Results 211 to 220 of about 663,231 (378)

Optimal antimicrobial duration for common bacterial infections [PDF]

open access: yes, 2019
Daveson, Kathryn   +2 more
core   +1 more source

A matter arising: When should inflammatory and autoimmune rheumatic diseases be considered ‘early’?

open access: yesEuropean Journal of Clinical Investigation, EarlyView.
Timely recognition of inflammatory and autoimmune rheumatic diseases (IARDs) is important to optimize the early diagnosis with tailored interventions and possible prevention of irreversible organ damage. This narrative review provides an update by summarizing the advances in identifying the early stages of rheumatoid arthritis, systemic sclerosis and ...
Elvis Hysa   +7 more
wiley   +1 more source

Exploring How Rheumatic Fever Is Portrayed on TikTok: A Descriptive Content Analysis. [PDF]

open access: yesInt J Environ Res Public Health
Tu'akoi S   +5 more
europepmc   +1 more source

Alert Card for Patients on Biologicals and Immunosuppressives: An EAACI Position Paper

open access: yes
Allergy, EarlyView.
Adam Chaker   +19 more
wiley   +1 more source

Public health reforms and the mortality decline in nineteenth‐century Italy

open access: yesThe Economic History Review, EarlyView.
Abstract This study examines the impact of Italy's 1887–8 health reforms on mortality, contributing to the historical debate on the state's role in Europe's health transition. Leveraging event‐study‐style difference‐in‐differences approach, we assess the effectiveness of the Crispi–Pagliani reforms, which strengthened public health governance and ...
Francesco Maria Salvatore Fiore Melacrinis   +1 more
wiley   +1 more source

Recurrent c.‐11C>T change located upstream of the normal ATG initiation codon of ANKH causes self‐limited familial infantile epilepsy

open access: yesEpilepsia, EarlyView.
Abstract Objective Pathogenic ANKH variants are a known cause of chondrocalcinosis (Online Mendelian Inheritance in Man [OMIM] #118600) and craniometaphyseal dysplasia (OMIM #123000). Here, we describe the phenotype and genotype of autosomal dominant infantile epilepsy caused by a c.‐11C>T change upstream of the gene's normal ATG initiation codon of ...
Josua Kegele   +7 more
wiley   +1 more source

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