B. Meissner

发表

Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance.

B. Steinhoff, K. Kallenberg, U. Heinemann, 2007, Brain : a journal of neurology.

Identification of toxic products of anthracene photomodification in simulated sunlight

B. Meissner, R. Altenburger, W. Brack, 2003, Environmental toxicology and chemistry.

MRI in the classical MM1 and the atypical MV2 subtypes of sporadic CJD: an inter‐observer agreement study

K. Kallenberg, U. Heinemann, A. Krasnianski, 2008, European journal of neurology.

Novel PRNP mutation in a patient with a slow progressive dementia syndrome.

H. Kretzschmar, U. Heinemann, A. Krasnianski, 2008, Medical science monitor : international medical journal of experimental and clinical research.

Sporadic Creutzfeldt-Jakob disease

B. Mollenhauer, B. Meissner, H. Kretzschmar, 2004, Neurology.

Brain-derived proteins in the CSF, do they correlate with brain pathology in CJD?

H. Kretzschmar, U. Heinemann, A. Krasnianski, 2006, BMC neurology.

Differenzialdiagnose rasch progredienter Demenzen

U. Heinemann, A. Krasnianski, B. Meissner, 2007 .

Fatal familial insomnia: Clinical features and early identification

U. Heinemann, A. Krasnianski, B. Meissner, 2008, Annals of neurology.

Quantitative analysis of transthyretin, tau and amyloid-beta in patients with dementia.

U. Heinemann, A. Krasnianski, B. Meissner, 2008, Journal of Alzheimer's disease : JAD.

Clinical Features and Diagnosis of the MM 2 Cortical Subtype of Sporadic Creutzfeldt-Jakob Disease

K. Kallenberg, H. Kretzschmar, U. Heinemann, 2006 .

Brain biopsy in patients with suspected Creutzfeldt-Jakob disease.

K. Kallenberg, H. Kretzschmar, U. Heinemann, 2008, Journal of neurosurgery.

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

C. Begue, R. G. Will, J. P. Brandel, 2009, Brain : a journal of neurology.

Explorer Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

G. Jansen, K. Kallenberg, P. Smith, 2016 .

Clinical Features of Rapidly Progressive Alzheimer’s Disease

H. Kretzschmar, B. Meissner, I. Zerr, 2010, Dementia and Geriatric Cognitive Disorders.

Clinical course in young patients with sporadic Creutzfeldt–Jakob disease

K. Kallenberg, H. Kretzschmar, U. Heinemann, 2005, Annals of neurology.

14-3-3 CSF levels in sporadic Creutzfeldt–Jakob disease differ across molecular subtypes

H. Kretzschmar, U. Heinemann, A. Krasnianski, 2009, Neurobiology of Aging.

MRI lesion profiles in sporadic Creutzfeldt–Jakob disease

D. Galanaud, G. Jansen, K. Kallenberg, 2009, Neurology.

MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease: a study on inter-observer agreement.

Horst Urbach, Kai Kallenberg, Michael Knauth, 2005, Brain : a journal of neurology.

MRI and clinical syndrome in dura materrelated Creutzfeldt-Jakob disease

K. Kallenberg, U. Heinemann, A. Krasnianski, 2009, Journal of Neurology.

Molecular subtype-specific clinical diagnosis of prion diseases.

H. Kretzschmar, U. Heinemann, A. Krasnianski, 2007, Veterinary microbiology.

Total prion protein levels in the cerebrospinal fluid are reduced in patients with various neurological disorders.

U. Heinemann, A. Krasnianski, B. Meissner, 2009, Journal of Alzheimer's disease : JAD.

Creutzfeldt-Jakob disease: comparative analysis of MR imaging sequences.

K. Kallenberg, B. Meissner, W. Schulz-Schaeffer, 2006, AJNR. American journal of neuroradiology.

Clinical features and diagnosis of the MM2 cortical subtype of sporadic Creutzfeldt-Jakob disease.

K. Kallenberg, H. Kretzschmar, U. Heinemann, 2006, Archives of neurology.

Sporadic Creutzfeldt–Jakob disease

K. Kallenberg, A. Krasnianski, B. Meissner, 2005, Neurology.

Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJD.

K. Kallenberg, H. Kretzschmar, U. Heinemann, 2006, Brain : a journal of neurology.

Clinical findings and diagnostic tests in Creutzfeldt-Jakob disease and variant Creutzfeldt-Jakob disease.

U. Heinemann, A. Krasnianski, B. Meissner, 2004, Folia neuropathologica.

Interleukin 4 and interleukin 10 levels are elevated in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.

U. Heinemann, B. Meissner, I. Zerr, 2005, Archives of neurology.

Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease

K. Kallenberg, U. Heinemann, A. Krasnianski, 2008, American Journal of Neuroradiology.

Pattern of Cortical Changes in Sporadic Creutzfeldt-Jakob Disease

H. Urbach, K. Kallenberg, B. Meissner, 2007, American Journal of Neuroradiology.

Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type

K. Kallenberg, H. Kretzschmar, A. Krasnianski, 2005 .

Increased frequency of positive family history of dementia in sporadic CJD

H. Kretzschmar, U. Heinemann, A. Krasnianski, 2009, Neurobiology of Aging.

Neuropsychological Symptoms in Sporadic Creutzfeldt-Jakob Disease Patients in Germany.

U. Heinemann, A. Krasnianski, B. Meissner, 2017, Journal of Alzheimer's disease : JAD.

ApoE Distribution and Family History in Genetic Prion Diseases in Germany

H. Kretzschmar, U. Heinemann, A. Krasnianski, 2007, Journal of Molecular Neuroscience.

ORIGINAL RESEARCH Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease

K. Kallenberg, U. Heinemann, A. Krasnianski, 2008 .

Total prion protein levels in the cerebrospinal fluid are reduced in patients with various neurological disorders.

U. Heinemann, A. Krasnianski, B. Meissner, 2009, Journal of Alzheimer's disease : JAD.

MRI lesion profiles in sporadic Creutzfeldt–Jakob disease

D. Galanaud, G. Jansen, K. Kallenberg, 2009, Neurology.