Results 271 to 280 of about 1,683,690 (332)

Use of calcium during pregnancy: far beyond pre-eclampsia. [PDF]

open access: yesRev Bras Ginecol Obstet
Amorim MMR   +4 more
europepmc   +1 more source

One Health Genomic Analysis of Methicillin‐Resistant Staphylococcus spp. From Humans, Cats, and Dogs in a Veterinary Hospital in Central Chile

open access: yesZoonoses and Public Health, EarlyView.
ABSTRACT Introduction The emergence of methicillin‐resistant Staphylococcus species (MRS) poses a growing threat to both human and veterinary health. Methods We performed a comparative genomic characterisation of 49 methicillin‐resistant Staphylococcus isolates collected from humans, dogs, and cats in a veterinary hospital from Central Chile.
Daniel Garrido   +7 more
wiley   +1 more source

[Evaluating the Effectiveness of Smoking Cessation Treatment Funding in Public Health Systems]. [PDF]

open access: yesAten Primaria
Camarelles Guillem F   +2 more
europepmc   +1 more source

Artificial Irrigation Impacts the Seasonal Occurrence of Pathogenic Leptospira in Its Wild Reservoirs in a Mediterranean Environment

open access: yesZoonoses and Public Health, EarlyView.
ABSTRACT Background Human activities play a significant role in the emergence of infectious diseases. We aimed to test whether artificial irrigation affects the occurrence of a zoonotic bacteria sensitive to desiccation, pathogenic Leptospira species (pathoLep), in micromammals inhabiting Mediterranean ecosystems.
Cristina Ruiz   +4 more
wiley   +1 more source

Immediate cortical glial alterations following spinal cord injury: Evidence from a novel in vitro model

open access: yesExperimental Physiology, EarlyView.
Abstract Spinal cord injury (SCI) triggers immediate and widespread pathophysiological changes not only at the site of impact but also beyond it, including alterations in remote cortical regions. Here, we report early astrocytic changes in the cerebral cortex following SCI at birth, identified using two specific glial markers in an innovative in vitro ...
Luca Mio   +4 more
wiley   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim   +9 more
wiley   +1 more source

A Retrospective Chart Review Study on the Burden of Illness of Acid Sphingomyelinase Deficiency in Brazil. [PDF]

open access: yesJ Clin Med
Giugliani R   +13 more
europepmc   +1 more source

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