6):332-9 (2002)
19	2007	Prions and prion diseases: fundamentals and mechanistic details.	+	-	nl	J Microbiol Biotechnol 17(7):1059-70 (2007)
20	2006	The infectivity of transmissible spongiform encephalopathy agent at low doses: the importance of phospholipid.	+	-	nl	J Appl Microbiol 101(2):261-74 (2006)
21	1985	Nature of the scrapie agent: current status of facts and hypotheses.	+	-	nl	J Gen Virol 66 ( Pt 7)(-):1357-68 (1985)
22	1978	Slow virus infections of the nervous system: virological, immunological and pathogenetic considerations.	+	-	nl	J Gen Virol 41(1):1-25 (1978)
23	1995	Prion diseases.	+	-	nl	Microbiol Immunol 39(12):923-8 (1995)
24	2006	The expanding universe of prion diseases.	+	-	nl	PLoS Pathog 2(3):e26 (2006)
25	2002	Involvement of macrophages in the pathogenesis of transmissible spongiform encephalopathies.	+	-	nl	Dev Immunol 9(1):19-27 (2002)
26	2006	The role of the cellular prion protein in the immune system.	+	-	nl	Clin Exp Immunol 146(1):1-8 (2006)
27	2003	Variant Creutzfeldt-Jakob disease: pathology, epidemiology, and public health implications.	+	-	nl	Am J Clin Nutr 78(3 Suppl):651S-656S (2003)
28	2009	Prion variants, species barriers, generation and propagation.	+	-	nl	J Biol 8(5):47 (2009)
29	2008	Chemical and biophysical insights into the propagation of prion strains.	+	-	nl	HFSP J 2(6):332-41 (2008)
30	2010	Emergence and natural selection of drug-resistant prions.	+	-	nl	Mol Biosyst 6(7):1115-30 (2010)
31	2008	Review. The origin of the prion agent of kuru: molecular and biological strain typing.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 363(1510):3747-53 (2008) Wadsworth JD
32	2008	Review. Understanding kuru: the contribution of anthropology and medicine.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 363(1510):3715-20 (2008) Lindenbaum S
33	2008	Review. The epidemiology of kuru: monitoring the epidemic from its peak to its end.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 363(1510):3707-13 (2008) Alpers MP
34	2008	Review. Kuru and its contribution to medicine.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 363(1510):3697-700 (2008) Gajdusek DC
35	2008	Review. Lessons of kuru research: background to recent studies with some personal reflections.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 363(1510):3689-96 (2008) Collinge J
36	2008	Review. The neuropathology of kuru and variant Creutzfeldt-Jakob disease.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 363(1510):3685-7 (2008) McLean CA
37	2008	Review. The changing face of kuru: a personal perspective.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 363(1510):3679-84 (2008) Mathews JD
38	2001	Prion protein interconversions.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 356(1406):197-200; discussion 200-2 (2001)
39	2001	The molecular biology of prion propagation.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 356(1406):185-95 (2001)
40	2001	Prions and the lymphoreticular system.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 356(1406):177-84 (2001)
41	2000	Scrapie infections initiated at varying doses: an analysis of 117 titration experiments.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 355(1400):1043-50 (2000)
42	2010	The role of GPI-anchored PrP C in mediating the neurotoxic effect of scrapie prions in neurons.	+	-	nl	Curr Issues Mol Biol 12(2):119-27 (2010)
43	2010	Targeting of the prion protein to the cytosol: mechanisms and consequences.	+	-	nl	Curr Issues Mol Biol 12(2):109-18 (2010)
44	2010	Prion protein and metal interaction: physiological and pathological implications.	+	-	nl	Curr Issues Mol Biol 12(2):99-107 (2010)
45	2010	Autophagy, prion infection and their mutual interactions.	+	-	nl	Curr Issues Mol Biol 12(2):87-97 (2010)
46	2010	Prion neurotoxicity: insights from prion protein mutants.	+	-	nl	Curr Issues Mol Biol 12(2):51-61 (2010)
47	1999	Cell biological studies of the prion protein.	+	-	nl	Curr Issues Mol Biol 1(1-2):65-75 (1999)
48	2008	Physiology of the prion protein.	+	-	nl	Physiol Rev 88(2):673-728 (2008)
49	1991	Prions and prion proteins.	+	-	nl	FASEB J 5(13):2799-807 (1991)
50	2008	Prion diseases: from protein to cell pathology.	+	-	nl	Am J Pathol 172(3):555-65 (2008)
51	1995	Etiology and pathogenesis of prion diseases.	+	-	nl	Am J Pathol 146(4):785-811 (1995)
52	1972	Subacute spongiform virus encephalopathies. Scrapie, Kuru and Creutzfeldt-Jakob disease: a review.	+	-	nl	Am J Pathol 68(3):626-52 (1972)
53	2006	Emerging pharmacotherapies for Creutzfeldt-Jakob disease.	+	-	nl	Arch Neurol 63(4):497-501 (2006)
54	2005	Human prion diseases: molecular and clinical aspects.	+	-	nl	Arch Neurol 62(4):545-52 (2005)
55	1999	Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting.	+	-	nl	Arch Neurol 56(3):357-62 (1999)
56	2004	Prions in control of cell glycosylation.	+	-	nl	Biochem J 380(Pt 2):e5-6 (2004) Hounsell EF
57	1990	Prion liposomes.	+	-	nl	Biochem J 266(1):1-14 (1990)
58	2006	Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.	+	-	nl	Brain 129(Pt 9):2297-317 (2006)
59	2006	A systematic review of prion therapeutics in experimental models.	+	-	nl	Brain 129(Pt 9):2241-65 (2006)
60	1999	How to improve the clinical diagnosis of Creutzfeldt-Jakob disease.	+	-	nl	Brain 122 ( Pt 12)(-):2345-51 (1999)
61	2000	Pathogenesis of prion diseases: a progress report.	+	-	nl	Cell Death Differ 7(10):889-902 (2000)
62	2006	Prion disease genetics.	+	-	nl	Eur J Hum Genet 14(3):273-81 (2006)
63	2002	A critical review of the nature of the spongiform encephalopathy agent: protein theory versus virus theory.	+	-	nl	Exp Biol Med (Maywood) 227(1):4-19 (2002)
64	2001	Lingering doubts about spongiform encephalopathy and Creutzfeldt-Jakob disease.	+	-	nl	Exp Biol Med (Maywood) 226(7):640-52 (2001)
65	2001	A critical review of atypical cerebellum-type Creutzfeldt-Jakob disease: its relationship to "new variant" CJD and bovine spongiform encephalopathy.	+	-	nl	Exp Biol Med (Maywood) 226(7):629-39 (2001)
66	2009	Transmissible mink encephalopathy - review of the etiology of a rare prion disease.	+	-	nl	Folia Neuropathol 47(2):195-204 (2009)
67	2009	Cannibalism, kuru and anthropology.	+	-	nl	Folia Neuropathol 47(2):138-44 (2009)
68	2009	Kuru and D. Carleton Gajdusek: a close encounter.	+	-	nl	Folia Neuropathol 47(2):114-37 (2009)
69	2009	Thoughts on mammalian prion strains.	+	-	nl	Folia Neuropathol 47(2):104-13 (2009)
70	2009	Reflections on a half-century in the field of transmissible spongiform encephalopathy.	+	-	nl	Folia Neuropathol 47(2):95-103 (2009)
71	2008	Prion diseases: a riddle wrapped in a mystery inside an enigma.	+	-	nl	Folia Neuropathol 46(2):93-116 (2008)
72	2008	Cell death and autophagy in prion diseases (transmissible spongiform encephalopathies).	+	-	nl	Folia Neuropathol 46(1):1-25 (2008)
73	2006	Variant CJD (vCJD) and bovine spongiform encephalopathy (BSE): 10 and 20 years on: part 2.	+	-	nl	Folia Neuropathol 44(2):102-10 (2006)
74	2006	Variant CJD (vCJD) and bovine spongiform encephalopathy (BSE): 10 and 20 years on: part 1.	+	-	nl	Folia Neuropathol 44(2):93-101 (2006)
75	2005	Neurodegeneration and oxidative stress: prion disease results from loss of antioxidant defence.	+	-	nl	Folia Neuropathol 43(4):229-43 (2005)
76	2004	Prions: proteins as genes and infectious entities.	+	-	nl	Genes Dev 18(5):470-85 (2004)
77	2005	Unraveling prion structures and biological functions.	+	-	nl	Genome Biol 6(13):366 (2005)
78	2005	Prions and the blood and immune systems.	+	-	nl	Haematologica 90(4):542-8 (2005)
79	1997	Human prion diseases and bovine spongiform encephalopathy (BSE).	+	-	nl	Hum Mol Genet 6(10):1699-705 (1997)
80	1995	Prion protein isoforms, a convergence of biological and structural investigations.	+	-	nl	J Biol Chem 270(33):19197-200 (1995)
81	1976	Scrapie: a review of its relation to human disease and ageing.	+	-	nl	J Med Genet 13(6):479-95 (1976)
82	2005	Molecular neurology of prion disease.	+	-	nl	J Neurol Neurosurg Psychiatry 76(7):906-19 (2005)
83	2004	Prion diseases.	+	-	nl	J Neurol Neurosurg Psychiatry 75 Suppl 1(-):i36-42 (2004)
84	1991	The spongiform encephalopathies.	+	-	nl	J Neurol Neurosurg Psychiatry 54(9):761-3 (1991)
85	2001	The molecular pathology of CJD: old and new variants.	+	-	nl	Mol Pathol 54(6):393-9 (2001)
86	1997	Creutzfeldt-Jakob disease in the elderly.	+	-	nl	Postgrad Med J 73(863):557-9 (1997)
87	1979	Slow viruses and chronic disease of the central nervous system.	+	-	nl	Postgrad Med J 55(640):143-9 (1979)
88	1978	Creutzfeldt--Jakob disease.	+	-	nl	Postgrad Med J 54(635):591-4 (1978)
89	2008	Prions in the environment: occurrence, fate and mitigation.	+	-	nl	Prion 2(4):162-9 (2008)
90	2007	An emerging concept of prion infections as a form of transmissible cerebral amyloidosis.	+	-	nl	Prion 1(4):223-7 (2007)
91	2007	Biological roles of prion domains.	+	-	nl	Prion 1(4):228-35 (2007)
92	2007	A structural overview of the vertebrate prion proteins.	+	-	nl	Prion 1(3):185-97 (2007)
93	2007	Prion stability.	+	-	nl	Prion 1(3):170-8 (2007)
94	2007	Prion-prion interactions.	+	-	nl	Prion 1(3):161-9 (2007)
95	2007	Yeast prions: evolution of the prion concept.	+	-	nl	Prion 1(2):94-100 (2007)
96	2007	Prions and related phenomena.	+	-	nl	Prion 1(2):81-2 (2007)
97	2007	Antiprion drugs as chemical tools to uncover mechanisms of prion propagation.	+	-	nl	Prion 1(1):48-52 (2007)
98	1998	Prions.	+	-	nl	Proc Natl Acad Sci U S A 95(23):13363-83 (1998)
99	1994	Inherited prion diseases.	+	-	nl	Proc Natl Acad Sci U S A 91(11):4611-4 (1994)
100	1994	Neurodegeneration in humans caused by prions.	+	-	nl	West J Med 161(3):264-72 (1994)
101	1988	Creutzfeldt-Jakob disease, 1988.	+	-	nl	West J Med 148(3):328-9 (1988)
102	2004	Mammalian prion biology: one century of evolving concepts.	+	-	nl	Cell 116(2):313-27 (2004)
103	1998	Prion protein biology.	+	-	nl	Cell 93(3):337-48 (1998)
104	2000	Prions: Portable prion domains.	+	-	nl	Curr Biol 10(9):R335-7 (2000)
105	2002	The utility of prions.	+	-	nl	Dev Cell 2(2):143-51 (2002)
106	2002	Prion diseases: pathogenesis and public health concerns.	+	-	nl	FEBS Lett 529(1):17-21 (2002)
107	2002	Cellular prion protein: on the road for functions.	+	-	nl	FEBS Lett 512(1-3):25-8 (2002)
108	1999	Prion protein interconversions and the transmissible spongiform encephalopathies.	+	-	nl	Structure 7(10):R231-40 (1999)
109	1994	MR diagnosis of Creutzfeldt-Jakob disease: significance of high signal intensity of the basal ganglia.	+	-	nl	AJR Am J Roentgenol 162(1):137-40 (1994)
110	2005	Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: the clinical phenotype of the "Heidenhain variant".	+	-	nl	Br J Ophthalmol 89(10):1341-2 (2005)
111	2006	Diffusion-weighted MR imaging of early-stage Creutzfeldt-Jakob disease: typical and atypical manifestations.	+	-	nl	Radiographics 26 Suppl 1(-):S191-204 (2006)
112	2009	Molecular pathology of human prion diseases.	+	-	nl	Int J Mol Sci 10(3):976-99 (2009)
113	2001	Insights into the physiological function of cellular prion protein.	+	-	nl	Braz J Med Biol Res 34(5):585-95 (2001)
114	2001	Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public health.	+	-	nl	CMAJ 165(1):51-8 (2001)
115	2005	Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis.	+	-	nl	AJNR Am J Neuroradiol 26(6):1551-62 (2005)
116	2002	Progress in understanding Creutzfeldt-Jakob disease.	+	-	nl	AJNR Am J Neuroradiol 23(7):1070-2 (2002)
117	2002	Emerging patterns of diffusion-weighted MR imaging in Creutzfeldt-Jakob disease: case report and review of the literature.	+	-	nl	AJNR Am J Neuroradiol 23(4):550-6 (2002)
118	2002	Molecular biology of prions.	+	-	nl	Acta Neurobiol Exp (Wars) 62(3):153-66 (2002)
119	2002	Variant Creutzfeldt-Jakob disease.	+	-	nl	Acta Neurobiol Exp (Wars) 62(3):167-73 (2002)
120	2002	Bovine spongiform encephalopathy. Update.	+	-	nl	Acta Neurobiol Exp (Wars) 62(3):183-95 (2002)
121	2002	Prion diseases: a dual view of the prion hypothesis as seen from a distance.	+	-	nl	Acta Neurobiol Exp (Wars) 62(3):197-224; discussion 224-6 (2002)
122	2008	The tubulovesicular structures - the ultrastructural hallmark for all prion diseases.	+	-	nl	Acta Neurobiol Exp (Wars) 68(1):113-21 (2008)
123	2011	Molecular pathology of human prion disease.	+	-	nl	Acta Neuropathol 121(1):69-77 (2011)
124	2011	Molecular biology and pathology of prion strains in sporadic human prion diseases.	+	-	nl	Acta Neuropathol 121(1):79-90 (2011)
125	2011	A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature.	+	-	nl	Acta Neuropathol 121(1):59-68 (2011)
126	2011	Tau, prions and Aβ: the triad of neurodegeneration.	+	-	nl	Acta Neuropathol 121(1):5-20 (2011)
127	2009	Prion protein misfolding and disease.	+	-	nl	Curr Opin Struct Biol 19(1):14-22 (2009)
128	2007	Chronic wasting disease.	+	-	nl	Biochim Biophys Acta 1772(6):610-8 (2007)
129	2007	The prion strain phenomenon: molecular basis and unprecedented features.	+	-	nl	Biochim Biophys Acta 1772(6):681-91 (2007)
130	2007	The cellular prion protein (PrP(C)): its physiological function and role in disease.	+	-	nl	Biochim Biophys Acta 1772(6):629-44 (2007)
131	2011	Self-propagation and transmission of misfolded mutant SOD1: prion or prion-like phenomenon?	+	-	nl	Cell Cycle 10(11):1711 (2011)
132	2004	A new kind of prion: a modified protein necessary for its own modification.	+	-	nl	Cell Cycle 3(2):100-3 (2004)
133	2006	Creutzfeldt-Jakob disease: a rare cause of dementia in elderly persons.	+	-	nl	Clin Infect Dis 43(3):340-6 (2006)
134	2008	Review. Reflections on amyloidosis in Papua New Guinea.	+	-	nl	Philos Trans R Soc Lond B Biol Sci 363(1510):3701-5 (2008) Westermark P
135	2006	The intriguing prion disorders.	+	-	nl	Cell Mol Life Sci 63(19-20):2342-51 (2006)
136	2009	Prions: protein aggregation and infectious diseases.	+	-	nl	Physiol Rev 89(4):1105-52 (2009)
137	2007	Prions.	+	-	nl	Biochemistry (Mosc) 72(13):1519-36 (2007)
138	2010	Redox control of prion and disease pathogenesis.	+	-	nl	Antioxid Redox Signal 12(11):1271-94 (2010)
139	2006	Self management of fatal familial insomnia. Part 1: what is FFI?	+	-	nl	MedGenMed 8(3):65 (2006)
140	2007	Neuroimaging findings in human prion disease.	+	-	nl	J Neurol Neurosurg Psychiatry 78(7):664-70 (2007)
141	2010	The prion hypothesis: from biological anomaly to basic regulatory mechanism.	+	-	nl	Nat Rev Mol Cell Biol 11(12):823-33 (2010)
142	2010	Prion-like transmission of protein aggregates in neurodegenerative diseases.	+	-	nl	Nat Rev Mol Cell Biol 11(4):301-7 (2010)

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