Results 91 to 100 of about 1,793,959 (342)
Inhalation therapy in the next decade : Determinants of adherence to treatment in asthma and COPD [PDF]
Peer reviewedPublisher ...
Amaducci, Sandro +36 more
core +5 more sources
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann +6 more
wiley +1 more source
Paradoxical embolism represents a critical and potentially fatal complication that can be associated with pulmonary embolism (PE). This case details a unique case of massive PE, further complicated by embolic stroke occurring during catheter-directed ...
Atefeh Ghorbanzadeh +2 more
doaj +1 more source
Although rare, pneumomediastinum and pneumopericardium should be considered in patients presenting with sudden onset post‐tussive chest discomfort.
Joseph Winterton, Simon Biart
doaj +1 more source
USSR Space Life Sciences Digest, issue 15 [PDF]
This is the 15th issue of NASA's USSR Space Life Sciences Digest. It contains abstracts of 59 papers published in Russian language periodicals or presented at conferences and of two new Soviet monographs.
Garshnek, Victoria +3 more
core +1 more source
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini +13 more
wiley +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source
Editorial: Evolution in respiratory pharmacology
Barbara Ruaro +6 more
doaj +1 more source
Screening and surveillance in respiratory medicine [PDF]
Dobler, Claudia C
core +1 more source
USSR Space Life Sciences Digest, issue 30 [PDF]
This is the thirtieth issue of NASA's Space Life Sciences Digest. It contains abstracts of 47 journal papers or book chapters published in Russian and of three Soviet monographs.
Rowe, Joseph +2 more
core +2 more sources

