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Chronic Kidney Disease from Polyvinylpyrrolidone Deposition in Persons with Intravenous Drug Use | American Society of Nephrology
Aquaporin-4-dependent glymphatic solute transport in the rodent brain. - Abstract - Europe PMC
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RPA Case Study in Healthcare - Helse Vest | UiPath
كثافة رحمه الله أصلي helse vest journal - jennifernoorbergen.com
The lower airways microbiome and antimicrobial peptides in idiopathic pulmonary fibrosis differ from chronic obstructive pulmonary disease | PLOS ONE
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Functional evaluation of 16 SCHAD missense variants: Only amino acid substitutions causing congenital hyperinsulinism of infancy lead to loss‐of‐function phenotypes in vitro - Velasco - 2021 - Journal of Inherited Metabolic Disease -
كثافة رحمه الله أصلي helse vest journal - jennifernoorbergen.com
An ocular glymphatic clearance system removes β-amyloid from the rodent eye | Science Translational Medicine
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Full article: Readiness for Change and Good Translations
The lower airways microbiome and antimicrobial peptides in idiopathic pulmonary fibrosis differ from chronic obstructive pulmonary disease | PLOS ONE
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كثافة رحمه الله أصلي helse vest journal - jennifernoorbergen.com
Prevalence of patients “at risk of malnutrition” and nutritional routines among surgical and non-surgical patients at a large university hospital during the years 2008–2018 - Clinical Nutrition
RPA Case Study in Healthcare - Helse Vest | UiPath
كثافة رحمه الله أصلي helse vest journal - jennifernoorbergen.com
Familial Diarrhea Syndrome Caused by an Activating GUCY2C Mutation
Implementation of recommended trauma system criteria in south-eastern Norway: a cross-sectional hospital survey | Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine | Full Text
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A Family History of Stroke Is Associated with Increased Intima-Media Thickness in Young Ischemic Stroke - The Norwegian Stroke i
Dynamic switching between intrinsic and extrinsic mode networks as demands change from passive to active processing | Scientific Reports
Prevalence of duplications and deletions of the 22q11 DiGeorge syndrome region in a populationâ•'based sample of infants wi
PDF) Familial Diarrhea Syndrome Caused by an Activating GUCY2C Mutation