Results 11 to 20 of about 44,691 (285)

Bronchopulmonary dysplasia in neonates born to mothers with preeclampsia: Impact of small for gestational age. [PDF]

open access: yesPLoS ONE, 2018
BACKGROUND AND OBJECTIVES:Small for gestational age and preeclampsia have both been described as risk factors for bronchopulmonary dysplasia in preterm neonates, but their respective role in the occurrence of bronchopulmonary dysplasia is debated.
Pauline Dravet-Gounot   +7 more
doaj   +1 more source

Treatment and prophylaxis of moderate and severe bronchopulmonary dysplasia in premature neonates

open access: yesMedičnì Perspektivi, 2021
Bronchopulmonary dysplasia in premature neonates leads to physical and mental developmental disorders and behavioral problems and associated with frequent rehospitalizations and long hospital stay.
A.V. Bolonska , O.Yu. Sorokina
doaj   +1 more source

Enteral lactoferrin supplementation for very preterm infants: a randomised placebo-controlled trial [PDF]

open access: yes, 2019
Background Infections acquired in hospital are an important cause of morbidity and mortality in very preterm infants. Several small trials have suggested that supplementing the enteral diet of very preterm infants with lactoferrin, an antimicrobial ...
Ainsworth, S   +59 more
core   +2 more sources

Bronchopulmonary Dysplasia: Executive Summary of a Workshop [PDF]

open access: yes, 2018
Comment in Bronchopulmonary Dysplasia: The Ongoing Search for One Definition to Rule Them All. [J Pediatr. 2018] Midlife crisis? In its 50th year, BPD redefines itself.
Bancalari, Eduardo   +17 more
core   +1 more source

Neuroendocrine cell hyperplasia of infancy (review of modern literature — 2018)

open access: yesZdorovʹe Rebenka, 2018
The review deals with the systematization of mo­dern world ideas about pulmonary neuroendocrine cells and a disease associated with their hyperplasia — neuroendocrine hyperplasia in infants. The pathogenesis, clinical and instrumental diagnostic criteria
O.L. Logvinova
doaj   +1 more source

Genetic variation in CRHR1 is associated with short-term respiratory response to corticosteroids in preterm infants at risk for bronchopulmonary dysplasia. [PDF]

open access: yes, 2019
BackgroundBronchopulmonary dysplasia (BPD) is an orphan disease and advances in prevention and treatment are lacking. The clinical efficacy of systemic corticosteroid therapy to reduce the severity of lung disease and BPD is highly variable.
Ballard, Philip L   +5 more
core   +1 more source

Role of serine proteases in the regulation of interleukin-877 during the development of bronchopulmonary dysplasia in preterm ventilated infants. [PDF]

open access: yesPLoS ONE, 2014
The chemokine interleukin-8 is implicated in the development of bronchopulmonary dysplasia in preterm infants. The 77-amino acid isoform of interleukin-8 (interleukin-877) is a less potent chemoattractant than other shorter isoforms. Although interleukin-
Mallinath Chakraborty   +11 more
doaj   +1 more source

Interstitial lungs diseases in infants: acinar, alveolar and alveolar capillary dysplasia (2018 review of modern literature)

open access: yesZdorovʹe Rebenka, 2018
The article presents a clinical сase of alveolar capillary dysplasia in a child aged 3 months. The discussion included terminological aspects, pathomorphological, diagnostic criteria of diffuse lung developmental disorders. Modern principles of treatment
O.L. Logvinova
doaj   +1 more source

Excessive gas exchange impairment during exercise in a subject with a history of bronchopulmonary dysplasia and high altitude pulmonary edema [PDF]

open access: yes, 2007
A 27-year-old male subject (V(O2 max)), 92% predicted) with a history of bronchopulmonary dysplasia (BPD) and a clinically documented case of high altitude pulmonary edema (HAPE) was examined at rest and during exercise.
Andrew T. Lovering   +6 more
core   +1 more source

Modern concept of the brain-lung-thyroid syndrome and its pulmonary manifestations

open access: yesZdorovʹe Rebenka, 2018
This article is a review of the modern world literature on the brain-lung-thyroid syndrome in children. The authors focused on the etiology and features of ontogenesis of the involved organs in the presence of NKX2-1 gene mutation.
O.L. Logvinova, M.A. Gonchar
doaj   +1 more source

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