The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease.

scientific article

The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1136/JNNP.2003.030320
P932PMC publication ID1739530
P698PubMed publication ID15716521
P5875ResearchGate publication ID8015861

P50authorMartin RossorQ56850440
P2093author name stringJ Collinge
A Kennedy
K Alner
L Cipolotti
M Ron
R J Cordery
P2860cites workPrion diseases of humans and animals: their causes and molecular basisQ28209943
Response Latencies in Naming ObjectsQ28256725
The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob diseaseQ30594575
First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological featuresQ33875443
Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.Q34403513
Diagnosis of new variant Creutzfeldt-Jakob diseaseQ34508722
New variant Creutzfeldt-Jakob disease: three case reports from LeicestershireQ35455461
Distinct neuropsychological characteristics in Creutzfeldt-Jakob disease.Q35560107
A neuropsychological-neuropathological case study of variant Creutzfeldt-Jakob disease.Q38439164
BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion proteinQ39686522
Letter: Possible person-to-person transmission of Creutzfeldt-Jakob diseaseQ43826201
Creutzfeldt-Jakob disease in pituitary growth hormone recipients in the United StatesQ44298550
Molecular classification of sporadic Creutzfeldt-Jakob disease.Q44451927
Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agentQ44592404
The neuropsychological profile associated with variant Creutzfeldt-Jakob diseaseQ47668167
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsQ48138886
Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgeryQ48313194
A modified card sorting test sensitive to frontal lobe defectsQ48346552
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological featuresQ48477322
Sporadic fatal insomnia: a case studyQ48712127
Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotypeQ48786927
Fatal familial insomnia: behavioral and cognitive features.Q52048639
Creutzfeldt-Jakob disease in a young womanQ56778195
The same prion strain causes vCJD and BSEQ57092996
Florid plaques and new variant Creutzfeldt-Jakob diseaseQ59691916
Creutzfeldt-Jakob disease after administration of human growth hormoneQ69867176
Sporadic Creutzfeldt-Jakob disease in a 18-year-old in the UKQ71520098
New variant Creutzfeldt-Jakob disease: neurological features and diagnostic testsQ73742650
The relation of laterality of lesion to performance on Weigl's sorting testQ76053741
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectneuropsychologyQ3872
prion protein familyQ24724413
P304page(s)330-336
P577publication date2005-03-01
P1433published inJournal of Neurology, Neurosurgery and PsychiatryQ1599804
P1476titleThe neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease
P478volume76

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cites work (P2860)
Q49076335Clinical and therapeutic aspects of prion disease
Q38942542Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation
Q49123512Isolated cortical signal increase on MR imaging as a frequent lesion pattern in sporadic Creutzfeldt-Jakob disease
Q37328569Multiparameter MR imaging in the 6-OPRI variant of inherited prion disease.
Q38734127Neuropsychological Symptoms in Sporadic Creutzfeldt-Jakob Disease Patients in Germany
Q35619208The cognitive profile of prion disease: a prospective clinical and imaging study.
Q48157168The utility of the recognition memory test and the graded naming test for monitoring neurological patients.
Q36901944Therapeutic approaches for prion disorders
Q44853053Variant Creutzfeldt-Jakob disease: neuropsychological profile in an extended series of cases.

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