| P2093 | author name string | Lueck CJ | |
| | McIlwaine GG | |
| | Zeidler M | |
| P2860 | cites work | Rapidly progressive cerebral degeneration (subacute vascular encephalopathy) with mental disorder, focal disturbances, and myoclonic epilepsy | Q30496228 |
| | MRI in sporadic Creutzfeldt-Jakob disease: correlation with clinical and neuropathological data | Q32068149 |
| | Creutzfeldt-Jakob disease with congophilic kuru plaques: CT and pathological findings of the cerebral white matter | Q33591493 |
| | Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation. | Q33591914 |
| | Creutzfeldt-Jakob disease in a recipient of human pituitary-derived gonadotrophin: a second case | Q33592086 |
| | A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I: Clinical features | Q33619404 |
| | Ataxic type of Creutzfeldt-Jakob disease with disproportionate enlargement of the fourth ventricle: a serial CT study | Q33715045 |
| | A case of Creutzfeldt-Jakob disease presenting with cortical deafness | Q33732846 |
| | Accidental transmission of Creutzfeldt-Jakob disease by dural cadaveric grafts | Q33733106 |
| | Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene | Q33733564 |
| | Creutzfeldt-Jakob disease and the eye. I. Background and patient management | Q34057654 |
| | Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population | Q34242490 |
| | Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter | Q34275815 |
| | Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene | Q34577743 |
| | Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei | Q34692172 |
| | "Friendly fire" in medicine: hormones, homografts, and Creutzfeldt-Jakob disease | Q35258054 |
| | Analysis of the prion protein gene in thalamic dementia | Q48883631 |
| | Pre-mortem diagnosis of Creutzfeldt-Jakob disease by detection of abnormal cerebrospinal fluid proteins | Q48886619 |
| | Positron emission tomography in Creutzfeldt-Jakob disease | Q48908409 |
| | Creutzfeldt-Jakob disease in a recipient of human pituitary-derived gonadotrophin | Q48924259 |
| | A prion disease with a novel 96-base pair insertional mutation in the prion protein gene | Q49103297 |
| | Slowly alternating skew deviation: Description of a pretectal syndrome in three patients | Q49140529 |
| | Creutzfeldt-Jakob disease in Japan. | Q50584781 |
| | Subacute spongiform encephalopathy. Spongiform cerebral atrophy. | Q51285794 |
| | The human diffusely projecting system. Evoked potentials and interactions. | Q51286599 |
| | Subacute spongiform encephalopathy--a subacute form of encephalopathy attributable to vascular dysfunction (spongiform cerebral atrophy). | Q51306039 |
| | Creutzfeldt-Jakob disease following pituitary-derived human growth hormone therapy: a new American case. | Q52069760 |
| | Transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease). Atypical clinical and pathological findings. | Q52101205 |
| | Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum. | Q52112739 |
| | Über eine eigenartige hereditär- familiäre Erkrankung des Zentralnervensystems | Q54302676 |
| | Pruritus in Creutzfeldt-Jakob disease | Q59416964 |
| | Creutzfeldt-Jakob disease after liver transplantation | Q59690477 |
| | Creutzfeldt-Jakob disease in a beef farmer | Q59691982 |
| | Combined Neurophysiological Studies in Creutzfeldt-Jakob Disease: A Case Report | Q62782506 |
| | Creutzfeldt-Jakob disease in individual occupationally exposed to BSE. | Q64986431 |
| | Two neurological cases. Demonstration at the Royal College of Physicians of London | Q66893615 |
| | Golgi and electronmicroscopic studies of spongifom encephalopathy | Q72634829 |
| | An Israeli family with Gerstmann-Sträussler-Scheinker disease manifesting the codon 102 mutation in the prion protein gene | Q72660032 |
| | The 14-3-3 brain protein and transmissible spongiform encephalopathy | Q73160982 |
| | Creutzfeldt-Jakob disease. A survey of 14 patients | Q73454900 |
| | New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests | Q73742650 |
| | Creutzfeldt-Jakob disease: neurophysiologic visual impairments | Q77441492 |
| | Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies | Q77738553 |
| | Polyopia and monocular diplopia of cerebral origin | Q82106658 |
| | Creutzfeldt-Jakob disease in Sweden | Q36319094 |
| | Pediatric Creutzfeldt-Jakob disease: probable transmission by a dural graft | Q36773085 |
| | Creutzfeldt-Jakob disease and lyophilised dura mater grafts: report of two cases. | Q36979622 |
| | Familial cerebral amyloidosis and spongiform encephalopathy | Q37017727 |
| | Electroencephalographic and clinicopathological studies on Creutzfeldt-Jakob syndrome | Q37047136 |
| | Subacute spongiform encephalopathy and its relation to Jakob-Creutzfeldt disease: report on six cases | Q37081580 |
| | Jakob-Creutzfeldt disease. Modification of clinical and electroencephalographic activity with methylphenidate and diazepam | Q37101553 |
| | AN ATAXIC FORM OF SUBACUTE PRESENILE POLIOENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE) | Q37122173 |
| | Inherited prion disease (PrP lysine 200) in Britain: two case reports | Q38950859 |
| | Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträussler syndrome | Q39102740 |
| | A rare presenile dementia associated with cortical blindness (Heidenhain's syndrome). | Q39662196 |
| | Creutzfeldt-Jakob disease. 1. Survey of the literature and clinical diagnosis | Q39977351 |
| | Creutzfeldt-Jakob disease in France: I. Retrospective study of the Paris area during the ten-year period 1968-1977 | Q41015598 |
| | Creutzfeldt-Jakob disease presenting as Wernicke-Korsakoff syndrome | Q41110307 |
| | Familial Creutzfeldt-Jakob disease | Q41135073 |
| | Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968-1977 | Q41141412 |
| | New variant Creutzfeldt-Jakob disease: psychiatric features | Q41604119 |
| | Panencephalopathic type of Creutzfeldt-Jakob disease associated with cadaveric dura mater graft | Q41620555 |
| | A retrospective study of Creutzfeldt-Jakob disease in Italy (1972-1986). | Q41890952 |
| | Argentophilic Plaques in Creutzfeldt-Jakob Disease | Q42439500 |
| | The Heidenhain variant of Creutzfeldt-Jakob disease | Q42467154 |
| | A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease | Q42601638 |
| | Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease | Q42643435 |
| | A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease. | Q42692446 |
| | Neurosurgery in a patient with Creutzfeldt-Jakob disease after pituitary derived growth hormone therapy in childhood | Q42714827 |
| | Magnetic resonance imaging in Creutzfeldt-Jakob disease: evidence of focal involvement of the cortex | Q42911562 |
| | Pituitary growth hormone and Creutzfeldt-Jakob disease | Q43164830 |
| | Creutzfeldt-Jakob disease from contaminated growth hormone extracts in France | Q43330320 |
| | Fatal familial insomnia: clinical and pathologic study of five new cases | Q43525616 |
| | Kuru--a subacute cerebellar degeneration. The natural history and clinical features | Q43630976 |
| | Early evolution and incidence of electroencephalographic abnormalities in Creutzfeldt-Jakob disease | Q43860274 |
| | A new case of Creutzfeldt-Jakob disease associated with human growth hormone therapy in New Zealand | Q43866816 |
| | Creutzfeldt-Jakob disease in pituitary growth hormone recipients in the United States | Q44298550 |
| | Transmission of Creutzfeldt-Jakob disease from man to squirrel monkey | Q44425262 |
| | Creutzfeldt-Jakob disease via dural and corneal transplants | Q44494777 |
| | MR imaging of Creutzfeldt-Jakob disease | Q44637990 |
| | Serial computed tomographic and electroencephalographic studies in Creutzfeldt-Jakob disease | Q44986599 |
| | Gerstmann-Sträussler-Scheinker disease with coincidental familial onset | Q45080832 |
| | Autonomic dysfunction in subacute spongiform encephalopathy | Q45306381 |
| | Geotropic ocular deviation with skew and absence of saccade in Creutzfelt-Jackob disease | Q45387066 |
| | Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies | Q45794286 |
| | Kuru with incubation periods exceeding two decades | Q46878269 |
| | Neurophysiological follow-up in two children with Creutzfeldt-Jakob disease after human growth hormone treatment | Q48087083 |
| | Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease | Q48126727 |
| | Reliability of EEG in the diagnosis of Creutzfeldt-Jakob disease | Q48137105 |
| | Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: a neuropathological study | Q48146155 |
| | Creutzfeldt-Jakob disease in a pregnant woman with an implanted dura mater graft | Q48150539 |
| | Posterior cortical atrophy. Neuropathologic correlations | Q48163005 |
| | Utility of 123I-IMP SPECT brain scans for the early detection of site-specific abnormalities in Creutzfeldt-Jakob disease (Heidenhain type): a case study | Q48215655 |
| | Diffusion-weighted MRI of right-hemisphere dysfunction in Creutzfeldt-Jakob disease | Q48221182 |
| | Abnormal eye movements in Creutzfeldt-Jakob disease | Q48239479 |
| | Early MRI findings in Creutzfeldt-Jakob disease. | Q48251976 |
| | Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features | Q48269420 |
| | Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases | Q48282299 |
| | Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples. | Q48297442 |
| | Neuropathologic verification of Creutzfeldt-Jakob disease in the exhumed American recipient of human pituitary growth hormone: epidemiologic and pathogenetic implications | Q48327715 |
| | Electrophysiological and pathological studies on Creutzfeldt-Jakob disease with retinal involvement | Q48332849 |
| | Functional integrity of benzodiazepine receptors of the geniculo-striate visual pathways in Creutzfeldt-Jakob disease. A pharmacological evoked potential study. | Q48370294 |
| | MRI abnormalities in Creutzfeldt-Jakob disease. | Q48378052 |
| | Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy | Q48408594 |
| | Replication of scrapie prions in hamster eyes precedes retinal degeneration | Q48411756 |
| | An autopsied case of Creutzfeldt-Jakob disease with the lateral geniculate body lesion showing antagonizing correlation between periodic synchronous discharges and photically induced giant evoked responses | Q48422651 |
| | Creutzfeldt-Jakob disease in a young adult with idiopathic hypopituitarism. Possible relation to the administration of cadaveric human growth hormone | Q48452739 |
| | Clinical and pathological features and laboratory confirmation of Creutzfeldt-Jakob disease in a recipient of pituitary-derived human growth hormone | Q48452766 |
| | Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features | Q48477322 |
| | Retinal degeneration in experimental scrapie after intraperitoneal or subcutaneous inoculation of hamsters | Q48492535 |
| | Creutzfeldt-Jakob disease in a husband and wife | Q48499224 |
| | Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation | Q48509318 |
| | Ataxic Creutzfeldt-Jakob disease: diagnostic techniques and neuropathologic observations in early disease | Q48529603 |
| | The ataxic (cerebellar) form of Creutzfeldt-Jakob disease | Q48610000 |
| | The Ataxic Form of Creutzfeldt-Jakob Disease | Q48622482 |
| | Evolution of EEG and visual evoked response changes in Jakob-Creutzfeldt disease | Q48642552 |
| | The clinical characteristics of transmissible Creutzfeldt-Jakob disease | Q48700797 |
| | Creutzfeldt-Jakob disease in a patient with a cadaveric dural graft | Q48709979 |
| | Different susceptibilities of the geniculate and extrageniculate visual pathways to human Creutzfeldt-Jakob disease (a combined neurophysiological-neuropathological study). | Q48717046 |
| | Creutzfeldt-Jakob disease after extracranial dura mater embolization for a nasopharyngeal angiofibroma | Q48718613 |
| | Supranuclear gaze palsy in familial Creutzfeldt-Jakob disease | Q48735161 |
| | An unusual case of Creutzfeldt-Jakob disease | Q48789369 |
| | Clinical and diagnostic findings in a patient with Creutzfeldt-Jakob disease (type Heidenhain). | Q48808752 |
| | Creutzfeldt-Jakob disease: a case with extensive white matter degeneration and optic atrophy | Q48852542 |
| | Unusual electroencephalographic and clinical evolution of a case of meningioma of the left temporo-occipital convexity | Q48869376 |
| | Creutzfeldt-Jakob disease with extensive degeneration of white matter | Q67251758 |
| | Spongiform encephalopathy of long duration: a family study | Q67254388 |
| | Electrophysiologic study of 2 cases of Creutzfeldt-Jakob disease | Q67491964 |
| | Analysis of clinical and electrophysiological findings in Jakob-Creutzfeldt disease | Q67501164 |
| | Abnormal Eye Movements in Gerstmann-Sträussler-Scheinker Disease | Q67731375 |
| | Serial MR imaging in Creutzfeldt-Jakob disease | Q68017678 |
| | A case of Creutzfeldt-Jakob disease related to familial retinitis pigmentosa patients | Q68132280 |
| | Jakob-Creutzfeldt disease associated with Wernicke encephalopathy | Q68144964 |
| | Creutzfeldt-Jakob disease in children treated with growth hormone | Q68295883 |
| | Panencephalopathic type of Creutzfeldt-Jakob disease with primary extensive involvement of white matter | Q68510978 |
| | Progressive fatal dementia (Creutzfeldt-Jakob disease) in a patient who received homograft tissue for tympanic membrane closure | Q68529065 |
| | Familial Creutzfeldt-Jakob disease without periodic EEG activity | Q68622166 |
| | Is applanation tonometry a risk factor for transmission of Creutzfeldt-Jakob disease? | Q68941951 |
| | Familial spongiform glioneuronal dystrophy (author's transl) | Q69351914 |
| | Creutzfeldt-Jakob disease after administration of human growth hormone | Q69867176 |
| | Computed tomography during Creutzfeldt-Jakob disease | Q69910293 |
| | [Subacute presenile spongiforme encephalopathy with occipital predilection and cortical blindness (Heidenhain-syndrome)] | Q69930672 |
| | [Subacute spongiform encephalopathy (Jakob-Cretzfeldt syndrome). Clinico-pathological evaluation of 9 cases] | Q69948923 |
| | Creutzfeldt-Jakob disease in an adolescent | Q70197668 |
| | Creutzfeldt-Jakob disease probably acquired from a cadaveric dura mater graft. Case report | Q70222127 |
| | Case records of the massachusetts general hospital. Weekly clinicopathological exercises. Case 49-1983. A 75-year-old man with progressive dementia | Q70294444 |
| | Positron emission tomography and histopathology in Creutzfeldt-Jakob disease | Q70514781 |
| | Retinopathy in Sheep Affected with Natural Scrapie | Q70563141 |
| | Morbus Gerstmann-Sträussler-Scheinker. The Sch. family-a report of three cases (author's transl) | Q70966460 |
| | Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene | Q70987295 |
| | Antagonizing correlation between periodic synchronous discharges and photically induced giant evoked responses in Creutzfeldt--Jakob disease (Heidenhain type): a case study | Q71018045 |
| | New variant of Creutzfeldt-Jakob disease in a 26-year-old French man | Q71021168 |
| | Gerstmann-Sträussler-Scheinker's disease. Electron-microscopic observations on a brain biopsy | Q71422167 |
| | Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation) | Q71512904 |
| | Sporadic Creutzfeldt-Jakob disease in a 18-year-old in the UK | Q71520098 |
| | 18F-fluorodeoxyglucose-PET and 99mTc-bicisate-SPECT in Creutzfeldt-Jakob disease | Q71550201 |
| | Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: first report from Japan | Q71761164 |
| | Supranuclear palsy of eyelid closure | Q72129421 |
| | Homonymous field defect as the first manifestation of Creutzfeldt-Jakob disease | Q72140785 |
| | Familial Creutzfeldt-Jakob disease. Autosomal dominance in 14 members over 3 generations | Q72153224 |
| | Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 45-1980 | Q72153727 |
| | Normal EEG in Creutzfeldt-Jakob disease | Q72153773 |
| | Transmission of Creutzfeldt-Jakob disease by handling of dura mater | Q72207948 |
| | Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients | Q72319642 |
| | Magnetic resonance imaging and neuropathological findings in two patients with Creutzfeldt-Jakob disease | Q72537918 |
| | A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob disease | Q72586596 |
| | Unilateral Creutzfeldt-Jakob disease presenting as rapidly progressive aphasia | Q72587943 |
| P921 | main subject | Creutzfeldt-Jakob disease | Q49989 |
| P304 | page(s) | 291-301 | |
| P577 | publication date | 2000-06-01 | |
| P1433 | published in | Eye | Q10278937 |
| P1476 | title | Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmic features | |
| P478 | volume | 14 ( Pt 3A) | |