نتایج جستجو برای: cdh

تعداد نتایج: 919  

Journal: :The European respiratory journal 2013
Paola E Cogo Manuela Simonato Olivier Danhaive Giovanna Verlato Giovanna Cobellis Francesco Savignoni Donatella Peca Aldo Baritussio Virgilio P Carnielli

Pulmonary hypoplasia and hypertension account for significant morbidity and mortality in neonates with congenital diaphragmatic hernia (CDH). Whether CDH is associated with surfactant dysfunction remains controversial. Therefore, we measured disaturated phosphatidylcholine (DSPC) and surfactant protein (SP)-B concentration in tracheal aspirates and their synthesis rate in infants with CDH compa...

Journal: :The Journal of biological chemistry 1993
C S Redwood S B Marston

We expressed the following fragments of chicken gizzard caldesmon in the pMW 172/BL21 (DE3) system at 0.4-2.2 mg of pure protein/liter of culture: full-length smooth muscle caldesmon (CDh) (amino acids 1-756), nonmuscle caldesmon (CDl), amino acids 1-128 (N128), 1-578 (N578), 230-419, 606-756 (606C), and 658-756 (658C). CDh bound tropomyosin with a Kd of 1.5 microM; N578, 230-419, and 606C boun...

2017
Daphne S. Mous Marjon J. Buscop-van Kempen Rene M. H. Wijnen Dick Tibboel Robbert J. Rottier

BACKGROUND Patients with congenital diaphragmatic hernia (CDH) have structural and functional different pulmonary vessels, leading to pulmonary hypertension. They often fail to respond to standard vasodilator therapy targeting the major vasoactive pathways, causing a high morbidity and mortality. We analyzed whether the expression of crucial members of these vasoactive pathways could explain th...

Journal: :Bioscience, biotechnology, and biochemistry 2009
Yuan Zhang Yue Zhou Jie Zhu Shiwu Dong Changqing Li Qiang Xiang

The limitations of specific adhesion and osteoblastic differentiation are current problems in bone tissue engineering. The aim of this study was to investigate the effect of a novel recombinant protein of fibronectin module III7-10/cadherin 11 EC1-2 (rFN/CDH) on cell adhesion and differentiation. Gene coding rFN/CDH was engineered by a homology modeling strategy, and an expression plasmid was c...

Journal: :Pediatrics 2014
Brendan T Campbell Katherine W Herbst Kelleigh E Briden Stephen Neff Kimberly A Ruscher James I Hagadorn

OBJECTIVE To describe the use of inhaled nitric oxide (INO) in newborns with congenital diaphragmatic hernia (CDH). METHODS Pediatric Health Information System data were queried for newborns with CDH admitted at <8 days of age at tertiary care US pediatric hospitals between 2003 and 2011. INO treatment status and timing in relation to CDH repair were determined for each infant. Hospital-speci...

Journal: :Annals of surgery 2015
Patrícia Pereira-Terra Jan A Deprest Ramin Kholdebarin Naghmeh Khoshgoo Philip DeKoninck Anne A Boerema-De Munck Jinxia Wang Fuqin Zhu Robbert J Rottier Barbara M Iwasiow Jorge Correia-Pinto Dick Tibboel Martin Post Richard Keijzer

OBJECTIVE AND BACKGROUND Our objective was to determine the fetal in vivo microRNA signature in hypoplastic lungs of human fetuses with severe isolated congenital diaphragmatic hernia (CDH) and changes in tracheal and amniotic fluid of fetuses undergoing fetoscopic endoluminal tracheal occlusion (FETO) to reverse severe lung hypoplasia due to CDH. METHODS We profiled microRNA expression in pr...

2017
Satyan Lakshminrusimha Martin Keszler Haresh Kirpalani Krisa Van Meurs Patricia Chess Namasivayam Ambalavanan Bradley Yoder Maria V Fraga Holly Hedrick Kevin P Lally Leif Nelin Michael Cotten Jonathan Klein Stephanie Guilford Ashley Williams Aasma Chaudhary Marie Gantz Jenna Gabrio Dhuly Chowdhury Kristin Zaterka-Baxter Abhik Das Rosemary D Higgins

Background Congenital diaphragmatic hernia (CDH) is commonly associated with pulmonary hypoplasia and pulmonary hypertension (PH). PH associated with CDH (CDH-PH) is frequently resistant to conventional pulmonary vasodilator therapy including inhaled nitric oxide (iNO) possibly due to right and left ventricular dysfunction. Milrinone is an intravenous inotrope and lusitrope with pulmonary vasod...

Journal: :American journal of physiology. Lung cellular and molecular physiology 2015
Karen Coste Leonardus W J E Beurskens Pierre Blanc Denis Gallot Amélie Delabaere Loïc Blanchon Dick Tibboel André Labbé Robbert J Rottier Vincent Sapin

Congenital diaphragmatic hernia (CDH) is a common life-threatening congenital anomaly resulting in high rates of perinatal death and neonatal respiratory distress. Some of the nonisolated forms are related to single-gene mutations or genomic rearrangements, but the genetics of the isolated forms (60% of cases) still remains a challenging issue. Retinoid signaling (RA) is critical for both diaph...

2012
S. Kotecha A. Barbato A. Bush F. Claus M. Davenport C. Delacourt J. Deprest E. Eber B. Frenckner A. Greenough A. G. Nicholson J. L. Antón - Pacheco F. Midulla

Infants with congenital diaphragmatic hernia (CDH) have significant mortality and long-term morbidity. Only 60–70% survive and usually those in high-volume centres. The current Task Force, therefore, has convened experts to evaluate the current literature and make recommendations on both the antenatal and post-natal management of CDH. The incidence of CDH varies from 1.7 to 5.7 per 10,000 live-...

Journal: :Prenatal diagnosis 2011
J Jani C Valencia M Cannie A Vuckovic M Sellars K H Nicolaides

OBJECTIVE To investigate tracheal dimensional differences seen at birth following fetal endoscopic tracheal occlusion (FETO) in cases of severe congenital diaphragmatic hernia (CDH) and to report on their clinical follow-up. PATIENTS AND METHODS In chest X-rays, taken within 48 h after birth, we measured the tracheal diameter at the level of the tracheal entry into the chest, 1 cm above the l...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید