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15.501  Articles
1 of 1.551 pages  |  10  records  |  more records»
Objectives: The Pierre Robin sequence (PRS) is defined by retromicrognathia, glossoptosis, and sleep apnea and can also be associated with cleft palate. Diagnosis, management and mandibular catch-up growth are still controversial issues in PRS patients. T... see more

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

The first symptom of esophageal atresia and tracheoesophageal fistula is the inability to eat and respiratory distress after feeding. The coexistence of Pierre Robin Sequence (PRS) with esophageal atresia and tracheoesophageal fistula is a rare clinical c... see more

BACKGROUND: Robinow Syndrome is an extremely rare genetic disorder characterised by abnormalities in head, face and external genitalia. This disorder exists in dominant pattern with moderate symptoms and recessive pattern with more physical and skeletal a... see more

OBJECTIVES To assess the impact of promoting self-care in nursing workload and associate it to the variables: age, gender, socioeconomic status, education, marital status and number of children of caregivers. METHODS Prospective study with 31 children ... see more

ORGANIZING INSTITUTIONSEuropean Society for Neonatology (ESN), European Society for Paediatric Research (ESPR), Union of European Neonatal & Perinatal Societies (UENPS), European Foundation for the Care of Newborn Infants (EFCNI), with the local host o... see more

RésuméObjectif : Revoir le traitement du syndrome de sécrétion inappropriée de l’hormone antidiurétique. Discuter les données probantes disponibles concernant les modalités thérapeutiques de cette pathologie.Source des données et sélection des études : Un... see more

RésuméObjectif : Revoir le traitement du syndrome de sécrétion inappropriée de l’hormone antidiurétique. Discuter les données probantes disponibles concernant les modalités thérapeutiques de cette pathologie.Source des données et sélection des études : Un... see more

RÉSUMÉLe syndrome de Fraser est un syndrome génétique malformatif rare dont les principales manifestations sont : une cryptophtalmie, des syndactylies, des anomalies laryngées, trachéales et des malformations urogénitales. Pour poser le diagnostic, il fau... see more

1 of 1.551 pages  |  10  records  |  more records»