Results 231 to 240 of about 95,782 (283)
Lymphatic Abnormalities in Noonan Syndrome Extend Beyond Clinically Apparent Disease
ABSTRACT Lymphatic disease represents a well‐described manifestation of Noonan syndrome (NS), yet the full phenotypic spectrum remains incompletely characterized, especially in asymptomatic individuals. We conducted a cross‐sectional study including 10 individuals with NS (four with peripheral lymphedema and six without) and 10 age‐ and sex‐matched ...
Inger Norlyk Sheyanth +7 more
wiley +1 more source
[Neutrophil-lymphocyte ratio and retinopathy in patients with type 2 diabetes mellitus]. [PDF]
Cuevas-Acuña MT +2 more
europepmc +1 more source
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli +18 more
wiley +1 more source
HISTÓRIA, CIÊNCIAS, SAÚDE - MANGUINHOS IN 2023: A YEAR OF CHANGE. [PDF]
Cerqueira RC, Cueto M.
europepmc +1 more source
Systematization of peer review in Epidemiologia e Serviços de Saúde. [PDF]
Silva MT, Galvão TF.
europepmc +1 more source
[CSP in 40 years of scientific publications]. [PDF]
Lima LD, Carvalho MS, Alves LC.
europepmc +1 more source

