Results 11 to 20 of about 7,669 (173)

Alice in Wonderland Syndrome as a Presenting Manifestation of Creutzfeldt-Jakob Disease [PDF]

Frontiers in Neurology, 2019
Background: Alice in Wonderland syndrome (AIWS) is a rare neurological disorder characterized by distortions of visual perception (metamorphopsias), the body image, and the experience of time, along with derealization and depersonalization.
Tirza Naarden, Bastiaan C. ter Meulen, Bastiaan C. ter Meulen, Sarah I. van der Weele, Jan Dirk Blom, Jan Dirk Blom, Jan Dirk Blom   +6 more
doaj   +4 more sources

Alice in wonderland syndrome as a manifestation of Creutzfeldt-Jakob disease

Annals of Indian Academy of Neurology, 2023
Shweta Pandey, D B Keerthiraj, Ravindra K Garg, Rajarshi Chakraborty   +3 more
doaj   +3 more sources

Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome [PDF]

Cureus, 2020
Corticobasal syndrome is an atypical parkinsonian syndrome consisting of a constellation of clinical findings that can be the result of various etiologies. While most cases are a result of a tauopathy, such as corticobasal degeneration, other etiologies must be considered in the evaluation of patients presenting with corticobasal syndrome. We present a
Gosden, Grant P, Okromelidze, Lela, Sandhu, Sukhwinder Johnny S, Middlebrooks, Erik H   +3 more
openaire   +2 more sources

Application value of real ⁃ time quaking ⁃ induced conversion technology in clinical diagnosis of Creutzfeldt⁃Jakob disease

Chinese Journal of Contemporary Neurology and Neurosurgery, 2023
Creutzfeldt⁃Jakob disease (CJD) is a group of clinically rare neurodegenerative diseases caused by misfolding of prion proteins, and is the most common type of human prion diseases.
Dian HE
doaj   +1 more source

Understanding the Phenotypic Heterogeneity Within the Sporadic Creutzfeldt-Jakob Disease MV1 Subtype. [PDF]

Neuropathol Appl Neurobiol
We present the clinical, pathological and prion biophysical features of three atypical cases of the MV1 subtype of sporadic Creutzfeldt–Jakob disease (sCJD). We propose that these heterozygous cases exist on a spectrum ranging from MM1‐like to VV1‐like phenotypes and recommend that subtyping be performed at pH 6.9 to avoid missing atypical or mixed ...
Nemani SK, Cortez LM, Myskiw J, Cali I, Booth SA, Jansen GH, Sim VL.   +6 more
europepmc   +2 more sources

Sporadic MM-1 Type Creutzfeldt-Jakob Disease With Hemiballic Presentation and No Cognitive Impairment Until Death: How New NCJDRSU Diagnostic Criteria May Allow Early Diagnosis

Frontiers in Neurology, 2018
Sporadic Creutzfeldt-Jakob disease is the most common human prion disorder. Although associated with heterogeneous clinical phenotypes, its distinctive feature is the presence of a rapidly progressive multidomain cognitive impairment.
Lorenzo Saraceno, Vito A. G. Ricigliano, Michele Cavalli, Alessandro Cagol, Giovanna Bosco, Fabio Moda, Paola Caroppo, Giovanni Meola, Giovanni Meola   +8 more
doaj   +1 more source

Negative Diffusion Weighted Imaging on Magnetic Resonance Imaging of the Brain in Creutzfeldt–Jakob Disease

Case Reports in Neurological Medicine, 2020
A 76-year-old Caucasian woman initially presented to the Duke Memory Disorders clinic with a 9-month history of a rapid decline in cognitive, motor, and neuropsychiatric function.
Elijah Lackey, Deepal P. Shah-Zamora, Jodi Hawes, Andy J. Liu   +3 more
doaj   +1 more source

Epilepsia partialis continua as the presenting manifestation of Creutzfeldt-Jakob disease: A video-polygraphic clinical vignette. [PDF]

Epileptic Disord
Epileptic Disorders, Volume 28, Issue 3, Page 920-924, June 2026.
Cutellè R, Pascarella A, Santoro A, Cianci V, Mammì A, Tripodi GG, Prestandrea C, Gasparini S, Ferlazzo E.   +8 more
europepmc   +2 more sources

Patients with Prion: Blocking Precautions Epidemiological

Revista de Epidemiologia e Controle de Infecção, 2017
Objective: To present the epidemiological blocking measures carried out in the hospital care of patients with Creutzfeldt-Jakob disease. Methodology: retrospective case series of four patients admitted to a referral hospital in southern Brazil, from June
Liarine Fernandes Bedin, Jaqueline Petittembert Fonseca, Ariane Baptista Monteiro, Luzia Fernandes Millão, Rita Catalina Aquino Caregnato   +4 more
doaj   +1 more source

Creutzfeldt-Jakob Disease Presenting as Posterior Reversible Encephalopathy Syndrome [PDF]

Cureus, 2020
Creutzfeldt-Jakob disease (CJD) is the most common human prion disease presenting with subacute cognitive decline. Common MRI findings for CJD include the T2 prolongation signal of the putamen and head of caudate. Diffusion-weighted MRI (DW-MRI) is considered to be the most sensitive technique for the detection of CJD-related abnormalities, especially ...
Bittar, Jan, Joshi, Parth, Genova, Justin, Yeboah, Kevin, Kafaie, Jafar   +4 more
openaire   +2 more sources