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4.814  Articles
1 of 482 pages  |  10  records  |  more records»
Pierre Robin sequence is described as a triad of micro- and/or retrognathia, glossoptosis, and upper airway obstruction, in 90% the triad is associated with cleft palate. In children with the Pierre Robin sequence, the main functional problems are upper r... see more

Neonatal alloimmune thrombocytopenia (FNAIT) results from transplacental transmission and binding of alloimmune antibodies on child's platelets antigens which were inherited from the father. Alloimmunization of the mother against platelet antigen can occu... see more

Background: Streptococcus agalactiae (group B streptococcus, GBS) is the leading cause of invasive neonatal infections in the developed world. We present epidemiological and clinical characteristics of invasive GBS disease among Slovenian neonates between... see more

Haemolytic disease of the foetus and newborn (HDFN) occurs when maternal alloimmune antibodies cross the placenta to the foetal circulation and cause destruction of erythrocytes, resulting in anaemia and hyperbilirubinemia. It can result from naturally pr... see more

Myocardial deformation derived by speckle tracking imaging (STI) is a novel method in echocardiography, that provides an insight into cardiac mechanics and is becoming more widely used in daily clinical practice. With this method a new global parameter of... see more

AbstractBackground: Streptococcus agalactiae is the leading cause of preventable invasive neonatal infections. Detection of maternal colonisation and use of antimicrobial prophylaxis during labour is a standard preventative approach. Very few data about t... see more

Mucopolysaccharidoses are a group of lysosomal storage diseases. Their common feature is the lack of enzymes that break down glycosaminoglycans, polysaccharides that bind to proteoglycans and form the extracellular matrix. Because there are no enzymes tha... see more


Duchenne muscular dystrophy (DMD) is the most common and one of the most serious childhood diseases. It is an X – linked recessive neuromuscular disease, caused by mutations in the dystrophin gene, primarily resulting in skeletal and heart muscle abnormal... see more

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