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Publications by Wolfgang Stremmel

Influence of Homozygosity for Methionine at Codon 129 of the Human Prion Gene on the Onset of Neurological and Hepatic Symptoms in Wilson Disease

Archives of Neurology

English

Related publications

Creutzfeldt-Jakob Disease Associated With a Missense Mutation at Codon 200 of the Prion Protein Gene in Brazil

Dementia e Neuropsychologia

Sensory Systems

Cognitive Neuroscience

English

Variant Creutzfeldt–Jakob Disease in a Patient With Heterozygosity at PRNP Codon 129

New England Journal of Medicine

English

The Homozygosity Index (HI) Approach Reveals High Allele Frequency for Wilson Disease in the Sardinian Population

European Journal of Human Genetics

English

Recent Advances in the Manipulation of Murine Gene Expression and Its Utility for the Study of Human Neurological Disease

Biochimica et Biophysica Acta - Molecular Basis of Disease

Molecular Medicine

Molecular Biology

English

The Evolutionary Scope and Neurological Disease Linkage of Yeast-Prion-Like Proteins in Humans

Molecular Biology

Applied Mathematics

Biological Sciences

English

Impact of Methionine Oxidation as an Initial Event on the Pathway of Human Prion Protein Conversion

Molecular Neuroscience

Infectious Diseases

English

Neuropsychiatric Symptoms, Endophenotypes, and Syndromes in Late-Onset Alzheimer's Disease: Focus on APOE Gene

International Journal of Alzheimer's Disease

Cognitive Neuroscience

Molecular Neuroscience

Behavioral Neuroscience

English

A Case of Anti-Cyclic Citrullinated Peptides Antibody Positive Rheumatoid Meningitis Without Arthritis at the Onset of Neurological Symptoms

Clinical Neurology

English

Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease

American Journal of Human Genetics

English