Pages that link to "Q49024516"
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The following pages link to Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein gene (Q49024516):
Displaying 23 items.
- First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases (Q28145109) (← links)
- PrP immunohistochemistry: different protocols, including a procedure for long formalin fixation, and a proposed schematic classification for deposits in sporadic Creutzfeldt-Jakob disease (Q33952863) (← links)
- Creutzfeldt-Jakob disease and the eye. I. Background and patient management (Q34057654) (← links)
- Cultured peripheral neuroglial cells are highly permissive to sheep prion infection (Q34553074) (← links)
- White matter involvement in sporadic Creutzfeldt-Jakob disease (Q34556043) (← links)
- Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia. (Q35122319) (← links)
- Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease (Q35486816) (← links)
- Prion disease genetics (Q36359872) (← links)
- Unusual presentations in patients with E200K familial Creutzfeldt-Jakob disease (Q36803341) (← links)
- Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis (Q37803365) (← links)
- Genetics of Prion Disease (Q37870102) (← links)
- Towards a functional pathology of hereditary neuropathies (Q39023144) (← links)
- Familial Creutzfeldt-Jakob Disease: Codon 200 Prion Disease in Libyan Jews (Q39241829) (← links)
- Genetic Creutzfeldt-Jakob disease mimicking chronic inflammatory demyelinating polyneuropathy (Q43191469) (← links)
- Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature. (Q45929842) (← links)
- Codon 200 mutation of the prion gene: genotype-phenotype correlations (Q47765383) (← links)
- Prion protein accumulation involving the peripheral nervous system in a sporadic case of Creutzfeldt-Jakob disease. (Q48136379) (← links)
- Peripheral nervous system hyperexcitability in VV2 sporadic Creutzfeldt-Jakob disease. (Q50007931) (← links)
- A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. (Q54093251) (← links)
- Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases (Q58781975) (← links)
- Severe and rapidly evolving peripheral neuropathy revealing sporadic Creutzfeldt-Jakob disease (Q62381830) (← links)
- Accumulation of prion protein in the vagus nerve in creutzfeldt-jakob disease. (Q64778987) (← links)
- Motor evoked potential studies in Creutzfeldt-Jakob disease (Q74239262) (← links)