Results 121 to 130 of about 7,037 (201)

Investigating the clinical correlation between sporadic Creutzfeldt Jakob disease and presence of other neurodegenerative pathologies [PDF]

INTRODUCTION: Sporadic Creutzfeldt Jakob Disease (sCJD) is a rapidly progressive and fatal neurodegenerative disorder. Age-specific mortality rates for sCJD have increased up to 65-79 years over the past four decades. Of interest is an apparent reduced
Lumsden, Jane Rebecca
core   +1 more source

Report of the Working Group `Overall Blood Supply Strategy with Regard to Variant Creutzfeldt-Jakob Disease (vCJD)' [PDF]

, 2009
von Koenig, Carl-Heinz Wirsing, Seitz, Rainer, Schlenkrich, Uwe, Gröner, Albrecht, Zerr, Inga, von Dewitz, Christian, Kretzschmar, Hans A., Bluemel, Johannes, Groener, Albrecht, Beekes, Michael, Strobel, Johanna, Heiden, Margarethe, Nuebling, Micha, Willkommen, Hannelore, Dewitz, Christian von, Blümel, Johannes, Burger, Reinhard, Kretzschmar, Hans, Wirsing von König, Carl-Heinz, Schottstedt, Volkmar   +19 more
core   +1 more source

Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy

, 2019
Sporadic Creutzfeldt-Jakob disease (CJD) is a rare neurodegenerative disease caused by prions that is randomly distributed in all countries, with an overall yearly mortality rate of about 1-2 cases per million people.
Capellari, Sabina, Puopolo, Maria, Fedele, Alberto, Biggeri, Annibale, Tiple, Dorina, Sanguedolce, Antonio, Turco, Giuseppa Lucia, Aprile, Valerio, Pocchiari, Maurizio, Colaizzo, Elisa, Ladogana, Anna, Parchi, Piero, Catelan, Dolores, Vaianella, Luana   +13 more
core   +1 more source

Evidence for sporadic Creutzfeldt-Jakob disease being an acquired disease [PDF]

, 2019
Sporadic Creutzfeldt-Jakob Disease (sCJD) is the most common form of human prion disease. It is a rapidly progressive dementia with other associated neurological abnormalities which is invariably fatal, usually within 4-6 months of first symptoms, and
Urwin, Patrick James Michael
core  

Development of a sensitive cell culture system to assess prion infectivity and the efficacy of prion decontamination technologies

, 2012
Creutzfeldt-Jakob disease (CJD) can be iatrogenically transmitted during transplants, grafts and transfusions from CJD infected donors and also contaminated surgical instruments.
Secker, Thomas
core  

The clinical analysis of 3 patients diagnosed with sporadic Creutzfeldt-Jakob disease: A case report. [PDF]

Medicine (Baltimore)
Abulimiti G, Yasheng A, Jiamaliding H, Abudula X, Ma X, Yibulaiyin H.   +5 more
europepmc   +1 more source

Sporadic Creutzfeldt Jakob disease

, 2010
P. GAMBETTI, PUOTI, Gianfranco, I. CALI, Q. KONG, WQ ZOU   +4 more
openaire   +3 more sources

Sporadic Creutzfeldt-Jakob Disease With Spinal Cord Lesions: A Case Report. [PDF]

Cureus
Akanuma H, Kanai K.
europepmc   +1 more source

Diagnosis of Sporadic Creutzfeldt-Jakob Disease in Both Kidney Recipients From the Same Donor: Was It Graft Transmission? [PDF]

Cureus
Ponczek MM, Jakubowska Z, Wojtaszek E, Malyszko J.   +3 more
europepmc   +1 more source

First Suspected Case of Sporadic Creutzfeldt-Jakob Disease in Syria. [PDF]

Int Med Case Rep J
Tarboosh H, Mansour R, Haidar N, Ghulam P, Gergy R, Nafla F.   +5 more
europepmc   +1 more source