Results 161 to 170 of about 92,292 (242)

Exploring the use of dalfampridine (4‐aminopyridine) for treatment of ataxia in cerebellar stroke

open access: yes
PM&R, EarlyView.
Arjun Kotwal   +4 more
wiley   +1 more source

Screening, characterising and assessing malnutrition in the hospital setting: A large‐scale point prevalence survey

open access: yesNutrition &Dietetics, EarlyView.
Abstract Aim To assess the prevalence of undernutrition, overnutrition, and simultaneous malnutrition in a hospital setting, as well as undernutrition risk and dietetic intervention rates. Methods A point prevalence survey was conducted annually from 2016 to 2024 (excluding 2020–2021 due to Coronavirus Disease 2019) across three metropolitan health ...
Kate Connell   +5 more
wiley   +1 more source

Therapeutic Value of Lactobacillus gasseri 345A in Chronic Constipation. [PDF]

open access: yesNeurogastroenterol Motil
Roos S   +7 more
europepmc   +1 more source

Slow Transit Constipation: Pathophysiological Perspectives and Management Updates

open access: yesJournal of Digestive Diseases, EarlyView.
Slow transit constipation (STC) is a complex neuromuscular disorder driven by interstitial cells of Cajal (ICCs) loss and enteric neuropathy. Diagnosis relies on objective transit testing while excluding pelvic floor dysfunction. Management follows a stepwise, phenotype‐driven approach, progressing from conventional laxatives to emerging targeted ...
Athanasios Syllaios   +8 more
wiley   +1 more source

Content validation of the nursing diagnosis “Adult Disuse Syndrome”: A quantitative study

open access: yesInternational Journal of Nursing Knowledge, EarlyView.
Abstract Purpose This study aimed to establish the content validity of the proposed nursing diagnosis (ND) “Adult Disuse Syndrome” and all its components. Method This is an exploratory descriptive study of diagnostic content validation under Fehring's proposal.
Edinson Fabian Ardila‐Suárez   +2 more
wiley   +1 more source

International Guideline on the Diagnosis and Management of Pediatric Patients With Hereditary Angioedema

open access: yesAllergy, EarlyView.
ABSTRACT Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare disease characterized by unpredictable episodes of tissue swelling (angioedema), which, in most cases, occur first under the age of 18 years, and entail a significant burden of disease not only for the patients but also for their families.
Henriette Farkas   +128 more
wiley   +1 more source

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