cystic fibrosis/albumin

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BODY MASS INDEX AND ALBUMIN LEVELS ARE ASSOCIATED WITH PULMONARY FUNCTION PARAMETERS IN PEDIATRIC SUBJECTS WITH CYSTIC FIBROSIS.

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To evaluate the association of body mass index (BMI) and albumin with pulmonary function in cystic fibrosis (CF) pediatric subjects.This is a cross-sectional study with clinically stable CF's subjects. Clinical (pulmonary function) and nutritional

[Coprologic anomaly in mucoviscidosis. Presence of albumin in low concentration in the feces].

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With an immunological technique, presence of albumin was searched in the stools of 47 patients with cystic fibrosis and 54 controls. Albumin was found in 93% of cystic fibrosis, at a mean level of 90 mg/100 g of fresh stools. The test was negative in the 54 healthy controls. It was positive in one

C-reactive protein/albumin ratio is associated with lung function among children/adolescents with cystic fibrosis: a three-year longitudinal study.

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Chronic lung infections, inflammation and depletion of nutritional status are considered to be prognostic indicators of morbidity in patients with cystic fibrosis. The aim of this study was to investigate the association between inflammatory markers and lung function, nutritional status and

A serine protease activity of human serum albumin towards 4-methylumbelliferyl-guanidinobenzoate (MUGB) and diisopropyl fluorophosphate (DEP): implications for the use of MUGB reactivity in amniotic fluid in prenatal diagnosis of cystic fibrosis.

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4-methylumbelliferylguanidinobenzoate (MUGB) reactivity in plasma from patients with cystic fibrosis and in amniotic fluid from pregnancies leading to children with cystic fibrosis, has been reported to be significantly decreased. We have so far been unable to confirm these findings and have

Automated immunoprecipitation of meconium albumin for cystic fibrosis screening in the newborn.

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Cystic fibrosis is the most frequent substantially lethal inherited disease in the United States. Newborn screening for cystic fibrosis has been suggested because early diagnosis permits genetic counselling of parents and improved treatment and prognosis for cystic fibrosis patients. The fact that

Screening for cystic fibrosis by analysis of meconium for albumin and protease inhibitors.

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A qualitative method of detecting elevated meconium protein concentration was compared with a method of determining meconium albumin concentration by electroimmunoassay since elevated meconium protein levels can indicate pancreatic insufficiency caused by cystic fibrosis. Between 5 and 10 per 1000

Screening for cystic fibrosis by analysis of albumin in meconium.

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A clinical study of the albumin content in meconium was performed on two categories of newborn infants: a screening series of 8,830 infants and a high-risk group for Cystic Fibrosis (CF) of 70 infants. A single radial immunodiffusion technique and test strips were used. Three CF infants were

Immunoglobulins and albumin in sputum from patients with cystic fibrosis. A study of protein stability and presence of proteases.

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Sputum sol phase from seventeen cystic fibrosis (CF) patients chronically infected in the lungs with mucoid Pseudomonas aeruginosa and presenting multiple precipitins in serum against this bacterium (CF + P) and 11 CF patients without P. aeruginosa infection (CF-P) were examined for proteolytic

Growth Status and Its Relationship with Serum Lipids and Albumin in Children with Cystic Fibrosis.

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Cystic fibrosis (CF) is an autosomal recessive disease, which affects many organs as it impairs chloride channel. This study was performed to evaluate growth status and its relationship with some laboratory indices such as Cholesterol (chol), Triglyceride (TG), albumin and total protein in children

Serum Albumin and Disease Severity of Non-Cystic Fibrosis Bronchiectasis.

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BACKGROUND A clinical classification system has been developed to define the severity and predict the prognosis of subjects with non-cystic fibrosis (CF) bronchiectasis. We aimed to identify laboratory parameters that are correlated with the bronchiectasis severity index (BSI) and FACED

Screening for cystic fibrosis-related diabetes and prediabetes: Evaluating 1,5-anhydroglucitol, fructosamine, glycated albumin, and hemoglobin A1c.

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Dysglycemia is prevalent in cystic fibrosis (CF) but screening with annual oral glucose tolerance tests (OGTT) can be burdensome. We investigated alternate glycemic markers-hemoglobin A1c (HbA1c), 1,5-anhydroglucitol (1,5AG), fructosamine (FA), and glycated albumin (GA)-as screening

β-Lactam antibiotics form distinct haptenic structures on albumin and activate drug-specific T-lymphocyte responses in multiallergic patients with cystic fibrosis.

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β-Lactam antibiotics provide the cornerstone of treatment for respiratory exacerbations in patients with cystic fibrosis. Unfortunately, approximately 20% of patients develop multiple nonimmediate allergic reactions that restrict therapeutic options. The purpose of this study was to explore the

Association of nutritional status, plasma, albumin levels and pulmonary function in cystic fibrosis.

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OBJECTIVE Malnutrition is related with pulmonary disease. The aim was to analyze the association of lung function respectively to nutritional status, identified pulmonary pathogens and socioeconomic condition of patients attending a pediatric CF reference center. METHODS Cross-sectional study

[Comment on the publication: "Qualitative Albumin Determination in meconium using tetrabrome phenol blue. A contribution to improvement of screening for familial cystic fibrosis"].

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[Qualitative albumin determination in meconium using tetrabrome phenol blue. Improvement of screening for familial cystic fibrosis].

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