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Publications by L. G. Goldfarb
Transmissible Familial Creutzfeldt-Jakob Disease Associated With Five, Seven, and Eight Extra Octapeptide Coding Repeats in the PRNP Gene.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Nonsense Mutation in the Phosphofructokinase Muscle Subunit Gene Associated With Retention of Intron 10 in One of the Isolated Transcripts in Ashkenazi Jewish Patients With Tarui Disease.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Related publications
Familial Creutzfeldt-Jakob Disease With D178n-129m Mutation of PRNP Presenting as Cerebellar Ataxia Without Insomnia
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Inherited Creutzfeldt-Jakob Disease in a Dutch Patient With a Novel Five Octapeptide Repeat Insertion and Unusual Cerebellar Morphology
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Variant Creutzfeldt–Jakob Disease in a Patient With Heterozygosity at PRNP Codon 129
New England Journal of Medicine
Medicine
Astrocyte Gene Expression in Creutzfeldt-Jakob Disease.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Rapidly Progressive Creutzfeldt-Jakob Disease in Patients With Familial Mediterranean Fever
European Journal of Neurology
Neurology
Creutzfeldt–Jakob Disease
E200k Familial Creutzfeldt-Jakob Disease Presenting With Subacute Multiple Cranial Neuropathy
Open Neurology Journal
Psychiatry
Mental Health
Neurology
Early Pathology in Sleep Studies of Patients With Familial Creutzfeldt-Jakob Disease
Journal of Sleep Research
Medicine
Behavioral Neuroscience
Cognitive Neuroscience
Creutzfeldt-Jakob Disease
The Lancet
Medicine
