Results 1 to 10 of about 3,186,351 (135)

Chronic heart failure phenotypes in prevalent patients treated with hemodialysis: A single-center experience [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2022
Introduction/Objective. Heart failure (HF) is the main cause of morbidity and mortality of hemodialysis (HD) patients. The aim of this cross-sectional single-center study was to examine the following: 1.
Dobričić Marija   +6 more
doaj   +1 more source

Acute Kidney Injury in Hospitalized Patients with COVID-19: Risk Factors and Serum Biomarkers

open access: yesBiomedicines, 2023
Background. AKI is one of the COVID-19 complications with high prognostic significance. In our research, we studied the prognostic role of several biomarkers that could help us understand AKI pathogenesis in patients with COVID-19. Methods.
Anastasia Shchepalina   +12 more
doaj   +1 more source

Tobacco smokers as target group for complicated coronavirus infection [PDF]

open access: yesPharmacia, 2022
The aim of current study was to determine, retrospectively, possible correlations between smoking and the incidence, course severity, intubation rate, and mortality (by gender and age) in patients treated for complicated coronavirus infection in the ...
Petar Atanasov   +8 more
doaj   +3 more sources

Paroxysmal states in internal diseases

open access: yesJournal of Education, Health and Sport, 2017
Borisenko О. А., Zaitseva T. A., Stoyanov A. N., Kolesnik Е. О. Paroxysmal states in internal diseases. Journal of Education, Health and Sport. 2017;7(1):437-448. eISSN 2391-8306.  DOI http://dx.doi.org/10.5281/zenodo.293018   http://ojs.ukw.edu.pl/index.
O. A. Borisenko   +3 more
doaj   +3 more sources

Understanding the ecosystem of patients with lysosomal storage diseases in Spain: a qualitative research with patients and health care professionals

open access: yesOrphanet Journal of Rare Diseases, 2022
Background Lysosomal Storage Diseases (LSDs) are a group of Rare Diseases (RDs) caused by lysosomal enzyme deficiencies. Patients with LSDs suffer from a wide range of symptoms with a strong impact in their daily routines.
Juan de Dios García-Díaz   +4 more
doaj   +1 more source

Current HHT genetic overview in Spain and its phenotypic correlation: data from RiHHTa registry

open access: yesOrphanet Journal of Rare Diseases, 2020
Background Hereditary hemorrhagic telangiectasia (HHT) is a rare vascular disease with autosomal dominant inheritance. Disease-causing variants in endoglin (ENG) and activin A receptor type II-like 1 (ACVRL1) genes are detected in more than 90% of cases ...
Rosario Sánchez-Martínez   +12 more
doaj   +1 more source

COVID-19 – the challenge to treat a disease and not a positive RT-PCR test [PDF]

open access: yesPharmacia, 2021
The new pandemic disease COVID is quick spread worldwide.The primary method used for diagnosing of COVID-19 is detecting viral nucleic acids. The main problem with RT-PCR test is the false negative results. The negative RT-PCR does not exclude a SARS-CoV-
Maria Georgieva Moneva-Sakelarieva   +5 more
doaj   +3 more sources

Studies on the clinical significance of nonesterified and total cholesterol in urine [PDF]

open access: yes, 1981
Gas-liquid chromatographic determinations of nonesterified and total urinary cholesterol were performed in 137 normals, 264 patients with various internal diseases without evidence of neoplasias or diseases of the kidney or urinary tract, 497 patients ...
A. Pickel   +35 more
core   +2 more sources

Hepatitis C identification and treatment in rural Pennsylvania, USA

open access: yesPreventive Medicine Reports, 2021
The opioid epidemic in the United States has led to increases in hepatitis C virus (HCV) infection especially in rural communities. It is recommended that persons who inject drugs undergo screening and treatment.
Tuesdae Stainbrook   +4 more
doaj   +1 more source

Development and preliminary validation of a new screening questionnaire for identifying atopic children [PDF]

open access: yes, 2017
Background: Allergic diseases represent a frequent and increasing condition affecting children. A screening questionnaire allowing an easy identification of children with symptoms of allergic diseases may improve management and clinical outcome.
BRUSCOLINI, ALICE   +5 more
core   +1 more source

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