Enfermedad rara - Search Results - UAB Digital Repository of Documents

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Articles, 1 records found Research literature, 1 records found

Articles	1 records found

24 p, 308.6 KB

El papel de la lengua inglesa en la neología científica en español / Moreno Navarro, Aránzazu (Universidad de Jaén) ; Zagalaz Sánchez, María Luisa (Universidad de Jaén) ; González González de Mesa, Carmen (Universidad de Oviedo)
El aprendizaje de una Lengua con Fines Profesionales (LPF) se ha caracte-rizado por su auge en los últimos años pues se ha convertido en una necesidad para numerosas personas interesadas en distintos ámbitos de especialidad. [...]
The interest in learning a Language for Specific Purposes (LSP) has been expanding in recent years, as it has become a necessity for many people studying different fields of expertise. In this regard, the first objective presented focuses on analyzing the characteristics of specialized language as well as establishing the simi-larities and differences with respect to the general language. [...]
2019
Language design : journal of theoretical and experimental linguistics, Vol. 21 (2019) , p. 59-82 (Articles)

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Research literature	1 records found

279 p, 5.1 MB

Desarrollo de modelos celulares de la enfermedad de Dent para la identificación de los mecanismos fisiopatológicos que subyacen a la progresión de la enfermedad / Durán Fernández, Mónica ; Meseguer Navarro, Anna, dir. ; Sarró Tauler, Eduard, dir. ; Ariceta Iraola, Gema, dir.
La malaltia de Dent de tipus 1 és un trastorn hereditari por freqüent caracteritzat per proteïnúria de baix pes molecular, hipercalciúria i nefrocalcinosi que progressa a la malaltia renal terminal. [...]
La enfermedad de Dent de tipo 1 es un trastorno hereditario poco frecuente caracterizado por proteinuria de bajo peso molecular (PBPM), hipercalciuria y nefrocalcinosis que progresa a enfermedad renal terminal. [...]
Dent's disease type 1 is a rare inherited disorder characterized by low molecular weight proteinuria (LMWP), hypercalciuria and nephrocalcinosis that progresses to end-stage renal disease. This disease is caused by mutations in the CLCN5 gene, that codifies for CLC-5, a Cl- channel which is mainly expressed in the proximal tubule of renal cells. [...]
2020

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