نتایج جستجو برای: cdh

تعداد نتایج: 919  

Journal: :Journal of applied physiology 1997
D W Allan J J Greer

Congenital diaphragmatic hernia (CDH) is a developmental anomaly characterized by the malformation of the diaphragm and impaired lung development. In the present study, we tested several hypotheses regarding the pathogenesis of CDH, including those suggesting that the primary defect is due to abnormal 1) lung development, 2) phrenic nerve formation, 3) developmental processes underlying diaphra...

Journal: :Journal of pediatric surgery 2009
Benjamin S Bryner Brady T West Ronald B Hirschl Robert A Drongowski Kevin P Lally Pamela Lally George B Mychaliska

PURPOSE Severe congenital diaphragmatic hernia (CDH) requiring extracorporeal membrane oxygenation (ECMO) is associated with high mortality. Timing of CDH repair relative to ECMO therapy remains controversial. Our hypothesis was that survival would significantly differ between those who underwent repair during ECMO and those who underwent repair after ECMO therapy. METHODS We examined deident...

Journal: :Mycologia 2013
Chiaki Hori Jill Gaskell Kiyohiko Igarashi Masahiro Samejima David Hibbett Bernard Henrissat Dan Cullen

To degrade the polysaccharides, wood-decay fungi secrete a variety of glycoside hydrolases (GHs) and carbohydrate esterases (CEs) classified into various sequence-based families of carbohydrate-active enzymes (CAZys) and their appended carbohydrate-binding modules (CBM). Oxidative enzymes, such as cellobiose dehydrogenase (CDH) and lytic polysaccharide monooxygenase (LPMO, formerly GH61), also ...

Journal: :American journal of physiology. Lung cellular and molecular physiology 2002
Randal P Babiuk John J Greer

Congenital diaphragmatic hernia (CDH) is a significant clinical problem in which a portion of the diaphragmatic musculature fails to form, resulting in a hole in the diaphragm. Here we use animal models of CDH to test two hypotheses regarding the pathogenesis. First, the origin of the defect results from the malformation of the amuscular mesenchymal component of the primordial diaphragm rather ...

Journal: :American journal of perinatology 2015
Theresa R Grover Karna Murthy Beverly Brozanski Jason Gien Natalie Rintoul Sarah Keene Tasnim Najaf Louis Chicoine Nicolas Porta Isabella Zaniletti Eugenia K Pallotto

OBJECTIVE The aim of this study is to characterize medical and surgical therapies and short-term outcomes in infants with congenital diaphragmatic hernia (CDH). STUDY DESIGN Retrospective analysis of CDH infants admitted to 27 children's hospitals submitting data to Children's Hospital Neonatal Database (CHND) from 2010 to 2013, stratified by gestational age, birth weight, and survival. RES...

2013
AYSE SOZEN MUSTAFA YILMAZ H. RIFAT KOYUNCUOGLU VEDAT ALI YUREKLI ERTUGRUL UZAR SULEYMAN KUTLUHAN

Objectives: Acupuncture is a traditional method for the treatment of many pain conditions, but the effectiveness of acupuncture remains controversial on chronic daily headache (CDH). We evaluated the efficacy of real acupuncture (RA) at CDH compared with sham acupuncture (SA). Method: The patients with CDH were selected from a Neurology Department of University Hospital. A total of 56 patients ...

Journal: :Genetics and molecular research : GMR 2011
I N Machado J K Heinrich R Barini C F A Peralta

Congenital diaphragmatic hernia (CDH) is a phenotypically and genetically heterogeneous disorder, with a complex inheritance pattern. Structural abnormalities of almost all chromosomes have been described in association with CDH. We made a molecular analysis through array comparative genomic hybridization (array CGH) of a group of fetuses with prenatal ultrasound diagnosis of CDH and normal G-b...

2017
Pei Li Ruijie Zhang Liyuan Wang Yibo Gan Yuan Xu Lei Song Lei Luo Chen Zhao Chengmin Zhang Bin Ouyang Bing Tu Qiang Zhou

Long-term exposure to a mechanical load causes degenerative changes in the disc nucleus pulposus (NP) tissue. A previous study demonstrated that N-cadherin (N-CDH)-mediated signalling can preserve the NP cell phenotype. However, N-CDH expression and the resulting phenotype alteration in NP cells under mechanical compression remain unclear. The present study investigated the effects of the compr...

Journal: :Journal of applied physiology 2000
J J Greer D Cote D W Allan W Zhang R P Babiuk L Ly R P Lemke K Bagnall

The goals of this study were to further our understanding of diaphragm embryogenesis and the pathogenesis of congenital diaphragmatic hernia (CDH). Past work suggests that the pleuroperitoneal fold (PPF) is the primary source of diaphragmatic musculature. Furthermore, defects associated with an animal model of CDH can be traced back to the formation of the PPF. This study was designed to elucid...

2016
Ba-Da Jeong Seo Hee Ahn Ji-Won Song Jae-Yoon Shim Mi-Young Lee Hye-Sung Won Pil-Ryang Lee Ahm Kim

We describe a case of an intrathoracic kidney combined with right congenital diaphragmatic hernia (CDH) that was diagnosed at 32 weeks of gestation. Although it has been well established that a right CDH shows a poorer outcome than a left CDH, our present case showed a good outcome because there was no herniation of other abdominal viscera, except for the right kidney. Our findings in this case...

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