Zobrazeno 1 - 10
of 20
pro vyhledávání: '"D E, deMello"'
Publikováno v:
Journal of Perinatology. 27:190-192
Thoracostomy tubes are commonly required to treat pnuemothoraces in premature infants. Evidence of impalement of the lungs by tube thoracostomy has been seen in autopsy studies. In neonates, there has been described a surprisingly high incidence of l
Publikováno v:
Clinical transplantation. 16(3)
We report a previously unrecognized late complication of allograft lung transplantation - persistent recurrent atelectasis of the transplanted lung. The patient developed sudden, severe respiratory distress about 2 yr after a right lung transplant, b
Autor:
D E, deMello, Z, Lin
Publikováno v:
Pediatric pathologymolecular medicine. 20(5)
Pulmonary alveolar proteinosis (PAP) is a disorder that rapidly leads to respiratory failure, because the alveolar spaces fill with a lipid-rich, proteinaceous material that impedes gas exchange. The pathogenesis of this life-threatening process rema
Publikováno v:
Histochemistry and cell biology. 115(4)
Two antisera, denoted R41 and R42, were raised against a synthetic peptide from the murine Clara cell-specific protein CC10, and one antiserum, denoted R40, was raised against human recombinant uteroglobin, the human homolog of murine CC10. Purified
Publikováno v:
Developmental dynamics : an official publication of the American Association of Anatomists. 220(2)
Vascular endothelial growth factor (VEGF), a factor that is critical for development of the vascular system in mouse embryos, exists as at least three isoforms, VEGF120, VEGF164, and VEGF188. The isoforms have different affinities for heparan sulfate
Publikováno v:
Clinical genetics. 57(5)
Mutations in the surfactant protein (SP)-B gene are responsible for SP-B deficiency in congenital alveolar proteinosis (CAP) (Nogee et al. J Clin Invest 1994: 93: 1860-1883; Lin et al. Mol Genet Metab 1998: 64: 25-35; Klein et al. Pediatrics 1998: 13
Publikováno v:
The Anatomical record. 252(1)
Recent availability of computerized image analysis has fostered hope that barium injection and landmarking of pulmonary arteries would be unnecessary for morphometric assessment when using this technique. We reasoned that if barium injection altered
Publikováno v:
Pediatric pulmonology. 24(6)
Publikováno v:
Pediatric pathologylaboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association. 17(2)
Congenital alveolar proteinosis is a recently described cause of lung dysfunction and respiratory distress in term neonates. In several cases a deficiency or insufficiency of surfactant apoprotein B (SP-B) has been caused by a frameshift mutation in
Autor:
R, Deidiker, D E, deMello
Publikováno v:
Pediatric pathologylaboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association. 16(5)
Propylthiouracil (PTU), a thyroid hormone inhibitor, is widely used for the treatment of hyperthyroidism. Rarely, the drug has been associated with severe hepatotoxicity. We present the case of a 13-year-old girl who developed jaundice and profound l