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[PDF] Top 20 Imaging in idiopathic pulmonary fibrosis: diagnosis and mimics

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Imaging in idiopathic pulmonary fibrosis: diagnosis and mimics

Imaging in idiopathic pulmonary fibrosis: diagnosis and mimics

... Idiopathic pulmonary fibrosis is a chronic disease of unknown etiology that usually has a progressive course and is commonly associated with a poor ...of idiopathic pulmonary ... See full document

7

Epidemiology of Idiopathic Pulmonary Fibrosis in Northern Italy.

Epidemiology of Idiopathic Pulmonary Fibrosis in Northern Italy.

... (GCD) and that identified as IPF cases all individuals with at least one hospitalization with diag- nosis of IPF or at least one outpatient visit with diagnosis of IPF (ICD-9-CM code ...onset. In ... See full document

15

Accelerated variant of idiopathic pulmonary fibrosis: clinical behavior and gene expression pattern.

Accelerated variant of idiopathic pulmonary fibrosis: clinical behavior and gene expression pattern.

... differs in clinical course and transcriptional profile, despite having similar lung function, chest imaging, and histology ...role in determining the eventual clinical phenotype, ... See full document

11

Comparison of two questionnaires which measure the health-related quality of life of idiopathic pulmonary fibrosis patients

Comparison of two questionnaires which measure the health-related quality of life of idiopathic pulmonary fibrosis patients

... Idiopathic pulmonary fibrosis (IPF) is a distinctive type of chronic fibrosing intersti- tial pneumonia of unknown cause associ- ated with a surgical lung biopsy showing a histological pattern of ... See full document

9

Análise semiquantitativa de biópsias cirúrgicas de diferentes lobos pulmonares de pacientes com pneumonia intersticial usual/fibrose pulmonar idiopática

Análise semiquantitativa de biópsias cirúrgicas de diferentes lobos pulmonares de pacientes com pneumonia intersticial usual/fibrose pulmonar idiopática

... lobes in terms of the histopathological features of usual interstitial pneumonia, using a semiquantitative ...with idiopathic pulmonary fibrosis and submitted to surgical biopsy ... See full document

7

PDF EN Jornal Brasileiro de Pneumologia 7 9 english

PDF EN Jornal Brasileiro de Pneumologia 7 9 english

... lobes in terms of the histopathological features of usual interstitial pneumonia, using a semiquantitative ...with idiopathic pulmonary fibrosis and submitted to surgical biopsy ... See full document

7

Survival in idiopathic pulmonary fibrosis - cytotoxic agents compared to corticosteroids

Survival in idiopathic pulmonary fibrosis - cytotoxic agents compared to corticosteroids

... possibility in patients studied in tertiary ...seen in our centers during the period of study, but were not included due to stringent inclusion ...biopsy in the study group was greater than ... See full document

8

Rev. Assoc. Med. Bras.  vol.62 número4

Rev. Assoc. Med. Bras. vol.62 número4

... mostly in young women and often after the lactation ...thickening and possible ulceration that mimics ...present and bilateral involvement may occur in up to 25% of cases. ... See full document

4

Six-minute walk test and idiopathic pulmonary fibrosis

Six-minute walk test and idiopathic pulmonary fibrosis

... a diagnosis of portopulmonary hypertension (POPH) secondary to alcoholic liver cirrhosis (Child-Pugh class C and Model for End-Stage Liver Disease = ...the Pulmonary Circulation of the Federal ... See full document

98

J. bras. pneumol.  vol.32 número6 en a06v32n6

J. bras. pneumol. vol.32 número6 en a06v32n6

... chronic idiopathic interstitial pneumonia, as defined in the American Thoracic Society/European Respiratory Society classification system made public in ...1977 and 1999, were reviewed, ... See full document

5

J. bras. pneumol.  vol.39 número1 en v39n1a17

J. bras. pneumol. vol.39 número1 en v39n1a17

... published. In conformity with the official 2011 American Thoracic Society Statement, idiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic, progressive fibrosing ... See full document

2

Editor’s Pick: PSMA-Specific Ligands in Prostate Cancer Diagnosis and Therapy

Editor’s Pick: PSMA-Specific Ligands in Prostate Cancer Diagnosis and Therapy

... biomarker and antigen of prostate cancer. It is overexpressed in almost all prostate cancers, and the expression level increases with prostate cancer ...expressed in the neovasculature of ... See full document

8

Protective roles of pulmonary rehabilitation mixture in experimental pulmonary fibrosis in vitro and in vivo

Protective roles of pulmonary rehabilitation mixture in experimental pulmonary fibrosis in vitro and in vivo

... FGF2 and PDGF expression were decreased significantly and HLF-1 proliferation was attenuated, as shown in Figure ...of pulmonary rehabilitation mixture (PRM) on epithelial-mesenchymal ... See full document

8

Coincidence of Cystic Fibrosis in Mother and her Child Related to Infertility

Coincidence of Cystic Fibrosis in Mother and her Child Related to Infertility

... known diagnosis of CF and radiographic findings, a sweat test was ...fat and contained undigested ...is in favor of a slight decrease in trypsin ... See full document

3

Rev. Hosp. Clin.  vol.55 número2

Rev. Hosp. Clin. vol.55 número2

... born in Guararapes (SP), presented a sudden increase in the anterior cervi- cal region, with fever and sweating, in October, ...antiinflammatories and antibiotics, she underwent ... See full document

8

Análise dos falsos AVCs admitidos na Unidade de AVC do Hospital de Santa Maria entre 2007 e 2013

Análise dos falsos AVCs admitidos na Unidade de AVC do Hospital de Santa Maria entre 2007 e 2013

... Posterior circulation stroke was found to be the most common provisional diagnosis in the emergency department. This is not surprising as location of stroke influences diagnostic accuracy. Anterior ... See full document

44

Evaluation of circulating proteins and hemodynamics towards predicting mortality in children with pulmonary arterial hypertension.

Evaluation of circulating proteins and hemodynamics towards predicting mortality in children with pulmonary arterial hypertension.

... investigation in a relatively large pediatric pulmonary hypertension population investigating the role of almost 30 proteins combined with clinical and demographic variables towards predicting ... See full document

7

Surfactant protein a in cystic fibrosis: supratrimeric structure and pulmonary outcome.

Surfactant protein a in cystic fibrosis: supratrimeric structure and pulmonary outcome.

... subjects in some of the groups were lower than ...octadecamers in BAL from healthy persons compared to BAL from birch pollen from 11 allergic persons [7] may play an as yet undetermined role in ... See full document

7

The in vivo fibrotic role of FIZZ1 in pulmonary fibrosis.

The in vivo fibrotic role of FIZZ1 in pulmonary fibrosis.

... the in vivo relevance of these findings, the effect of FIZZ1 deficiency on BM recruitment to the lung was assessed in the BLM model using GFP BM chimera mice to allow tracking of BM cell movement using ... See full document

11

Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations.

Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations.

... function and increased ...Pseudomonas in samples with low diversity, similar to previous CF studies ...progresses and chronic infection develops, normal microbiota are disrupted and diversity ... See full document

13

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