ライフサイエンスコーパス: sporadic Creutzfeldt-Jakob disease

1 ensitivity of 80 to 90% for the diagnosis of sporadic Creutzfeldt-Jakob disease.

2 enerally symmetric pattern of involvement in sporadic Creutzfeldt-Jakob disease.

3 ) diffusivities in the total white matter in sporadic Creutzfeldt-Jakob disease.

4 wed by the correct histological diagnosis of sporadic Creutzfeldt-Jakob disease.

5 xist in the most common human prion disease, sporadic Creutzfeldt-Jakob disease.

6 erentiating autoimmune encephalopathies from sporadic Creutzfeldt-Jakob disease.

7 tients had either inherited prion disease or sporadic Creutzfeldt-Jakob disease.

8 incorporated into the diagnostic criteria of sporadic Creutzfeldt-Jakob disease.

9 rebellar abnormalities that closely resemble sporadic Creutzfeldt-Jakob disease.

10 es and some have met diagnostic criteria for sporadic Creutzfeldt-Jakob disease.

11 ted individuals resembled those of classical sporadic Creutzfeldt-Jakob disease.

12 (Sc) exists both between and within cases of sporadic Creutzfeldt-Jakob disease.

13 olecular basis for a novel classification of sporadic Creutzfeldt-Jakob disease.

14 blot and immunohistochemistry in 19 cases of sporadic Creutzfeldt-Jakob disease.

15 ting observed in experimental, acquired, and sporadic Creutzfeldt-Jakob diseases.

16 zfeldt-Jakob disease (15 of 15 with definite sporadic Creutzfeldt-Jakob disease, 13 of 14 with probab

17 is detectable at low levels in some cases of sporadic Creutzfeldt-Jakob disease and conversely, that

18 ble spongiform encephalopathies (variant and sporadic Creutzfeldt-Jakob disease and genetic forms of

19 forms found in all of the major subtypes of sporadic Creutzfeldt-Jakob disease and in a case of iatr

20 Twenty-six patients with sporadic Creutzfeldt-Jakob disease and nine age- and gen

21 ples from patients with and patients without sporadic Creutzfeldt-Jakob disease and tested them using

22 zfeldt-Jakob disease, 13 of 14 with probable sporadic Creutzfeldt-Jakob disease, and 2 of 2 with inhe

23 al PrP aggregates derived from patients with sporadic Creutzfeldt-Jakob disease are taken up and degr

24 the prion, in brain samples from humans with sporadic Creutzfeldt-Jakob disease, as well as in rodent

25 rogeneous and may be clinically mistaken for sporadic Creutzfeldt-Jakob disease because of a negative

26 of abnormal prion protein that characterizes sporadic Creutzfeldt-Jakob disease can be found in certa

27 ting on PrP(Sc) aggregates extracted from 60 sporadic Creutzfeldt-Jakob disease (CJD) and 6 variant C

28 Fourth, protease-resistant PrPSc cores in sporadic Creutzfeldt-Jakob disease (CJD) and Gerstmann-S

29 that prions from the brains of patients with sporadic Creutzfeldt-Jakob disease (CJD) bind to very lo

30 al and molecular data from a large number of sporadic Creutzfeldt-Jakob disease (CJD) cases.

31 Sporadic Creutzfeldt-Jakob disease (CJD) is the most pre

32 ted elk and deer with those in subjects with sporadic Creutzfeldt-Jakob disease (CJD), as well as CJD

33 els of the most common human prion disorder, sporadic Creutzfeldt-Jakob disease (CJD), in which prion

34 and amniotic fluid, in a pregnant woman with sporadic Creutzfeldt-Jakob disease (CJD).

35 these were classified as either familial or sporadic Creutzfeldt-Jakob disease (CJD); there was no c

36 tensor imaging to study the white matter in sporadic Creutzfeldt-Jakob disease compared to healthy c

37 In sporadic Creutzfeldt-Jakob disease, disease-associated P

38 EEG has long been used in the diagnosis of sporadic Creutzfeldt-Jakob disease; however, the charact

39 eases cohorts (FTLD, ALS, Alzheimer disease, sporadic Creutzfeldt-Jakob disease, Huntington disease-l

40 Definite diagnosis of sporadic Creutzfeldt-Jakob disease in living patients re

41 ings from olfactory epithelium in diagnosing sporadic Creutzfeldt-Jakob disease in living patients.

42 Sporadic Creutzfeldt-Jakob disease is considered primari

43 Sporadic Creutzfeldt-Jakob disease is the most common of

44 o distinct disease phenotypes, identified as sporadic Creutzfeldt-Jakob disease (M/M2 sCJD) and spora

45 ity within the white matter of patients with sporadic Creutzfeldt-Jakob disease, mainly in the left h

46 ase (n = 59) and compare these with cases of sporadic Creutzfeldt-Jakob disease (n = 170) in the Unit

47 iseases can occur as an idiopathic disorder (sporadic Creutzfeldt-Jakob disease) or can be acquired,

48 eas extracts from the brains of familial and sporadic Creutzfeldt-Jakob disease patients produced the

49 Cumulatively, the data show that sporadic Creutzfeldt-Jakob disease PrP(Sc) is not a sing

50 of PRNP thought to confer susceptibility to sporadic Creutzfeldt-Jakob disease (rs1029273), all pati

51 list prion clinic who were suspected to have sporadic Creutzfeldt-Jakob disease (sCJD) and yet were f

52 Current cerebrospinal fluid (CSF) tests for sporadic Creutzfeldt-Jakob disease (sCJD) are based on t

53 oradic fatal insomnia (sFI) and a subtype of sporadic Creutzfeldt-Jakob disease (sCJD) identified as

54 A case of sporadic Creutzfeldt-Jakob disease (sCJD) is described i

55 Phenotypic heterogeneity in sporadic Creutzfeldt-Jakob disease (sCJD) is well docume

56 e CSF RT-QuIC differentiated 94% of cases of sporadic Creutzfeldt-Jakob disease (sCJD) MM1 from the s

57 hological studies confirmed the diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) MM1 subtype.

58 activate both hamster Sc237 prions and human sporadic Creutzfeldt-Jakob disease (sCJD) prions.

59 in misfolding, the most common subtype being sporadic Creutzfeldt-Jakob disease (sCJD), a rapidly pro

60 sfolding, with the most common subtype being sporadic Creutzfeldt-Jakob disease (sCJD), a rapidly pro

61 ly distinct subtypes have been identified in sporadic Creutzfeldt-Jakob disease (sCJD), based on the

62 cts from brains of two patients, who died of sporadic Creutzfeldt-Jakob disease (sCJD), contained eit

63 Human sporadic Creutzfeldt-Jakob disease (sCJD), endemic sheep

64 ans on bound PrP species present in control, sporadic Creutzfeldt-Jakob disease (sCJD), or variant CJ

65 served in the heart tissue of a patient with sporadic Creutzfeldt-Jakob Disease (sCJD), the most comm

66 ibodies to neuronal antigens misdiagnosed as sporadic Creutzfeldt-Jakob disease (sCJD).

67 horless PrP species has been also claimed in sporadic Creutzfeldt-Jakob disease (sCJD).

68 l and ethnic differences in individuals with sporadic Creutzfeldt-Jakob disease (sCJD).

69 are susceptible to prions from patients with sporadic Creutzfeldt-Jakob disease (sCJD).

70 mean diffusivity within the white matter in sporadic Creutzfeldt-Jakob disease, suggesting possible

71 Cases diagnosed as sporadic Creutzfeldt-Jakob disease with atypical neuropa