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Background Cellulitis is a common cause of hospital admission, yet the clinical relevance and predictors of bacteremia remain incompletely characterized. Identifying patients at risk of bloodstream infection may help optimize diagnostic strategies and clinical management. Methods We conducted a retrospective observational study at a tertiary-care hospital including all consecutive patients hospitalized with cellulitis between...
Mercury and lead legacy pollution from a coal-fired power plant recorded in lake Chiprana sedimentary record (NE Spain)NARA Subscribed
Purpose The Ebro Basin is one of the most industrialised regions of the Iberian Peninsula, yet its long-term legacy of metal contamination remains poorly constrained due to the scarcity of continuous sedimentary archives in semi-arid environments. This study reconstructs the history of mercury (Hg) and lead (Pb) pollution in the Ebro Basin using Lake Chiprana, the only permanent hypersaline lake providing a continuous, high-re...
Invasive fungal infections (IFI) are a significant cause of morbidity and mortality in hematologic malignancy patients and hematopoietic cell transplant (HCT) recipients. Mold cholecystitis has rarely been described. We present a case of disseminated Lomentospora prolificans , that had recrudescence of symptoms with acute cholecystitis. Treatment included a temporary cholecystostomy and administration of the novel antifungal f...
Decoupled Climatic Drivers of Tree and Ground‐Layer Carbon Uptake in Mountain Ecosystems Around the WorldNARA Subscribed
One of the key ecological processes affected by climate change is plant carbon uptake. However, there is substantial uncertainty about how plant carbon uptake will respond to warming in mountain ecosystems, which are known for sharp temperature gradients and abrupt shifts in vegetation structure. Specifically, we lack an understanding of whether these response trajectories over time will be linear or non‐linear, and how they m...
Functional connectivity alterations in spinocerebellar ataxia type 10: insights from gray matter atrophyNARA Subscribed
Spinocerebellar ataxia type 10 (SCA10) is a rare, inherited neurological disease caused by an expansion of the non-coding ATTCT pentanucleotide repeat in the ATAXIN 10 gene. It is characterized by cerebellar ataxia and epilepsy. Previous research has demonstrated extensive white and gray matter degeneration, particularly in the cerebellum. However, the impact of the SCA10 mutation on functional connectivity (FC) remains unexpl...