Variably protease-sensitive prionopathy
Human disease
Variably protease-sensitive prionopathy (VPSPr) (formerly known as Protease Sensitive Prionopathy) is a sporadic transmissible spongiform encephalopathy first described in an abstract for a conference on prions in 2006. The study was published in a 2008 report on 11 cases.
Nº Q7915745 ★★
Poco común · Saberes
Variably protease-sensitive prionopathy
Human disease
Variably protease-sensitive prionopathy (VPSPr) (formerly known as Protease Sensitive Prionopathy) is a sporadic transmissible spongiform encephalopathy first described in an abstract for a conference on prions in 2006. The study was published in a 2008 report on 11 cases.
Último precio
—
Precio mínimo
—
Mediana 7 d
—
Ventas 30 d
0
Rango 30 d
—
En circulación
0
Cotización
mediana
mín – máx
ventas
Sin ventas en el periodo
Ver tabla
| Fecha | mediana | Mín | Máx | ventas |
|---|
Historial de ventas
- Última venta
- —
- Media 30 d
- —
- Mínimo 30 d
- —
- Máximo 30 d
- —
- Ventas 7 d
- 0
- Ventas 30 d
- 0
Aún no hay ventas.
Ventas anónimas: sin comprador ni vendedor. Las cifras solo cuentan ventas entre jugadores.
En Wikipedia
Texto en inglés Aún no hay artículo en tu idioma: extracto en inglés.
Variably protease-sensitive prionopathy (VPSPr) (formerly known as Protease Sensitive Prionopathy) is a sporadic transmissible spongiform encephalopathy first described in an abstract for a conference on prions in 2006. The study was published in a 2008 report on 11 cases. It was first identified as a distinct disease in 2010 by Zou W.Q. and coworkers from the United States National Prion Disease Pathology Surveillance Center. VPSPr shares similarities to other neurodegenerative disorders such as Creutzfeldt-Jakob disease and Alzheimer's, but there are unique markers of the disease in its clinical manifestations and electrophoretic profile.
Texto: Wikipedia en inglés, CC BY-SA 4.0. · Imagen: Rodríguez-Martínez AB, López de Munain A, Ferrer I, Zarranz... (CC BY 2.0) ·
Cartas cercanas
Progressive rubella panencephalitis
Human disease
Nº Q7248868 ★
Parálisis supranuclear progresiva
Enfermedad degenerativa cerebral
Nº Q945930 ★★★
Transmissible mink encephalopathy
Prion disease of mink
Nº Q3657255 ★
Encefalopatía espongiforme transmisible
Grupo de enfermedades generalmente neurodegenerativas presentes en varias especies producidas por priones
Nº Q703961 ★★★★
Vestibular paroxysmia
Disease
Nº Q130548951 ★
Parálisis bulbar progresiva
Condición médica
Nº Q7248833 ★★