نتایج جستجو برای: cystic lung disease

تعداد نتایج: 1751468  

Journal: :iranian journal of radiology 0
umit aksoy ozcan department of radiology, school of medicine, acibadem university, acibadem kozyatagi, hastanesi inonu ave., okur st., turkey +90-2165714426, [email protected];[email protected]; department of radiology, school of medicine, acibadem university, acibadem kozyatagi, hastanesi inonu ave., okur st., turkey +90-2165714426, [email protected];[email protected] ersan altun department of radiology, school of medicine, acibadem university, acibadem kozyatagi, hastanesi inonu ave., okur st., turkey +90-2165714426, [email protected];[email protected] latif abbasoglu department of pediatric surgery, acibadem, turkey

background the most common space occupying lesions of the fetal thorax are congenital diaphragmatic hernia (cdh), congenital cystic adenomatoid malformation (ccam), and bronchopulmonary sequestration (bps). although applications of prenatal mri have been vastly improved in the recent years, its use in the assessment of space occupying lesions of the fetal chest differs among centers. objectives...

Journal: :iranian journal of veterinary medicine 2015
reza youssefi parviz tajik vrya tohidi vahid akbarinejad

in the present report, diagnosis and treatment of a case with follicular ovarian cysts in a 5-year-old persian queen cat is described. in response to palpation of spines, the queen cat presented herself in lordosis and danced up and down with her rear legs. trans-abdominal ultrasonography examination showed 2 cysts  in the left ovary of the queen. serum estrogen assay indicated elevated level o...

2013
Hendrik Suhling Jessica Rademacher Mark Greer Axel Haverich Gregor Warnecke Jens Gottlieb Tobias Welte

References 1 Speich R, van der Bij W. Epidemiology and management of infections after lung transplantation. Clin Infect Dis 2001; 33: Suppl. 1, S58–S65. 2 Gottlieb J, Mattner F, Weissbrodt H, et al. Impact of graft colonization with gram-negative bacteria after lung transplantation on the development of bronchiolitis obliterans syndrome in recipients with cystic fibrosis. Respir Med 2009; 103: ...

2010
Hartmut Grasemann

Cystic fibrosis affects multiple organs but lung disease remains the major determinant of patient morbidity and mortality. Cystic fibrosis lung disease is characterized by chronic infection and inflammation. The amino acid L-arginine is substrate for both nitric oxide synthases and arginases. The activity of arginase in sputum is increased while the production of nitric oxide is reduced in the ...

Journal: :BMJ case reports 2012
Lokesh Shahani

1 of 1 DESCRIPTION Lymphangioleiomyomatosis (LAM) is a rare disease which predominantly affects young females and is commonly found in association with tuberous sclerosis. 1 The clinical features result from progressive cystic destruction of the lungs and the accumulation of LAM cells within the lungs and axial lymphatics. 2 The gold standard for the diagnosis of LAM is a tissue biopsy which sh...

Farzaneh Mohammadi Zia Seyed Jaber Mousavi,

  Human hydatid cyst is a wide spread disease. It is an endemic disease in Iran. Hydatid cyst is extremely rare in the female reproductive organs. This is a case report of ovarian hydatid cyst in a 42-year-old woman. She presented with feeling of enlargement of abdomen and abdominal pain. On physical examination, a large mass in lower abdomen palpated. Ultrasonography reported a heterogeneous ...

2015
Paul J. McKiernan Catherine M. Greene

The cystic fibrosis lung is a complex milieu comprising multiple factors that coordinate its physiology. MicroRNAs are regulatory factors involved in most biological processes and it is becoming increasingly clear that they play a key role in the development and manifestations of CF lung disease. These small noncoding RNAs act posttranscriptionally to inhibit protein production. Their involveme...

2017
Magdalena Kołodziej Michael J. de Veer Marian Cholewa Gary F. Egan Bruce R. Thompson

Monitoring of pulmonary physiology is fundamental to the clinical management of patients with Cystic Fibrosis. The current standard clinical practise uses spirometry to assess lung function which delivers a clinically relevant functional readout of total lung function, however does not supply any visible or localised information. High Resolution Computed Tomography (HRCT) is a well-established ...

Journal: :JOP : Journal of the pancreas 2001
R D Coakley R C Boucher

In gastrointestinal tissues, cumulative evidence from both in vivo and in vitro studies suggests a role for the cystic fibrosis transmembrane conductance regulator (CFTR) in apical epithelial bicarbonate conductance. Abnormal lumenal acidification is thus hypothesized to play a role in the genesis of cystic fibrosis (CF) pancreatic disease. However, consensus regarding CFTR's participation in p...

Journal: :Seminars in respiratory and critical care medicine 2009
Brian P O'Sullivan Patrick Flume

There is strong evidence that early, aggressive therapy of lung disease leads to improved quality and quantity of life for patients with cystic fibrosis (CF). The treatment of pulmonary disease associated with CF is multifactorial, encompassing prophylaxis, aggressive treatment of infection, use of antiinflammatory agents, and treatment of severe complications. Chest physiotherapy on a regular ...

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