Claudia Ponto

Robert Koch Str. 40
Goettingen, NI 37075, Germany

Last Updated: 09/26/2026

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Found 14 publications

Age at onset in genetic prion disease and the design of preventive clinical trials.

Age at onset in genetic prion disease and the design of preventive clinical trials.

Journal: Neurology

Published: November 02, 2018

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

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

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: March 14, 2016

Quantifying prion disease penetrance using large population control cohorts.

Quantifying prion disease penetrance using large population control cohorts.

Journal: Science translational medicine

Published: January 22, 2016

A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk.

A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk.

Journal: PloS one

Published: January 12, 2015

Clinical findings and diagnosis in genetic prion diseases in Germany.

Clinical findings and diagnosis in genetic prion diseases in Germany.

Journal: European journal of epidemiology

Published: December 03, 2014

Rare structural genetic variation in human prion diseases.

Rare structural genetic variation in human prion diseases.

Journal: Neurobiology of aging

Published: October 24, 2014

Cerebrospinal fluid tau levels are a marker for molecular subtype in sporadic Creutzfeldt-Jakob disease.

Cerebrospinal fluid tau levels are a marker for molecular subtype in sporadic Creutzfeldt-Jakob disease.

Journal: Neurobiology of aging

Published: October 19, 2014

Ascertainment bias causes false signal of anticipation in genetic prion disease.

Ascertainment bias causes false signal of anticipation in genetic prion disease.

Journal: American journal of human genetics

Published: April 06, 2014

Detection of infectivity in blood of persons with variant and sporadic Creutzfeldt-Jakob disease.

Detection of infectivity in blood of persons with variant and sporadic Creutzfeldt-Jakob disease.

Journal: Emerging infectious diseases

Published: January 01, 2014

A proposal of new diagnostic pathway for fatal familial insomnia.

A proposal of new diagnostic pathway for fatal familial insomnia.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: November 20, 2013

Diagnostic profiles of patients with late-onset Creutzfeldt-Jakob disease differ from those of younger Creutzfeldt-Jakob patients: a historical cohort study using data from the German National Reference Center.

Diagnostic profiles of patients with late-onset Creutzfeldt-Jakob disease differ from those of younger Creutzfeldt-Jakob patients: a historical cohort study using data from the German National Reference Center.

Journal: Journal of neurology

Published: October 17, 2013

R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia.

R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association

Published: September 17, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026