نتایج جستجو برای: alpha interleukins child heart defects

تعداد نتایج: 861547  

Journal: :American journal of medical genetics 2001
Shi-Min Yuan

BACKGROUND Kabuki syndrome (KS) is an entity of multiple congenital malformations with mental retardation with undetermined etiology. Congenital heart defects are one of the clinical manifestations of KS with insufficient elucidations. METHODS Literature of congenital heart defects associated with KS was comprehensively retrieved, collected and reviewed. The clinical features of the congenita...

Journal: :Journal of medical genetics 1978
N C Nevin A Ritchie F McKeown G Roberts

Raised alpha-fetoprotein concentrations were found at 29 and 30 weeks' gestation in the amniotic fluid and maternal serum of a woman who presented in her seventh pregnancy with apparent polyhydramnios. The fetus had multiple abnormalities including gross distension of the bladder resulting from absence of the urethra, intestinal artresia, and a congenital heart defect.

Journal: :Circulation 1985
P C Ursell J M Byrne B A Strobino

We investigated the impact of heart defects on the developing human fetus by examining 412 hearts from consecutive spontaneous abortuses. In each case, the cardiac morphology was correlated with the autopsy findings and the karyotype (unavailable in 115 hearts not successfully cultured). Of the 412 hearts, 10 (2.4%) contained structural defects (six ventricular septal defects, one atrial septal...

Journal: :Indian pediatrics 2014
Sunil Karande Varsha Patil Archana Kher Mamta Muranjan

OBJECTIVES To assess the proportion and pattern of extracardiac birth defects in children with congenital heart defects referred to a tertiary care institute. METHODS Cross-sectional observational study from January 2010 to June 2011. RESULTS Out of 560 children with congenital heart defects, 98 (17.5%) had extracardiac birth defects. Fifty-six had multiple congenital defects; 36 were syndr...

Journal: :Circulation 1987
M Rabinovitch M Andrew H Thom G A Trusler W G Williams R D Rowe P M Olley

In patients with pulmonary hypertension associated with congenital heart defects, ultrastructural abnormalities are observed in endothelial cells, which suggest heightened metabolic function. If endothelial production of the von Willebrand factor (vWF) is increased, this may be associated with abnormal interactions with platelets leading to worsening of the pulmonary hypertension. We therefore ...

2015
Nathan J. Palpant Peter Hofsteen Lil Pabon Hans Reinecke Charles E. Murry

BACKGROUND Maternal smoking is a risk factor for low birth weight and other adverse developmental outcomes. OBJECTIVE We sought to determine the impact of standard tobacco cigarettes and e-cigarettes on heart development in vitro and in vivo. METHODS Zebrafish (Danio rerio) were used to assess developmental effects in vivo and cardiac differentiation of human embryonic stem cells (hESCs) wa...

Journal: :Circulation 2006
René R Marty Stephan Dirnhofer Nora Mauermann Sacha Schweikert Shizuo Akira Lukas Hunziker Josef M Penninger Urs Eriksson

BACKGROUND Experimental autoimmune myocarditis (EAM) is a CD4+ T-cell-mediated mouse model of postviral cardiomyopathy. Activation of interleukin-1 type 1 and Toll-like receptors that share the common downstream adaptor molecule MyD88 is required for disease induction. The specific role of MyD88 in myocarditis, however, is not known. METHODS AND RESULTS In contrast to control littermates, MyD...

Journal: :Diabetes 2005
So-Young Park You-Ree Cho Brian N Finck Hyo-Jeong Kim Takamasa Higashimori Eun-Gyoung Hong Mi-Kyung Lee Cheryl Danton Swati Deshmukh Gary W Cline Julie J Wu Anton M Bennett Beverly Rothermel April Kalinowski Kerry S Russell Young-Bum Kim Daniel P Kelly Jason K Kim

Diabetic heart failure may be causally associated with alterations in cardiac energy metabolism and insulin resistance. Mice with heart-specific overexpression of peroxisome proliferator-activated receptor (PPAR)alpha showed a metabolic and cardiomyopathic phenotype similar to the diabetic heart, and we determined tissue-specific glucose metabolism and insulin action in vivo during hyperinsulin...

Journal: :Revista Española de Enfermedades Digestivas 2005

2017

Tetralogy of Fallot is the most common cyanotic congenital heart disease worldwide [1]. Among other conotruncal abnormalities, 13-16% of Tetralogy of Fallot individuals are reported to have 22q11.2 deletion syndrome which is characterized by thymic hypoplasia, endocrine abnormalities and hypocalcaemia [2]. Individuals with micro deletion 22q11.2 deletion syndrome are prone to auto immune disord...

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