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Changes of the microbial population structure in an overloaded fed-batch biogas reactor digesting maize silage

Bioresource technology, 2014-12, Vol.174, p.108-117

2014

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Transformation of Sulfonamides and Tetracyclines during Anaerobic Fermentation of Liquid Manure

Journal of environmental quality, 2017, Vol.46 (1), p.160-168

2017

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Methane Yields and Digestion Dynamics of Press Fluids from Mechanically Dehydrated Maize Silages Using Different Types of Digesters

Bioenergy research, 2012-06, Vol.5 (2), p.294-305

2012

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Versuchsanlage zur energetischen Beurteilung von Substraten und Kofermentaten für Biogasanlagen

Umweltwissenschaften und Schadstoff-Forschung, 2006-11, Vol.18 (4), p.219-227

Zerr, Walter

2006

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Versuchsanlage zur energetischen Beurteilung von Substraten und Kofermentaten für Biogasanlagen

Umweltwissenschaften und Schadstoff-Forschung, 2006-11, Vol.18 (4), p.219

Zerr, Walter

2006

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Validation and utilization of amended diagnostic criteria in Creutzfeldt-Jakob disease surveillance

Neurology, 2018-07, Vol.91 (4)

2018

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The real-time quaking-induced conversion assay for detection of human prion disease and study of other protein misfolding diseases

Nature protocols, 2016-11, Vol.11 (11), p.2233-2242

2016

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Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Annals of neurology, 1999-08, Vol.46 (2), p.224-233

1999

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Hereditary Human Prion Diseases: an Update

Molecular neurobiology, 2017-08, Vol.54 (6), p.4138-4149

2017

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Validation and utilization of amended diagnostic criteria in Creutzfeldt-Jakob disease surveillance

Neurology, 2018-07, Vol.91 (4), p.e331

2018

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Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease

Annals of neurology, 2004-11, Vol.56 (5), p.702-708

2004

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Deletion of cellular prion protein results in reduced akt activation, enhanced postischemic caspase-3 activation, and exacerbation of ischemic brain injury

Stroke (1970), 2006-05, Vol.37 (5), p.1296-1300

2006

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Application of an in vitro-amplification assay as a novel pre-screening test for compounds inhibiting the aggregation of prion protein scrapie

Scientific reports, 2016-07, Vol.6 (1), p.28711-28711, Article 28711

2016

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Doxycycline in early CJD: a double-blinded randomised phase II and observational study

Journal of neurology, neurosurgery and psychiatry, 2017-02, Vol.88 (2), p.119-125

2017

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Upregulation of cellular prion protein (PrP c) after focal cerebral ischemia and influence of lesion severity

Neuroscience letters, 2004-11, Vol.372 (1), p.146-150

2004

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Application of real-time quaking-induced conversion in Creutzfeldt–Jakob disease surveillance

Journal of neurology, 2023-04, Vol.270 (4), p.2149-2161

2023

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Auditory Deficits in Audiovisual Speech Perception in Adult Asperger’s Syndrome: fMRI Study

Frontiers in psychology, 2019-10, Vol.10, p.2286-2286

2019

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Proteomics Approach to Identify the Interacting Partners of Cellular Prion Protein and Characterization of Rab7a Interaction in Neuronal Cells

Journal of proteome research, 2011-07, Vol.10 (7), p.3123-3135

2011

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Current clinical diagnosis in Creutzfeldt-Jakob disease: Identification of uncommon variants

Annals of neurology, 2000-09, Vol.48 (3), p.323-329

2000

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Clinical findings and diagnosis in genetic prion diseases in Germany

European journal of epidemiology, 2016-02, Vol.31 (2), p.187-196

2016

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Filtration of Protein Aggregates Increases the Accuracy for Diagnosing Prion Diseases in Brain Biopsies

Journal of neuropathology and experimental neurology, 2013-08, Vol.72 (8), p.758-767

2013

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Cellular prion protein directly interacts with and enhances lactate dehydrogenase expression under hypoxic conditions

Experimental neurology, 2015-09, Vol.271, p.155-167

2015

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The comorbidity profiles and medication issues of patients with multiple system atrophy: a systematic cross-sectional analysis

Journal of neurology, 2024-05, Vol.271 (5), p.2639-2648

2024

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Neuropsychological Symptoms in Sporadic Creutzfeldt-Jakob Disease Patients in Germany

Journal of Alzheimer's disease, 2017-01, Vol.59 (1), p.329-337

2017

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Prevalence of Health Care and Hospital Worker SARS-CoV-2 IgG Antibody in a Pediatric Hospital

Hospital pediatrics, 2021-03, Vol.11 (3), p.e48-e53

2021

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Changes of the microbial population structure in an overloaded fed-batch biogas reactor digesting maize silage

Transformation of Sulfonamides and Tetracyclines during Anaerobic Fermentation of Liquid Manure

Methane Yields and Digestion Dynamics of Press Fluids from Mechanically Dehydrated Maize Silages Using Different Types of Digesters

Versuchsanlage zur energetischen Beurteilung von Substraten und Kofermentaten für Biogasanlagen

Versuchsanlage zur energetischen Beurteilung von Substraten und Kofermentaten für Biogasanlagen

Validation and utilization of amended diagnostic criteria in Creutzfeldt-Jakob disease surveillance

The real-time quaking-induced conversion assay for detection of human prion disease and study of other protein misfolding diseases

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Hereditary Human Prion Diseases: an Update

Validation and utilization of amended diagnostic criteria in Creutzfeldt-Jakob disease surveillance

Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease

Deletion of cellular prion protein results in reduced akt activation, enhanced postischemic caspase-3 activation, and exacerbation of ischemic brain injury

Application of an in vitro-amplification assay as a novel pre-screening test for compounds inhibiting the aggregation of prion protein scrapie

Doxycycline in early CJD: a double-blinded randomised phase II and observational study

Upregulation of cellular prion protein (PrP c) after focal cerebral ischemia and influence of lesion severity

Application of real-time quaking-induced conversion in Creutzfeldt–Jakob disease surveillance

Auditory Deficits in Audiovisual Speech Perception in Adult Asperger’s Syndrome: fMRI Study

Proteomics Approach to Identify the Interacting Partners of Cellular Prion Protein and Characterization of Rab7a Interaction in Neuronal Cells

Current clinical diagnosis in Creutzfeldt-Jakob disease: Identification of uncommon variants

Clinical findings and diagnosis in genetic prion diseases in Germany

Filtration of Protein Aggregates Increases the Accuracy for Diagnosing Prion Diseases in Brain Biopsies

Cellular prion protein directly interacts with and enhances lactate dehydrogenase expression under hypoxic conditions

The comorbidity profiles and medication issues of patients with multiple system atrophy: a systematic cross-sectional analysis

Neuropsychological Symptoms in Sporadic Creutzfeldt-Jakob Disease Patients in Germany

Prevalence of Health Care and Hospital Worker SARS-CoV-2 IgG Antibody in a Pediatric Hospital

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