Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias

نویسندگان

  • Katharina Stoeck
  • Pascual Sanchez-Juan
  • Joanna Gawinecka
  • Alison Green
  • Anna Ladogana
  • Maurizio Pocchiari
  • Raquel Sanchez-Valle
  • Eva Mitrova
  • Theodor Sklaviadis
  • Jerzy Kulczycki
  • Dana Slivarichova
  • Albert Saiz
  • Miguel Calero
  • Richard Knight
  • Adriano Aguzzi
  • Jean-Louis Laplanche
  • Katell Peoc’h
  • Gabi Schelzke
  • Andre Karch
  • Cornelia M. van Duijn
  • Inga Zerr
چکیده

Citation for published version: Stoeck, K, Sanchez-Juan, P, Gawinecka, J, Green, A, Ladogana, A, Pocchiari, M, Sanchez-Valle, R, Mitrova, E, Sklaviadis, T, Kulczycki, J, Slivarichova, D, Saiz, A, Calero, M, Knight, R, Aguzzi, A, Laplanche, J-L, Peoc'h, K, Schelzke, G, Karch, A, van Duijn, CM & Zerr, I 2012, 'Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years' Brain, vol 135, no. 10, pp. 3051-3061., 10.1093/brain/aws238

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Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt–Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years

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Op-brai120155 3051..3061

Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt–Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years Katharina Stoeck, Pascual Sanchez-Juan, Joanna Gawinecka, Alison Green, Anna Ladogana, Maurizio Pocchiari, Raquel Sanchez-Valle, Eva Mitrova, Theodor Sklaviadis, Jerzy Kulczycki, Dana Slivarichova, Albert Saiz, Miguel Calero, Richard Knight, Adriano ...

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CSF lactate dehydrogenase activity in patients with Creutzfeldt-Jakob disease exceeds that in other dementias.

The diagnosis of Creutzfeldt-Jakob disease (CJD) is still made by exclusion of other dementias. We now evaluated lactate dehydrogenase (LDH) in the cerebrospinal fluid (CSF) as a possible additional diagnostic tool. CSF LDH levels of patients with CJD (n = 26) were compared with those in other dementias (n = 28). LDH isoenzymes were determined in a subset (n = 9). Total LDH and isoenzyme LDH-1 ...

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Creutzfeldt-Jakob disease accounts for more than 90% of all sporadic prion disease cases. The molecular MM2 genotype has been divided into cortical and thalamic subtypes based on structures involved and is characterized clinically by progressive dementia without ataxia or typical electroencephalography changes. Proposed diagnostic criteria for MM2 cortical type sporadic Creutzfeldt-Jakob diseas...

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تاریخ انتشار 2016