Differential (Click to cross reference) affect, flat agitation agnosia, visual Alice in Wonderland syndrome alternating rapid movement, impaired anorexia arm weakness ataxia ataxia, cerebellar ataxia, progressive ataxia, truncal ataxic gait atypical Balint's syndrome basal ganglia, lesion of basal ganglia, lesion, bilateral bedridden bradykinesia CAT scan, emission, abnormal caudate nucleus, lesion of, bilateral cerebellar lesion cerebral cortex cerebrospinal fluid cerebrospinal fluid, abnormal Clinical Pathologic Conference(C.P.C.) cognition, slowed color vision, impaired Creutzfeldt-Jakob disease, genetic deep gray nuclei delay in diagnosis dementia dementia, familial dementia, presenile dementia, rapidly progressive depression difficulty climbing stairs diplopia dissociated sensory loss dizziness dysarthria dyschromatopsia dysdiadochokinesia dysmetria electroencephalogram, abnormalities of electroencephalogram, periodic complexes episodic disorders eye movement, disorders of falling false negative false positive familial fibrillations finger nose finger test gait disorder gene mutation genetic counselling genetic neurologic disorders genetic testing hallucination, visual handwriting headache headache, episodic heel-knee-shin test hemianopia, homonymous heralding manifestation hot cross bun sign hyporeflexia imbalance immunohistochemistry incoordination insomnia Jakob-Creutzfeldt disease Jakob-Creutzfeldt disease, cerebellar variant Jakob-Creutzfeldt disease, Heidenhain variant Jakob-Creutzfeldt disease, variant Jakob-Creutzfeldt disease, young adult life expectancy linear lesion macropsia memory, defect of recent memory, impairment of mental status, abnormal metamorphopsia micropsia Mini Mental Status Examination monoparesis mortality motor cortex MRI MRI pattern MRI, abnormal MRI, diffusion weighted MRI, diffusion weighted, pattern MRI, false negative MRI, negative MRI, punctate pattern MRI, spinal cord MRI, susceptibility weighted myelitis myelitis, longitudinal myelitis, transverse myelopathy myoclonic jerks myoclonus myoclonus, cortical myoclonus, stimulus sensitive nasal brushings nerve conduction studies neurologic disease, diagnoses of neuropathology neuropathology, brain neuropathy nystagmus occipital cortex occipital lobe, lesion of pathognomonic perseveration PLEDs PLEDs, bilateral independent polyneuropathy polyneuropathy, chronic inflammatory demyelinating prion disease prognosis progressive neurologic disorder proprioception prosopagnosia protein 14-3-3, cerebrospinal fluid psychiatric problems in neurologic disorders pursuit eye movements, abnormal rapidly progressing neurologic illness real-time quaking-induced conversion Romberg's sign saccadic eye movements, abnormal skin, biopsy spinal cord spinal cord, lesion of spongy degeneration of brain square wave jerks startle myoclonus symmetric brain lesions tandem gait, ataxic tau protein thalamus, lesion of-bilateral vertigo vertigo, episodic vibratory sensation vision, blurred visual distortions visual loss visual loss, progressive walking frame walking, difficulty with weakness, acute weakness, focal weight loss wide based gait workup

Showing articles 0 to 16 of 16 Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease NEJM 386;674-687, Case 5-2022, 2022 Laboratory Diagnosis of Creutzfeldt-Jakob Disease NEJM 386:1345-1350, Zerr, I., 2022 More Than a Little Unsteady NEJM 387:e9, Kraft, A.W.,et al, 2022 Sporadic Creutzfeldt-Jakob Disease in a Very Young Person Neurol 97:813-816,801, Appleby, B.S.,et al, 2021 An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome Cureus DOI:10.7759/cureus,8608, Gupta,A. & Dhingra,A., 2020 Homonymous Hemianopia with Normal Magnetic Resonance Imaging JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020 Rapid Progression of Prion Disease Associated with Transverse Myelitis Neurol 94:e1670-e1672, Hussein, O.,et al, 2020 Long Survival Sporadic Creutzfeldt-Jakob Disease Neurol 95:87-88, Liu, X.Y.,et al, 2020 A 57-Year-Old Woman with Progressive Ataxia and Falls Neurol 95:650-656, Badahdah, A., 2020 RT-QuIC: A New Test for Sporadic CJD Pract Neurol 19:49-55, Green, A.J.E., 2019 Clinicopathologic Conference, Creutzfeldt-Jakob Disease NEJM 381:1569-1578, Case 32-2019, 2019 Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples JAMA Neurol 74:155-162,144, Bongianni, M.,et al, 2017 Cerebrospinal Fluid Real-Time Quaking-Induced Conversion is a Robust and Reliable Test for Sporadic Creutzfeldt-Jakob Disease: An International Study Ann Neurol 80:160-165, McGuire, L.I.,et al, 2016 A 64-year-old Man with Visual Distortions Neurol 87:e252-e256, McGrath, E.R.,et al, 2016 Rapid and Sensitive RT-QuIC Detection of Human Creutzfeldt-Jakob Disease Using Cerebrospinal Fluid mBio 6:e02451-14, Orru,C.D.,et al, 2015 A Test for Creutzfeldt-Jakob Disease Using Nasal Brushings NEJM 371:519-529, Orru, C.D.,et al, 2014 Showing articles 0 to 16 of 16