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neonatal congenital pulmonaiy fibrosis相关文献:
NKX2-1-Related Disorders.
Patel NJ, Jankovic J.
2014 Feb 20 [updated 2023 Jun 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:24555207
Congenital Deletion of Nedd4-2 in Lung Epithelial Cells Causes Progressive Alveolitis and Pulmonary Fibrosis in Neonatal Mice.
Leitz DHW, Duerr J, Mulugeta S, Seyhan Agircan A, Zimmermann S, Kawabe H, Dalpke AH, Beers MF, Mall MA.
Int J Mol Sci. 2021 Jun 7;22(11):6146. doi: 10.3390/ijms22116146.
PMID:34200296
A neonatal rat model of pulmonary vein stenosis.
Li D, Qiu L, Hong H, Chen H, Zhao P, Xiao Y, Zhang H, Sun Q, Ye L.
Cell Biosci. 2023 Jun 19;13(1):112. doi: 10.1186/s13578-023-01058-8.
PMID:37337290
Congenital rubella.
Dudgeon JA.
J Pediatr. 1975 Dec;87(6 Pt 2):1078-86. doi: 10.1016/s0022-3476(75)80119-3.
PMID:1102644
Multifactorial origin of pulmonary hypertension in a child with congenital heart disease, Down syndrome, and BMPR-2 mutation.
Bajolle F, Malekzadeh-Milani S, Lévy M, Bonnet D.
Pulm Circ. 2021 Jul 5;11(3):20458940211027433. doi: 10.1177/20458940211027433. eCollection 2021 Jul-Sep.
PMID:34285797
Pathological Roles for Endothelial Colony-Forming Cells in Neonatal and Adult Lung Disease.
Robertson JO, Erzurum SC, Asosingh K.
Am J Respir Cell Mol Biol. 2023 Jan;68(1):13-22. doi: 10.1165/rcmb.2022-0318PS.
PMID:36215049
The Management of Asymptomatic Congenital Pulmonary Airway Malformation: Results of a European Delphi Survey.
Kersten CM, Hermelijn SM, Mullassery D, Muthialu N, Cobanoglu N, Gartner S, Bagolan P, Mesas Burgos C, Sgrò A, Heyman S, Till H, Suominen J, Schurink M, Desender L, Losty P, Steyaert H, Terheggen-Lagro S, Metzelder M, Bonnard A, Sfeir R, Singh M, Yardley I, Rikkers-Mutsaerts NRVM, van der Ent CK, Qvist N, Cox DW, Peters R, Bannier MAGE, Wessel L, Proesmans M, Stanton M, Hannon E, Zampoli M, Morini F, Tiddens HAWM, Wijnen RMH, Schnater JM.
Children (Basel). 2022 Jul 30;9(8):1153. doi: 10.3390/children9081153.
PMID:36010044
Pulmonary Manifestations of Genetic Disorders in Children.
Pletcher BA, Turcios NL.
Pediatr Clin North Am. 2021 Feb;68(1):1-24. doi: 10.1016/j.pcl.2020.09.010.
PMID:33228926
Cerebropulmonary dysgenetic syndrome.
Shanklin DR, Mullins AC, Baldwin HS.
Exp Mol Pathol. 2008 Oct;85(2):112-6. doi: 10.1016/j.yexmp.2008.04.006. Epub 2008 May 28.
PMID:18603241
Cutaneous histiocytosis syndromes.
Roper SS, Spraker MK.
Pediatr Dermatol. 1985 Nov;3(1):19-30. doi: 10.1111/j.1525-1470.1985.tb00480.x.
PMID:2999740
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