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A case study of Legionnaire's Disease in 15 year old childA case study of Legionnaire's Disease in 15 year old child
A case study of congenital deficiency of surfactant protein C in 4 months old childA case study of congenital deficiency of surfactant protein C in 4 months old child
Diseases associated with mutations in the filamin A gene (FLNA) [Заболевания, ассоциированные с мутациями в гене филамина А (FLNA)] encoding filamin A, which is a cytoskeleton protein with polymorphic functions. The mutations of this gene
The technique of multi-criterial and multi-level assessment of contract quality under uncertainty of constructing desirability functions of private criteria, a comparison is made with the analytic hierarchy
Outpatient management of children with bronchopulmonary dysplasia: What is important to know for a neonatologist and a pediatrician? is the most common chronic lung disease in infants and a serious complication of prematurity and respiratory
Pharmacotherapy of bronchopulmonary dysplasia: A personalized approachPharmacotherapy of bronchopulmonary dysplasia: A personalized approach
Общественный стереотип тренерской профессииThe article deals with the results of a study on the choice of future employment in the field
Mukolipidosis type II as the cause of pulmonary hypertension in children with hypoxemia on the basis of a long-term clinical observation of the child with type II mucosolipidosis (ML
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